144 results on '"Yüksel, Hüsniye"'
Search Results
2. Mild-to-Moderate Kidney Dysfunction and Cardiovascular Disease: Observational and Mendelian Randomization Analyses
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Gaziano, Liam, primary, Sun, Luanluan, additional, Arnold, Matthew, additional, Bell, Steven, additional, Cho, Kelly, additional, Kaptoge, Stephen K., additional, Song, Rebecca J., additional, Burgess, Stephen, additional, Posner, Daniel C., additional, Mosconi, Katja, additional, Robinson-Cohen, Cassianne, additional, Mason, Amy M., additional, Bolton, Thomas R., additional, Tao, Ran, additional, Allara, Elias, additional, Schubert, Petra, additional, Chen, Lingyan, additional, Staley, James R., additional, Staplin, Natalie, additional, Altay, Servet, additional, Amiano, Pilar, additional, Arndt, Volker, additional, Ärnlöv, Johan, additional, Barr, Elizabeth L.M., additional, Björkelund, Cecilia, additional, Boer, Jolanda M.A., additional, Brenner, Hermann, additional, Casiglia, Edoardo, additional, Chiodini, Paolo, additional, Cooper, Jackie A., additional, Coresh, Josef, additional, Cushman, Mary, additional, Dankner, Rachel, additional, Davidson, Karina W., additional, de Jongh, Renate T., additional, Donfrancesco, Chiara, additional, Engström, Gunnar, additional, Freisling, Heinz, additional, de la Cámara, Agustín Gómez, additional, Gudnason, Vilmundur, additional, Hankey, Graeme J., additional, Hansson, Per-Olof, additional, Heath, Alicia K., additional, Hoorn, Ewout J., additional, Imano, Hironori, additional, Jassal, Simerjot K., additional, Kaaks, Rudolf, additional, Katzke, Verena, additional, Kauhanen, Jussi, additional, Kiechl, Stefan, additional, Koenig, Wolfgang, additional, Kronmal, Richard A., additional, Kyrø, Cecilie, additional, Lawlor, Deborah A., additional, Ljungberg, Börje, additional, MacDonald, Conor, additional, Masala, Giovanna, additional, Meisinger, Christa, additional, Melander, Olle, additional, Moreno Iribas, Conchi, additional, Ninomiya, Toshiharu, additional, Nitsch, Dorothea, additional, Nordestgaard, Børge G., additional, Onland-Moret, Charlotte, additional, Palmieri, Luigi, additional, Petrova, Dafina, additional, Garcia, Jose Ramón Quirós, additional, Rosengren, Annika, additional, Sacerdote, Carlotta, additional, Sakurai, Masaru, additional, Santiuste, Carmen, additional, Schulze, Matthias B., additional, Sieri, Sabina, additional, Sundström, Johan, additional, Tikhonoff, Valérie, additional, Tjønneland, Anne, additional, Tong, Tammy, additional, Tumino, Rosario, additional, Tzoulaki, Ioanna, additional, van der Schouw, Yvonne T., additional, Monique Verschuren, W.M., additional, Völzke, Henry, additional, Wallace, Robert B., additional, Wannamethee, S. Goya, additional, Weiderpass, Elisabete, additional, Willeit, Peter, additional, Woodward, Mark, additional, Yamagishi, Kazumasa, additional, Zamora-Ros, Raul, additional, Akwo, Elvis A., additional, Pyarajan, Saiju, additional, Gagnon, David R., additional, Tsao, Philip S., additional, Muralidhar, Sumitra, additional, Edwards, Todd L., additional, Damrauer, Scott M., additional, Joseph, Jacob, additional, Pennells, Lisa, additional, Wilson, Peter W.F., additional, Harrison, Seamus, additional, Gaziano, Thomas A., additional, Inouye, Michael, additional, Baigent, Colin, additional, Casas, Juan P., additional, Langenberg, Claudia, additional, Wareham, Nick, additional, Riboli, Elio, additional, Gaziano, J.Michael, additional, Danesh, John, additional, Hung, Adriana M., additional, Butterworth, Adam S., additional, Wood, Angela M., additional, Di Angelantonio, Emanuele, additional, Koettgen, Anna, additional, Shaw, Jonathan, additional, Atkins, Robert, additional, Zimmet, Paul, additional, Whincup, Peter, additional, Willeit, Johann, additional, Leitner, Christoph, additional, Tybjaerg-Hansen, Anne, additional, Schnohr, Peter, additional, Afzal, Shoaib, additional, Pablos, David Lora, additional, Arriscado, Cristina Martin, additional, Ferreiro, Carmen Romero, additional, Stocker, Hannah, additional, Schöttker, Ben, additional, Holleczek, Bernd, additional, Chetrit, Angela, additional, Welin, Lennart, additional, Svärdsudd, Kurt, additional, Lissner, Lauren, additional, Hange, Dominique, additional, Mehlig, Kirsten, additional, Nagel, Dorothea, additional, Norman, Paul E., additional, Almeida, Osvaldo, additional, Flicker, Leon, additional, Hata, Jun, additional, Honda, Takanori, additional, Furuta, Yoshihiko, additional, Iso, Hiroyasu, additional, Kitamura, Akihiko, additional, Muraki, Isao, additional, Salonen, Jukka T., additional, Tuomainen, Tomi-Pekka, additional, van Zutphen, E. M., additional, van Schoor, N. M., additional, Lo Noce, Cinzia, additional, Kronmal, Richard, additional, Lappas, Georg, additional, Nilsson, Peter M., additional, Hedblad, Bo, additional, Shaffer, Jonathan, additional, Schwartz, Joseph, additional, Shimbo, Daichi, additional, Sato, Shinichi, additional, Hayama-Terada, Mina, additional, Jassal, Simerjot, additional, Aspelund, Thor, additional, Thorsson, Bolli, additional, Sigurdsson, Gunnar, additional, Chaker, Layal, additional, Ikram, Kamran M., additional, Kavousi, Maryam, additional, Tunstall-Pedoe, Hugh, additional, Can, Günay, additional, Yüksel, Hüsniye, additional, Özkan, Uğur, additional, Nakagawa, Hideaki, additional, Morikawa, Yuko, additional, Ishizaki, Masao, additional, Feskens, Edith, additional, Geleijnse, Johanna M, additional, and Kromhout, Daan, additional
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- 2022
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3. Serum total and high-density lipoprotein phospholipids: Independent predictive value for cardiometabolic risk
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Onat, Altan, Altuğ Çakmak, H., Can, Günay, Yüksel, Murat, Köroğlu, Bayram, and Yüksel, Hüsniye
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- 2014
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4. Coronary disease risk and fasting glucose levels in a non-diabetic population
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Onat, Altan, Can, Günay, Çiçek, Gökhan, Doğan, Yüksel, and Yüksel, Hüsniye
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- 2011
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5. Visceral adipose tissue and body fat mass: Predictive values for and role of gender in cardiometabolic risk among Turks
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Onat, Altan, Uğur, Murat, Can, Günay, Yüksel, Hüsniye, and Hergenç, Gülay
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- 2010
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6. Serum complement C3: a determinant of cardiometabolic risk, additive to the metabolic syndrome, in middle-aged population
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Onat, Altan, Hergenç, Gülay, Can, Günay, Kaya, Zekeriya, and Yüksel, Hüsniye
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- 2010
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7. Sex-Specific Predictors of Metabolic Syndrome Independent of Its Components
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Onat, Altan, Can, Günay, Çakr, Hakan, Özpamuk-Karadeniz, Fatma, Karadeniz, Yusuf, Yüksel, Hüsniye, Şimşek, Barş, and Ademoğlu, Evin
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- 2015
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8. Neck circumference as a measure of central obesity: Associations with metabolic syndrome and obstructive sleep apnea syndrome beyond waist circumference
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Onat, Altan, Hergenç, Gülay, Yüksel, Hüsniye, Can, Günay, Ayhan, Erkan, Kaya, Zekeriya, and Dursunoğlu, Dursun
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- 2009
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9. Associations of alcohol consumption with blood pressure, lipoproteins, and subclinical inflammation among Turks
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Onat, Altan, Hergenc, Gülay, Dursunoglu, Dursun, Ordu, Serkan, Can, Günay, Bulur, Serkan, and Yüksel, Hüsniye
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- 2008
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10. Comment on Ye et al. The Association Between Circulating Lipoprotein(a) and Type 2 Diabetes: Is It Causal? Diabetes 2014;63: 332–342
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Onat, Altan, Altay, Servet, and Yüksel, Hüsniye
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- 2014
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11. Equalization of four cardiovascular risk algorithms after systematic recalibration: individual-participant meta-analysis of 86 prospective studies
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Pennells, Lisa, Kaptoge, Stephen, Wood, Angela, Sweeting, Mike, Zhao, Xiaohui, White, Ian, Burgess, Stephen, Willeit, Peter, Bolton, Thomas, Moons, Karel G M, van der Schouw, Yvonne T, Selmer, Randi, Khaw, Kay-Tee, Gudnason, Vilmundur, Assmann, Gerd, Amouyel, Philippe, Salomaa, Veikko, Kivimaki, Mika, Nordestgaard, Børge G, Blaha, Michael J, Kuller, Lewis H, Brenner, Hermann, Gillum, Richard F, Meisinger, Christa, Ford, Ian, Knuiman, Matthew W, Rosengren, Annika, Lawlor, Debbie A, Völzke, Henry, Cooper, Cyrus, Marín Ibañez, Alejandro, Casiglia, Edoardo, Kauhanen, Jussi, Cooper, Jackie A, Rodriguez, Beatriz, Sundström, Johan, Barrett-Connor, Elizabeth, Dankner, Rachel, Nietert, Paul J, Davidson, Karina W, Wallace, Robert B, Blazer, Dan G, Björkelund, Cecilia, Donfrancesco, Chiara, Krumholz, Harlan M, Nissinen, Aulikki, Davis, Barry R, Coady, Sean, Whincup, Peter H, Jørgensen, Torben, Ducimetiere, Pierre, Trevisan, Maurizio, Engström, Gunnar, Crespo, Carlos J, Meade, Tom W, Visser, Marjolein, Kromhout, Daan, Kiechl, Stefan, Daimon, Makoto, Price, Jackie F, Gómez de la Cámara, Agustin, Wouter Jukema, J, Lamarche, Benoît, Onat, Altan, Simons, Leon A, Kavousi, Maryam, Ben-Shlomo, Yoav, Gallacher, John, Dekker, Jacqueline M, Arima, Hisatomi, Shara, Nawar, Tipping, Robert W, Roussel, Ronan, Brunner, Eric J, Koenig, Wolfgang, Sakurai, Masaru, Pavlovic, Jelena, Gansevoort, Ron T, Nagel, Dorothea, Goldbourt, Uri, Barr, Elizabeth L M, Palmieri, Luigi, Njølstad, Inger, Sato, Shinichi, Monique Verschuren, W M, Varghese, Cherian V, Graham, Ian, Onuma, Oyere, Greenland, Philip, Woodward, Mark, Ezzati, Majid, Psaty, Bruce M, Sattar, Naveed, Jackson, Rod, Ridker, Paul M, Cook, Nancy R, D'Agostino, Ralph B, Thompson, Simon G, Danesh, John, Di Angelantonio, Emanuele, Simpson, Lara M, Pressel, Sara L, Couper, David J, Nambi, Vijay, Matsushita, Kunihiro, Folsom, Aaron R, Shaw, Jonathan E, Magliano, Dianna J, Zimmet, Paul Z, Wannamethee, S Goya, Willeit, Johann, Santer, Peter, Egger, Georg, Casas, Juan Pablo, Amuzu, Antointtte, Tikhonoff, Valérie, Sutherland, Susan E, Cushman, Mary, Søgaard, Anne Johanne, Håheim, Lise Lund, Ariansen, Inger, Tybjærg-Hansen, Anne, Jensen, Gorm B, Schnohr, Peter, Giampaoli, Simona, Vanuzzo, Diego, Panico, Salvatore, Balkau, Beverley, Bonnet, Fabrice, Marre, Michel, de la Cámara, Agustin Gómez, Rubio Herrera, Miguel Angel, Friedlander, Yechiel, McCallum, John, McLachlan, Stela, Guralnik, Jack, Phillips, Caroline L, Wareham, Nick, Schöttker, Ben, Saum, Kai-Uwe, Holleczek, Bernd, Tolonen, Hanna, Vartiainen, Erkki, Jousilahti, Pekka, Harald, Kennet, D’Agostino, Ralph B, Massaro, Joseph M, Pencina, Michael, Vasan, Ramachandran, Kayama, Takamasa, Kato, Takeo, Oizumi, Toshihide, Jespersen, Jørgen, Møller, Lars, Bladbjerg, Else Marie, Chetrit, A, Wilhelmsen, Lars, Lissner, Lauren, Dennison, Elaine, Kiyohara, Yutaka, Ninomiya, Toshiharu, Doi, Yasufumi, Nijpels, Giel, Stehouwer, Coen D A, Kazumasa, Yamagishi, Iso, Hiroyasu, Kurl, Sudhir, Tuomainen, Tomi-Pekka, Salonen, Jukka T, Deeg, Dorly J H, Nilsson, Peter M, Hedblad, Bo, Melander, Olle, De Boer, Ian H, DeFilippis, Andrew Paul, Verschuren, W M Monique, Watt, Graham, Tverdal, Aage, Kirkland, Susan, Shimbo, Daichi, Shaffer, Jonathan, Bakker, Stephan J L, van der Harst, Pim, Hillege, Hans L, Dallongeville, Jean, Schulte, Helmut, Trompet, Stella, Smit, Roelof A J, Stott, David J, Després, Jean-Pierre, Cantin, Bernard, Dagenais, Gilles R, Laughlin, Gail, Wingard, Deborah, Aspelund, Thor, Eiriksdottir, Gudny, Gudmundsson, Elias Freyr, Ikram, Arfan, van Rooij, Frank J A, Franco, Oscar H, Rueda-Ochoa, Oscar L, Muka, Taulant, Glisic, Marija, Tunstall-Pedoe, Hugh, Howard, Barbara V, Zhang, Ying, Jolly, Stacey, Davey-Smith, George, Can, Günay, Yüksel, Hüsniye, Nakagawa, Hideaki, Morikawa, Yuko, Miura, Katsuyuki, Ingelsson, Martin, Giedraitis, Vilmantas, Gaziano, J Michael, Shipley, Martin, Arndt, Volker, Cook, Nancy, Ibañez, Alejandro Marín, Geleijnse, Johanna M, Epidemiology, Læknadeild (HÍ), Faculty of Medicine (UI), Heilbrigðisvísindasvið (HÍ), School of Health Sciences (UI), Háskóli Íslands, University of Iceland, Pennells, Lisa [0000-0002-8594-3061], Kaptoge, Stephen [0000-0002-1155-4872], Wood, Angela [0000-0002-7937-304X], Sweeting, Michael [0000-0003-0980-8965], Zhao, Xiaohui [0000-0001-9922-2815], Burgess, Stephen [0000-0001-5365-8760], Danesh, John [0000-0003-1158-6791], Di Angelantonio, Emanuele [0000-0001-8776-6719], Apollo - University of Cambridge Repository, Nutrition and Health, APH - Aging & Later Life, APH - Societal Participation & Health, APH - Health Behaviors & Chronic Diseases, Cardiovascular Centre (CVC), Groningen Kidney Center (GKC), Groningen Institute for Organ Transplantation (GIOT), Lifestyle Medicine (LM), Life Course Epidemiology (LCE), AGEM - Endocrinology, metabolism and nutrition, Internal medicine, Epidemiology and Data Science, İÜC, Lisa, Pennell, Stephen, Kaptoge, Angela, Wood, Mike, Sweeting, Xiaohui, Zhao, Ian, White, Stephen, Burge, Peter, Willeit, Thomas, Bolton, Karel G M, Moon, Yvonne T, van der Schouw, Randi, Selmer, Kay-Tee, Khaw, Vilmundur, Gudnason, Gerd, Assmann, Philippe, Amouyel, Veikko, Salomaa, Mika, Kivimaki, Børge G, Nordestgaard, Michael J, Blaha, Lewis H, Kuller, Hermann, Brenner, Richard F, Gillum, Christa, Meisinger, Ian, Ford, Matthew W, Knuiman, Annika, Rosengren, Debbie A, Lawlor, Henry, Völzke, Cyrus, Cooper, Alejandro, Marín Ibañez, Edoardo, Casiglia, Jussi, Kauhanen, Jackie A, Cooper, Beatriz, Rodriguez, Johan, Sundström, Elizabeth, Barrett-Connor, Rachel, Dankner, Paul J, Nietert, Karina W, Davidson, Robert B, Wallace, Dan G, Blazer, Cecilia, Björkelund, Chiara, Donfrancesco, Harlan M, Krumholz, Aulikki, Nissinen, Barry R, Davi, Sean, Coady, Peter H, Whincup, Torben, Jørgensen, Pierre, Ducimetiere, Maurizio, Trevisan, Gunnar, Engström, Carlos J, Crespo, Tom W, Meade, Marjolein, Visser, Daan, Kromhout, Stefan, Kiechl, Makoto, Daimon, Jackie F, Price, Agustin, Gómez de la Cámara, J, Wouter Jukema, Benoît, Lamarche, Altan, Onat, Leon A, Simon, Maryam, Kavousi, Yoav, Ben-Shlomo, John, Gallacher, Jacqueline M, Dekker, Hisatomi, Arima, Nawar, Shara, Robert W, Tipping, Ronan, Roussel, Eric J, Brunner, Wolfgang, Koenig, Masaru, Sakurai, Jelena, Pavlovic, Ron T, Gansevoort, Dorothea, Nagel, Uri, Goldbourt, Elizabeth L M, Barr, Luigi, Palmieri, Inger, Njølstad, Shinichi, Sato, W M, Monique Verschuren, Cherian V, Varghese, Ian, Graham, Oyere, Onuma, Philip, Greenland, Mark, Woodward, Majid, Ezzati, Bruce M, Psaty, Sattar, W Tipping, Naveerobert, M Simpson, Lara, L Pressel, Sara, J Couper, David, Nambi, Vijay, Matsushita, Kunihiro, R Folsom, Aaron, E Shaw, Jonathan, J Magliano, Dianna, Z Zimmet, Paul, W Knuiman, Matthew, H Whincup, Peter, Goya Wannamethee, S, Willeit, Johann, Santer, Peter, Egger, Georg, Pablo Casas, Juan, Amuzu, Antoinette, Ben-Shlomo, Yoav, Gallacher, John, Tikhonoff, Valérie, Casiglia, Edoardo, E Sutherland, Susan, J Nietert, Paul, Cushman, Mary, M Psaty, Bruce, Johanne Søgaard, Anne, Lund Håheim, Lise, Ariansen, Inger, Tybjærg-Hansen, Anne, B Jensen, Gorm, Schnohr, Peter, Giampaoli, Simona, Vanuzzo, Diego, Panico, Salvatore, Palmieri, Luigi, Balkau, Beverley, Bonnet, Fabrice, Marre, Michel, Gómez de la Cámara, Agustin, Angel Rubio Herrera, Miguel, Friedlander, Yechiel, Mccallum, John, Mclachlan, Stela, Guralnik, Jack, L Phillips, Caroline, Khaw, Kay-Tee, Wareham, Nick, Schöttker, Ben, Saum, Kai-Uwe, Holleczek, Bernd, Nissinen, Aulikki, Tolonen, Hanna, Donfrancesco, Chiara, Vartiainen, Erkki, Jousilahti, Pekka, Harald, Kennet, B D’Agostino, Ralph, M Massaro, Joseph, Pencina, Michael, Vasan, Ramachandran, Kayama, Takamasa, Kato, Takeo, Oizumi, Toshihide, Jespersen, Jørgen, Møller, Lar, Marie Bladbjerg, Else, Chetrit, A, Rosengren, Annika, Wilhelmsen, Lar, Björkelund, Cecilia, Lissner, Lauren, Nagel, Dorothea, Dennison, Elaine, Kiyohara, Yutaka, Ninomiya, Toshiharu, Doi, Yasufumi, Rodriguez, Beatriz, Nijpels, Giel, A Stehouwer, Coen D, Sato, Shinichi, Kazumasa, Yamagishi, Iso, Hiroyasu, Goldbourt, Uri, Salomaa, Veikko, Kurl, Sudhir, Tuomainen, Tomi-Pekka, T Salonen, Jukka, Visser, Marjolein, H Deeg, Dorly J, W Meade, Tom, M Nilsson, Peter, Hedblad, Bo, Melander, Olle, H De Boer, Ian, Paul DeFilippis, Andrew, M Monique Verschuren, W, Sattar, Naveed, Watt, Graham, Meisinger, Christa, Koenig, Wolfgang, H Kuller, Lewi, Tverdal, Aage, F Gillum, Richard, A Cooper, Jackie, Kirkland, Susan, Shimbo, Daichi, Shaffer, Jonathan, Ducimetiere, Pierre, L Bakker, Stephan J, van der Harst, Pim, L Hillege, Han, J Crespo, Carlo, Amouyel, Philippe, Dallongeville, Jean, Assmann, Gerd, Schulte, Helmut, Trompet, Stella, J Smit, Roelof A, J Stott, David, T van der Schouw, Yvonne, Després, Jean-Pierre, Cantin, Bernard, R Dagenais, Gille, Laughlin, Gail, Wingard, Deborah, Trevisan, Maurizio, Aspelund, Thor, Eiriksdottir, Gudny, Freyr Gudmundsson, Elia, Ikram, Arfan, A van Rooij, Frank J, H Franco, Oscar, L Rueda-Ochoa, Oscar, Muka, Taulant, Glisic, Marija, Tunstall-Pedoe, Hugh, Völzke, Henry, V Howard, Barbara, Zhang, Ying, Jolly, Stacey, Davey-Smith, George, Can, Günay, Yüksel, Hüsniye, Nakagawa, Hideaki, Morikawa, Yuko, Miura, Katsuyuki, Njølstad, Inger, Ingelsson, Martin, Giedraitis, Vilmanta, M Ridker, Paul, Michael Gaziano, J, Kivimaki, Mika, Shipley, Martin, J Brunner, Eric, Arndt, Volker, Brenner, Hermann, Cook, Nancy, Ford, Ian, Marín Ibañez, Alejandro, M Geleijnsed, Johanna, Rod, Jackson, Paul M, Ridker, Nancy R, Cook, Ralph B, D'Agostino, Simon G, Thompson, John, Danesh, and Emanuele, Di Angelantonio
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Male ,Cardiac & Cardiovascular Systems ,Nutrition and Disease ,Prevention and Epidemiology ,PREDICTION ,Áhættuþættir ,030204 cardiovascular system & hematology ,GUIDELINES ,0302 clinical medicine ,Risk Factors ,Voeding en Ziekte ,FRAMINGHAM ,Discrimination ,Medicine ,Cardiac and Cardiovascular Systems ,Blóðrásarsjúkdómar ,Prospective Studies ,Prospective cohort study ,Non-U.S. Gov't ,1102 Cardiorespiratory Medicine and Haematology ,CALIBRATION ,Kardiologi ,Framingham Risk Score ,Emerging Risk Factors Collaboration ,SCORES ,Research Support, Non-U.S. Gov't ,Incidence (epidemiology) ,Middle Aged ,Cardiovascular disease ,Justice and Strong Institutions ,Risk prediction ,ddc ,3. Good health ,Cardiovascular Diseases ,Meta-analysis ,Cohort ,Calibration ,Female ,Risk assessment ,Cardiology and Cardiovascular Medicine ,Algorithm ,Life Sciences & Biomedicine ,Algorithms ,SDG 16 - Peace ,Risk algorithms ,DISEASE PREVENTION ,Research Support ,Risk Assessment ,VALIDATION ,03 medical and health sciences ,Clinical Research ,Journal Article ,Humans ,ddc:610 ,Risk factor ,VLAG ,Aged ,Science & Technology ,business.industry ,SDG 16 - Peace, Justice and Strong Institutions ,030229 sport sciences ,R1 ,STATIN USE ,Cardiovascular System & Hematology ,Cardiovascular System & Cardiology ,business ,PRIMARY PREVENTION ,TASK-FORCE - Abstract
Publisher's version (útgefin grein), Aims: There is debate about the optimum algorithm for cardiovascular disease (CVD) risk estimation. We conducted head-to-head comparisons of four algorithms recommended by primary prevention guidelines, before and after 'recalibration', a method that adapts risk algorithms to take account of differences in the risk characteristics of the populations being studied. Methods and results: Using individual-participant data on 360 737 participants without CVD at baseline in 86 prospective studies from 22 countries, we compared the Framingham risk score (FRS), Systematic COronary Risk Evaluation (SCORE), pooled cohort equations (PCE), and Reynolds risk score (RRS). We calculated measures of risk discrimination and calibration, and modelled clinical implications of initiating statin therapy in people judged to be at 'high' 10 year CVD risk. Original risk algorithms were recalibrated using the risk factor profile and CVD incidence of target populations. The four algorithms had similar risk discrimination. Before recalibration, FRS, SCORE, and PCE over-predicted CVD risk on average by 10%, 52%, and 41%, respectively, whereas RRS under-predicted by 10%. Original versions of algorithms classified 29-39% of individuals aged ≥40 years as high risk. By contrast, recalibration reduced this proportion to 22-24% for every algorithm. We estimated that to prevent one CVD event, it would be necessary to initiate statin therapy in 44-51 such individuals using original algorithms, in contrast to 37-39 individuals with recalibrated algorithms. Conclusion: Before recalibration, the clinical performance of four widely used CVD risk algorithms varied substantially. By contrast, simple recalibration nearly equalized their performance and improved modelled targeting of preventive action to clinical need., The work of the co-ordinating centre was funded by the UK Medical Research Council (G0800270), British Heart Foundation (SP/09/ 002), British Heart Foundation Cambridge Cardiovascular Centre of Excellence, UK National Institute for Health Research Cambridge Biomedical Research Centre, European Research Council (268834), and European Commission Framework Programme 7 (HEALTH-F2-2012-279233). The Emerging Risk Factor Collaboration’s website https://www.phpc.cam.ac.uk/ceu/erfc/list-of-studies/ has compiled a list provided by investigators of some of the funders of the component studies in this analysis. I.W. was supported by the Medical Research Council Unit Programme MC_UU_12023/21. M.K. is supported by the Netherlands Organization for Scientific Research (NWO) Veni grant (Veni, 91616079). J.P. is supported by Erasmus Mundus Western Balkans (ERAWEB), a project funded by the European Commission.
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- 2019
12. Abdominal obesity with hypertriglyceridaemia, lipoprotein(a) and apolipoprotein A-I determine marked cardiometabolic risk
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Onat, Altan, Can, Günay, Örnek, Ender, Sansoy, Vedat, Aydn, Mesut, and Yüksel, Hüsniye
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- 2013
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13. High Absolute Coronary Disease Risk among Turks: Involvement of Risk Factors Additional to Conventional Ones
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Onat, Altan, Can, Günay, Hergenç, Gülay, Küçükdurmaz, Zekeriya, Uğur, Murat, and Yüksel, Hüsniye
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- 2010
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14. Contribution of TEKHARF Study to Medical Science in Recent Years
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Yüksel, Hüsniye, primary
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- 2018
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15. Additional file 1: Figure S1. of Gender-modulated risk of coronary heart disease, diabetes and coronary mortality among Turks for three major risk factors, and residual adiposity risk
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Can, Günay, Onat, Altan, Yurtseven, Eray, Karadeniz, Yusuf, Tuğba Akbaş-Şimşek, Ayşem Kaya, and Yüksel, Hüsniye
- Abstract
Comparative sex distribution of the proportions in the three adiposity categories is shown. Though men prevail in “normal weight” and overweight categories, women predominate in obesity by over two-fold. (DOCX 15 kb)
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- 2016
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16. Lower circulating migration inhibitory factor protein is associated with metabolic syndrome and diabetes
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Onat, Altan, primary, Ademoğlu, Evin, additional, Can, Günay, additional, Çoban, Neslihan, additional, Kaya, Ayşem, additional, and Yüksel, Hüsniye, additional
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- 2017
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17. Lipoprotein(a)-activated immunity, insulin resistance and new-onset diabetes
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Kaya, Ayşem, primary, Onat, Altan, additional, Yüksel, Hüsniye, additional, Can, Günay, additional, Yüksel, Murat, additional, and Ademoğlu, Evin, additional
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- 2017
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18. In memory of Prof. Dr. Altan Onat
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Yüksel, Hüsniye, primary
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- 2017
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19. Sex-dependent independent prediction of incident diabetes by depressive symptoms
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Akbaş-Şimşek, Tuğba, primary, Onat, Altan, additional, Kaya, Adnan, additional, Tusun, Eyyup, additional, Yüksel, Hüsniye, additional, and Can, Günay, additional
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- 2016
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20. TEKHARF çalışmasının son yıllarda tıp bilimine katkıları.
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Yüksel, Hüsniye
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- 2018
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21. Advances in understanding gender difference in cardiometabolic disease risk.
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Onat, Altan, Karadeniz, Yusuf, Tusun, Eyyup, Yüksel, Hüsniye, Kaya, Ayşem, Yüksel, Hüsniye, and Kaya, Ayşem
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GENDER differences (Psychology) ,CARDIOVASCULAR diseases risk factors ,LIPOPROTEINS ,OBESITY ,POSTMENOPAUSE ,CARDIOVASCULAR disease prevention ,PREVENTION of obesity ,CARDIOVASCULAR diseases ,COMPARATIVE studies ,ESTROGEN ,HIGH density lipoproteins ,IMMUNITY ,INFLAMMATION ,INSULIN resistance ,RESEARCH methodology ,MEDICAL cooperation ,RESEARCH ,SEX distribution ,PHENOTYPES ,DISEASE management ,EVALUATION research ,METABOLIC syndrome - Abstract
Gender differences exist in cardiovascular or metabolic disease risk, beyond the protective effect of estrogens, mostly burdening the postmenopausal female. We aimed to review herein sex differences in pro-inflammatory states, the independence of inflammation from insulin resistance, differences in high-density lipoprotein dysfunction, in gene-environment interactions, and in the influence of current and former smoking on cardiometabolic risk. Sex differences in absorption of long-chain fatty acids are highlighted. Differences exist in the first manifestation of cardiovascular disease, men being more likely to develop coronary heart disease as a first event, compared to women who have cerebrovascular disease or heart failure as a first event. Autoimmune activation resulting from pro-inflammatory states, a fundamental mechanism for numerous chronic diseases in people prone to metabolic syndrome, is much more common in women, and these constitute major determinants. Therapeutic approaches to aspects related to sex difference are briefly reviewed. [ABSTRACT FROM AUTHOR]
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- 2016
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22. Gender-modulated risk of coronary heart disease, diabetes and coronary mortality among Turks for three major risk factors, and residual adiposity risk
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Can, Günay, primary, Onat, Altan, additional, Yurtseven, Eray, additional, Karadeniz, Yusuf, additional, Akbaş-Şimşek, Tuğba, additional, Kaya, Ayşem, additional, and Yüksel, Hüsniye, additional
- Published
- 2016
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23. The roles of the GPX1 Pro198Leu and OGG1 Ser326Cys variants in coronary artery disease / GPX1 geni Pro198Leu ve OGG1 geni Ser326Cys varyantlarının koroner arter hastalığındaki rolleri
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Bayoğlu, Burcu, primary, Çakmak, Hüseyin Altuğ, additional, Yüksel, Hüsniye, additional, Kurt, Esin, additional, and Cengiz, Müjgan, additional
- Published
- 2016
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24. Lipoprotein(A) Level and Mif Gene Variant Predict Incident Metabolic Syndrome and Mortality
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Onat, Altan, primary, Can, Günay, additional, Çoban, Neslihan, additional, Dönmez, İbrahim, additional, Çakır, Hakan, additional, Ademoğlu, Evin, additional, Erginel-Ünaltuna, Nihan, additional, and Yüksel, Hüsniye, additional
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- 2016
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25. Sex-dependent independent prediction of incident diabetes by depressive symptoms.
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Akbaş‐Şimşek, Tuğba, Onat, Altan, Kaya, Adnan, Tusun, Eyyup, Yüksel, Hüsniye, and Can, Günay
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MENTAL depression ,REGRESSION analysis ,DIABETES ,GENDER differences (Psychology) ,OBESITY ,DIAGNOSIS of mental depression ,TYPE 2 diabetes ,SEX distribution ,PREDICTIVE tests ,DISEASE incidence ,PROPORTIONAL hazards models ,WAIST circumference - Abstract
Objective: To study the predictive value of depressive symptoms (DeprSs) in a general population of Turkey for type 2 diabetes.Methods: Responses to three questions served to assess the sense of depression. Cox regression analyses were used regarding risk estimates for incident diabetes, after exclusion of prevalent cases of diabetes. Mean follow-up consisted of 5.15 (±1.4) years.Results: Depressive symptoms were present at baseline in 16.2% of the whole study sample, threefold in women than men. Reduced physical activity grade was the only significant covariate at baseline in men, while younger age and lower blood pressure were significantly different in women compared with those without DeprS. In men, presence of DeprS predicted incident diabetes at a significant 2.58-fold relative risk (95% confidence interval 1.03; 6.44), after adjustment for age, systolic blood pressure, and antidepressant drug usage. When further covariates were added, waist circumference remained the only significant predictor, while DepS was attenuated to a relative risk of 2.12 (95% confidence interval 0.83; 5.40). DeprS was not associated with diabetes in women, whereas antidepressant drug usage only tended to be positively associated.Conclusion: Gender difference existed in the relationship between DeprS and incident diabetes. DeprS predicted subsequent development of diabetes in men alone, not in women. Copyright © 2016 John Wiley & Sons, Ltd. [ABSTRACT FROM AUTHOR]- Published
- 2017
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26. Tenth categories of total and HDL cholesterol fail to independently predict death risk in middle-aged Turkish adults.
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Onat, Altan, Can, Günay, Keskin, Muhammed, Çamkıran, Volkan, Uzun, Ahmet Okan, and Yüksel, Hüsniye
- Abstract
Copyright of Archives of the Turkish Society of Cardiology / Türk Kardiyoloji Derneği Arşivi is the property of KARE Publishing and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)
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- 2017
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27. An inverse-to-anticipated relationship of Lp-PLA2 activity in diabetes: Reflection of underlying autoimmune activation
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Onat, Altan, primary, Akbaş, Tuğba, additional, and Yüksel, Hüsniye, additional
- Published
- 2015
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28. Türk halkında kronik atriyal fibrilasyon insidansı, prevalansı ve mortalitesine ilişkin tahminler
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Uyarel, Hüseyin, Onat, Altan, Yüksel, Hüsniye, Can, Günay, Ordu, Serkan, and Dursunoğlu, Dursun
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Kalp ve Kalp Damar Sistemi - Abstract
Amaç: Bu çalışmada, Türk toplumunda kronik atriyal fibrilasyonun (AF) prevalansı, insidansı ve mortalitesi araştırıldı. Ça lış ma pla nı: Türk Erişkinlerinde Kalp Hastalığı ve Risk Faktörleri (TEKHARF) Çalışması’nın son olarak 2006/07 taramasına kadar izlenen kohortu öne dönük ve kesitsel olarak analiz edildi. Katılımcı sayısı 3450 (1707 erkek, 1743 kadın; ort. yaş 5213) idi. Atriyal fibrilasyon prevalansı için ölen katılımcılar, insidansı için başlangıçta AF bulunan bireyler dışlandı. Bul gu lar: Altmış yedi kişide AF belirlendi. Toplam takip süresi 34 100 kişi-yılı (ortalama 9.9 yıl) idi. Prevalan AF 43, insidan AF 46 katılımcıda saptandı. Genel prevalans %1.25 idi ve dağılımı 32-59, 60-69 ve 70 yaş gruplarında sırasıyla %0.46, %2.09 ve %2.49 idi. Genel insidans 1000 kişi-yılı başına 1.35 bulundu ve aynı yaş gruplarına dağılımı sırasıyla 0.31, 1.98 ve 3.50 idi. Prevalans ve insidans oranları tüm yaş gruplarında kadınlarda erkeklerden daha yüksek idi (kadın/erkek oranı, prevalans için 1.69, insidans için 1.19). İnsidan olgularda sağkalım iki cinsiyette de 5-9 yıl arasındaydı. Toplam mortalite 100 kişi-yılı başına 6.8 bulundu. Hipertansiyon AF için en önemli etken iken, bunu ileri yaş takip etmekteydi. Atriyal fibrilasyonlu erkeklerin bel çevresi, beklenenin aksine kadınlara göre 1.9 cm daha dardı. C-reaktif protein düzeyleri AF’li erkeklerde ortalama 1.21 mg/l ile, hem AF’li kadınlara (ort. 2.62 mg/l), hem de AF bulunmayan erkeklere (ort. 1.78 mg/l) göre anlamlı derecede düşüktü. So nuç: Türk yetişkinlerinde, kronik AF insidansının yılda 35 bin (22 bini kadın), prevalansının ise halen 310 bin (200 bini kadın) olduğu tahmin edilmektedir. İnflamasyon sürecinin erkeklerimizde bu aritminin patogenezinde daha az önemle yer alması olasılığının AF’nin daha sık gelişmemesinde rolü olabilir. Objectives: We investigated the incidence, prevalence, and mortality of chronic atrial fibrillation (AF) in Turkish adults. Study design: In a prospective and cross-sectional design, we analyzed 3,450 eligible participants (1707 men, 1743 women; mean age 52±13 years) of the Turkish Adult Risk Factor Study, who had been surveyed until 2006/07. Those who were dead and were found to have AF at baseline were excluded in the estimation of AF prevalence and incidence, respectively. Results: Atrial fibrillation was determined in 67 participants. The total follow-up was 34,100 person-years (mean 9.9 years). There were 43 prevalent and 46 incident cases, which corresponded to 1.25% and 1.35 per 1000 personyears, respectively. For age brackets of 32-59, 60-69, and ≥70 years, the prevalence rates were 0.46%, 2.09%, and 2.49%, and the incidence rates were 0.31, 1.98, and 3.50 per 1000 person-years, respectively. Both were higher in women of all age groups, with female-to-male ratios for overall prevalence and incidence being 1.69 and 1.19, respectively. Survival after onset of AF was 5 to 9 years and overall mortality was 6.8 per 100 person-years. Hypertension was the most common cause of AF, followed by advanced age. Contrary to expectations, waist circumference of men with AF was smaller by 1.9 cm than that of women. Serum C-reactive protein levels in men with AF (mean 1.21 mg/l) were significantly lower than women with AF (mean 2.62 mg/l) and than males without AF (mean 1.78 mg/l). Conclusion: In Turkish adults, the current incidence and prevalence of chronic AF can be extrapolated to be 35,000 per year (22,000 in women) and 310,000 (200,000 in women), respectively. Considering the low incidence in males, it seems that inflammatory processes may play a minor role in the development of AF in Turkish men.
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- 2008
29. Algorithm for predicting CHD death risk in Turkish adults: conventional factors contribute only moderately in women.
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Onat, Altan, Can, Günay, Kaya, Ayşem, Keskin, Muhammed, Hayıroğlu, Mert İ., and Yüksel, Hüsniye
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DIAGNOSIS ,CORONARY disease ,CARDIOVASCULAR disease related mortality ,HIGH density lipoproteins ,HYPERTENSION ,HEALTH of adults ,AUTOIMMUNITY ,WOMEN ,HEALTH - Abstract
Objective: To assist the management strategy of individuals, we determined an algorithm for predicting the risk of coronary heart disease (CHD) death in Turkish adults with a high prevalence of metabolic syndrome (MetS). Methods: The risk of CHD death was estimated in 3054 middle-aged adults, followed over 9.08±4.2 years. Cox proportional hazard regression was used to predict risk. Discrimination was assessed using C-statistics. Results: CHD death was identified in 233 subjects. In multivariable analysis, the serum high-density lipoprotein-cholesterol (HDL-C) level was not predictive in men and the non-HDL-C level was not predictive in women. Age, presence of diabetes, systolic blood pressure =160 mm Hg, smoking habit, and low physical activity were predictors in both sexes. The exclusion of coronary disease at baseline did not change the risk estimates materially. Using an algorithm of the 7 stated variables, individuals in the highest category of risk score showed a 19-to 50-fold higher spread in the absolute risk of death from CHD than those in the second lowest category. C-index of the model using age alone was as high as 0.774 in men and 0.836 in women (p<0.001 each), while the incorporation of 6 conventional risk factors contributed to a C-index of 0.058 in males and 0.042 in females. Conclusion: In a middle-aged population with prevalent MetS, men disclosed anticipated risk parameters (except for high HDL-C levels) as determinants of the risk of CHD death. On the other hand, serum non-HDL-C levels and moderate systolic hypertension were not relevant in women. The moderate contribution of conventional risk factors (beyond age) to the estimation of the risk of CHD death in women is consistent with the operation of autoimmune activation. [ABSTRACT FROM AUTHOR]
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- 2017
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30. Fasting glycemia and glycated hemoglobin categories: Relationship to serum lipoprotein(a) level and disparity in 2 geographic regional groups of Turkey.
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Onat, Altan, Karadeniz, Yusuf, Can, Günay, Karakoyun, Süleyman, Özpamuk-Karadeniz, Fatma, Kaya, Ayşem, and Yüksel, Hüsniye
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BLOOD lipoproteins ,GLUCOSE analysis ,GLYCOSYLATED hemoglobin ,REGRESSION analysis ,CREATININE - Abstract
Objective: The goal of the present study was to determine covariates of serum lipoprotein (Lp) (a) within fasting glucose and glycated hemoglobin (HbA1c) categories, and to detect features that were different among covariates based on residence in Marmara and Central Anatolia (Marm-CA) regions or remaining 5 geographic regions of Turkey. Methods: Data of randomly-selected group of 1167 men and women (mean age 61 years) who participated in biennial surveys of 2013 and 2015 were cross-sectionally analyzed in 6 categories. Results: In multiple linear regression analysis of nondiabetic women, homeostatic model assessment (HOMA) index score was inversely associated with Lp(a) (β coefficient 0.49; p=0.001); this was not true for men. In the whole sample, Lp(a) was significantly positively associated with female sex and with serum creatinine, and inversely in each sex with HOMA index (β coefficient 0.63; p<0.001). Linear models within separate categories showed significant associations of Lp(a) only in individuals with no evidence of diabetes other than HbA1c >6.5%: in women, positive association with total cholesterol and inverse relationship with creatinine were found, and in men, positive association with apolipoprotein (apo) B was determined. Similar age, diastolic blood pressure, fasting glucose, triglyceride, uric acid, and C-reactive protein values were obtained from participants of 2 regional groups. Residents of the Marm-CA region who were nondiabetic exhibited significantly (by 23%) lower serum Lp(a) among individuals with HbA1c ≥5.7%, significantly higher HOMA index score, concentrations of apoB, and low-density lipoprotein cholesterol. Conclusion: Hallmark of prediabetic and diabetic glycemia/HbA1c categories seems to be an independent inverse association between Lp(a) protein (yet not of apoB) and HOMA score, this being primarily so in residents of Marm-CA region. [ABSTRACT FROM AUTHOR]
- Published
- 2017
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31. Low acylation stimulating protein levels are associated with cardiometabolic disorders-secondary to autoimmune activation?
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Onat, Altan, Altay, Servet, Yüksel, Murat, Karadeniz, Yusuf, Can, Günay, Yüksel, Hüsniye, and Ademoğlu, Evin
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ACYLATION ,DEACYLATION ,AUTOIMMUNE diseases ,TESTOSTERONE ,METABOLIC disorders - Abstract
Objective: We investigated the possible association of serum acylation stimulating protein (ASP) with cardiometabolic disorders and the evidence of autoimmune activation. Methods: Population-based randomly selected 1024 participants were cross-sectionally and prospectively analyzed. ASP concentrations were measured with a validated ELISA kit. Correlations were sought separately in subjects with no cardiometabolic disorders (n=427) designated as "healthy." Results: ASP was positively correlated with total testosterone and inversely correlated with platelet activating factor (PAF), PAF-acetylhydrolase (AH), in each gender, and positively correlated in "healthy" men with lipoprotein [Lp](a) and apolipoprotein B. Correlations of ASP with PAF values ≥22 nmol/L were abolished, contrasted to a strongly inverse one in subjects with PAF <22 nmol/L. In linear regression analyses in the whole sample, ASP was inversely associated independently with PAF and PAF-AH and, in men, positively with Lp(a) and sex hormone-binding globulin. Prevalent and (at 2.0 years' follow-up) incident metabolic syndrome (MetS, n=393), diabetes (n=154), and coronary heart disease (CHD, n=171) were analyzed by sex-, age-, and Lp(a)-adjusted logistic regression, using tertiles of ASP and PAF. The lower two (<42 nmol/L) ASP tertiles were a risk factor in combined sexes for MetS and diabetes. In women, incident CHD was predicted by either reduced or elevated ASP tertiles. Conclusion: Findings can be explained by the notion of operation of immune responses against both ASP and oxidized PAF-like lipids of Lp(a) to yield for "reduced" values and increased likelihood of cardiometabolic disorders. [ABSTRACT FROM AUTHOR]
- Published
- 2017
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32. Serum creatinine is associated with coronary disease risk even in the absence of metabolic disorders
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Onat, Altan, primary, Yüksel, Hüsniye, additional, Can, Günay, additional, Köroğlu, Bayram, additional, Kaya, Ayşem, additional, and Altay, Servet, additional
- Published
- 2013
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33. The serious adjustment bias and competing outcomes in hypertriglyceridemic waist phenotype
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Onat, Altan, primary, Köroglu, Bayram, additional, and Yüksel, Hüsniye, additional
- Published
- 2013
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34. Rheumatoid factor mediates excess serum lipoprotein(a) for independent association with type 2 diabetes in men.
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Onat, Altan, Ademoğlu, Evin, Can, Günay, Altay, Servet, Karagöz, Ahmet, Köroglu, Bayram, and Yüksel, Hüsniye
- Abstract
Objective: The potential association of rheumatoid factor (RF) and lipoprotein (Lp)(a) levels, as well as with the likelihood of type 2 diabetes and hypertension, needs exploring. Methods: Cross-sectional associations were sought in this unselected and population-based 1539-adult cohort (age 58.8±10.6 years). RF was assayed nephelometrically. Multiple logistic regression analyses were used for covariates of RF positivity and for the latter's association with diabetes and hypertension. Results: RF-positive individuals were older, fewer current smokers, had significantly lower fasting triglycerides (by 13%), higher fibrinogen, and tended to higher sex hormone-binding globulin (SHBG) levels. Whereas, women had a similar risk profile irrespective of RF status, RF-positive men had significantly higher Lp(a). In contrast to Lp(a) being positively correlated with SHBG in RF-negative subjects (r=0.08; p=0.007), an inverse correlation existed in seropositive individuals (r=-0.32, p=0.011), suggesting the interplay of an immune complex. In regression analyses, RF positivity was associated with Lp(a) in men but not in women, [OR 1.53 (1.19; 1.96)], independent of age, SHBG, and C-reactive protein (CRP). RF positivity was further associated with diabetes [OR 1.98 (95% CI 1.11; 3.52)] in the whole sample, additively to waist circumference and CRP, major determinants of diabetes. RF-positive subjects were not significantly associated independently with hypertension. Conclusion: Autoimmune activation linked to Lp(a) is mediated by the autoantibody RF in contributing to the development of type 2 diabetes. [ABSTRACT FROM AUTHOR]
- Published
- 2015
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35. Diverging sex-specific long-term effects of cigarette smoking on fasting insulin and glucose levels in non-diabetic people
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Onat, Altan, primary, Can, Günay, additional, Çiçek, Gökhan, additional, Doğan, Yüksel, additional, Kaya, Hasan, additional, Gümrükçüoğlu, Hasan Ali, additional, and Yüksel, Hüsniye, additional
- Published
- 2012
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36. APOC3 482C>T polymorphism, circulating apolipoprotein C-III and smoking: Interrelation and roles in predicting type-2 diabetes and coronary disease
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Onat, Altan, primary, Erginel-Unaltuna, Nihan, additional, Çoban, Neslihan, additional, Çiçek, Gökhan, additional, and Yüksel, Hüsniye, additional
- Published
- 2011
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37. An Alarming Increase in Blood Triglyceride Levels for Community Health Reflects Protective Protein Defects
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ONAT, Altan, primary, HERGENÇ, Gülay, additional, CAN, Günay, additional, YÜKSEL, Hüsniye, additional, UĞUR, Murat, additional, and KAYA, Hasan, additional
- Published
- 2010
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38. Evaluation of association between common genetic variants on chromosome 9p21 and coronary artery disease in Turkish population.
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Çakmak, Hüseyin Altuğ, Bayoğlu, Burcu, Durmaz, Eser, Can, Günay, Karadag, Bilgehan, Cengiz, Müjgan, Vural, Vural Ali, and Yüksel, Hüsniye
- Subjects
CORONARY disease ,CARDIOVASCULAR diseases risk factors ,SINGLE nucleotide polymorphisms ,DISEASE susceptibility ,POLYMERASE chain reaction ,MULTIPLE regression analysis ,GENETICS - Abstract
Objective: Coronary artery disease (CAD), which develops from complex interactions between genetic and enviromental factors, is a leading cause of death worldwide. Based on genome-wide association studies (GWAS), the chromosomal region 9p21 has been identified as the most relevant locus presenting a strong association with CAD in different populations. The aim of the present study was to investigate the association of two SNPs on chromosome 9p21 on susceptibility to CAD and the effect of these SNPs along with cardiovascular risk factors on the severity of CAD in the Turkish population. Methods: This study had an observational case-control design. We genotyped 460 subjects, aged 30-65 years, to investigate the association of 2 SNPs (rs1333049, rs2383207) on chromosome 9p21 and CAD risk in Turkish population. Real-time polymerase chain reaction (RT-PCR) was used to analyze the 2 SNPs in CAD patients and healthy controls. The genotype and allelic variations of these SNPs with the severity of CAD was also assessed using semi-quantitative methods such as the Gensini score. Student's t test and multiple regression analysis were used for statistical analysis. Results: The SNPs rs1333049 and rs2383207 were found to be associated with CAD with an adjusted OR of 1.81 (95% Cl 1.05-3.12) and 2.12 (95% CI 1.19-4.10) respectively. After adjustment of CAD risk factors such as smoking, family history of CAD and diabetes, the homozygous AA genotype for rs2383207 increased the CAD risk with an OR 3.69. Also a very strong association was found between rs1333049 and rs2383207 and Gensini scores representing the severity of CAD (p<0.001). Conclusion: The rs2383207 and rs1333049 SNPs on 9p21 chromosome were significantly associated with the risk and severity of CAD in the Turkish population. [ABSTRACT FROM AUTHOR]
- Published
- 2015
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39. Short and Long Term Survival of Surgical Treatment of Left Ventricular Aneurysms. Ten Years Experience.
- Author
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Ural, Ertan, primary, Yüksel, Hüsniye, additional, Pehlivanoglu, Seçkin, additional, Bakay, Cihat, additional, and Olga, Rüstem, additional
- Published
- 2002
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40. Long-Term Prognosis after a First Myocardial Infarction in Turkey: Determinants of Mortality and Reinfarction
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Yüksel, Hüsniye, primary, Güzelsoy, Deniz, additional, Yazicioğlu, Nuran, additional, Şenocak, Mustafa, additional, Öztürk, Muzaffer, additional, and Demiroglu, Cemi, additional
- Published
- 1994
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41. Increased apolipoprotein A-I levels mediate the development of prehypertension among Turks.
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Onat, Altan, Can, Günay, Örnek, Ender, Çiçek, Gökhan, Murat, Sani N., and Yüksel, Hüsniye
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APOLIPOPROTEIN A ,PREHYPERTENSION ,TYPE 2 diabetes ,CORONARY disease ,HYPERTENSION ,TURKS ,DISEASES - Abstract
Copyright of Anatolian Journal of Cardiology / Anadolu Kardiyoloji Dergisi is the property of KARE Publishing and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)
- Published
- 2013
- Full Text
- View/download PDF
42. Dissection of the interventricular septum by unruptured right and left sinus of Valsalva aneurysms
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Yüksel, Hüsniye, primary, Yazicioǧlu, Nuran, additional, Sarioǧlu, Tayyar, additional, Çeliker, Cengiz, additional, Paker, Tufan, additional, Enar, Rasim, additional, Aytaç, Aydin, additional, and Demiroǧlu, Cem'i, additional
- Published
- 1991
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43. İloprost ile tedavi edilen bir kolesterol emboli sendromu olgusu.
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Karadağ, Berrin, DöventaŞ, Alper, Özkan, Hasan, Erdinçler, Deniz Suna, Beğer, Tanju, and Yüksel, Hüsniye
- Published
- 2007
44. Autoimmune activation, a fundamental mechanism of coronary artery disease risk, missed by inadequate analysis.
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Onat, Altan and Yüksel, Hüsniye
- Published
- 2013
45. Tenth categories of total and HDL cholesterol fail to independently predict death risk in middle-aged Turkish adults
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Volkan Çamkıran, Altan Onat, Muhammed Keskin, Günay Can, Ahmet Okan Uzun, Hüsniye Yüksel, Çamkıran, Volkan, Altan Onat, Altan, Can,Günay, Keskin, Muhammed, Uzun, Ahmet Okan, Yüksel, Hüsniye, Koç University Hospital, and Department of Cardiology
- Subjects
Male ,lcsh:Diseases of the circulatory (Cardiovascular) system ,Turkey ,lcsh:Medicine ,030204 cardiovascular system & hematology ,Cohort Studies ,Decile ,Medicine ,Cardiology ,Cardiovascular system ,0302 clinical medicine ,Risk Factors ,turkish adult risk factor study ,Longitudinal Studies ,030212 general & internal medicine ,Aged, 80 and over ,Mortality rate ,Hazard ratio ,Middle Aged ,High-density lipoprotein cholesterol ,Mortality risk ,Sex ,Turkish adult risk factor study ,Total cholesterol ,Cholesterol ,Predictive value of tests ,Regression Analysis ,Female ,Cardiology and Cardiovascular Medicine ,Cohort study ,lcsh:Internal medicine ,medicine.medical_specialty ,Hypercholesterolemia ,03 medical and health sciences ,Sex Factors ,Predictive Value of Tests ,high-density lipoprotein cholesterol ,Diabetes mellitus ,Internal medicine ,medicine ,Humans ,sex ,Mortality ,Risk factor ,lcsh:RC31-1245 ,Aged ,Proportional Hazards Models ,Proportional hazards model ,business.industry ,Cholesterol, HDL ,lcsh:R ,medicine.disease ,Endocrinology ,total cholesterol ,lcsh:RC666-701 ,mortality risk ,business ,Demography - Abstract
Objective: The aim of this study was to delineate in detail the longitudinal association of total cholesterol (TC) and high-density lipoprotein cholesterol (HDL-C) levels with overall mortality in middle-aged partici pants of the biennial Turkish Adult Risk Factor study.Methods: Baseline lipid variables were analyzed in sex-specific deciles. A baseline age of 45 to 84 years as an inclusion criterion led to the enrollment of 2121 men and women. Cox regression analyses were performed. Results: Deaths were recorded in 237 and 306 women and men, respectively, during a mean 8.85 +/- 4.4 years of follow-up. Afte r adjustment for age, smoking status, lipid-lowering and antihypertensive drug usage, prevalent diabetes, and coronary heart disease, and using the lowest decile as referent, neither TC (p trend=0.94 and 0.96, respectively), nor HDL-C categories (p trend=0.20 and 0.31, respectively) were significantly predictive of mortality in either gender. TC deciles exhibited a gender difference insofar as hazard ratios in females tended to be reciprocal to those in males in deciles 2 through 5. Conclusion: The findings on TC deciles may be attributed to a comparatively higher death rate in the female (compared with male) bottom decile, reflecting the autoimmune process-induced elevated risk in the lowest decile. Observations on HDLC confirmed presumed pro-inflammatory conversion in levels >50 mg/dL. These results have important clinical implications., TOFAS; Turkish Society of Cardiology
- Published
- 2017
46. Female and urban participants demonstrate an adverse trend in overall mortality in Turkey – and a report on the TARF survey 2016
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Çamkıran, Volkan, Altan Onat, Altan, Can,Günay, Keskin, Muhammed, Uzun, Ahmet Okan, Yüksel, Hüsniye, Koç University Hospital, and Department of Cardiology
- Subjects
Mortality trend ,Sex ,Turkey-epidemiology ,Medicine ,Cardiology ,Cardiovascular system - Abstract
Objective: This study is an examination of 1) overall mortality trend in the Turkish Adult Risk Factor (TARF) study stratified by sex and place of residence, and 2) brief report on main aspects of the 2016 survey. Methods: The period of last 18 years was divided into 2 for trend analysis of data. Required information on deaths was obtained. Baseline age >= 40 years at the beginning of each period was the inclusion criterion. Cox regression analyses were performed. Results: Among over 2500 participants in each, deaths were recorded in 281 and 334 individuals in Periods 1 and 2, respectively, and baseline mean age was 54.6 years and 56.4 years, respectively, in each period. Age-adjusted hazard ratio for mortality in Period 2 remained virtually the same for rural males, rose to borderline significance for urban males and rural females (p=0.06, p=0.09), and increased 1.72-fold for urban females (p=0.006), as compared to Period 1. Whereas males gained an average of 3.8 years of survival in the later period compared with the earlier period, females gained only 1.8 years. This narrowed the difference in mean age at death in favor of women from 2.5 years to 0.5 year. Of 1144 participants to be surveyed in the TARF 2016, 48 were lost to follow-up, 695 were examined, and 39 participants were ascertained to be deceased. In 362 cases, verbal information was obtained regarding health status. Conclusion: Gain in survival in Turkish women has distinctly stagnated compared with men, and hazard of death has risen significantly for women and urban residents in the past decade, suggesting interaction between female sex and urban residence. Both phenomena require recognition and adoption of appropriate measures., TOFAS; Turkish Society of Cardiology
- Published
- 2017
47. Mitral anulus kalsifikasyonun kardiyovasküler risk faktörleri ve global kardiyovasküler risk skorları ile ilişkisi
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Ajouz, Bassam, Yüksel, Hüsniye, and Kardiyoloji Ana Bilim Dalı
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Kardiyoloji ,Cardiovascular system ,Cardiovascular diseases ,Risk factors ,Cardiology ,Mitral valve ,Scales ,Mitral valve stenosis ,Mitral valve insufficiency ,Calcification - Abstract
Amaç: Mitral anulus kalsifikasyonu (MAK) yaşla artış gösteren mitral kapağın fibröz iskeletinin kronik dejeneratif kalsifikasyonudur. Patolojik çalışmalar MAK'ın ateroskleroza benzer etyolojiye sahip olduğunu göstermiştir. Bu çalışmanın amacı MAK ile kardiyovasküler risk faktörleri ve kardiyovasküler risk skorları arasındaki ilişkiyi değerlendirmektir.Metod: Çalışmamızda Cerrrahpaşa Tıp Fakültesi Kardiyoloji Anabilim Dalın'da Nisan 2010 - Nisan 2012 tarihleri arasında takip edilen 2075 hastanın tıbbi kayıtları retrospektif olarak incelendi, 2075 hastadan ekokardiyografi ile MAK olan 400 hastadan oluşan özel bir çalışma grubu seçildi. Bu 400 hasta, klasik kardiyovasküler risk faktörleri ve kardiyovasküler risk skorları (Türk Kardiyoloji Derneği risk skoru, Framingham risk skoru ve Amerikan Kalp Derneği ACC/AHA 2013 risk skoru) yönünden incelenip, yaş ve cinsiyet özellikleri benzer olan MAK olmayan 400 hastadan oluşan bir kontrol grubu ile karşılaştırıldı.Dört yüz MAK olan hastanın arasında, akut koroner sendromu tanısıyla (AKS) hastaneye başvuran ve daha önceden kardiyak hastalığı olmayan 83 hasta alt grubu oluşturdu. AKS alt grubu ile diğer gruplar arasında aynı yönlerden karşılaştırmalar yapıldı.Bulgular: Kardiyovasküler aile öyküsü MAK ve kontrol grupları arasında anlamlı farklılık göstermedi (p>0,05). Diğer kardiyovasküler risk faktörleri ise dislipidemi, hipertansiyon, sigara kullanımı ve diyabet MAK grubunda kontrol grubuna göre istatistiksel olarak anlamlı (p0,05). The other cardiovascular risk factors dislipidemia, hipertension, smoking and diabetes mellitus were significantly higher in the MAC group (p
- Published
- 2015
48. Vitronektin düzeyinin akut koroner sendromlu hastalarda diagnostik ve prognostik önemi
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Aslan, Serkan, Yüksel, Hüsniye, and Kardiyoloji Ana Bilim Dalı
- Subjects
Kardiyoloji ,Coronary disease ,Cardiovascular system ,Diagnosis-differential ,Coronary vessels ,Cardiology ,Vitronectin ,Atherosclerosis - Abstract
Giriş ve Amaç: Vitronektin (VN) bir plazma glikoproteini olup ateroskleroz patogenezindeki rolü aratırılmaktadır. Çalımamızın amacı tek ölçümle akut koroner sendromda (AKS) tanı belirteci olarak kullanılabilirliini, hastane içi ve altı aylık takipte major kardiyovasküler olay (MACE) öngörü deerini belirlemektir. Materyal ve Metod: Çalıma popülasyonu ST elevasyonlu akut miyokard infarktüslü (STEM) 30, non-ST elevasyonlu akut koroner sendromlu (NSTE-AKS) 32 hasta ve koroner arterleri anjiyografik olarak normal 18 bireyden olutu. Bavuruda VN serum düzeyi ELISA yöntemi ile belirlendi. Hasta özellikleri, yapılan tedavi ve kardiyovasküler olaylar, prognostik risk belirteçleri kaydedildi. Hastalar 6 ay takip edildi. Ölüm, tekrarlayan AM, kalp yetersizlii, major ventriküler aritmi ve inme MACE olarak belirlendi. AKS?lerdeki VN düzeyleri normal grup ile kıyaslanarak tanı deeri aratırıldı. Bulgular: VN düzeyleri AKS?li hastalarda kontrol grubuna kıyasla yüksekti (p=0,001). AKS tanısı için ROC analizinde elde edilen 1.59 µg/ml?lik kestirim deeri %64 duyarlılık, %83 özgüllük gösterdi (p=0,004). 1.59 µg/ml üzerindeki deerler %93 pozitif prediktif deere sahipti. VN?nin üst iki kuartilinde alt iki kuartile göre hastane içi ve 6 ay izlemde MACE geliimi fazlaydı (Hastane içi p=0,026, 6 ay izlem p=0,001). Dier prognoz belirleyicileri ile çoklu regresyon analizinde baımsız olarak MACE?yi öngördü (p=0,001). KAH yaygınlıı ile VN kuartilleri arasında anlamlı bir korelasyon gözlendi (p=0.016). Gensini skoru NSTE-AKS kolunda VN düzeyi ile pozitif korelasyon bulundu (p=0,013). Sonuç: Çalımamıza dayanarak VN?nin AKS?lerde klinik ile birlikte deerlendirildiinde tanı testi olarak kullanılabileceini söyleyebiliriz. Ancak yüksek hasta katılımlı çalımalarla desteklenmelidir. AKS?lerde güçlü bir MACE öngörücüsü olduu ve KAH?ın yaygınlıının bir belirteci olduu dier çalımalara benzer ekilde bizim çalımamızla da desteklenmitir. Anahtar kelimeler: Vitronektin, akut koroner sendrom, koroner arter hastalıı, ateroskleroz, major kardiyovasküler olay Background: Vitronectin (VN) is a novel plasma glycoprotein. Its role in the pathogenesis of atherosclerosis is a subject of active investigation. The aim of this study is to determine the utility of single VN measurement in the diagnosis of acute coronary syndromes (ACS), as well as its value in predicting major cardiovascular events (MACE) in-hospital and six month period after ACS. Material and Methods: Study population consisted of 30 ST segment elevation acute myocardial infarction (STEMI), 32 non-ST segment elevation acute coronary syndrome (NSTE-ACS) patients and 18 control cases with documented normal coronary arteries. VN serum level was measured on admission for ACS, using ELISA method. Patient characteristics, administered treatments, and prognostic risk markers for cardiovascular events were recorded. Patients were followed up for six months for MACE including death, ACS, heart failure, ventricular arrhythmias and stroke. VN levels in ACS patients were compared with VN levels in control subjects in order to determine its diagnostic value. VN's predictive value was investigated in comparison with recognized prognostic markers. Findings: VN levels were higher in ACS patients compared to controls (p=0.001). VN's cut-off value was 1.59 µg/ml in the diagnosis of ACS with a sensitivity of 64% and specificity of 83% using ROC analysis (p=0.004). VN levels >1.59 µg/ml had a positive predictive value of 93%. When upper two quartiles were compared to the lower quartiles, in-hospital and 6-month MACE values were found to be significantly higher (p=0.026 and p=0.001 respectively). VN was also able to predict MACE independent of other prognostic markers in multivariate regression analysis (p=0.001). There were significant correlations between CAD severity and VN quartiles (p=0.016). A positive correlation was found between Gensini score and VN levels in the NSTE-ACS group (p=0.013). Conclusion: Based on these data, we can state that VN may be used as a diagnostic test in ACS patients together with clinical evaluation. These findings should be supported with additional studies performed in larger patient groups. The VN's strong predictive value for MACE in ACS, along with its relation with CAD severity was supported with our findings, which were in line with several previous studies. Key words: Vitronectin, acute coronary syndrome, coronary artery disease, atherosclerosis, major cardiovascular event 93
- Published
- 2012
49. Diyabetes mellitus ve sistemik arter hipertansiyonu olan hastalarda aort sertliğinin serum hyaluronidaz düzeyi ile ilişkisinin araştırılması
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Firincioğullari, Habbaş, Yüksel, Hüsniye, and Kardiyoloji Ana Bilim Dalı
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Kardiyoloji ,Cardiology - Abstract
Amaç: Aort sertliği gelisiminde meydana gelen bozukluklardan bir tanesi de vaskülerglikokaliks tabakasındaki değisimlerdir. Yüksek oksidatif stres durumlarında glikokalikstabakası hasar görmektedir ve nitrik oksid (NO) üretimine bağlı akım iliskili vazodilatasyonbozulmaktadır. Bu çalısmada diyabetes mellitus (DM) ve sistemik arter hipertansiyonu (HT)olan hastalarda aort duvarı elastikiyetini gösteren parametrelerin serum hyaluronidaz ve NOdüzeyleri ile iliskisi arastırıldı.Yöntem: Çalısmaya ?stanbul Üniversitesi Cerrahpasa Tıp Fakültesi Hastanesine tip 2DM (21 hasta), HT (30 hasta) ve DM artı HT (50 hasta) tanısı ile basvuran 101 hasta(ortalama yas 56.77±6.78, 35 erkek, 66 kadın) alındı. Çalısmaya alınan hastalaraekokardiyografik olarak aortik strain, aortik strain indeksi ve aort distensibilitesi ölçümleri, vees zamanlı olarak alınan kandan serum hyaluronidaz ve NO düzeyi ölçümleri yapıldı. Aortsertliği parametreleri serum hyaluronidaz ve NO düzeyleriyle karsılastırıldı.Bulgular: Hastalarda serum hyaluronidaz düzeyleri yüksekliği ile aortik strain, aortikstrain indeksi ve aort distensibilitesi artısı arasında anlamlı iliski saptandı (sırasıyla p
- Published
- 2009
50. Çözünür CD40 ligandının koroner arter hastalığının yaygınlığı ve şiddeti ile ilişkisi
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Cengiz, Betül, Yüksel, Hüsniye, and Kardiyoloji Ana Bilim Dalı
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Kardiyoloji ,Cardiology - Abstract
GİRİŞ VE AMAÇ: CD40/CD40 ligandı sistemi, hücresel ve humoral immün yanıtın değişik fazlarını düzenleyen bir sistemdir. CD40 ligandının hem membrana bağlı hem de çözünür haldeki formu (sCD40L), reseptörü olan CD40 ile etkileşerek birçok değişik inflamatuvar yanıta sebep olur. sCD40L, özellikle aktif trombositlerden salınmaktadır. Günümüzde aktif trombositlerin aterosklerotik lezyon gelişiminin ve restenoz sürecinin bir parçası olduğu bilinmektedir. Bu bilgilerden yola çıkarak tasarlanan çalışmamızın amacı, sCD40L düzeyleri ile koroner arter hastalığının (KAH) yaygınlığı ve şiddetinin ilişkisini araştırmaktır.YÖNTEM: Çalışmaya alınan 102 hastadan 37'si akut koroner sendrom (AKS), 41'i kararlı angina pektoris (SAP), 24' ü de kontrol grubunda yer aldı. sCD40L ölçümü için kan örnekleri, AKS grubunda hastaneye kabulde, SAP grubu ve kontrol grubunda ise koroner anjiyografi sonrasında alındı. KAH yaygınlığı ve şiddetinin göstergesi olan Gensini skoru, her darlığın derecesi ve bölgesel önemi göz önünde bulundurularak hesaplandı.BULGULAR: Ortalama sCD40L düzeyi, AKS grubunda diğer gruplara göre anlamlı olarak yüksek bulundu (p0.05). AKS alt grupları arasında ortalama sCD40L değerleri arasında anlamlı fark saptanmadı (p>0.05). AKS ve SAP grubunda, Gensini skoru ile sCD40L düzeyleri arasında anlamlı bir ilişki bulunamadı (p>0.05).SONUÇ: Koroner arter hastalığının farklı klinik tiplerinde bakılan sCD40L düzeyleri ile KAH şiddeti ve yaygınlığı arasında ilişki gösterilemedi. AKS grubunda, sCD40L düzeyleri diğer gruplara göre anlamlı olarak yüksek bulundu, ancak AKS grubunun alt grupları arasında anlamlı farklılık gözlenmedi. Bu da artmış sCD40L düzeylerinin, plak rüptürü gelişip, miyokard nekrozu oluşmadan kararsız plağın tespitinde kullanılabileceğini desteklemektedir. BACKGROUND AND OBJECTIVE: The CD40 and CD40 ligand system regulates multiple phases of the humoral and cellular immune response. Both membrane-bound and soluble forms of this ligand may interact with CD40, resulting in various inflammatory responses. Soluble CD40 ligand (sCD40L) especially releases from activated platelets. Platelets are involved in atherosclerotic lesion formation and restenosis processes. According to this knowledge, the aim of our study is to evaluate whether there is a relationship between the level of sCD40L and angiographic extent and severity of coronary artery disease (CAD).METHOD: 102 participants were included to our study (37 patients in acute coronary syndrome (ACS) group, 41 patients in stable angina pectoris group (SAP), 24 patients in control group). Peripheral venous blood samples were drawn at the Coronary Care Unit admission of ACS group patients. From SAP group patients and controls, blood samples collected after coronary angiography. The Gensini score was computed for each patient by assigning the severity score to each coronary stenosis in accordance with the degree of the vessel narrowing and its geographic importance.RESULTS: Mean serum sCD40L level was significantly higher in patients with ACS than the controls and SAP patients (p0.05).CONCLUSION: Our study doesn?t show relation between sCD40L levels and Gensini scores in patients with different clinical sub-types of CAD. In ACS group sCD40L levels were significantly higher than other groups, but there was no significant difference between ACS sub-groups. This finding suggest that increased sCD40L levels can be used as a marker for determining the unstable plaque before ruptured and occuring miyocardial necrosis. 41
- Published
- 2007
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