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8,090 results on '"K, Okada"'

1. Bulk evidence of anisotropic s-wave pairing with no sign change in the kagome superconductor CsV3Sb5

Author

M. Roppongi, K. Ishihara, Y. Tanaka, K. Ogawa, K. Okada, S. Liu, K. Mukasa, Y. Mizukami, Y. Uwatoko, R. Grasset, M. Konczykowski, B. R. Ortiz, S. D. Wilson, K. Hashimoto, and T. Shibauchi

Subjects
Science
Abstract

In the kagome superconductor CsV3Sb5 the symmetry of the superconducting gap is still in question, both at ambient pressure and under high pressure. Here, via controlled introduction of impurities, the authors report evidence for a non-chiral full superconducting gap with no sign change.

Published
2023
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4. DEVELOPMENT OF DETAILED BUILDING DISTRIBUTION MAP TO SUPPORT SMART CITY PROMOTION -AN APPROACH USING SATELLITE IMAGE AND DEEP LEARNING–

Author

K. Okada, N. Nishiyama, Y. Akiyama, H. Miyazaki, and S. Miyazawa

Subjects
Technology, Engineering (General). Civil engineering (General), TA1-2040, Applied optics. Photonics, TA1501-1820
Abstract

Detailed demographics play an important role in the development of smart cities. However, especially in developing countries, the maintenance and management of this data is incomplete, which hinders the promotion of smart cities. The objective of this study is to develop a method to create detailed building distribution maps from satellite images, which will serve as a basis for developing detailed demographic data to support the promotion of smart cities around the world. The target area is several areas of Tokyo where validation data is available. We first developed a method for extracting buildings from satellite images and then estimating the building use to determine the buildings where residents are distributed. Both methods use deep learning. As a result, it was possible to extract buildings with an extraction rate (the number of buildings in the automatically extracted building data divided by the number of buildings in the data for verification) of up to 60.3% for the entire target area. In addition, in the estimation of building use, our method was able to classify detached and non-detached buildings with an average accuracy of 78.7% for the entire target area.

Published
2022
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5. Dietary salt with nitric oxide deficiency induces nocturnal polyuria in mice via hyperactivation of intrarenal angiotensin II-SPAK-NCC pathway

Author

Y. Sekii, H. Kiuchi, K. Takezawa, T. Imanaka, S. Kuribayashi, K. Okada, Y. Inagaki, N. Ueda, S. Fukuhara, R. Imamura, H. Negoro, and N. Nonomura

Subjects
Biology (General), QH301-705.5
Abstract

This study reports a mouse model of nocturnal polyuria - increased urine production at night that causes compromised quality of life and may impact mortality in older people. The authors identify a molecular pathway in the kidney that could prove to be a promising drug target for nocturnal polyuria.

Published
2022
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6. Lysine acetylation regulates the interaction between proteins and membranes

Author

Alan K. Okada, Kazuki Teranishi, Mark R. Ambroso, Jose Mario Isas, Elena Vazquez-Sarandeses, Joo-Yeun Lee, Arthur Alves Melo, Priyatama Pandey, Daniel Merken, Leona Berndt, Michael Lammers, Oliver Daumke, Karen Chang, Ian S. Haworth, and Ralf Langen

Subjects
Science
Abstract

Lysine acetylation regulates the function of soluble proteins in vivo, yet it remains largely unexplored whether lysine acetylation regulates the function of membrane proteins. Here, the authors map lysine acetylation predominantly in membrane-interaction regions in peripheral membrane proteins and show with three candidate proteins how lysine acetylation is a regulator of membrane protein function.

Published
2021
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7. Huntingtin fibrils with different toxicity, structure, and seeding potential can be interconverted

Author

J. Mario Isas, Nitin K. Pandey, Hui Xu, Kazuki Teranishi, Alan K. Okada, Ellisa K. Fultz, Anoop Rawat, Anise Applebaum, Franziska Meier, Jeannie Chen, Ralf Langen, and Ansgar B. Siemer

Subjects
Science
Abstract

Huntingtin exon-1 (HTTex1) consists of a N-terminal N17 domain, the disease causing polyQ domain and a C-terminal proline-rich domain (PRD). Here, the authors combine electron paramagnetic resonance (EPR), solid-state NMR with other biophysical method to characterise the structural differences of various HTTex1 fibril types with different toxicity and find that the dynamics and entanglement of the PRD domain differs among them and that the HTTex1 fibrils can be interconverted.

Published
2021
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9. Phase-field crack analysis using estimated transition zone of crack by molecular dynamics simulation

Author

K. Satake, K. Okada, and M. Muramatsu

Subjects
Physics, QC1-999
Abstract

We calculate the parameter that governs the width of the transition zone by molecular dynamics (MD) simulation and use it in a phase-field crack (PFC) simulation with the mechanical properties of iron. First, a quantitative evaluation of intactness is conducted by examining the change in atomic conformation induced by crack propagation, whose numerical data are taken from the result of the MD simulation. The spatial distribution of the intactness is fitted to the same function as the damage parameter in the PFC model, namely, an exponential function, by the least-squares method. From this distribution, the transition zone parameter is estimated. The result of the PFC simulation using this newly determined transition zone parameter is discussed in terms of the crack path by comparison with the result of crack propagation analysis based on the MD simulation.

Published
2021
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10. Risk profiles and one-year outcomes of patients with newly diagnosed atrial fibrillation in India: Insights from the GARFIELD-AF Registry

Author

Jitendra PS. Sawhney, Veerappa A. Kothiwale, Vikas Bisne, Rajashekhar Durgaprasad, Praveen Jadhav, Manoj Chopda, Velam Vanajakshamma, Ramdhan Meena, Govindan Vijayaraghavan, Kamaldeep Chawla, Jagan Allu, Karen S. Pieper, A. John Camm, Ajay K. Kakkar, Jean-Pierre Bassand, David A. Fitzmaurice, Samuel Z. Goldhaber, Shinya Goto, Sylvia Haas, Werner Hacke, Lorenzo G. Mantovani, Frank Misselwitz, Alexander G.G. Turpie, Martin van Eickels, Freek W.A. Verheugt, Gloria Kayani, Keith A.A. Fox, Bernard J. Gersh, Hector Lucas Luciardi, Harry Gibbs, Marianne Brodmann, Frank Cools, Antonio Carlos Pereira Barretto, Stuart J. Connolly, Alex Spyropoulos, John Eikelboom, Ramon Corbalan, Dayi Hu, Petr Jansky, Jørn Dalsgaard Nielsen, Hany Ragy, Pekka Raatikainen, Jean-Yves Le Heuzey, Harald Darius, Matyas Keltai, Sanjay Kakkar, Jitendra Pal Singh Sawhney, Giancarlo Agnelli, Giuseppe Ambrosio, Yukihiro Koretsune, Carlos Jerjes Sánchez Díaz, Hugo Ten Cate, Dan Atar, Janina Stepinska, Elizaveta Panchenko, Toon Wei Lim, Barry Jacobson, Seil Oh, Xavier Viñolas, Marten Rosenqvist, Jan Steffel, Pantep Angchaisuksiri, Ali Oto, Alex Parkhomenko, Wael Al Mahmeed, David Fitzmaurice, D.Y. Hu, K.N. Chen, Y.S. Zhao, H.Q. Zhang, J.Z. Chen, S.P. Cao, D.W. Wang, Y.J. Yang, W.H. Li, Y.H. Yin, G.Z. Tao, P. Yang, Y.M. Chen, S.H. He, Ying Wang, Yong Wang, G.S. Fu, X. Li, T.G. Wu, X.S. Cheng, X.W. Yan, R.P. Zhao, M.S. Chen, L.G. Xiong, P. Chen, Y. Jiao, Y. Guo, L. Xue, F.Z. Wang, H. Li, Z.M. Yang, C.L. Bai, J. Chen, J.Y. Chen, X. Chen, S. Feng, Q.H. Fu, X.J. Gao, W.N. Guo, R.H. He, X.A. He, X.S. Hu, X.F. Huang, B. Li, J. Li, L. Li, Y.H. Li, T.T. Liu, W.L. Liu, Y.Y. Liu, Z.C. Lu, X.L. Luo, T.Y. Ma, J.Q. Peng, X. Sheng, X.J. Shi, Y.H. Sun, G. Tian, K. Wang, L. Wang, R.N. Wu, Q. Xie, R.Y. Xu, J.S. Yang, L.L. Yang, Q. Yang, Y. Ye, H.Y. Yu, J.H. Yu, T. Yu, H. Zhai, Q. Zhan, G.S. Zhang, Q. Zhang, R. Zhang, Y. Zhang, W.Y. Zheng, B. Zhou, Z.H. Zhou, X.Y. Zhu, S. Kakkar, J.P.S. Sawhney, P. Jadhav, R. Durgaprasad, A.G. Ravi Shankar, R.K. Rajput, K. Bhargava, R. Sarma, A. Srinivas, D. Roy, U.M. Nagamalesh, M. Chopda, R. Kishore, G. Kulkarni, P. Chandwani, R.A. Pothiwala, M. Padinhare Purayil, S. Shah, K. Chawla, V.A. Kothiwale, B. Raghuraman, G. Vijayaraghavan, V.M. Vijan, G. Bantwal, V. Bisne, A. Khan, J.B. Gupta, S. Kumar, D. Jain, S. Abraham, D. Adak, A. Barai, H. Begum, P. Bhattacharjee, M. Dargude, D. Davies, B. Deshpande, P. Dhakrao, V. Dhyani, S. Duhan, M. Earath, A. Ganatra, S. Giradkar, V. Jain, R. Karthikeyan, L. Kasala, S. Kaur, S. Krishnappa, A. Lawande, B. Lokesh, N. Madarkar, R. Meena, P. More, D. Naik, K. Prashanth, M. Rao, N.M. Rao, N. Sadhu, D. Shah, M. Sharma, P. Shiva, S. Singhal, S. Suresh, V. Vanajakshamma, S.G. Panse, Y. Koretsune, S. Kanamori, K. Yamamoto, K. Kumagai, Y. Katsuda, K. Sadamatsu, F. Toyota, Y. Mizuno, I. Misumi, H. Noguchi, S. Ando, T. Suetsugu, M. Minamoto, Hiroshi Oda, K. Shiraishi, S. Adachi, K. Chiba, H. Norita, M. Tsuruta, T. Koyanagi, H. Ando, T. Higashi, K. Okada, S. Azakami, S. Komaki, K. Kumeda, T. Murayama, J. Matsumura, Y. Oba, R. Sonoda, K. Goto, K. Minoda, Y. Haraguchi, H. Suefuji, H. Miyagi, H. Kato, Tadashi Nakamura, Tsugihiro Nakamura, H. Nandate, R. Zaitsu, Yoshihisa Fujiura, A. Yoshimura, H. Numata, J. Ogawa, H. Tatematsu, Y. Kamogawa, K. Murakami, Y. Wakasa, M. Yamasawa, H. Maekawa, S. Abe, H. Kihara, S. Tsunoda, Katsumi Saito, Kazuyuki Saito, T. Fudo, K. Obunai, H. Tachibana, I. Oba, T. Kuwahata, S. Higa, M. Gushiken, T. Eto, H. Yoshida, D. Ikeda, Yoshitake Fujiura, M. Ishizawa, M. Nakatsuka, K. Murata, C. Ogurusu, M. Shimoyama, M. Akutsu, I. Takamura, F. Hoshino, N. Yokota, T. Iwao, K. Tsuchida, M. Takeuchi, Y. Hatori, Y. Kitami, Yoichi Nakamura, R. Oyama, M. Ageta, Hiroyuki Oda, Y. Go, K. Mishima, T. Unoki, S. Morii, Yuhei Shiga, H. Sumi, T. Nagatomo, K. Sanno, K. Fujisawa, Y. Atsuchi, T. Nagoshi, T. Seto, T. Tabuchi, M. Kameko, K. Nii, K. Oshiro, H. Takezawa, S. Nagano, N. Miyamoto, M. Iwaki, Yuichiro Nakamura, M. Fujii, M. Okawa, Masahiko Abe, Masatake Abe, Mitsunori Abe, T. Saito, T. Mito, K. Nagao, J. Minami, T. Mita, I. Sakuma, T. Taguchi, S. Marusaki, H. Doi, M. Tanaka, T. Fujito, M. Matsuta, T. Kusumoto, S. Kakinoki, K. Ashida, N. Yoshizawa, J. Agata, O. Arasaki, M. Manita, M. Ikemura, S. Fukuoka, H. Murakami, S. Matsukawa, Y. Hata, T. Taniguchi, T. Ko, H. Kubo, M. Imamaki, M. Akiyama, M. Inagaki, H. Odakura, T. Ueda, Y. Katsube, A. Nakata, H. Watanabe, M. Techigawara, M. Igarashi, K. Taga, T. Kimura, S. Tomimoto, M. Shibuya, M. Nakano, K. Ito, T. Seo, S. Hiramitsu, H. Hosokawa, M. Hoshiai, M. Hibino, K. Miyagawa, Hajime Horie, N. Sugishita, Yukio Shiga, A. Soma, K. Neya, Tetsuro Yoshida, Tomoki Yoshida, M. Mizuguchi, M. Ishiguro, T. Minagawa, M. Wada, H. Mukawa, F. Okuda, S. Nagasaka, Y. Abe, Sen Adachi, Susumu Adachi, T. Adachi, K. Akahane, T. Amano, K. Aoki, T. Aoyama, H. Arai, S. Arima, T. Arino, H. Asano, T. Asano, J. Azuma, T. Baba, T. Betsuyaku, H. Chibana, H. Date, J. Doiuchi, Y. Emura, M. Endo, Y. Fujii, R. Fujiki, A. Fujisawa, Y. Fujisawa, T. Fukuda, T. Fukui, N. Furukawa, T. Furukawa, W. Furumoto, T. Goto, M. Hamaoka, N. Hanazono, K. Hasegawa, T. Hatsuno, Y. Hayashi, K. Higuchi, K. Hirasawa, H. Hirayama, M. Hirose, S. Hirota, M. Honda, Hideki Horie, T. Ido, O. Iiji, H. Ikeda, K. Ikeda, K. Ikeoka, M. Imaizumi, H. Inaba, T. Inoue, F. Iseki, A. Ishihara, N. Ishioka, N. Ito, T. Iwase, H. Kakuda, J. Kamata, H. Kanai, H. Kanda, M. Kaneko, H. Kano, T. Kasai, T. Kato, Y. Kato, Y. Kawada, K. Kawai, K. Kawakami, S. Kawakami, T. Kawamoto, S. Kawano, J. Kim, T. Kira, H. Kitazawa, H. Kitazumi, T. Kito, T. Kobayashi, T. Koeda, J. Kojima, H. Komatsu, I. Komatsu, Y. Koshibu, T. Kotani, T. Kozuka, Y. Kumai, T. Kumazaki, I. Maeda, K. Maeda, Y. Maruyama, S. Matsui, K. Matsushita, Y. Matsuura, K. Mineoi, H. Mitsuhashi, N. Miura, S. Miyaguchi, S. Miyajima, H. Miyamoto, A. Miyashita, S. Miyata, I. Mizuguchi, A. Mizuno, T. Mori, O. Moriai, K. Morishita, O. Murai, Sho Nagai, Shunichi Nagai, E. Nagata, H. Nagata, A. Nakagomi, S. Nakahara, M. Nakamura, R. Nakamura, N. Nakanishi, T. Nakayama, R. Nakazato, T. Nanke, J. Nariyama, Y. Niijima, H. Niinuma, Y. Nishida, Y. Nishihata, K. Nishino, H. Nishioka, K. Nishizawa, I. Niwa, K. Nomura, S. Nomura, M. Nozoe, T. Ogawa, N. Ohara, M. Okada, K. Okamoto, H. Okita, M. Okuyama, H. Ono, T. Ono, Y. Onuki Pearce, S. Oriso, A. Ota, E. Otaki, Y. Saito, H. Sakai, N. Sakamoto, Y. Sakamoto, Y. Samejima, Y. Sasagawa, H. Sasaguri, A. Sasaki, T. Sasaki, Kazuki Sato, Kiyoharu Sato, M. Sawano, S. Seki, Y. Sekine, Y. Seta, K. Sezaki, N. Shibata, Y. Shiina, H. Shimono, Y. Shimoyama, T. Shindo, H. Shinohara, R. Shinohe, T. Shinozuka, T. Shirai, T. Shiraiwa, Y. Shozawa, T. Suga, C. Sugimoto, Kazuo Suzuki, Keita Suzuki, Shu Suzuki, Shunji Suzuki, Susumu Suzuki, Y. Suzuki, M. Tada, A. Taguchi, T. Takagi, Y. Takagi, K. Takahashi, S. Takahashi, H. Takai, C. Takanaka, S. Take, H. Takeda, K. Takei, K. Takenaka, T. Tana, G. Tanabe, K. Taya, H. Teragawa, S. Tohyo, S. Toru, Y. Tsuchiya, T. Tsuji, K. Tsuzaki, H. Uchiyama, O. Ueda, Y. Ueyama, N. Wakaki, T. Wakiyama, T. Washizuka, M. Watanabe, T. Yamada, T. Yamagishi, H. Yamaguchi, Kenichi Yamamoto, Kentaro Yamamoto, Kunihiko Yamamoto, T. Yamamoto, M. Yamaura, M. Yamazoe, K. Yasui, Y. Yokoyama, K. Yoshida, T.W. Lim, C.K. Ching, C.G. Foo, J.H. Chow, D.D. Chen, F.R. Jaufeerally, Y.M. Lee, G. Lim, W.T. Lim, S. Thng, S.Y. Yap, C. Yeo, S. Oh, H.N. Pak, J.-B. Kim, J.H. Kim, S.-W. Jang, D.H. Kim, D.R. Ryu, S.W. Park, D.-K. Kim, D.J. Choi, Y.S. Oh, M.-C. Cho, S.-H. Kim, H.-K. Jeon, D.-G. Shin, J.S. Park, H.K. Park, S.-J. Han, J.H. Sung, J.-G. Cho, G.-B. Nam, Y.K. On, H.E. Lim, J.J. Kwak, T.-J. Cha, T.J. Hong, S.H. Park, J.H. Yoon, N.-H. Kim, K.-S. Kim, B.C. Jung, G.-S. Hwang, C.-J. Kim, D.B. Kim, J.J. Ahn, H.J. An, H. Bae, A.L. Baek, W.J. Chi, E.A. Choi, E.H. Choi, H.K. Choi, H.S. Choi, S. Han, E.S. Heo, K.O. Her, S.W. Hwang, E.M. Jang, H.-S. Jang, S. Jang, H.-G. Jeon, S.R. Jeon, Y.R. Jeon, H.K. Jeong, I.-A. Jung, Hyeon Jeong Kim, Hyun Ju Kim, Ji Seon Kim, Jung Sook Kim, J.A. Kim, K.T. Kim, M.S. Kim, Sang Hee Kim, Sang Hyun Kim, Y.-I. Kim, C.S. Lee, E.H. Lee, G.H. Lee, H.Y. Lee, H.-Y. Lee, K.H. Lee, K.R. Lee, M.S. Lee, M.-Y. Lee, R.W. Lee, S.E. Lee, S.H. Lee, S. Lee, W.Y. Lee, I.K. Noh, A.R. Park, B.R. Park, H.N. Park, J.H. Park, M. Park, Y. Park, S.-Y. Seo, J. Shim, J.H. Sim, Y.M. Sohn, W.S. Son, Y.S. Son, H.J. Song, H.K. Wi, J.J. Woo, S. Ye, K.H. Yim, K.M. Yoo, E.J. Yoon, S.Y. Yun, P. Angchaisuksiri, S. Chawanadelert, P. Mongkolwongroj, K. Kanokphatcharakun, S. Cheewatanakornkul, T. Laksomya, S. Pattanaprichakul, T. Chantrarat, S. Rungaramsin, S. Silaruks, W. Wongcharoen, K. Siriwattana, K. Likittanasombat, P. Katekangplu, W. Boonyapisit, D. Cholsaringkarl, B. Chatlaong, P. Chattranukulchai, Y. Santanakorn, P. Hutayanon, P. Khunrong, T. Bunyapipat, S. Jai-Aue, P. Kaewsuwanna, P. Bamungpong, S. Gunaparn, S. Hongsuppinyo, R. Inphontan, R. Khattaroek, K. Khunkong, U. Kitmapawanont, C. Kongsin, B. Naratreekoon, S. Ninwaranon, J. Phangyota, A. Phrommintikul, P. Phunpinyosak, K. Pongmorakot, S. Poomiphol, N. Pornnimitthum, S. Pumprueg, S. Ratchasikaew, K. Sanit, K. Sawanyawisuth, B. Silaruks, R. Sirichai, A. Sriwichian, W. Suebjaksing, P. Sukklad, T. Suttana, A. Tangsirira, O. Thangpet, W. Tiyanon, Y. Vorasettakarnkij, T. Wisaratapong, W. Wongtheptien, A. Wutthimanop, S. Yawila, A. Oto, A. Altun, I. Ozdogru, K. Ozdemir, O. Yilmaz, A. Aydinlar, M.B. Yilmaz, E. Yeter, Z. Ongen, M. Cayli, H. Pekdemir, M. Ozdemir, M. Sucu, T. Sayin, M. Demir, H. Yorgun, M. Ersanli, E. Okuyan, D. Aras, H. Abdelrahman, O. Aktas, D. Alpay, F. Aras, M.F. Bireciklioglu, S. Budeyri, M. Buyukpapuc, S. Caliskan, M. Esen, M.A. Felekoglu, D. Genc, B. Ikitimur, E.B. Karaayvaz, S. Kılıç Karataş, S. Okutucu, E. Ozcelik, A. Quisi, H. Sag, L. Sahiner, B.Y. Sayin, T. Seker, D. Uzun Alkan, E. Yildirim, R. Yildirim, F. Yilmaz, V. Yuksekdag, H.L. Luciardi, N. Vensentini, A.C. Ingaramo, G.A. Sambadaro, V. Fernandez Caputi, S.G. Berman, P. Dragotto, A.J. Kleiban, N. Centurion, G. Giacomi, R.A. Ahuad Guerrero, D. Conde, G. Zapata, L.A. Di Paola, J.L. Ramos, R.D. Dran, J. Egido, A.A. Fernandez, M.J. Fosco, S. Sassone, V.A. Sinisi, L.R. Cartasegna, M.A. Berli, O.A. Gomez Vilamajo, F. Ferroni, E.D. Alaguibe, A. Alvarez D'Amelio, C. Arabetti, L. Arias, J.A. Belardi, L. Bergesio, F. Berli, M. Berli, S. Borchowiec, C. Buzzetti, R. Cabrini, V. Campisi, A.L. Cappi, R. Carrizo, F. Colombo Berra, J.P. Costabel, O.J.A. Costamagna, A.A. Damonte, I.N. De Urquiza, F. Diez, M.F. Edén, M. Fanuele, F. Fernandez Voena, M. Foa Torres, C. Funosas, M.P. Giacomi, C.H. Gimenez, E.P. Gurfinkel, M. de L.M. Had, V. Hansen, A.D. Hrabar, M. Ingratta, A. Lopez, G. Maehara, L. Maffei, A. Martinelli, C. Martinelli, J. Matkovich, B. Mautner, A. Meirino, R. Munguia, A. Navarro, V. Novas, G. Perez Prados, J. Pontoriero, R.N. Potito, C. Ricotti, M.A. Rodriguez, F. Rolandi, M.E. Said Palladino, M. Salinger, L.S. Sanziani, P.O. Schygiel, A. Sossich, J.F. Tinto, L. Tonelli, A.L. Tufare, M. Vallejo, M.E. Yunis, M. Zillo, F.J. Zurbrigk, A.C.P. Barretto, D.C. Sobral Filho, J. Jaber, D. Armaganijan, J. Faria Neto, A. Steffens, W. Kunz Sebba Barroso de Souza, J.D. de Souza Neto, J.M. Ribeiro, M. Silveira Teixeira, P.R. Ferreira Rossi, L. Pires, D. Moreira, J.C. Moura Jorge, A. Menezes Lorga Filho, L.C. Bodanese, M. Westerlund Montera, C.H. Del Carlo, T. Da Rocha Rodrigues, F.A. Alves da Costa, A. Lopes, R. Lopes, G.R. Araújo, E.R. Fernandes Manenti, J.F. Kerr Saraiva, J.C. Ferreira Braga, A. Negri, L. Souto, C. Moncada, D. Bertolim Precoma, F. Roquette, G. Reis, R.A. Ramos Filho, E. Lanna Figueiredo, R. Vieira Botelho, C. Munhoz da Fontoura Tavares, C.R. Costantini Frack, J. Abdalla Saad, H.C. Finimundi, C. Pisani, D. Chemello, M. Pereira Martins, C.C. Broilo França, F. Alban, G.B. Aranha Rosito, J.B. de Moura Xavier Moraes Junior, R.T. Tumelero, L. Nigro Maia, R. Simões de Almeida, N.C. do Carmo Borges, L.G. Gomes Ferreira, P. Agliardi, J. Alves de Oliveira Gomes, V. Araujo, M. Arruda Nakazone, T. Barbosa, S. Barroso, E. Belisario Falchetto, H. Bellotti Lopes, M.A. Benez Teixeira Lemos, G. Biazus, L. Borges Queiroz, F.E. Camazzola, M. Caporale, S. Cardoso Boscato, F. Chieza, M.O. Chokr, R. Clemente Mingireanov, N. Codonho Góes, C. Correa, M. Costa, C. Costantini Ortiz, L.S. da Silva, F. da Silva Paulitsch, J.A. da Silveira, E. Daros, G.R. de Araújo, M.I. Del Monaco, C. Dias, M.A. Dias, A.P. Drummond Wainstein, P. Ely Pizzato, D.C. Esteves, P. Fabri, T. Félix Lorenzato Fonseca, E. Fernandes, C. Fonseca, C.R. Frack Costantini, R. Franchin Ferraz, F. Freire, P. Gottardo, D. Guanaes, S. Guizzardi, E. Hettwer Magedanz, F. Igansi, F. Jannuzzi, G. Junior, D. Komar, E.G. Lino, D. Lopes, O. Lourenço da Silva Júnior, E. Lustosa, A.P. Macagnan, M.C. Marinho, M. Mazzoni, G. Melo, L. Mortari, O.M.C.C. Mouco, C. Nanzer Vital, C. Ormundo, S. Oss Emmer, E. Palmegiani, R. Pavani, L. Pereira, V.L. Pereira, R. Perreira, S. Poletti, S.C. Quaia Fortunato, C. Queirantes, N. Ramos Pereira, R.L. Rech, S. Ribeiro, A. Rodrigues, H. Roesch, T. Ruaro Reichert, D. Santos, I. Santos, M. Santos, M.V. Seroqui, S. Silva, L. Soares, L. Spolaor, C. Stoll, N. Toazza Duda, L. Trama, B. Unterkircher, M.V. Valois, T. Vargas, T. Viana, C. Vicente, L. Vidal Armaganijan, R. Vieira Homem, L.G. Vieira Torres, L. Vila Boas, F. Villaça Guimarães Filho, R. Corbalan, G. Eggers, C. Bugueño Gutiérrez, G. Arriagada, S. Potthoff Cardenas, B.A.J. Stockins Fernandez, C. Conejeros, C. 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Domenech Borras, A. Elorriaga Madariaga, A. Espallargas, M. Fernandez, E. Fernandez Escobar, E. Fernandez Mas, A. Ferrer, J. Fosch, M. Garcia Bermudez, V. Garcia Millan, M. Gavira Saenz, C. Gines Garcia, C. Gomez, Y. Gomez Perez, A. Gonzales Segovia, P. Gonzalez, L. Grigorian, A. Guerrero Molina, M. del C. Gutierrez del Val, B. Herrero Maeso, E. Hevia Rodriguez, A. Iglesias Garcia, M.J. Jimenez Fernandez, B. Jimeno Besa, P. Juan Salvadores, M.B. Lage Bouzamayor, I. Lasuncion, L.E. Lezcano Gort, M. Llobet Molina, M. Lopez, A. Manzanal Rey, J. Mara Guerra, S. Marcus, A. Martin Vila, M. Martinez Mena, P. Mazon, F. Mendez Zurita, G. Millán, M. Molina, P. Montero Alia, D. Montes, M. Moure Gonzalez, R.B. Munoz Munoz, A. Negrete Palma, H.N. Orellana Figueroa, V.M. Ortega, C. Ortiz Cortes, D. Otero Tomera, N. Palomo Merchan, I. Pareja Ibar, E. Pena Garcia, M. Pereda Armayor, M. Perez Carasa, I. Prieto, V. Quintern, R. Renom, L.M. Rincon Diaz, V. Rios, L. Riquelme Sola, R. Rivera, X. Robiro Robiro, M. Roca, C. Roca Saumell, C. Rodrigo, E. Rodriguez, M. Rodriguez Garcia, S. Saez Jimenez, P. Sanchez Calderon, L. Sanchez Mendez, S. Sanchez Parra, C. Santolaya, M.R. Senan Sanz, A. Seoane Blanco, E. Serralvo, N. Sierra, C. Simon Valero, J. Sorribes Lopez, M. Teixido Fontanillas, M. Terns Riera, G. Tobajas, C. Torres, J. Torres Marques, M. Ubeda Pastor, M. Rosenqvist, A. Wirdby, J. Linden, K. Henriksson, M. Elmersson, A. Egilsson, U. Börjesson, G. Svärd, B. Liu, A. Lindh, L.-B. Olsson, M. Gustavsson, Lars Andersson, Lisbeth Andersson, L. Benson, C. Bothin, A. Hajimirsadeghi, K. Kadir, M. Ericsson, A. Ohlsson, H. Lindvall, P. Svensson, K. Thorne, H. Handel, P. Platonov, B. Eriksson, I. Timberg, K. Romberg, M. Crisby, J.-E. Karlsson, S.A. Jensen, A. Andersson, L. Malmqvist, B. Martinsson, F. Bernsten, J. Engdahl, J. Thulin, A. Hot-Bjelac, P. Stalby, H. Aaröe, E. Ahbeck, H. Ahlmark, F. Al-Khalili, G. Bonkowski, S. Dzeletovic, A.-B. Ekstrand, G.-B. Eriksson, K. Floren, C. Grässjö, S. Hahn, P. Jaensson, B. Jansson, J.-H. Jansson, R.-M. Kangert, A. Koch, D. Kusiak, A. Lettenström, A. Lindberg, C.-J. Lindholm, A. Mannermyr, K. Mansson, M. Millborg, C. Nilsson, A.-M. Ohlin, A. Olofsson, A. Osberg, A. Pedersen, K. Risbecker, K. Rosenberg, J. Samuelsson, M. Shayesteh, K. Skoglund, M. Stjernberg, C. Thorsen, J. Steffel, J.H. Beer, J. Debrunner, D. Amstutz, J. Bruegger, G. Elise, A. Grau, A. Guinand, I. Henriette, E. Saga, S. Winnik, A. Parkhomenko, I. Rudyk, V. Tseluyko, O. Karpenko, S. Zhurba, I. Kraiz, I. Kupnovytska, N. Serediuk, Y. Mostovoy, O. Ushakov, O. Koval, I. Kovalskyi, Y. Svyshchenko, O. Sychov, M. Stanislavchuk, O. Kraydashenko, A. Yagensky, S. Tykhonova, I. Fushtey, R. Belegai, G. Berko, L. Burdeuna, O. Chabanna, I. Daniuk, A. Ivanov, E. Kamenska, P. Kaplan, O. Khyzhnyak, S. Kizim, O. Matova, O. Medentseva, V. Mochonyi, M. Mospan, V. Nemtsova, T. Ovdiienko, O. Palamarchuk, M. Pavelko, R. Petrovskyy, D. Plevak, O. Proshak, S. Pyvovar, L. Rasputina, O. Romanenko, O. Romanova, A. Sapatyi, O. Shumakov, R. Stets, L. Todoriuk, V. Varenov, D. Fitzmaurice, N. Chauhan, D. Goodwin, P. Saunders, R. Evans, J. Leese, P.S. Jhittay, A. Ross, M.S. Kainth, G. Pickavance, J. McDonnell, A. Williams, T. Gooding, H. Wagner, S. Suryani, A. Singal, S. Sircar, R. Bilas, P. Hutchinson, A. Wakeman, M. Stokes, N. Paul, M. Aziz, C. Ramesh, P. Wilson, S. Franklin, S. Fairhead, J. Thompson, V. St Joseph, G. Taylor, D. Tragen, D. Seamark, C. Paul, M. Richardson, A. Jefferies, H. Sharp, H. Jones, C. Giles, M. Page, O. Oginni, J. Aldegather, S. Wetherwell, W. Lumb, P. Evans, F. Scouller, N. Macey, Y. Stipp, R. West, S. Thurston, P. Wadeson, J. Matthews, P. Pandya, A. Gallagher, T. Railton, B. Sinha, D. Russell, J.A. Davies, P. Ainsworth, C.P. Jones, P. Weeks, J. Eden, D. Kernick, W. Murdoch, L. Lumley, R.P. Patel, S.W. Wong, M. Saigol, K. Ladha, K. Douglas, D.F. Cumberlidge, C. Bradshaw, G. Van Zon, K.P. Jones, M.J. Thomas, E. Watson, B. Sarai, N. Ahmad, W. Willcock, J. Cairns, S. Sathananthan, N. de Kare-Silver, A. Gilliland, E. Strieder, A. Howitt, B. Vishwanathan, N. Bird, D. Gray, M. Clark, J. Bisatt, J. Litchfield, E. Fisher, T. Fooks, A.R. Kelsall, E. Alborough, J. Wakeling, M. Parfitt, K. Milne, S. Rogers, R. Priyadharshan, J.L. Oliver, E. Davies, S. Abushal, M. Jacobs, C. Hutton, N.I. Walls, R. Thompson, C. Chigbo, S.M.A. Zaidi, M. Howard, K.C. Butter, S. Barrow, H. Little, I.U. Haq, L. Gibbons, S. Glencross, A.J. McLeod, K. Poland, C. Mulholland, A. Warke, P. Conn, G. Burns, R.N. Smith, S. Lowe, R. Kamath, H.S. Dau, J. Webster, I. Hodgins, S. Vercoe, P.C. Roome, H. Pinnock, J.R.A. Patel, A. Ali, N. Hart, R. Davies, E. Stuart, C.A. Neden, M. Danielsen, R. Heath, P. Sharma, S. Galloway, C. Hawkins, R. Oliver, M. Aylward, S. Mannion, M. Braddick, D. Edwards, A.C. Rothwell, A. Sabir, F. Choudhary, S. Khalaque, A. Wilson, S. Peters, W. Coulson, N. Roberts, A. Heer, S. Coates, B. Ward, D. Jackson, S. Walton, D. Shepherd, M. Sterry, T. Wong, M. Boon, R. Bunney, R. Haria-Shah, R.T. Baron, S. Davies, T. Schatzberger, N. Hargreaves, T. Stephenson, H. Choi, R. Batson, L. Lucraft, T. Myhill, S. Estifano, D. Geatch, J. Wilkinson, R. Veale, K. Forshaw, T. Davies, K. Zaman, P. Vinson, C. Liley, M. Bandrapalli, P. McGinty, R. Wastling, P. McEleny, A. Beattie, P. Cooke, M. Wong, J. Gunasegaram, M. Pugsley, S. Ahmad, C. A'Court, J. Ayers, J. Bennett, S. Cartwright, S. Dobson, C. Dooldeniya, A. Flynn, R. Fox, J. Goram, A. Halpin, A. Hay, P. Jacobs, L. Jeffers, L. Lomax, I. Munro, R. Muvva, M. Nadaph, K. Powell, S. Randfield, D. Redpath, R. Reed, M. Rickenbach, G. Rogers, P.B. Saunders, C. Seamark, J. Shewring, P. Simmons, H. Simper, H. Stoddart, A. Sword, N. Thomas, A. Thomson, H. Gibbs, A. Blenkhorn, B. Singh, W. Van Gaal, W. Abhayaratna, R. Lehman, P. Roberts-Thomson, J. Kilian, D. Coulshed, A. Catanchin, D. Colquhoun, H. Kiat, D. Eccleston, J. French, L. Zimmett, B. Ayres, T. Phan, P. Blombery, D. Crimmins, D. O'Donnell, A. Choi, P. Astridge, M. Arstall, N. Jepson, M. Binnekamp, A. Lee, J. Rogers, G. Starmer, P. Carroll, J. Faunt, A. Aggarwala, L. Barry, C. Batta, R. Beveridge, A. Black, M. Bonner, J. Boys, E. Buckley, M. Campo, L. Carlton, A. Connelly, B. Conway, D. Cresp, H. Dimitri, S. Dixon, M. Dolman, M. Duroux, M. Eskandari, R. Eslick, A. Ferreira-Jardim, T. Fetahovic, D. Fitzpatrick, R. Geraghty, J. Gibbs, T. Grabek, M.H. Modi, K. Hayes, M.P. Hegde, L. Hesketh, B. Hoffmann, B. Jacobson, K. Johnson, C. Juergens, I. Kassam, V. Lawlor, M. Lehman, S. Lehman, D. Leung, S. Mackay, M. MacKenzie, C. McCarthy, C. McIntosh, L. McKeon, H. Morrison, C. Mussap, J.-D. Myers, V. Nagalingam, G. Oldfield, V. O'May, J. Palmer, L. Parsons, K. Patching, T. Patching, V. Paul, M. Plotz, S. Preston, H. Rashad, M. Ratcliffe, S. Raynes, J. Rose, L. Sanders, M. Seremetkoska, H. Setio, S. Shone, P. Shrestha, C. Singh, C. Singleton, N. Stoyanov, S. Sutcliffe, K. Swaraj, J. Tarrant, S. Thompson, I.M. Tsay, M. Vorster, A. Waldman, L. Wallis, E. Wilford, K. Wong, S.J. Connolly, A. Spyropoulos, J. Eikelboom, R. Luton, M. Gupta, A.S. Pandey, S. Cheung, R. Leader, P. Beaudry, F. Ayala-Paredes, J. Berlingieri, J. Heath, G. Poirier, M. Du Preez, R. Nadeau, G. Dresser, R. Dhillon, T. Hruczkowski, B. Schweitzer, B. Coutu, P. Angaran, P. MacDonald, S. Vizel, S. Fikry, R. Parkash, A. Lavoie, J. Cha, B. Ramjattan, J. Bonet, K. Ahmad, L. Aro, T. Aves, K. Beaudry, C. Bergeron, J. Bigcanoe, N. Bignell, L. Breakwell, E. Burke, L. Carroll, B. Clarke, T. Cleveland, S. Daheb, P. Dehghani, I. Denis, Z. Djaidani, P. Dorian, S. Douglass, J. Dunnigan, A. Ewert, D. Farquhar, A. Fearon, L. Ferleyko, D. Fournier, B. Fox, M.-C. Grenier, W. Gulliver, K. Haveman, C. Hines, K. Hines, A.M. Jackson, C. Jean, G. Jethoo, R. Kahlon, S. Kelly, R. Kim, V. Korley, J. Kornder, L. Kwan, J. Largy, C. Lewis, S. Lewis, I. Mangat, R. Moor, J. Navratil, I. Neas, J. Otis, R. Otis, M. Pandey, F. Petrie, A. Pinter, M. Raines, P. Roberts, M. Robinson, G. Sas, S. Schulman, L. Snell, S. Spearson, J. Stevenson, T. Trahey, S. Wong, D. Wright, H. Ragy, A. Abd El-Aziz, S.K. Abou Seif, M.G. El Din, S. El Etriby, A. Elbahry, A. El-Etreby, M. Elkhadem, A. Katta, T. Khairy, A. Mowafy, M. Nawar, A. Ohanissian, A. Reda, M. Reda, H. Salem, N. Sami, S. Samir, M. Setiha, M. Sobhy, A. Soliman, N. Taha, M. Tawfik, E. Zaatout, D. Kettles, J. Bayat, H. Siebert, A. Horak, Y. Kelfkens, R. Garda, T. Pillay, M. Guerra, L. van Zyl, H. Theron, A. Murray, R. Louw, D. Greyling, P. Mntla, V. Ueckermann, R. Loghdey, S. Ismail, F. Ahmed, J. Engelbrecht, A. Ramdass, S. Maharajh, W. Oosthuysen, G. Angel, C. Bester, M. Booysen, C. Boshoff, C. Cannon, S. Cassimjee, C. Chami, G. Conway, A. Davids, L. de Meyer, G. Du Plessis, T. Ellis, L. Henley, M. Karsten, E. Loyd, J. Marks, L. Mavhusa, M. Mostert, A. Page, L. Rikhotso, M. Salie, J. Sasto, F. Shaik, A. Skein, L. Smith, G. Tarr, T. Tau, F. van Zyl, W. Al Mahmeed, G. Yousef, A. Agrawal, M. Nathani, M. Ibrahim, E.M. Esheiba, R. Singh, A. Naguib, M. Abu-Mahfouz, M. Al Omairi, A. Al Naeemi, R. Maruthanayagam, N. Bazargani, A. Wassef, R. Gupta, M. Khan, B. Subbaraman, A. Abdul, A. Al Mulla, S. El Bardisy, P. Haridas, S. Jadhav, K. Magdaluyo, M. Makdad, I. Maqsood, R. Mohamed, N. Sharma, R. Sharma, M. Thanzeel, S.Z. Goldhaber, R. Canosa, P. Rama, E. Blumberg, J. Garcia, P. Mullen, V. Wilson, A. Quick, K. Ferrick, W.M. Kutayli, M. Cox, M. Franco, S. Falkowski, R. Mendelson, M. Williams, S. Miller, S. Beach, A. Alfieri, T. Gutowski, I. Haque, R. Reddy, W. Ahmed, P. Delafontaine, D. Diercks, D. Theodoro, K. Remmel, M. Alberts, R. Ison, H. Noveck, P. Duffy, S. Pitta, D. Nishijima, C. Treasure, N. Asafu-Adjaye, K. Ball, M. Bartlett, M. Bentley, S. Bowers, A. Brown, A. Browne, J. Cameron-Watts, M. Canova, D. Cassidy, K. Cervellione, S. Congal, J. DePauw, A. Dickerson, M. Eley, L. Evans, S. Felpel, K. Ferdinand, D. Fielder, P. Gentry, A. Haideri, F. Hakimi, T. Harbour, E. Hartranft, B. Hawkins, M. Headlee, L. Henson, C. Herrick, T. Hicks, S. Jasinski, A. Jones, L. Jones, P. Jones, S. Karl, M. Keeling, J. Kerr, P. Knowles, J. Langdon, M. Lay, J.A. Lee, T. Lincoln, E. Malone, A. Merliss, D. Merritt, J. Minardo, B. Mooso, C. Orosco, V. Palumbo, M. Parker, T. Parrott, S. Paserchia, G. Pearl, J. Peterson, N. Pickelsimer, T. Purcell, J. Raynor, S. Raziano, C. Richard, T. Richardson, C. Robertson, A. Sage, T. Sanghera, P. Shaw, J. Shoemaker, K. Smith, B. Stephanie, A. Thatcher, H. Theobald, N. Thompson, L. Treasure, T. Tripti, C. Verdi, and V. Worthy

Subjects
Surgery, RD1-811, Diseases of the circulatory (Cardiovascular) system, RC666-701
Abstract

Background: The Global Anticoagulant Registry in the FIELD–Atrial Fibrillation (GARFIELD-AF) is an ongoing prospective noninterventional registry, which is providing important information on the baseline characteristics, treatment patterns, and 1-year outcomes in patients with newly diagnosed non-valvular atrial fibrillation (NVAF). This report describes data from Indian patients recruited in this registry. Methods and results: A total of 52,014 patients with newly diagnosed AF were enrolled globally; of these, 1388 patients were recruited from 26 sites within India (2012–2016). In India, the mean age was 65.8 years at diagnosis of NVAF. Hypertension was the most prevalent risk factor for AF, present in 68.5% of patients from India and in 76.3% of patients globally (P

Published
2018
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12. The Mitochondrial-Derived Peptides, HumaninS14G and Small Humanin-like Peptide 2, Exhibit Chaperone-like Activity

Author

Alan K. Okada, Kazuki Teranishi, Fleur Lobo, J. Mario Isas, Jialin Xiao, Kelvin Yen, Pinchas Cohen, and Ralf Langen

Subjects
Medicine, Science
Abstract

Abstract Mitochondrial-derived peptides (MDPs) and their analogs have emerged as wide-spectrum, stress response factors protective in amyloid disease models. MDP cytoprotective functions are generally attributed to anti-apoptotic activity, however, little is known about their capacity to facilitate the cell’s unfolded protein response via direct interactions with amyloidogenic proteins. Here, we explored the effects of the MDP-analog, humaninS14G (HNG), and the MDP, small humanin-like peptide 2 (SHLP2), on the misfolding of islet amyloid polypeptide (IAPP), a critical pathogenic step in type 2 diabetes mellitus (T2DM). Our thioflavin T fluorescence studies show that HNG inhibits IAPP misfolding at highly substoichiometric concentrations. Seeded fluorescence and co-sedimentation studies demonstrate MDPs block amyloid seeding and directly bind misfolded, seeding-capable IAPP species. Furthermore, our electron paramagnetic resonance spectroscopy and circular dichroism data indicate MDPs do not act by binding IAPP monomers. Taken together our results reveal a novel chaperone-like activity wherein these MDPs specifically target misfolded amyloid seeds to inhibit IAPP misfolding which, along with direct anti-apoptotic activity and beneficial metabolic effects, make HNG and SHLP2 exciting prospects as T2DM therapeutics. These data also suggest that other mitochondrial stress response factors within the MDP family may be amenable to development into therapeutics for protein-misfolding diseases.

Published
2017
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14. Neotropical freshwater fisheries : A dataset of occurrence and abundance of freshwater fishes in the Neotropics

Author

Lívia Helena Tonella, Renata Ruaro, Vanessa Salete Daga, Diego Azevedo Zoccal Garcia, Oscar Barroso Vitorino, Tatiana Lobato‐de Magalhães, Roberto Esser dos Reis, Fabio Di Dario, Ana Cristina Petry, Michael Maia Mincarone, Luciano Fogaça de Assis Montag, Paulo Santos Pompeu, Adonias Aphoena Martins Teixeira, Alberto Luciano Carmassi, Alberto J. Sánchez, Alejandro Giraldo Pérez, Alessandra Bono, Aléssio Datovo, Alexander S. Flecker, Alexandra Sanches, Alexandre Lima Godinho, Alexandre Matthiensen, Alexandre Peressin, Alexandre Wagner Silva Hilsdorf, Alexéia Barufatti, Alice Hirschmann, Aline Jung, Allan K. Cruz‐Ramírez, Alline Braga Silva, Almir Manoel Cunico, Amanda Saldanha Barbosa, Amauri de Castro Barradas, Ana Carolina Lacerda Rêgo, Ana Clara Sampaio Franco, Ana Paula Lula Costa, Ana Paula Vidotto‐Magnoni, Anderson Ferreira, Anderson Kassner Filho, André Batista Nobile, André Lincoln Barroso Magalhães, André Teixeira da Silva, Andréa Bialetzki, Andréa Cristina dos Santos Maroclo Gomes, Andrezza Bellotto Nobre, Armando Cesar Rodrigues Casimiro, Arturo Angulo Sibaja, Arthur Alexandre Capelli dos Santos, Átila Rodrigues de Araújo, Augusto Frota, Bárbara Angélio Quirino, Beatriz Moreira Ferreira, Bianca Weiss Albuquerque, Bruna Arbo Meneses, Brunno Tolentino Oliveira, Bruno Augusto Torres Parahyba Campos, Bruno Bastos Gonçalves, Bruno Busnello Kubiak, Bruno da Silveira Prudente, Bruno Gorini de Araujo Passos Pacheco, Bruno Kazuo Nakagawa, Bruno Tayar Marinho do Nascimento, Calebe Maia, Camila Cantagallo Devids, Carla Ferreira Rezende, Carla Muñoz‐Mendoza, Carlos A. Peres, Carlos Alberto de Sousa Rodrigues Filho, Carlos Alberto Santos de Lucena, Carlos Alexandre Fernandes, Carlos Benhur Kasper, Carlos Donascimiento, Carmino Emidio, Carolina Carrillo‐Moreno, Carolina Machado, Carolina Pera, Caroline Hartmann, Catherine M. Pringle, Cecília Gontijo Leal, Céline Jézéquel, Chris Harrod, Clarissa Alves da Rosa, Claudio Quezada‐Romegialli, Crisla Maciel Pott, Crislei Larentis, Cristiane A. S. Nascimento, Cristina da Silva Gonçalves, Cristina Jaques da Cunha, Cristina Moreira Pisicchio, Daniel Cardoso de Carvalho, Daniel Galiano, Daniel Gomez‐Uchida, Daniel Oliveira Santana, Daniel Salas Johnson, Danielle Katharine Petsch, Danielly Torres Hashiguti de Freitas, Dayani Bailly, Débora Ferreira Machado, Débora Reis de Carvalho, Dhyego Hamilton Topan, Diego Cañas‐Rojas, Diego da Silva, Diogo Freitas‐Souza, Dilermando Pereira Lima‐Júnior, Diovani Piscor, Djalma Pereira Moraes, Douglas Viana, Dyego Leonardo Ferraz Caetano, Éder André Gubiani, Edson K. Okada, Eduardo Cazuni do Amaral, Eduardo Meneguzzi Brambilla, Eduardo Ribeiro Cunha, Elaine Antoniassi Luiz Kashiwaqui, Elise Amador Rocha, Elisete Ana Barp, Elmary da Costa Fraga, Elvira D'Bastiani, Eugenia Zandonà, Eurizângela Pereira Dary, Evanilde Benedito, Everardo Barba‐Macías, Evelyn Vanessa Calvache Uvidia, Fabiana Luques Fonseca, Fabiane Silva Ferreira, Fábio Lima, Fábio Maffei, Fábio Porto‐Foresti, Fabrício Barreto Teresa, Fabrício de Andrade Frehse, Fagner Júnior M. Oliveira, Felipe Pessoa da Silva, Felipe Pontieri de Lima, Fernanda Dotti do Prado, Fernando Camargo Jerep, Fernando Emmanuel Gonçalves Vieira, Fernando Gertum Becker, Fernando Rogério de Carvalho, Flávio Kulaif Ubaid, Francisco Keilo Teixeira, Francisco Provenzano Rizzi, Francisco Severo‐Neto, Francisco Villamarín, Franco Teixeira de Mello, Friedrich Wolfgang Keppeler, Gabriel de Avila Batista, Gabriel de Menezes Yazbeck, Giancarlo Tesitore, Gilberto Nepomuceno Salvador, Gita Juan Soteroruda Brito, Giulianna Rondineli Carmassi, Gregório Kurchevski, Guillermo Goyenola, Hasley Rodrigo Pereira, Helen Jamille Fernandes Silva Alvez, Helena Alves do Prado, Henrique Ledo Lopes Pinho, Híngara Leão Sousa, Hugo Bornatowski, Hugo de Oliveira Barbosa, Ibon Tobes, Igor de Paiva Affonso, Igor Raposo Queiroz, Irma Vila, Iván Vinicio Jácome Negrete, Ivo Gavião Prado, Jean Ricardo Simões Vitule, Jessé Figueiredo‐Filho, Jessica Antúnez Gonzalez, Jéssica Caroline de Faria Falcão, Jéssica Vieira Teixeira, Jimmy Pincheira‐Ulbrich, Jislaine Cristina da Silva, João Antonio de Araujo Filho, João Fernando Marques da Silva, João Gabriel Genova, João Gabriel Ribeiro Giovanelli, João Vitor Perin Andriola, Jonatas Alves, Jonathan Valdiviezo‐Rivera, Jorge Brito, Jorge Iván Sánchez Botero, Jorge Liotta, Jorge Luis Ramirez, Jorge Reppold Marinho, José Luís Olivan Birindelli, Jose Luis Costa Novaes, Joseph E. Hawes, Josiane Ribolli, Juan Francisco Rivadeneira, Juan Jacobo Schmitter‐Soto, Juliana Camara Assis, Juliana Paulo da Silva, Juliana Silveira dos Santos, Juliana Wingert, Juliana Wojciechowski, Juliano André Bogoni, Juliano Ferrer, Julio César Jut Solórzano, Júlio César Sá‐Oliveira, Jussara Oliveira Vaini, Kamila Contreras Palma, Karine Orlandi Bonato, Karla Dayane de Lima Pereira, Kassiano dos Santos Sousa, Kevin Giancarlo Borja‐Acosta, Laís Carneiro, Larissa Faria, Leonardo Brito de Oliveira, Leonardo Cardoso Resende, Leonardo Ferreira da Silva Ingenito, Leonardo Oliveira Silva, Leydiane Nunes Rodrigues, Lida Guarderas‐Flores, Lidiane Martins, Lorena Tonini, Lorrana Thaís Máximo Durville Braga, Louise Cristina Gomes, Lucas de Fries, Lucas Gonçalves da Silva, Lucas Ribeiro Jarduli, Luciano Benedito Lima, Luciano Gomes Fischer, Luciano Lazzarini Wolff, Luciano Neves dos Santos, Luis Artur Valões Bezerra, Luisa Maria Sarmento Soares, Luisa Resende Manna, Luiz Fernando Duboc, Luiz Guilherme dos Santos Ribas, Luiz Roberto Malabarba, Marcelo Fulgêncio Guedes Brito, Marcelo Rennó Braga, Marcelo Silva de Almeida, Maria Cecília Sily, Maria Claudene Barros, Maria Histelle Sousa do Nascimento, Maria Laura de Souza Delapieve, Maria Teresa Fernandez Piedade, Marina Tagliaferro, Mário Cesar Cardoso de Pinna, Mario H. Yánez‐Muñoz, Mário Luís Orsi, Marlon Ferraz da Rosa, Marlos Bastiani, Marta Severino Stefani, Martha Buenaño‐Carriel, Martha Elena Valdez Moreno, Mateus Moreira de Carvalho, Mateus Tavares Kütter, Matheus Oliveira Freitas, Mauricio Cañas‐Merino, Mauricio Cetra, Mauricio Herrera‐Madrid, Mauricio Mello Petrucio, Mauro Galetti, Miguel Ángel Salcedo, Miguel Pascual, Milton Cezar Ribeiro, Milza Celi Fedatto Abelha, Mônica Andrade da Silva, Mônica Pacheco de Araujo, Murilo Sversut Dias, Naiara Guimaraes Sales, Naraiana Loureiro Benone, Natane Sartor, Nelson Ferreira Fontoura, Nicholas Silvestre de Souza Trigueiro, Nicolás Álvarez‐Pliego, Oscar Akio Shibatta, Pablo A. Tedesco, Pablo Cesar Lehmann Albornoz, Pablo Henrique Fernandes Santos, Pâmela Virgolino Freitas, Patricia Calegari Fagundes, Patrícia Domingues de Freitas, Patricio Mena‐Valenzuela, Paul Tufiño, Paula Araujo Catelani, Paula Peixoto, Paulo Ilha, Pedro De Podestà Uchôa de Aquino, Pedro Gerhard, Pedro Hollanda Carvalho, Pedro Jiménez‐Prado, Pedro Manoel Galetti, Pedro Paulino Borges, Pedro Peixoto Nitschke, Pedro Sartori Manoel, Phamela Bernardes Perônico, Philip Teles Soares, Pitágoras Augusto Piana, Priscila de Oliveira Cunha, Priscila Plesley, Rafael Couto Rosa de Souza, Rafael Rogério Rosa, Rana W. El‐Sabaawi, Raoni Rosa Rodrigues, Raphael Covain, Raquel Coelho Loures, Raul Rennó Braga, Reginaldo Ré, Rémy Bigorne, Renata Cassemiro Biagioni, Renato Azevedo Matias Silvano, Renato Bolson Dala‐Corte, Renato Tavares Martins, Ricardo Rosa, Ricardo Sartorello, Rodrigo de Almeida Nobre, Ronald D. Bassar, Ronaldo César Gurgel‐Lourenço, Ronaldo Fernando Martins Pinheiro, Ronaldo Leal Carneiro, Rosa Florido, Rosana Mazzoni, Rosane Silva‐Santos, Rosiane de Paula Santos, Rosilene Luciana Delariva, Sandra Maria Hartz, Sebastien Brosse, Sérgio Luiz Althoff, Shaka Nóbrega Marinho Furtado, Sidnei Eduardo Lima‐Junior, Silvia Yasmin Lustosa Costa, Solange Arrolho, Sonya K. Auer, Sybelle Bellay, Taís de Fátima Ramos Guimarães, Talitha Mayumi Francisco, Tatiane Mantovano, Tatyana Gomes, Telton Pedro Anselmo Ramos, Thaís de Assis Volpi, Thais Moura Emiliano, Thiago Augusto Pedroso Barbosa, Thiago José Balbi, Thiago Nascimento da Silva Campos, Thiago Teixeira Silva, Thiago Vinícius Trento Occhi, Thiely Oliveira Garcia, Tiago Magalhães da Silva Freitas, Tiago Octavio Begot, Tony Leandro Rezende da Silveira, Ueslei Lopes, Uwe Horst Schulz, Valéria Fagundes, Valéria Flávia Batista da Silva, Valter M. Azevedo‐Santos, Vanessa Ribeiro, Vanessa Graciele Tibúrcio, Vera Lúcia Lescano de Almeida, Victoria J. Isaac‐Nahum, Vinicius Abilhoa, Vinicius Farias Campos, Vinicius Tavares Kütter, Vivian de Mello Cionek, Viviane Prodocimo, Wagner Vicentin, Waldney Pereira Martins, Walna Micaelle de Moraes Pires, Weferson Júnio da Graça, Welber Senteio Smith, Wesley Dáttilo, Windsor Efren Aguirre Maldonado, Yuri Gomes Ponce de Carvalho Rocha, Yzel Rondon Súarez, and Zilda Margarete Seixas de Lucena

Subjects
biodiversity hotspot, ichthyology, Landschapsarchitectuur en Ruimtelijke Planning, Landscape Architecture and Spatial Planning, conservation, species distribution, Neotropical region, occurrence, Ecology, Evolution, Behavior and Systematics, data paper
Abstract

The Neotropical region hosts 4225 freshwater fish species, ranking first among the world's most diverse regions for freshwater fishes. Our NEOTROPICAL FRESHWATER FISHES data set is the first to produce a large-scale Neotropical freshwater fish inventory, covering the entire Neotropical region from Mexico and the Caribbean in the north to the southern limits in Argentina, Paraguay, Chile, and Uruguay. We compiled 185,787 distribution records, with unique georeferenced coordinates, for the 4225 species, represented by occurrence and abundance data. The number of species for the most numerous orders are as follows: Characiformes (1289), Siluriformes (1384), Cichliformes (354), Cyprinodontiformes (245), and Gymnotiformes (135). The most recorded species was the characid Astyanax fasciatus (4696 records). We registered 116,802 distribution records for native species, compared to 1802 distribution records for nonnative species. The main aim of the NEOTROPICAL FRESHWATER FISHES data set was to make these occurrence and abundance data accessible for international researchers to develop ecological and macroecological studies, from local to regional scales, with focal fish species, families, or orders. We anticipate that the NEOTROPICAL FRESHWATER FISHES data set will be valuable for studies on a wide range of ecological processes, such as trophic cascades, fishery pressure, the effects of habitat loss and fragmentation, and the impacts of species invasion and climate change. There are no copyright restrictions on the data, and please cite this data paper when using the data in publications.

Published
2023

15. First observation of long-lived π+π− atoms

Author

B. Adeva, L. Afanasyev, A. Anania, S. Aogaki, A. Benelli, V. Brekhovskikh, T. Cechak, M. Chiba, P. Chliapnikov, P. Doskarova, D. Drijard, A. Dudarev, M. Duma, D. Dumitriu, D. Fluerasu, A. Gorin, O. Gorchakov, K. Gritsay, C. Guaraldo, M. Gugiu, M. Hansroul, Z. Hons, S. Horikawa, Y. Iwashita, V. Karpukhin, J. Kluson, M. Kobayashi, V. Kruglov, L. Kruglova, A. Kulikov, E. Kulish, A. Kuptsov, A. Lamberto, A. Lanaro, R. Lednicky, C. Mariñas, J. Martincik, L. Nemenov, M. Nikitin, K. Okada, V. Olchevskii, V. Ovsiannikov, M. Pentia, A. Penzo, M. Plo, P. Prusa, G. Rappazzo, A. Romero Vidal, A. Ryazantsev, V. Rykalin, J. Saborido, J. Schacher, A. Sidorov, J. Smolik, F. Takeutchi, L. Tauscher, T. Trojek, S. Trusov, T. Urban, T. Vrba, V. Yazkov, Y. Yoshimura, M. Zhabitsky, and P. Zrelov

Subjects
Physics, QC1-999
Abstract

After observing and investigating the double-exotic (a double-exotic atom is a bound system, in which both oppositely charged components are unstable particles like μ,π,K,…) π+π− atom with the ground state lifetime τ of about 3×10−15 s, the upgraded DIRAC experiment at the CERN PS accelerator observes for the first time long-lived states of the same atom with lifetimes of about 10−11 s and more. The number of characteristic pion pairs resulting from the breakup (ionisation) of long-lived π+π− atoms amounts to 436±61, corresponding to a signal-to-error ratio of better than 7 standard deviations. This observation opens a new possibility to measure energy differences between p and s atomic states and so to determine ππ scattering lengths.

Published
2015
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16. Lysine acetylation regulates the interaction between proteins and membranes

Author

Leona Berndt, Elena Vazquez-Sarandeses, Arthur Alves de Melo, Kazuki Teranishi, Ralf Langen, Mark R. Ambroso, Michael Lammers, Daniel Merken, Oliver Daumke, Ian S. Haworth, Joo-Yeun Lee, Alan K Okada, Jose Mario Isas, Karen Chang, and Priyatama Pandey

Subjects
Cancer Research, Science, Lysine, General Physics and Astronomy, Nerve Tissue Proteins, Membrane curvature, complex mixtures, Article, General Biochemistry, Genetics and Molecular Biology, Membrane biophysics, Computational biophysics, Animals, Membrane lipids, Multidisciplinary, Chemistry, Peripheral membrane protein, Acetylation, General Chemistry, Subcellular localization, Cell biology, Membrane, Membrane protein, Mutation, Amphiphysin, bacteria, Drosophila, 500 Naturwissenschaften und Mathematik::540 Chemie::540 Chemie und zugeordnete Wissenschaften, Function (biology)
Abstract

Lysine acetylation regulates the function of soluble proteins in vivo, yet it remains largely unexplored whether lysine acetylation regulates membrane protein function. Here, we use bioinformatics, biophysical analysis of recombinant proteins, live-cell fluorescent imaging and genetic manipulation of Drosophila to explore lysine acetylation in peripheral membrane proteins. Analysis of 50 peripheral membrane proteins harboring BAR, PX, C2, or EHD membrane-binding domains reveals that lysine acetylation predominates in membrane-interaction regions. Acetylation and acetylation-mimicking mutations in three test proteins, amphiphysin, EHD2, and synaptotagmin1, strongly reduce membrane binding affinity, attenuate membrane remodeling in vitro and alter subcellular localization. This effect is likely due to the loss of positive charge, which weakens interactions with negatively charged membranes. In Drosophila, acetylation-mimicking mutations of amphiphysin cause severe disruption of T-tubule organization and yield a flightless phenotype. Our data provide mechanistic insights into how lysine acetylation regulates membrane protein function, potentially impacting a plethora of membrane-related processes., Lysine acetylation regulates the function of soluble proteins in vivo, yet it remains largely unexplored whether lysine acetylation regulates the function of membrane proteins. Here, the authors map lysine acetylation predominantly in membrane-interaction regions in peripheral membrane proteins and show with three candidate proteins how lysine acetylation is a regulator of membrane protein function.

Published
2021

17. Different mechanism of two-proton emission from proton-rich nuclei 23Al and 22Mg

Author

Y.G. Ma, D.Q. Fang, X.Y. Sun, P. Zhou, Y. Togano, N. Aoi, H. Baba, X.Z. Cai, X.G. Cao, J.G. Chen, Y. Fu, W. Guo, Y. Hara, T. Honda, Z.G. Hu, K. Ieki, Y. Ishibashi, Y. Ito, N. Iwasa, S. Kanno, T. Kawabata, H. Kimura, Y. Kondo, K. Kurita, M. Kurokawa, T. Moriguchi, H. Murakami, H. Ooishi, K. Okada, S. Ota, A. Ozawa, H. Sakurai, S. Shimoura, R. Shioda, E. Takeshita, S. Takeuchi, W.D. Tian, H.W. Wang, J.S. Wang, M. Wang, K. Yamada, Y. Yamada, Y. Yasuda, K. Yoneda, G.Q. Zhang, and T. Motobayashi

Subjects
Physics, QC1-999
Abstract

Two-proton relative momentum (qpp) and opening angle (θpp) distributions from the three-body decay of two excited proton-rich nuclei, namely Al23→p+p+Na21 and Mg22→p+p+Ne20, have been measured with the projectile fragment separator (RIPS) at the RIKEN RI Beam Factory. An evident peak at qpp∼20 MeV/c as well as a peak in θpp around 30° are seen in the two-proton break-up channel from a highly-excited 22Mg. In contrast, such peaks are absent for the 23Al case. It is concluded that the two-proton emission mechanism of excited 22Mg is quite different from the 23Al case, with the former having a favorable diproton emission component at a highly excited state and the latter dominated by the sequential decay process.

Published
2015
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18. Association between prognosis and the use of angiotensin-converting enzyme inhibitors and/or angiotensin II receptor blocker in frail patients with heart failure with preserved ejection fraction

Author

A Sunaga, S Hikoso, S Tamaki, M Yano, T Hayashi, B Oeun, H Kida, Y Sotomi, T Dohi, K Okada, H Mizuno, D Nakatani, T Yamada, Y Yasumura, and Y Sakata

Subjects
Cardiology and Cardiovascular Medicine
Abstract

Background The effectiveness of angiotensin-converting enzyme inhibitors (ACE-I) and angiotensin II receptor blockers (ARB) has not been demonstrated in patients with heart failure with preserved ejection fraction (HFpEF). We recently reported significant interaction between the use of ACE-I and/or ARB (ACE-I/ARB) and frailty on prognosis in patients with HFpEF. Purpose In the present study, we examined the association between ACE-I/ARB and prognosis in patients with HFpEF stratified by the presence or absence of frailty. Methods We examined the association between the use of ACE-I/ARB and prognosis according to the presence (Clinical Frailty Scale (CFS) ≥5) or absence (CFS ≤4) of frailty in patients with HFpEF in a post-hoc analysis of registry data. Primary endpoint was the composite of all-cause mortality and heart failure admission. Secondary endpoints were all-cause mortality and heart failure admission. Results Of 1059 patients, median age was 83 years and 45% were male. Kaplan-Meier analysis showed that the risk of composite endpoint (log-rank P=0.001) and all-cause death (log-rank P=0.005) in patients with ACE-I/ARB was lower in those with CFS ≥5, but similar between patients with and without ACE-I/ARB in patients with CFS ≤4 (composite endpoint: log-rank P=0.830; all-cause death: log-rank P=0.192). In a multivariable Cox proportional hazards model, use of ACE-I/ARB was significantly associated with lower risk of the composite endpoint (hazard ratio = 0.52, 95% CI: 0.33–0.83, P=0.005) and heart failure admission (hazard ratio = 0.45, 95% CI: 0.25–0.83, P=0.010) in patients with CFS ≥5, but not in patients with CFS ≤4 (composite endpoint: hazard ratio = 1.41, 95% CI: 0.99–2.02, P=0.059; heart failure admission: hazard ratio = 1.43, 95% CI: 0.94–2.18, P=0.091). The association between ACE-I or ARB and prognosis did not significantly differ by CFS (CFS ≤4: log-rank P=0.562; CFS ≥5: log-rank P=0.100, for with ACE-I vs. ARB, respectively). Adjusted HRs for CFS 1–4 were higher than 1.0, but were less than 1.0 at CFS 5. Conclusions In patients with HFpEF, use of ACE-I/ARB was associated with better prognosis in patients with frailty as assessed with the CFS, but not in those without frailty. Funding Acknowledgement Type of funding sources: Private company. Main funding source(s): Roche

Published
2022

19. Clinical trajectory and outcomes of patients with heart failure with preserved ejection fraction with normal or indeterminate diastolic function

Author

B Oeun, S Hikoso, D Nakatani, K Okada, T Dohi, Y Sotomi, H Kida, A Sunaga, T Sato, M Seo, M Yano, T Hayashi, T Yamada, Y Yasumura, and Y Sakata

Subjects
Cardiology and Cardiovascular Medicine
Abstract

Background Heart failure (HF) with preserved ejection fraction (HFpEF) is a chronic and progressive disease, but limited therapeutic strategies are currently available. Although left ventricular diastolic dysfunction (DD) is a prominent mechanism of HFpEF, a certain number of patients with HFpEF have a normal diastolic function (ND) or indeterminate diastolic function (ID). With the progressive nature of HFpEF, diastolic function may change over time. However, the change of diastolic function, its predictor and prognosis in patients with clinically established HFpEF remains unknown. Purpose To investigate the clinical trajectory and outcomes of patients with HFpEF with ND or ID and to identify factors associated with progression from ND or ID at discharge to DD at 1-year follow-up. Methods Using data from a prospective multicenter observational study of patients with HFpEF, we extracted 289 patients with HFpEF with ND or ID at discharge who had echocardiographic data at 1-year follow-up for the re-evaluation of diastolic function. Diastolic function was assessed according to the 2016 American Society of Echocardiography recommendations. Patients were classified according to the absence or presence of progression from ND or ID to DD at 1 year. The primary endpoint was a composite of all-cause death and HF rehospitalization. Results Median age was 81 years, and 138 (47.8%) patients were female. At 1 year, 107 (37%) patients progressed to DD. During a median follow-up of 709 days, the composite endpoint occurred in 90 (31.1%) patients. Compared to patients without progression to DD, those with progression to DD had a significantly higher cumulative incidence rate of the composite endpoint (incidence rate: 11.7/100 person-year versus 23.3/100 person-year, P Conclusion More than one-third of patients with HFpEF with ND or ID progressed to DD at 1 year and had poor clinical outcomes. Age, BMI, and serum albumin were independently associated with this progression. Funding Acknowledgement Type of funding sources: Public grant(s) – National budget only. Main funding source(s): This work was supported by grants from Japan Society for the Promotion of Science KAKENHI (No. JP 17K09496) and Japan Agency for Medical Research and Development (No. JP16lk1010013).

Published
2022

20. Premature atrial contraction on Holter electrocardiogram predicts the recurrence of atrial fibrillation after catheter ablation

Author

A Sunaga, N Tanaka, M Masuda, T Watanabe, H Kida, B Oeun, T Sato, Y Sotomi, T Dohi, K Okada, H Mizuno, D Nakatani, S Hikoso, K Inoue, and Y Sakata

Subjects
Cardiology and Cardiovascular Medicine
Abstract

Introduction It is important to detect the recurrence of atrial fibrillation (AF) after catheter ablation (CA) early, but the method of detection has not been established. The purpose of this study is to determine whether 24-h Holter electrocardiogram (ECG) can predict the recurrence of AF after CA. Methods We studied 336 patients of 497 patients enrolled in EARNEST-PVI trial to investigate whether the total number of premature atrial contraction (PAC) and the maximum number of PAC run by 24-h Holter ECG at 6 months after CA predicted AF recurrence after 6 months. We excluded 86 patients with recurrence by 6 months after CA and 75 patients without Holter ECG at 6 months after CA. Results Median age was 66 years, male were 77% and median follow-up period was 1138 days. Receiver operating characteristic curve analysis identified the total number of PAC ≥270 beats and the maximum number of PAC run ≥8 beats as the optimal cutoff for prediction of AF recurrence. Kaplan-Meier analysis showed patients with the total number of PAC ≥270 beats had more frequent AF recurrence than those without (Kaplan-Meier estimated 3-year AF recurrence rate 34% vs. 17%, Log-rank P=0.001) and patients with the maximum number of PAC run ≥8 beats had more frequent AF recurrence than those without (Kaplan-Meier estimated 3-year AF recurrence rate 33% vs. 20%, Log-rank P=0.006). Multivariate analysis revealed that the total number of PAC ≥270 beats and the maximum number of PAC run were significantly associated with AF recurrence (hazard ratio [95% confidence interval] 1.83 [1.16–2.91], P=0.01 and 1.01 [1.01–1.02], P=0.001, respectively) Conclusion The total number of PAC and the maximum number of PAC run on the Holter ECG may be useful in predicting AF recurrence after CA. Funding Acknowledgement Type of funding sources: None.

Published
2022

21. Aging and growth parameter from the Piaractus mesopotamicus (pacu) from the Cuiabá river, Mato Grosso, Brazil

Author

Angela M. Ambrosio, Thiago J. Balbi, Talitha M. Francisco, Luiz C. Gomes, Marina S. Zuliani, and Edson K. Okada

Subjects
Marcas de aposição, escamas, modelo de von Bertalanffy, Ford-walford, Zoology, QL1-991
Abstract

This study has aims to determine the age and to estimate the growth parameters using scales of the species. Individuals of Piaractus mesopotamicus (Holmberg, 1887) used in this study were captured in the commercial fishery conducted in the region, along the year 2006. The model selected to express the growth of the species was the von Bertalanffy Sl= Sl∞*[1-exp-k(t-to)]. To determine if scales are suitable for studying the growth of pacu, we analyzed the relation between standard length (Sl) and the radius of the scales through linear regression. The period of annuli formation was determined analyzing the variations in the marginal increment and evaluating the consistency of the readings through the analysis of the coefficient of variations (CVs) for the average standard lengths of each age (number of rings) observed in the scales. The relationship between Ls of the fish and the radius of the scales showed that scales can be used to study the age and growth of P. mesopotamicus (R= 0.79). CVs were always below 20%, demonstrating the consistency of the readings. Annuli formation occurred in February, probably related to trophic migration that occurs in this month in the region. Equations that represents the growth in length obtained for P. mesopotamicus are Sl=50.00*[1-exp-0.18(t-(-3.00)] for males and Sl=59.23*[1-exp-0.14(t-(-3.36)] for females. The growth parameters obtained in this study were lower compared to other studies previously conducted for the same species and can related to overexploitation that species is submitted by fishing in the region. These values show also that females of pacu attain greater asymptotic length than males that growth faster.

Published
2014
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25. Short communication: Detection of mastication speed during rumination in cattle using 3-axis, neck-mounted accelerometers and fast Fourier transfer algorithm

Author

K. Okada, T. Tamura, and Y. Chida

Subjects
Holstein Cattle, Computer science, Fast Fourier transform, Accelerometer, 03 medical and health sciences, Accelerometry, Genetics, medicine, Animals, Mastication, 030304 developmental biology, 0303 health sciences, Fourier Analysis, Spectrum Analysis, Limits of agreement, 0402 animal and dairy science, 04 agricultural and veterinary sciences, 040201 dairy & animal science, Vibration, Rumination, Cattle, Female, Animal Science and Zoology, Spectrum analysis, medicine.symptom, Algorithm, Algorithms, Food Science
Abstract

There have been limited reports on mastication speed during cattle rumination. The objective of this study was to establish a method to detect mastication speed based on data obtained during rumination through the use of a 3-axis accelerometer attached to the neck. A 3-axis accelerometer was attached to 6 dry Holstein cattle. When rumination behavior was observed, the accelerometer and the high-speed camera simultaneously recorded acceleration at the neck and moving image of the head movement. Based on the number of mastication movements recorded on video, mastication speed A was calculated. Data obtained from the 3-axis accelerometer were analyzed with fast Fourier transfer algorithm and identified as mastication speed B. The vibration of the neck recorded in the accelerometer during rumination was considered as mastication movement. Using Bland-Altman plot analysis, the mean difference between mastication speed A and mastication speed B was 0.041 s/bite, and the 95% limits of agreement ranged from -0.080 to 0.161. Since mastication movement occurred periodically, it was possible to detect the movement using spectrum analysis, as mastication speed B. Although there were some differences between calculated speeds and speeds obtained from spectrum analysis, there was clinical compatibility between mastication speed A and B. This study showed the feasibility of establishing a detection method for mastication speed during rumination, which might provide a basic procedure for studying the purpose of mastication and the variable factors involved.

Published
2020

26. Perioperative strategies for the reduction of postoperative pulmonary complications

Author

Charles J. Fox, Rachel J. Kaye, Alan D. Kaye, Alex D. Pham, Richard D. Urman, Anusha Kallurkar, Chizoba Mosieri, Lindsey K. Okada, Debbie Chandler, and Elyse M. Cornett

Subjects
Lung Diseases, medicine.medical_specialty, medicine.medical_treatment, Population, Atelectasis, Risk Assessment, Perioperative Care, 03 medical and health sciences, Postoperative Complications, 0302 clinical medicine, Risk Factors, 030202 anesthesiology, medicine, Humans, Intensive care medicine, education, Early Ambulation, Mechanical ventilation, education.field_of_study, Lung, business.industry, Smoking, Perioperative, medicine.disease, Asthma, Respiratory Function Tests, Pneumonia, Anesthesiology and Pain Medicine, medicine.anatomical_structure, Respiratory failure, Bronchitis, business, 030217 neurology & neurosurgery
Abstract

Postoperative pulmonary complications (PPCs), estimated between 2.0% and 5.6% in the general surgical population and 20-70% for upper abdominal and thoracic surgeries, are a significant factor leading to poor patient outcomes. Efforts to decrease the incidence of PPCs such as bronchospasm, atelectasis, exacerbations of underlying chronic lung conditions, infections (bronchitis and pneumonia), prolonged mechanical ventilation, and respiratory failure, begins with a detailed preoperative risk evaluation. There are several available preoperative tests to estimate the risk of PPCs. However, the value of some of these studies to estimate PPCs remains controversial and is still debated. In this review, the preoperative risk assessment of PPCs is examined along with preoperative pulmonary tests to estimate risk, intraoperative, and procedure-associated risk factors for PPCs, and perioperative strategies to decrease PPCs. The importance of minimizing these events is reflected in the fact that nearly 25% of postoperative deaths occurring in the first week after surgery are associated with PPCs. This review provides important information to help clinical anesthesiologists to recognize potential risks for pulmonary complications and allows strategies to create an appropriate perioperative plan for patients.

Published
2020

27. Cryptic Species Account for the Seemingly Idiosyncratic Secondary Metabolism of Sarcophyton glaucum Specimens Collected in Palau

Author

Pieter C. Dorrestein, Christopher A. Leber, Marcy J. Balunas, Bethany K Okada, Kim Quach, Camille M. Sultana, Catherine S. McFadden, Viqqi Kurnianda, Robert M. Samples, Oscar Alvarado, Charlie Brayton, Andrés Mauricio Caraballo-Rodríguez, Sydney R Davis, Taylor S Davis, Junichi Tanaka, J Chance Crompton, Vincent Shieh, Samantha M. Gromek, Katherine N. Maloney, Ryan T. Botts, Brent J.-A. Chicoine, Jason V. Chari, and Elizabeth M Maloney

Subjects
Pharmacology, Species complex, biology, Phylogenetic tree, 010405 organic chemistry, Sarcophyton, Organic Chemistry, Pharmaceutical Science, Zoology, Interspecific competition, biology.organism_classification, 01 natural sciences, Intraspecific competition, 0104 chemical sciences, Analytical Chemistry, 010404 medicinal & biomolecular chemistry, Complementary and alternative medicine, Sarcophyton glaucum, Drug Discovery, Molecular Medicine, Clade, Secondary metabolism
Abstract

Sarcophyton glaucum is one of the most abundant and chemically studied soft corals with over 100 natural products reported in the literature, primarily cembrane diterpenoids. Yet, wide variation in the chemistry observed from S. glaucum over the past 50 years has led to its reputation as a capricious producer of bioactive metabolites. Recent molecular phylogenetic analysis revealed that S. glaucum is not a single species but a complex of at least seven genetically distinct species not distinguishable using traditional taxonomic criteria. We hypothesized that perceived intraspecific chemical variation observed in S. glaucum was actually due to differences between cryptic species (interspecific variation). To test this hypothesis, we collected Sarcophyton samples in Palau, performed molecular phylogenetic analysis, and prepared chemical profiles of sample extracts using gas chromatography-flame ionization detection. Both unsupervised (principal component analysis) and supervised (linear discriminant analysis) statistical analyses of these profiles revealed a strong relationship between cryptic species membership and chemical profiles. Liquid chromatography with tandem mass spectrometry-based analysis using feature-based molecular networking permitted identification of the chemical drivers of this difference between clades, including cembranoid diterpenes (2R,11R,12R)-isosarcophytoxide (5), (2S,11R,12R)-isosarcophytoxide (6), and isosarcophine (7). Our results suggest that early chemical studies of Sarcophyton may have unknowingly conflated different cryptic species of S. glaucum, leading to apparently idiosyncratic chemical variation.

Published
2020

28. Bulk evidence of anisotropic $s$-wave pairing with no sign change in the kagome superconductor CsV$_3$Sb$_5$

Author

M. Roppongi, K. Ishihara, Y. Tanaka, K. Ogawa, K. Okada, S. Liu, K. Mukasa, Y. Mizukami, Y. Uwatoko, R. Grasset, M. Konczykowski, B. R. Ortiz, S. D. Wilson, K. Hashimoto, T. Shibauchi, University of Tokyo [Kashiwa Campus], Institute for Solid State Physics [Tokyo] (ISSP), The University of Tokyo (UTokyo), Laboratoire des Solides Irradiés (LSI), Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-École polytechnique (X)-Centre National de la Recherche Scientifique (CNRS), Défauts, Désordre et Structuration de la Matière (DDSM), Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-École polytechnique (X)-Centre National de la Recherche Scientifique (CNRS)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-École polytechnique (X)-Centre National de la Recherche Scientifique (CNRS), University of California [Santa Barbara] (UC Santa Barbara), and University of California (UC)

Subjects
[PHYS.COND.CM-S]Physics [physics]/Condensed Matter [cond-mat]/Superconductivity [cond-mat.supr-con], Superconductivity (cond-mat.supr-con), Condensed Matter - Strongly Correlated Electrons, Multidisciplinary, Strongly Correlated Electrons (cond-mat.str-el), Condensed Matter - Superconductivity, Condensed Matter::Superconductivity, General Physics and Astronomy, FOS: Physical sciences, General Chemistry, General Biochemistry, Genetics and Molecular Biology
Abstract

The recently discovered kagome superconductors $A$V$_3$Sb$_5$ ($A$ = K, Rb, Cs) possess a unique band structure with van Hove singularities and Dirac dispersions, in which unusual charge-density-wave (CDW) orders with time-reversal and rotational symmetry breaking have been reported. One of the most crucial unresolved issues is identifying the symmetry of the superconductivity that develops inside the CDW phase. Theory predicts a variety of unconventional superconducting symmetries, including exotic states with chiral and topological properties accompanied by a sign-changing superconducting gap. Experimentally, however, the phase information on the superconducting gap in $A$V$_3$Sb$_5$ is still lacking. Here we report the electron irradiation effects in CsV$_3$Sb$_5$ using introduced impurities as a phase-sensitive probe of superconductivity. Our magnetic penetration depth measurements reveal that with increasing impurities, a highly anisotropic fully-gapped state changes gradually to an isotropic full-gap state without passing through a nodal state. Furthermore, transport measurements under high pressure show that the double superconducting dome in the pressure-temperature phase diagram survives against sufficient impurities. These results are strong bulk evidence that CsV$_3$Sb$_5$ is a non-chiral, anisotropic $s$-wave superconductor with no sign change both at ambient and high pressure, which provides a clue to understanding the relationship between CDW and superconductivity in kagome superconductors., Comment: 22 pages, 4 figures

Published
2022
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29. Age and growth parameters of cachara Pseudoplastystoma reticulatum (Siluriformes, Pimelodidae) from the Cuiabá River, Brazil

Author

Talitha M. Francisco, Angela Maria Ambrósio, Thiago José Balbi, Marina S. Zuliani, Edson K. Okada, and Luiz C. Gomes

Subjects
Marcas de aposição, nadadeira peitoral, modelo de von Bertalanffy, Ford-Walford, Zoology, QL1-991
Abstract

Age and growth parameters of cachara Pseudoplatystoma reticulatum (Eigenmann & Eigenmann, 1889) (Siluriformes, Pimelodidae) (males and females) were estimated through the analysis of growth rings in spines of pectoral fins. Fish were collected from January to December 2007, in the area directly influenced by the Aproveitamento Múltiplo de Manso (APM Manso) and in the Cuiabá River (upper parts of the Pantanal). The maximum number of growth rings was seven for males, and eight, for females. The analysis of temporal variations in mean marginal increment showed that rings found in the spines were formed annually, in December. Growth rings were associated to spawning (in the study region from November to March) of the species. The growth curve in length was obtained by the von Bertalanffy model adjusted by the Ford-Walford transformation. The equations are: Ls = 72.7*[1-e-0.44(t+1.5974)] for males, and Ls = 84.5*[1-e-0.33(t+2.0943)] for females. The equations that describe the growth curve in weight are: Wt = 4991.61*[1-e-0.44 (t+1.5974] 2.70 for males and Wt = 7503.17*[1-e-0.33 (t+2.0943] 2.99 for females.

Published
2011
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30. Genome reprogramming during the first cell cycle in in vitro produced porcine embryos

Author

I. Barnetová and K. Okada

Subjects
epigenetics, pig, icsi, ivf, methylation, Animal culture, SF1-1100
Abstract

Conflicting data still exist regarding the extent of paternal pronuclear DNA demethylation in one cell-stage mammalian embryos. Demethylation of paternal pronuclear DNA was observed in in vitro produced porcine zygotes, whereas in vitro produced embryos do not show any or only weak paternal genome demethylation. In our experiments, we have used and compared two in vitro techniques commonly used for in vitro embryo production (in vitro fertilization and intracytoplasmic sperm injection) and then we evaluated the extent of labelling in both these groups after 5-methylcytosine (5-MeC) or dimethyl H3/K9 labelling. We have found no differences in the methylation pattern between both those techniques used for the production of embryos. Moreover, we did not detect any demethylation of paternal DNA after 5-MeC labelling at all. Contrary to this, labelling with dimethyl H3/K9 antibodies showed differences in labelling intensity between maternal and paternal genomes in 42% of zygotes after in vitro fertilization and in 44% of zygotes after intracytoplasmic sperm injection. Our results indicate that in vitro matured pig oocytes exhibit rather inconsistent methylation patterns. This inconsistency probably resulted from insufficient cytoplasmic maturation of oocytes and to a lesser extent from the in vitro technique for embryo production.

Published
2010
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31. Guided Wave Transceive Technique Using Magnetostrictive Effect of STPG370 Pipe itself and High-Temperature Superconductor SQUID

Author

K Watanabe, K Okada, S Masumitsu, T Munkhnyam, W Sun, Y Hatsukade, Y Shoyama, and A Tomotoshi

Subjects
History, Computer Science Applications, Education
Abstract

We developed a non-contacting ultrasonic guided wave testing technique using magnetostrictive effects and high-temperature superconductor (HTS) SQUID for STPG370 steel pipes. A pair of C-shaped electromagnets was used to magnetize the STPG370 pipe while rotating the pipe, in order to give uniform remnant fields as bias fields. Conditions to give larger remnant field in the pipe were investigated using an electromagnetic field simulation. The simulation results indicated that C-shaped pb permalloy iron cores with an aperture angle of 20 degree and a diameter of 20 mm should be utilized for the magnetization. An excitation coil was wound around one of the magnetized parts, which is used as a transmitter. One cycle sine current of 9 App at 50 kHz was repeatedly supplied to the coil to generate T(0,1) mode guided waves in the pipe. The other magnetized part, which was used as a receiver, was combined with the HTS-SQUID gradiometer, which was located above the pipe with a lift-off of 4 mm. In measurements, the pipe was rotated to perform all-round measurements. A contour map of the time-series signal distribution of T(0, 1) mode guided wave was obtained around the pipe.

Published
2022

36. Piperacillin triggers virulence factor biosynthesis via the oxidative stress response in

Author

Anran, Li, Bethany K, Okada, Paul C, Rosen, and Mohammad R, Seyedsayamdost

Subjects
Piperacillin, Transcription, Genetic, Burkholderia, Virulence Factors, Secondary Metabolism, Gene Expression Regulation, Bacterial, Biological Sciences, beta-Lactams, Models, Biological, Biosynthetic Pathways, Oxidative Stress, Antibiosis, Reactive Oxygen Species, Oxidation-Reduction
Abstract

Natural products have been an important source of therapeutic agents and chemical tools. The recent realization that many natural product biosynthetic genes are silent or sparingly expressed during standard laboratory growth has prompted efforts to investigate their regulation and develop methods to induce their expression. Because it is difficult to intuit signals that induce a given biosynthetic locus, we recently implemented a forward chemical-genetic approach to identify such inducers. In the current work, we applied this approach to nine silent biosynthetic loci in the model bacterium Burkholderia thailandensis to systematically screen for elicitors from a library of Food and Drug Administration–approved drugs. We find that β-lactams, fluoroquinolones, antifungals, and, surprisingly, calcimimetics, phenothiazine antipsychotics, and polyaromatic antidepressants are the most effective global inducers of biosynthetic genes. Investigations into the mechanism of stimulation of the silent virulence factor malleicyprol by the β-lactam piperacillin allowed us to elucidate the underlying regulatory circuits. Low-dose piperacillin causes oxidative stress, thereby inducing redox-sensing transcriptional regulators, which activate malR, a pathway-specific positive regulator of the malleicyprol gene cluster. Malleicyprol is thus part of the OxyR and SoxR regulons in B. thailandensis, allowing the bacterium to initiate virulence in response to oxidative stress. Our work catalogs a diverse array of elicitors and a previously unknown regulatory input for secondary metabolism in B. thailandensis.

Published
2021

37. Piperacillin triggers virulence factor biosynthesis via the oxidative stress response in Burkholderia thailandensis

Author

Bethany K. Okada, Paul Rosen, Anran Li, and Mohammad R. Seyedsayamdost

Subjects
Genetics, Multidisciplinary, Burkholderia thailandensis, Regulator, Virulence, Biology, biology.organism_classification, Virulence factor, Regulon, Gene cluster, medicine, Secondary metabolism, Piperacillin, medicine.drug
Abstract

Natural products have been an important source of therapeutic agents and chemical tools. The recent realization that many natural product biosynthetic genes are silent or sparingly expressed during standard laboratory growth has prompted efforts to investigate their regulation and develop methods to induce their expression. Because it is difficult to intuit signals that induce a given biosynthetic locus, we recently implemented a forward chemical-genetic approach to identify such inducers. In the current work, we applied this approach to nine silent biosynthetic loci in the model bacterium Burkholderia thailandensis to systematically screen for elicitors from a library of Food and Drug Administration–approved drugs. We find that β-lactams, fluoroquinolones, antifungals, and, surprisingly, calcimimetics, phenothiazine antipsychotics, and polyaromatic antidepressants are the most effective global inducers of biosynthetic genes. Investigations into the mechanism of stimulation of the silent virulence factor malleicyprol by the β-lactam piperacillin allowed us to elucidate the underlying regulatory circuits. Low-dose piperacillin causes oxidative stress, thereby inducing redox-sensing transcriptional regulators, which activate malR, a pathway-specific positive regulator of the malleicyprol gene cluster. Malleicyprol is thus part of the OxyR and SoxR regulons in B. thailandensis, allowing the bacterium to initiate virulence in response to oxidative stress. Our work catalogs a diverse array of elicitors and a previously unknown regulatory input for secondary metabolism in B. thailandensis.

Published
2021

40. The Mitochondrial Peptide Humanin Targets but Does Not Denature Amyloid Oligomers in Type II Diabetes

Author

Joan-Emma Shea, Zachary A. Levine, Ralf Langen, Kazuki Teranishi, and Alan K. Okada

Subjects
chemistry.chemical_classification, endocrine system, Amyloid, Peptidomimetic, Mutant, Intracellular Signaling Peptides and Proteins, Endogeny, Peptide, General Chemistry, Molecular Dynamics Simulation, 010402 general chemistry, Fibril, 01 natural sciences, Biochemistry, Catalysis, Islet Amyloid Polypeptide, Mitochondria, 0104 chemical sciences, Type ii diabetes, Colloid and Surface Chemistry, Diabetes Mellitus, Type 2, chemistry, Biophysics, Humans, Humanin
Abstract

Mitochondrially derived peptides (MDPs) such as humanin (HN) have shown a remarkable ability to modulate neurological amyloids and apoptosis-associated proteins in cells and animal models. Recently, we found that humanin-like peptides also inhibit amyloid formation outside of neural environments in islet amyloid polypeptide (IAPP) fibrils and plaques, which are hallmarks of Type II diabetes. However, the biochemical basis for regulating amyloids through endogenous MDPs remains elusive. One hypothesis is that MDPs stabilize intermediate amyloid oligomers and discourage the formation of insoluble fibrils. To test this hypothesis, we carried out simulations and experiments to extract the dominant interactions between the S14G-HN mutant (HNG) and a diverse set of IAPP structures. Replica-exchange molecular dynamics suggests that MDPs cap the growth of amyloid oligomers. Simulations also indicate that HNG-IAPP heterodimers are 10 times more stable than IAPP homodimers, which explains the substoichiometric ability of HNG to inhibit amyloid growth. Despite this strong attraction, HNG does not denature IAPP. Instead, HNG binds IAPP near the disordered NFGAIL motif, wedging itself between amyloidogenic fragments. Shielding of NFGAIL-flanking fragments reduces the formation of parallel IAPP β-sheets and subsequent nucleation of mature amyloid fibrils. From ThT spectroscopy and electron microscopy, we found that HNG does not deconstruct mature IAPP fibrils and oligomers, consistent with the simulations and our proposed hypothesis. Taken together, this work provides new mechanistic insight into how endogenous MDPs regulate pathological amyloid growth at the molecular level and in highly substoichiometric quantities, which can be exploited through peptidomimetics in diabetes or Alzheimer's disease.

Published
2019

41. PHENIX Collaboration

Author

A. Adare, S. Afanasiev, C. Aidala, N.N. Ajitanand, Y. Akiba, R. Akimoto, H. Al-Bataineh, J. Alexander, M. Alfred, A. Al-Jamel, H. Al-Ta'ani, K.R. Andrews, V. Andrieux, A. Angerami, K. Aoki, N. Apadula, L. Aphecetche, E. Appelt, Y. Aramaki, R. Armendariz, S.H. Aronson, J. Asai, H. Asano, E.C. Aschenauer, E.T. Atomssa, R. Averbeck, T.C. Awes, C. Ayuso, B. Azmoun, V. Babintsev, A. Bagoly, M. Bai, X. Bai, G. Baksay, L. Baksay, A. Baldisseri, N.S. Bandara, B. Bannier, K.N. Barish, P.D. Barnes, B. Bassalleck, A.T. Basye, S. Bathe, S. Batsouli, V. Baublis, F. Bauer, C. Baumann, S. Baumgart, A. Bazilevsky, M. Beaumier, S. Beckman, S. Belikov, R. Belmont, J. Ben-Benjamin, R. Bennett, A. Berdnikov, Y. Berdnikov, J.H. Bhom, A.A. Bickley, M.T. Bjorndal, D. Black, D.S. Blau, M. Boer, J.G. Boissevain, J.S. Bok, H. Borel, K. Boyle, M.L. Brooks, D.S. Brown, D. Broxmeyer, J. Bryslawskyj, D. Bucher, H. Buesching, V. Bumazhnov, G. Bunce, J.M. Burward-Hoy, C. Butler, S. Butsyk, C.M. Camacho, S. Campbell, V. Canoa Roman, A. Caringi, P. Castera, R. Cervantes, J.-S. Chai, B.S. Chang, W.C. Chang, J.-L. Charvet, C.-H. Chen, S. Chernichenko, C.Y. Chi, J. Chiba, M. Chiu, I.J. Choi, J.B. Choi, S. Choi, R.K. Choudhury, P. Christiansen, T. Chujo, P. Chung, A. Churyn, O. Chvala, V. Cianciolo, Z. Citron, C.R. Cleven, Y. Cobigo, B.A. Cole, M.P. Comets, Z. Conesa del Valle, M. Connors, P. Constantin, N. Cronin, N. Crossette, M. Csanád, T. Csörgő, T. Dahms, S. Dairaku, I. Danchev, T.W. Danley, K. Das, A. Datta, M.S. Daugherity, G. David, M.K. Dayananda, M.B. Deaton, K. DeBlasio, K. Dehmelt, H. Delagrange, A. Denisov, D. d'Enterria, A. Deshpande, E.J. Desmond, K.V. Dharmawardane, O. Dietzsch, L. Ding, A. Dion, P.B. Diss, D. Dixit, J.H. Do, M. Donadelli, L. D'Orazio, J.L. Drachenberg, O. Drapier, A. Drees, K.A. Drees, A.K. Dubey, M. Dumancic, J.M. Durham, A. Durum, D. Dutta, V. Dzhordzhadze, S. Edwards, Y.V. Efremenko, J. Egdemir, T. Elder, F. Ellinghaus, W.S. Emam, T. Engelmore, A. Enokizono, H. En'yo, B. Espagnon, S. Esumi, K.O. Eyser, B. Fadem, W. Fan, N. Feege, D.E. Fields, M. Finger, F. Fleuret, S.L. Fokin, B. Forestier, Z. Fraenkel, J.E. Frantz, A. Franz, A.D. Frawley, K. Fujiwara, Y. Fukao, Y. Fukuda, S.-Y. Fung, T. Fusayasu, S. Gadrat, K. Gainey, C. Gal, P. Gallus, P. Garg, A. Garishvili, I. Garishvili, F. Gastineau, H. Ge, M. Germain, F. Giordano, A. Glenn, H. Gong, X. Gong, M. Gonin, J. Gosset, Y. Goto, R. Granier de Cassagnac, N. Grau, S.V. Greene, G. Grim, M. Grosse Perdekamp, Y. Gu, T. Gunji, L. Guo, H. Guragain, H.-Å. Gustafsson, T. Hachiya, A. Hadj Henni, C. Haegemann, J.S. Haggerty, M.N. Hagiwara, K.I. Hahn, H. Hamagaki, J. Hamblen, H.F. Hamilton, R. Han, S.Y. Han, J. Hanks, H. Harada, C. Harper, E.P. Hartouni, K. Haruna, M. Harvey, S. Hasegawa, T.O.S. Haseler, K. Hashimoto, E. Haslum, K. Hasuko, R. Hayano, S. Hayashi, X. He, M. Heffner, T.K. Hemmick, T. Hester, J.M. Heuser, H. Hiejima, J.C. Hill, K. Hill, R. Hobbs, M. Hohlmann, R.S. Hollis, M. Holmes, W. Holzmann, K. Homma, B. Hong, T. Horaguchi, Y. Hori, D. Hornback, T. Hoshino, N. Hotvedt, J. Huang, S. Huang, M.G. Hur, T. Ichihara, R. Ichimiya, J. Ide, H. Iinuma, Y. Ikeda, K. Imai, Y. Imazu, J. Imrek, M. Inaba, Y. Inoue, A. Iordanova, D. Isenhower, L. Isenhower, M. Ishihara, A. Isinhue, T. Isobe, M. Issah, A. Isupov, Y. Ito, D. Ivanishchev, Y. Iwanaga, B.V. Jacak, M. Javani, S.J. Jeon, M. Jezghani, Z. Ji, J. Jia, X. Jiang, J. Jin, O. Jinnouchi, D. John, B.M. Johnson, T. Jones, E. Joo, K.S. Joo, V. Jorjadze, D. Jouan, D.S. Jumper, F. Kajihara, S. Kametani, N. Kamihara, J. Kamin, S. Kanda, M. Kaneta, S. Kaneti, B.H. Kang, J.H. Kang, J.S. Kang, H. Kanou, D. Kapukchyan, J. Kapustinsky, K. Karatsu, S. Karthas, M. Kasai, T. Kawagishi, D. Kawall, M. Kawashima, A.V. Kazantsev, S. Kelly, T. Kempel, J.A. Key, V. Khachatryan, P.K. Khandai, A. Khanzadeev, K. Kihara, K.M. Kijima, J. Kikuchi, A. Kim, B.I. Kim, C. Kim, D.H. Kim, D.J. Kim, E. Kim, E.-J. Kim, G.W. Kim, H.-J. Kim, H.J. Kim, K.-B. Kim, M. Kim, M.H. Kim, S.H. Kim, Y.-J. Kim, Y.K. Kim, Y.-S. Kim, B. Kimelman, D. Kincses, E. Kinney, K. Kiriluk, Á. Kiss, E. Kistenev, R. Kitamura, A. Kiyomichi, J. Klatsky, J. Klay, C. Klein-Boesing, D. Kleinjan, P. Kline, T. Koblesky, L. Kochenda, V. Kochetkov, M. Kofarago, Y. Komatsu, B. Komkov, M. Konno, J. Koster, D. Kotchetkov, D. Kotov, A. Kozlov, A. Král, A. Kravitz, F. Krizek, P.J. Kroon, J. Kubart, S. Kudo, G.J. Kunde, N. Kurihara, K. Kurita, M. Kurosawa, M.J. Kweon, Y. Kwon, G.S. Kyle, R. Lacey, Y.S. Lai, J.G. Lajoie, E.O. Lallow, D. Layton, A. Lebedev, Y. Le Bornec, S. Leckey, B. Lee, D.M. Lee, G.H. Lee, J. Lee, K. Lee, K.B. Lee, K.S. Lee, M.K. Lee, S. Lee, S.H. Lee, S.R. Lee, T. Lee, M.J. Leitch, M.A.L. Leite, M. Leitgab, E. Leitner, B. Lenzi, Y.H. Leung, B. Lewis, N.A. Lewis, X. Li, X.H. Li, P. Lichtenwalner, P. Liebing, H. Lim, S.H. Lim, L.A. Linden Levy, T. Liška, A. Litvinenko, H. Liu, L.D. Liu, M.X. Liu, V.-R. Loggins, S. Lokos, K. Lovasz, B. Love, R. Luechtenborg, D. Lynch, C.F. Maguire, T. Majoros, Y.I. Makdisi, M. Makek, M. Malaev, A. Malakhov, M.D. Malik, A. Manion, V.I. Manko, E. Mannel, Y. Mao, L. Mašek, H. Masuda, H. Masui, S. Masumoto, F. Matathias, M.C. McCain, M. McCumber, P.L. McGaughey, D. McGlinchey, C. McKinney, N. Means, A. Meles, M. Mendoza, B. Meredith, W.J. Metzger, Y. Miake, T. Mibe, J. Midori, A.C. Mignerey, D.E. Mihalik, P. Mikeš, K. Miki, A.J. Miller, T.E. Miller, A. Milov, S. Mioduszewski, D.K. Mishra, G.C. Mishra, M. Mishra, J.T. Mitchell, M. Mitrovski, G. Mitsuka, Y. Miyachi, S. Miyasaka, S. Mizuno, A.K. Mohanty, S. Mohapatra, P. Montuenga, H.J. Moon, T. Moon, Y. Morino, A. Morreale, D.P. Morrison, S.I.M. Morrow, M. Moskowitz, J.M. Moss, S. Motschwiller, T.V. Moukhanova, D. Mukhopadhyay, T. Murakami, J. Murata, A. Mwai, T. Nagae, K. Nagai, S. Nagamiya, K. Nagashima, T. Nagashima, Y. Nagata, J.L. Nagle, M. Naglis, M.I. Nagy, I. Nakagawa, H. Nakagomi, Y. Nakamiya, K.R. Nakamura, T. Nakamura, K. Nakano, S. Nam, C. Nattrass, A. Nederlof, P.K. Netrakanti, J. Newby, M. Nguyen, M. Nihashi, T. Niida, S. Nishimura, B.E. Norman, R. Nouicer, T. Novák, N. Novitzky, R. Novotny, A. Nukariya, A.S. Nyanin, J. Nystrand, C. Oakley, H. Obayashi, E. O'Brien, S.X. Oda, C.A. Ogilvie, H. Ohnishi, H. Oide, I.D. Ojha, M. Oka, K. Okada, O.O. Omiwade, Y. Onuki, J.D. Orjuela Koop, J.D. Osborn, A. Oskarsson, I. Otterlund, G.J. Ottino, M. Ouchida, K. Ozawa, R. Pak, D. Pal, A.P.T. Palounek, V. Pantuev, V. Papavassiliou, B.H. Park, I.H. Park, J. Park, J.S. Park, S. Park, S.K. Park, W.J. Park, S.F. Pate, L. Patel, M. Patel, H. Pei, J.-C. Peng, W. Peng, H. Pereira, D.V. Perepelitsa, G.D.N. Perera, V. Peresedov, D.Yu. Peressounko, C.E. PerezLara, J. Perry, R. Petti, M. Phipps, C. Pinkenburg, R. Pinson, R.P. Pisani, M. Proissl, A. Pun, M.L. Purschke, A.K. Purwar, H. Qu, P.V. Radzevich, J. Rak, A. Rakotozafindrabe, B.J. Ramson, I. Ravinovich, K.F. Read, S. Rembeczki, M. Reuter, K. Reygers, D. Reynolds, V. Riabov, Y. Riabov, E. Richardson, D. Richford, T. Rinn, N. Riveli, D. Roach, G. Roche, S.D. Rolnick, A. Romana, M. Rosati, C.A. Rosen, S.S.E. Rosendahl, P. Rosnet, Z. Rowan, J.G. Rubin, P. Rukoyatkin, J. Runchey, P. Ružička, V.L. Rykov, M.S. Ryu, S.S. Ryu, A.S. Safonov, B. Sahlmueller, N. Saito, T. Sakaguchi, S. Sakai, K. Sakashita, H. Sakata, H. Sako, V. Samsonov, M. Sano, S. Sano, M. Sarsour, H.D. Sato, K. Sato, S. Sato, T. Sato, M. Savastio, S. Sawada, B. Schaefer, B.K. Schmoll, K. Sedgwick, J. Seele, R. Seidl, Y. Sekiguchi, A.Yu. Semenov, V. Semenov, A. Sen, R. Seto, P. Sett, A. Sexton, D. Sharma, A. Shaver, T.K. Shea, I. Shein, A. Shevel, T.-A. Shibata, K. Shigaki, H.H. Shim, M. Shimomura, T. Shioya, T. Shohjoh, K. Shoji, P. Shukla, A. Sickles, C.L. Silva, D. Silvermyr, C. Silvestre, K.S. Sim, B.K. Singh, C.P. Singh, V. Singh, M.J. Skoby, M. Skolnik, S. Skutnik, M. Slunečka, K.L. Smith, W.C. Smith, M. Snowball, T. Sodre, S. Solano, A. Soldatov, R.A. Soltz, W.E. Sondheim, S.P. Sorensen, I.V. Sourikova, N.A. Sparks, F. Staley, P.W. Stankus, P. Steinberg, E. Stenlund, M. Stepanov, A. Ster, S.P. Stoll, M.R. Stone, T. Sugitate, C. Suire, A. Sukhanov, J.P. Sullivan, T. Sumita, J. Sun, S. Syed, J. Sziklai, T. Tabaru, S. Takagi, E.M. Takagui, A. Takahara, A. Takeda, A. Taketani, R. Tanabe, K.H. Tanaka, Y. Tanaka, S. Taneja, K. Tanida, M.J. Tannenbaum, S. Tarafdar, A. Taranenko, P. Tarján, G. Tarnai, E. Tennant, H. Themann, D. Thomas, T.L. Thomas, R. Tieulent, A. Timilsina, T. Todoroki, M. Togawa, A. Toia, J. Tojo, L. Tomášek, M. Tomášek, Y. Tomita, H. Torii, C.L. Towell, M. Towell, R. Towell, R.S. Towell, V.-N. Tram, I. Tserruya, Y. Tsuchimoto, T. Tsuji, S.K. Tuli, H. Tydesjö, N. Tyurin, Y. Ueda, B. Ujvari, K. Utsunomiya, C. Vale, H. Valle, H.W. van Hecke, M. Vargyas, S. Vazquez-Carson, E. Vazquez-Zambrano, A. Veicht, J. Velkovska, R. Vértesi, A.A. Vinogradov, M. Virius, B. Voas, A. Vossen, V. Vrba, N. Vukman, E. Vznuzdaev, M. Wagner, D. Walker, X.R. Wang, Z. Wang, D. Watanabe, K. Watanabe, Y. Watanabe, Y.S. Watanabe, F. Wei, R. Wei, J. Wessels, S. Whitaker, A.S. White, S.N. White, N. Willis, D. Winter, S. Wolin, C.P. Wong, J.P. Wood, C.L. Woody, R.M. Wright, M. Wysocki, B. Xia, W. Xie, C. Xu, Q. Xu, L. Xue, S. Yalcin, Y.L. Yamaguchi, H. Yamamoto, K. Yamaura, R. Yang, A. Yanovich, Z. Yasin, P. Yin, J. Ying, S. Yokkaichi, J.H. Yoo, J.S. Yoo, I. Yoon, Z. You, G.R. Young, I. Younus, H. Yu, I.E. Yushmanov, W.A. Zajc, O. Zaudtke, A. Zelenski, C. Zhang, S. Zharko, S. Zhou, J. Zimamyi, L. Zolin, and L. Zou

Subjects
Nuclear and High Energy Physics
Published
2019

43. 188 Improvement of Erectile Dysfunction in Germ Cell Tumor Survivors

Author

K. Okada, K. Fujita, S. Fukuhara, T. Imanaka, S. Kuribayashi, Y. Sekii, K. Takezawa, H. Kiuchi, and N. Nonomura

Subjects
Psychiatry and Mental health, Endocrinology, Reproductive Medicine, Urology, Endocrinology, Diabetes and Metabolism
Abstract

Introduction Germ cell tumors (GCTs) are the most common malignant neoplasms in adolescents and young adults, and most patients with these tumors can be completely cured. Therefore, maintaining quality of life (QOL) is important. Erectile dysfunction (ED) is one factor that reduces the QOL of GCT survivors. Objective We aimed to clarify the relationship between ED and age, follow-up period, serum levels of hormones, and treatment methods for GCT survivors. Methods We evaluated ED using the Sexual Health Inventory for Men questionnaire (SHIM) and measured serum levels of hormones in survivors after GCT treatment. The relationships between the SHIM score responses and age, serum levels of hormones, follow-up period, and treatment methods were assessed using a logistic analysis. Results Fifty-two GCT survivors were enrolled and 46 survivors completed the SHIM. The median age, follow-up period, and SHIM score were 38 years, 35 months, and 18, respectively. Regarding the SHIM scores, 85% had scores Conclusions Improvement of SHIM score can be expected after GCT treatment regardless of age, serum levels of hormone, and treatment method. Disclosure Work supported by industry: no.

Published
2022

44. 133 Outcomes of Treatment for LOH Syndrome Assessed by Free Testosterone

Author

Y Kaku, K Sato, A Ooishi, T Ishida, K Okada, K Chiba, and M Fujisawa

Subjects
Psychiatry and Mental health, Endocrinology, Reproductive Medicine, Urology, Endocrinology, Diabetes and Metabolism
Abstract

Objective Late-onset hypogonadism (LOH) is defined by reduced serum testosterone levels, and androgen replacement therapy (ART) is widely used. While serum total testosterone (TT) is used as an indicator for diagnosis and treatment for LOH in the United States and Europe, serum free testosterone (FT) is used in Japan. Patients with low FT levels (less than 8.5 pg/mL) are to be indicated for ART as LOH, and patients with moderate FT levels (between 8.5 pg/mL and 11.8 pg/mL) are also to be considered for ART as LOH borderline. In this study, we examined the outcomes of LOH and LOH borderline patients who were treated by ART. Methods We examined Aging Male Symptom (AMS) scale scores of LOH (n=76) and LOH borderline patients (n=16) who were treated with ART for at least 6 months at our hospital. Results In LOH patients, AMS score decreased from 52.1±12.3 to 41.5±12.2 (p Conclusion ART improves AMS score both in LOH and LOH borderline patients, but there were no significant differences between two groups in this study. Disclosure Work supported by industry: no.

Published
2022

45. 213 Effect of Clomiphene Citrate Therapy for Male Infertility

Author

K Okada, K Sato, A Ohnishi, Y Kaku, T Ishida, K Chiba, and M Fujisawa

Subjects
Psychiatry and Mental health, Endocrinology, Reproductive Medicine, Urology, Endocrinology, Diabetes and Metabolism
Abstract

Introduction & Objectives To assess the efficacy and safety of clomiphene citrate (CC) for idiopathic male infertility. Methods We identified low testosterone (T) and male infertility patients treated with CC at our institution in the period September 2017 to May 2020. Data were gathered on patient characteristics and laboratory values at baseline. We retrospectively evaluated patients whose sperm concentration < 15*106/mL and/or sperm motility < 40%. FSH, LH and total T were measured before and 6-8 weeks after CC therapy. Sperm concentration, sperm motility were evaluated 3 month after CC therapy. Side effects were also recorded. In this series, 25 mg of CC was added every morning in all patients. Results A total of 37 men were included, with a mean age of 36.7 years. After 3month of CC therapy, sperm concentration was significantly increased from 14.07±16.21*106/ml to 30.52±38.10*106/ml. Sperm motility was also increased from 22.61±17.32% to 29.01±17.11%, but not significantly. Total T, FSH, and LH levels all significantly increased. 2 couples (5.4%) got pregnant. 2 patients experienced side effects: acne, n = 1; increased hepatic enzymes, n = 1. There were 5 patients who complained low libido and/or ED, but no improvement by T elevation. Conclusions According to our data, CC therapy increased sperm concentration significantly. CC therapy may be an effective and safe alternative for patients with low T and low sperm concentration. We have to evaluate more cases to know the CC therapy effect for low libido and ED. Disclosure Work supported by industry: no.

Published
2022

46. 126 Relationship Between Sexual Function Improvement and Treatment Satisfaction by TRT in LOH Patients

Author

K Chiba, K Sato, A Onishi, Y Kaku, T Ishida, K Okada, and M Fujisawa

Subjects
Psychiatry and Mental health, Endocrinology, Reproductive Medicine, Urology, Endocrinology, Diabetes and Metabolism
Abstract

Introduction In the treatment of LOH (late-onset hypogonadism) syndrome, TRT (testosterone replacement therapy) is effective for various LOH related symptoms including sexual function. However, among Japanese population, sexual desire is not always strong in elderly men. Even if the patients do not have opportunities of sexual intercourse, TRT may still be beneficial for other symptoms derived from LOH syndrome. Objectives To examine patients’ satisfaction by TRT, we examined the relationship between TRT effect on sexual function and whole treatment satisfaction in our patient cohort. Methods Patients who have LOH symptoms and low serum free-testosterone (FT) levels were diagnosed as LOH syndrome. FT was diagnosed as “low” when Results Median patients’ age was 54 years (n=95). Before treatment, total testosterone was 4.5±1.8ng/ml and free testosterone was 6.2±2.3pg/ml. The majority of chief complaint before treatment were psychological or somatic symptoms. After treatment, SHIM score showed significant improvement in all questions of 1 to 5, and total SHIM score increased from 6.4 to 9.4. The number of patients who have few opportunities for sexual intercourse (0 point for SHIM Q3.4.5) decreased from 66% to 48% after treatment. Using the questionnaire for patients’ satisfaction, 71% were classified into the effective group. The number of patients who still had few opportunities of sexual intercourse after treatment was 39% in the effective group and 71% in the ineffective group. Conclusions From the point of patient satisfaction, TRT for LOH syndrome was effective in 71% of patients. Almost 40 percent of the patients who were satisfied with the treatment answered that there were few opportunities of sexual intercourse even after treatment. The improvement in sexual function may not be always required in a cohort of our patient population. Disclosure Work supported by industry: no.

Published
2022

47. Crop production and energy generation in a greenhouse integrated with semi-transparent organic photovoltaic film

Author

K. Okada, Ibrahim Yehia, Murat Kacira, and Meir Teitel

Subjects
0106 biological sciences, Photovoltaic system, Environmental engineering, Greenhouse, Environment controlled, 02 engineering and technology, Horticulture, 021001 nanoscience & nanotechnology, Semi transparent, 01 natural sciences, Electricity generation, Crop production, Environmental science, 0210 nano-technology, 010606 plant biology & botany
Published
2018

48. A slow mode wave as a possible source of Pi 2 and associated particle precipitation: a case study

Author

O. Saka, O. Watanabe, K. Okada, and D. N. Baker

Subjects
Science, Physics, QC1-999, Geophysics. Cosmic physics, QC801-809
Abstract

An intensification of auroral luminosity referred to as an auroral break-up often accompanies the onset of geomagnetic pulsation (Pi 2) at the dip-equator. One such auroral break-up occurred at 2239 UT on 16 June, 1986, being accompanied by weak substorm activity (AE~50 nT) which was recorded in all-sky image of Syowa Station, Antarctica (66.2°S, 71.8°E in geomagnetic coordinates). The associated Pi 2 magnetic pulsation was detected by a fluxgate magnetometer in the afternoon sector at the dip-equator (Huancayo, Peru; 1.44°N, 355.9° in geomagnetic coordinates; 12.1°S, 75.2°W in geographic coordinates; L=1.00). In spite of the large separation of the two stations in longitude and latitude, the auroral break-up and subsequent luminosity modulation were seen to be correlated with the wave form of the ground Pi 2 pulsation. This occurred in such a way that the luminosity maximum was seen to occur at the phase of maximum amplitudes of Pi 2 wave form. We argue that the observed correlation could be interpreted as indicating a Pi 2-modulation of a field-aligned acceleration of the low energy electrons that may occur near the equator of the midnight magnetosphere.Key words. Magnetospheric physics (auroral phenomena; energetic particles · precipitating; MHD waves and instabilities)

Published
1999
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49. Autoantibodies neutralizing type I IFNs are present in ~4% of uninfected individuals over 70 years old and account for ~20% of COVID-19 deaths

Author

Bastard, P. Gervais, A. Voyer, T.L. Rosain, J. Philippot, Q. Manry, J. Michailidis, E. Hoffmann, H.-H. Eto, S. Garcia-Prat, M. Bizien, L. Parra-Martínez, A. Yang, R. Haljasmägi, L. Migaud, M. Särekannu, K. Maslovskaja, J. De Prost, N. Tandjaoui-Lambiotte, Y. Luyt, C.-E. Amador-Borrero, B. Gaudet, A. Poissy, J. Morel, P. Richard, P. Cognasse, F. Troya, J. Trouillet-Assant, S. Belot, A. Saker, K. Garçon, P. Rivière, J.G. Lagier, J.-C. Gentile, S. Rosen, L.B. Shaw, E. Morio, T. Tanaka, J. Dalmau, D. Tharaux, P.-L. Sene, D. Stepanian, A. Megarbane, B. Triantafyllia, V. Fekkar, A. Heath, J.R. Franco, J.L. Anaya, J.-M. Solé-Violán, J. Imberti, L. Biondi, A. Bonfanti, P. Castagnoli, R. Delmonte, O.M. Zhang, Y. Snow, A.L. Holland, S.M. Biggs, C.M. Moncada-Vélez, M. Arias, A.A. Lorenzo, L. Boucherit, S. Coulibaly, B. Anglicheau, D. Planas, A.M. Haerynck, F. Duvlis, S. Nussbaum, R.L. Ozcelik, T. Keles, S. Bousfiha, A.A. El Bakkouri, J. Ramirez-Santana, C. Paul, S. Pan-Hammarström, Q. Hammarström, L. Dupont, A. Kurolap, A. Metz, C.N. Aiuti, A. Casari, G. Lampasona, V. Ciceri, F. Barreiros, L.A. Dominguez-Garrido, E. Vidigal, M. Zatz, M. Van De Beek, D. Sahanic, S. Tancevski, I. Stepanovskyy, Y. Boyarchuk, O. Nukui, Y. Tsumura, M. Vidaur, L. Tangye, S.G. Burrel, S. Duffy, D. Quintana-Murci, L. Klocperk, A. Kann, N.Y. Shcherbina, A. Lau, Y.-L. Leung, D. Coulongeat, M. Marlet, J. Koning, R. Reyes, L.F. Chauvineau-Grenier, A. Venet, F. Monneret, G. Nussenzweig, M.C. Arrestier, R. Boudhabhay, I. Baris-Feldman, H. Hagin, D. Wauters, J. Meyts, I. Dyer, A.H. Kennelly, S.P. Bourke, N.M. Halwani, R. Sharif-Askari, N.S. Dorgham, K. Sallette, J. Sedkaoui, S.M. AlKhater, S. Rigo-Bonnin, R. Morandeira, F. Roussel, L. Vinh, D.C. Ostrowski, S.R. Condino-Neto, A. Prando, C. Bondarenko, A. Spaan, A.N. Gilardin, L. Fellay, J. Lyonnet, S. Bilguvar, K. Lifton, R.P. Mane, S. Anderson, M.S. Boisson, B. Béziat, V. Zhang, S.-Y. Andreakos, E. Hermine, O. Pujol, A. Peterson, P. Mogensen, T.H. Rowen, L. Mond, J. Debette, S. De Lamballerie, X. Duval, X. Mentré, F. Zins, M. Soler-Palacin, P. Colobran, R. Gorochov, G. Solanich, X. Susen, S. Martinez-Picado, J. Raoult, D. Vasse, M. Gregersen, P.K. Piemonti, L. Rodríguez-Gallego, C. Notarangelo, L.D. Su, H.C. Kisand, K. Okada, S. Puel, A. Jouanguy, E. Rice, C.M. Tiberghien, P. Zhang, Q. Cobat, A. Abel, L. Casanova, J.-L. Alavoine, L. Behillil, S. Burdet, C. Charpentier, C. Dechanet, A. Descamps, D. Ecobichon, J.-L. Enouf, V. Frezouls, W. Houhou, N. Kafif, O. Lehacaut, J. Letrou, S. Lina, B. Lucet, J.-C. Manchon, P. Nouroudine, M. Piquard, V. Quintin, C. Thy, M. Tubiana, S. Van Der Werf, S. Vignali, V. Visseaux, B. Yazdanpanah, Y. Chahine, A. Waucquier, N. Migaud, M.-C. Deplanque, D. Djossou, F. Mergeay-Fabre, M. Lucarelli, A. Demar, M. Bruneau, L. Gerardin, P. Maillot, A. Payet, C. Laviolle, B. Laine, F. Paris, C. Desille-Dugast, M. Fouchard, J. Malvy, D. Nguyen, D. Pistone, T. Perreau, P. Gissot, V. Le Goas, C. Montagne, S. Richard, L. Chirouze, C. Bouiller, K. Desmarets, M. Meunier, A. Lefevre, B. Jeulin, H. Legrand, K. Lomazzi, S. Tardy, B. Gagneux-Brunon, A. Bertholon, F. Botelho-Nevers, E. Christelle, K. Nicolas, L. Roufai, L. Amat, K. Couffin-Cadiergues, S. Esperou, H. Hendou, S. Townsend, L. Cheallaigh, C.N. Bergin, C. Martin-Loeches, I. Dunne, J. Conlon, N. O'Farrelly, C. Abad, J. Accordino, G. Achille, C. Aguilera-Albesa, S. Aguilo-Cucurull, A. Ozkan, E.A. Darazam, I.A. Albisures, J.A.R. Aldave, J.C. Ramos, M.A. Khan, T.A. Aliberti, A. Nadji, S.A. Alkan, G. AlKhater, S.A. Allardet-Servent, J. Allende, L.M. Alonso-Arias, R. Alshahrani, M.S. Alsina, L. Alyanakian, M.-A. Borrero, B.A. Amoura, Z. Antoli, A. Aubart, M. Auguet, T. Avramenko, I. Aytekin, G. Azot, A. Bahram, S. Bajolle, F. Baldanti, F. Baldolli, A. Ballester, M. Feldman, H.B. Barrou, B. Barzaghi, F. Basso, S. Bayhan, G.I. Bezrodnik, L. Bilbao, A. Blanchard-Rohner, G. Blanco, I. Blandinieres, A. Blazquez-Gamero, D. Bleibtreu, A. Bloomfield, M. Bolivar-Prados, M. Borghesi, A. Borie, R. Botdhlo-Nevers, E. Bousquet, A. Boutolleau, D. Bouvattier, C. Bravais, J. Briones, M.L. Brunner, M.-E. Bruno, R. Bueno, M.R.P. Bukhari, H. Bustamante, J. Agra, J.J.C. Capra, R. Carapito, R. Carrabba, M. Casasnovas, C. Caseris, M. Cassaniti, I. Castelle, M. Castelli, F. De Vera, M.C. Castro, M.V. Catherinot, E. Celik, J.B. Ceschi, A. Chalumeau, M. Charbit, B. Cheng, M.P. Clave, P. Clotet, B. Codina, A. Cohen, Y. Comarmond, C. Combes, A. Comoli, P. Corsico, A.G. Coşkuner, T. Cvetkovski, A. Cyrus, C. Danion, F. Darley, D.R. Das, V. Dauby, N. Dauger, S. De Munter, P. De Pontual, L. Dehban, A. Delplancq, G. Demoule, A. Desguerre, I. Di Sabatino, A. Diehl, J.-L. Dobbelaere, S. Dubost, C. Ekwall, O. Bozdemir, Ş.E. Elnagdy, M.H. Emiroglu, M. Endo, A. Erdeniz, E.H. Aytekin, S.E. Lasa, M.P.E. Euvrard, R. Fabio, G. Faivre, L. Falck, A. Fartoukh, M. Faure, M. Arquero, M.F. Ferrer, R. Ferreres, J. Flores, C. Francois, B. Fumado, V. Fung, K.S.C. Fusco, F. Gagro, A. Solis, B.G. Gaussem, P. Gayretli, Z. Gil-Herrera, J. Gatineau, A.G. Girona-Alarcon, M. Godinez, K.A.C. Goffard, J.-C. Gonzales, N. Gonzalez-Granado, L.I. Gonzalez-Montelongo, R. Guerder, A. Gulhan, B. Gumucio, V.D. Hanitsch, L.G. Gunst, J. Gut, M. Hadjadj, J. Hancerli, S. Hariyan, T. Hatipoglu, N. Heppekcan, D. Hernandez-Brito, E. Ho, P.-K. Holanda-Pena, M.S. Horcajada, J.P. Hraiech, S. Humbert, L. Hung, I.F.N. Iglesias, A.D. Inigo-Campos, A. Jamme, M. Arranz, M.J. Jimeno, M.-T. Jordan, I. Kanik-Yuksek, S. Kara, Y.B. Karahan, A. Karbuz, A. Yasar, K.K. Kasapcopur, O. Kashimada, K. Demirkol, Y.K. Kido, Y. Kizil, C. Kilic, A.O. Koutsoukou, A. Krol, Z.J. Ksouri, H. Kuentz, P. Kwan, A.M.C. Kwan, Y.W.M. Kwok, J.S.Y. Lam, D.S.Y. Lampropoulou, V. Lanternier, F. Le Bourgeois, F. Leo, Y.-S. Lopez, R.L. Levin, M. Levy, M. Levy, R. Li, Z. Lilleri, D. Lima, E.J.A.B. Linglart, A. Lopez-Collazo, E. Lorenzo-Salazar, J.M. Louapre, C. Lubetzki, C. Lung, K.-C. Lye, D.C. Magnone, C. Mansouri, D. Marchioni, E. Marioli, C. Marjani, M. Marques, L. Pereira, J.M. Martin-Nalda, A. Pueyo, D.M. Marzana, I. Mata-Martinez, C. Mathian, A. Matos, L.R.B. Matthews, G.V. Mayaux, J. McLaughlin-Garcia, R. Meersseman, P. Mege, J.-L. Mekontso-Dessap, A. Melki, I. Meloni, F. Meritet, J.-F. Merlani, P. Akcan, O.M. Mezidi, M. Migeotte, I. Millereux, M. Million, M. Mirault, T. Mircher, C. Mirsaeidi, M. Mizoguchi, Y. Modi, B.P. Mojoli, F. Moncomble, E. Melian, A.M. Martinez, A.M. Morange, P.-E. Mordacq, C. Morelle, G. Mouly, S.J. Munoz-Barrera, A. Nafati, C. Nagashima, S. Nakagama, Y. Neven, B. Neves, J.F. Ng, L.F.P. Ng, Y.-Y. Nielly, H. Medina, Y.N. Cuadros, E.N. Ocejo-Vinyals, J.G. Okamoto, K. Oualha, M. Ouedrani, A. Ozkaya-Parlakay, A. Pagani, M. Papadaki, M. Parizot, C. Parola, P. Pascreau, T. Paz-Artal, E. Pedraza, S. Pellecer, N.C.G. Pellegrini, S. De Diego, R.P. Perez-Fernandez, X.L. Philippe, A. Picod, A. De Chambrun, M.P. Piralla, A. Planas-Serra, L. Ploin, D. Poncelet, G. Poulakou, G. Pouletty, M.S. Pourshahnazari, P. Qiu-Chen, J.L. Quentric, P. Rambaud, T. Raoult, V. Rebillat, A.-S. Redin, C. Resmini, L. Ricart, P. Richard, J.-C. Rivet, N. Rocamora-Blanch, G. Rodero, M.P. Rodrigo, C. Rodriguez, L.A. Rodriguez-Palmero, A. Romero, C.S. Rothenbuhler, A. Roux, D. Rovina, N. Rozenberg, F. Ruch, Y. Ruiz, M. Del Prado, M.Y.R. Ruiz-Rodriguez, J.C. Sabater-Riera, J. Saks, K. Salagianni, M. Sanchez, O. Sanchez-Montalva, A. Sanchez-Ramon, S. Schidlowski, L. Schluter, A. Schmidt, J. Schmidt, M. Schuetz, C. Schweitzer, C.E. Scolari, F. Sediva, A. Seijo, L. Seminario, A.G. Seng, P. Senoglu, S. Seppanen, M. Llovich, A.S. Shahrooei, M. Siguret, V. Siouti, E. Smadja, D.M. Smith, N. Sobh, A. Soler, C. Sozeri, B. Stella, G.M. Stepanovskiy, Y. Stoclin, A. Taccone, F. Taupin, J.-L. Tavernier, S.J. Terrier, B. Thiery, G. Thorball, C. Thorn, K. Thumerelle, C. Tipu, I. Tolstrup, M. Tomasoni, G. Toubiana, J. Alvarez, J.T. Tsang, O.T.Y. Tserel, L. 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CoV-Contact Cohort St James's Hospital, SARS CoV2 Interest group COVID Clinicians French COVID Cohort Study Group NIAID Immune Response to COVID Group Danish CHGE COVID Human Genetic Effort HGID Lab COVID-STORM Clinicians NH-COVAIR Study Group The Danish Blood Donor Study (DBDS) Imagine COVID-Group The Milieu Interieur Consortium Amsterdam UMC Covid-19 Biobank CONSTANCES cohort 3C-Dijon Study Cerba HealthCare Etablissement du Sang study group

Abstract

Circulating autoantibodies (auto-Abs) neutralizing high concentrations (10 ng/ml; in plasma diluted 1:10) of IFN-α and/or IFN-ω are found in about 10% of patients with critical COVID-19 (coronavirus disease 2019) pneumonia but not in individuals with asymptomatic infections. We detect auto-Abs neutralizing 100-fold lower, more physiological, concentrations of IFN-α and/or IFN-ω (100 pg/ml; in 1:10 dilutions of plasma) in 13.6% of 3595 patients with critical COVID-19, including 21% of 374 patients >80 years, and 6.5% of 522 patients with severe COVID-19. These antibodies are also detected in 18% of the 1124 deceased patients (aged 20 days to 99 years; mean: 70 years). Moreover, another 1.3% of patients with critical COVID-19 and 0.9% of the deceased patients have auto-Abs neutralizing high concentrations of IFN-β. We also show, in a sample of 34,159 uninfected individuals from the general population, that auto-Abs neutralizing high concentrations of IFN-α and/or IFN-ω are present in 0.18% of individuals between 18 and 69 years, 1.1% between 70 and 79 years, and 3.4% >80 years. Moreover, the proportion of individuals carrying auto-Abs neutralizing lower concentrations is greater in a subsample of 10,778 uninfected individuals: 1% of individuals 80 years. By contrast, auto-Abs neutralizing IFN-β do not become more frequent with age. Auto-Abs neutralizing type I IFNs predate SARS-CoV-2 infection and sharply increase in prevalence after the age of 70 years. They account for about 20% of both critical COVID-19 cases in the over 80s and total fatal COVID-19 cases. © 2021 The Authors, some rights reserved.

Published
2021

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