8 results on '"Kaori Muto"'
Search Results
2. Learning to listen: A complementary approach to informed consent for patients with visual impairments
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Kayo Takashima, Takeshi Soma, Kaori Muto, Kohji Nishida, and Jusaku Minari
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Genetics ,Cell Biology ,Biochemistry ,Developmental Biology - Abstract
This forum describes an exploratory approach for assisting individuals with visual impairment during the informed consent (IC) process to participate in a cutting-edge trial. Our approach has been developed to focus on potential participants' preparedness to give IC, along with the creation of supporting audio material.
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- 2022
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3. CKD, Brain Atrophy, and White Matter Lesion Volume: The Japan Prospective Studies Collaboration for Aging and Dementia
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Kenji Maki, Tomoyuki Ohara, Jun Hata, Mao Shibata, Naoki Hirabayashi, Takanori Honda, Satoko Sakata, Yoshihiko Furuta, Masato Akiyama, Keisuke Yamasaki, Yasuko Tatewaki, Yasuyuki Taki, Takanari Kitazono, Tatsuya Mikami, Tetsuya Maeda, Kenjiro Ono, Masaru Mimura, Kenji Nakashima, Jun-ichi Iga, Minoru Takebayashi, Toshiharu Ninomiya, Shigeyuki Nakaji, Koichi Murashita, Songee Jung, Mina Misawa, Naoki Ishizuka, Hiroshi Akasaka, Yasuo Terayama, Hisashi Yonezawa, Junko Takahashi, Moeko Noguchi-Shinohara, Junji Komatsu, Shutaro Shibata, Sohshi Yuki-Nozaki, Shogyoku Bun, Hidehito Niimura, Ryo Shikimoto, Hisashi Kida, Yasuyo Fukada, Hisanori Kowa, Toshiya Nakano, Kenji Wada, Masafumi Kishi, Tomoki Ozaki, Ayumi Tachibana, Yuta Yoshino, Jun-ichi Iga Shu-ichi Ueno, Tomohisa Ishikawa, Seiji Yuki, Asuka Koyama, Naoto Kajitani, Mamoru Hashimoto, Manabu Ikeda, Yoshihiro Kokubo, Kazuhiro Uchida, Midori Esaki, Benjamin Thyreau, Koji Yonemoto, Hisako Yoshida, Kaori Muto, Yusuke Inoue, Izen Ri, Yukihide Momozawa, Chikashi Terao, Michiaki Kubo, and Yutaka Kiyohara
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Nephrology ,Internal Medicine - Published
- 2023
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4. Cross-sectional analysis of BioBank Japan clinical data: A large cohort of 200,000 patients with 47 common diseases
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Makoto Hirata, Yoichiro Kamatani, Akiko Nagai, Yutaka Kiyohara, Toshiharu Ninomiya, Akiko Tamakoshi, Zentaro Yamagata, Michiaki Kubo, Kaori Muto, Taisei Mushiroda, Yoshinori Murakami, Koichiro Yuji, Yoichi Furukawa, Hitoshi Zembutsu, Toshihiro Tanaka, Yozo Ohnishi, Yusuke Nakamura, Koichi Matsuda, Masaki Shiono, Kazuo Misumi, Reiji Kaieda, Hiromasa Harada, Shiro Minami, Mitsuru Emi, Naoya Emoto, Hajime Arai, Ken Yamaji, Yoshimune Hiratsuka, Satoshi Asai, Mitsuhiko Moriyama, Yasuo Takahashi, Tomoaki Fujioka, Wataru Obara, Seijiro Mori, Hideki Ito, Satoshi Nagayama, Yoshio Miki, Akihide Masumoto, Akira Yamada, Yasuko Nishizawa, Ken Kodama, Hiromu Kutsumi, Yoshihisa Sugimoto, Yukihiro Koretsune, Hideo Kusuoka, and Takashi Yoshiyama
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Male ,0301 basic medicine ,Pathology ,medicine.medical_specialty ,Cross-sectional study ,Epidemiology ,Common disease ,Family history ,Disease ,Logistic regression ,Cohort Studies ,03 medical and health sciences ,0302 clinical medicine ,Japan ,Internal medicine ,Databases, Genetic ,Humans ,Medicine ,Precision Medicine ,Medical History Taking ,Aged ,Biological Specimen Banks ,Biobank ,lcsh:R5-920 ,business.industry ,BioBank Japan Project ,General Medicine ,Odds ratio ,Middle Aged ,Cross-Sectional Studies ,030104 developmental biology ,030220 oncology & carcinogenesis ,Cohort ,Female ,Original Article ,Clinical information ,lcsh:Medicine (General) ,business ,Body mass index - Abstract
Background To implement personalized medicine, we established a large-scale patient cohort, BioBank Japan, in 2003. BioBank Japan contains DNA, serum, and clinical information derived from approximately 200,000 patients with 47 diseases. Serum and clinical information were collected annually until 2012. Methods We analyzed clinical information of participants at enrollment, including age, sex, body mass index, hypertension, and smoking and drinking status, across 47 diseases, and compared the results with the Japanese database on Patient Survey and National Health and Nutrition Survey. We conducted multivariate logistic regression analysis, adjusting for sex and age, to assess the association between family history and disease development. Results Distribution of age at enrollment reflected the typical age of disease onset. Analysis of the clinical information revealed strong associations between smoking and chronic obstructive pulmonary disease, drinking and esophageal cancer, high body mass index and metabolic disease, and hypertension and cardiovascular disease. Logistic regression analysis showed that individuals with a family history of keloid exhibited a higher odds ratio than those without a family history, highlighting the strong impact of host genetic factor(s) on disease onset. Conclusions Cross-sectional analysis of the clinical information of participants at enrollment revealed characteristics of the present cohort. Analysis of family history revealed the impact of host genetic factors on each disease. BioBank Japan, by publicly distributing DNA, serum, and clinical information, could be a fundamental infrastructure for the implementation of personalized medicine., Highlights • The BioBank Japan Project (BBJ) annually collected clinical information. • Analysis of the clinical information at enrollment characterized the BBJ cohort. • Analysis of family history revealed impacts of host genetic factors on the diseases.
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- 2017
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5. Statin use and all-cause and cancer mortality: BioBank Japan cohort
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Hiroshi Yokomichi, Akiko Nagai, Makoto Hirata, Akiko Tamakoshi, Yutaka Kiyohara, Yoichiro Kamatani, Kaori Muto, Toshiharu Ninomiya, Koichi Matsuda, Michiaki Kubo, Yusuke Nakamura, Zentaro Yamagata, Kazuo Misumi, Nobuyoshi Higa, Sunao Matsubayashi, Kei Matsuura, Shiro Minami, Hitoshi Sugihara, Naoya Emoto, Hirotoshi Ohmura, Akihiro Inui, Michihiro Ogasawara, Satoshi Asai, Mitsu- hiko Moriyama, Yasuo Takahashi, Tomoaki Fujioka, Wataru Obara, Seijiro Mori, Hideki Ito, Satoshi Nagayama, Yoshio Miki, Akihide Masumoto, Akira Yamada, Yasuko Nishizawa, Ken Kodama, Satoshi Ugi, Hiroshi Maegawa, Yukihiro Koretsune, Hideo Kusuoka, and Masako Ueyama
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Male ,Dyslipidaemia ,medicine.medical_specialty ,Statin ,Colorectal cancer ,medicine.drug_class ,Epidemiology ,Hyperlipidemias ,Disease ,030204 cardiovascular system & hematology ,Cohort Studies ,03 medical and health sciences ,0302 clinical medicine ,Japan ,Anti-cholesterol agents ,Cause of Death ,Neoplasms ,Internal medicine ,medicine ,Humans ,cardiovascular diseases ,Survival analysis ,Aged ,Biological Specimen Banks ,lcsh:R5-920 ,business.industry ,Mortality rate ,Statins ,nutritional and metabolic diseases ,General Medicine ,Middle Aged ,Statin treatment ,medicine.disease ,Biobank ,Colon cancer ,Endocrinology ,030220 oncology & carcinogenesis ,Cohort ,Female ,Original Article ,lipids (amino acids, peptides, and proteins) ,Hydroxymethylglutaryl-CoA Reductase Inhibitors ,lcsh:Medicine (General) ,business ,Kaplan–Meier estimate - Abstract
Background Statins are the first-line agents used to treat patients with high serum low-density lipoprotein cholesterol levels, thus reducing the risk of death from arterial sclerotic cardiovascular disease; however, little is known about the effects of non-statin pharmacological interventions on mortality as well as about the potential protective effects of statin use against cancer death. This work aimed to compare all-cause and cancer mortality among patients with hyperlipidaemia who did and did not receive statin treatment. Methods Between 2003 and 2007 fiscal years, we recruited Japanese patients diagnosed with hyperlipidaemia from 66 hospitals. Patients in our cohort were followed up for a maximum of 12 years to observe the causes of death. Kaplan–Meier estimates from the baseline were used to compare the mortality of patients based on the administered medicine. All-cause mortality were compared among patients with/without administration of statins and other agents; any-organ and colorectal cancer mortality were compared between patients with/without administration of statins. Results Our cohort included 41,930 patients with mean ages of 64–66 years and mean body mass indices of 24–25 kg/m2. Patients who received statin monotherapy and were treated with lifestyle modification exhibited nearly identical survival curves, whereas statin use represented a non-significant but potentially protective effect against colorectal cancer-related mortality. The lowest mortality in this cohort was associated with resin monotherapy. Conclusions Mortality rate has been similar for patients treated with statin monotherapy and lifestyle modification. Statin monotherapy could potentially reduce any-organ- and colorectal cancer-related mortality., Highlights • Statin-mediated reduction of low-density lipoprotein levels reduces mortality. • Little is known on the effect of non-statin hyperlipidaemia medicines on mortality. • Statin monotherapy is safe in terms of cancer mortality. • Statin use may reduce colorectal cancer-related mortality. • Resin monotherapy was associated with the lowest mortality.
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- 2017
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6. Demographic and lifestyle factors and survival among patients with esophageal and gastric cancer: The Biobank Japan Project
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Emiko Okada, Shigekazu Ukawa, Koshi Nakamura, Makoto Hirata, Akiko Nagai, Koichi Matsuda, Toshiharu Ninomiya, Yutaka Kiyohara, Kaori Muto, Yoichiro Kamatani, Zentaro Yamagata, Michiaki Kubo, Yusuke Nakamura, Akiko Tamakoshi, Rai Shimoyama, Shinichiro Makimoto, Hiromasa Harada, Tomoaki Fujikawa, Shiro Minami, Eiji Uchida, Masao Miyashita, Yoshiaki Kajiyama, Natsumi Tomita, Akihito Nagahara, Satoshi Asai, Mitsuhiko Moriyama, Yasuo Takahashi, Tomoaki Fujioka, Wataru Obara, Seijiro Mori, Hideki Ito, Satoshi Nagayama, Yoshio Miki, Akihide Masumoto, Akira Yamada, Yasuko Nishizawa, Ken Kodama, Hiromitsu Ban, Satoshi Murata, Yukihiro Koretsune, Motohiro Hirao, and Hideo Ogata
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Male ,Esophageal Neoplasms ,Survival ,Epidemiology ,Esophageal cancer ,Gastroenterology ,0302 clinical medicine ,Japan ,Risk Factors ,Young adult ,Biological Specimen Banks ,Aged, 80 and over ,lcsh:R5-920 ,Hazard ratio ,General Medicine ,Middle Aged ,Prognosis ,030220 oncology & carcinogenesis ,Carcinoma, Squamous Cell ,Female ,Original Article ,030211 gastroenterology & hepatology ,Esophageal Squamous Cell Carcinoma ,Underweight ,medicine.symptom ,lcsh:Medicine (General) ,Cohort study ,Adult ,medicine.medical_specialty ,Young Adult ,03 medical and health sciences ,Stomach Neoplasms ,Internal medicine ,medicine ,Humans ,Life Style ,Survival analysis ,Aged ,Proportional Hazards Models ,business.industry ,Proportional hazards model ,Cancer ,medicine.disease ,Survival Analysis ,digestive system diseases ,business ,Gastric cancer ,Follow-Up Studies - Abstract
Background Several studies have evaluated associations between the characteristics of patients with esophageal and gastric cancer and survival, but these associations remain unclear. We described the distribution of demographic and lifestyle factors among patients with esophageal and gastric cancer in Japan, and investigated their potential effects on survival. Methods Between 2003 and 2007, 24- to 95-year-old Japanese patients with esophageal and gastric cancer were enrolled in the BioBank Japan Project. The analysis included 365 patients with esophageal squamous cell carcinoma (ESCC) and 1574 patients with gastric cancer. Hazard ratios (HRs) and 95% confidence intervals (CIs) for mortality were estimated using medical institution-stratified Cox proportional hazards models. Results During follow-up, 213 patients with ESCC (median follow-up, 4.4 years) and 603 patients with gastric cancer (median follow-up, 6.1 years) died. Among patients with ESCC, the mortality risk was higher in ever drinkers versus never drinkers (multivariable HR = 2.37, 95% CI: 1.24, 4.53). Among patients with gastric cancer, the mortality risk was higher in underweight patients versus patients of normal weight (multivariable HR = 1.66, 95% CI: 1.34, 2.05). Compared to patients with gastric cancer with no physical exercise habit, those who exercised ≥3 times/week had a lower mortality risk (multivariate HR = 0.75, 95% CI = 0.61, 0.93). However, lack of stage in many cases was a limitation. Conclusions Among patients with ESCC, alcohol drinkers have a poor prognosis. Patients with gastric cancer who are underweight also have a poor prognosis, whereas patients with physical exercise habits have a good prognosis., Highlights • Among ESCC patients, alcohol drinkers had a poor prognosis. • Underweight gastric cancer patients had a poor prognosis. • Gastric cancer patients who exercised had a good prognosis. • No association between esophageal or gastric cancer and smoking was observed.
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- 2017
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7. Characteristics and prognosis of Japanese male and female lung cancer patients: The BioBank Japan Project
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Koshi Nakamura, Shigekazu Ukawa, Emiko Okada, Makoto Hirata, Akiko Nagai, Zentaro Yamagata, Toshiharu Ninomiya, Kaori Muto, Yutaka Kiyohara, Koichi Matsuda, Yoichiro Kamatani, Michiaki Kubo, Yusuke Nakamura, Akiko Tamakoshi, Hiromasa Harada, Makoto Hibino, Atsushi Okuyama, Nobuyasu Kano, Shiro Minami, Akihiko Genma, Jitsuo Usuda, Kenji Suzuki, Mitsuaki Sekiya, Satoru Takeda, Satoshi Asai, Mitsuhiko Moriyama, Yasuo Takahashi, Tomoaki Fujioka, Wataru Obara, Seijiro Mori, Hideki Ito, Satoshi Nagayama, Yoshio Miki, Akihide Masumoto, Akira Yamada, Yasuko Nishizawa, Ken Kodama, Noriaki Tezuka, Yasutaka Nakano, Yukihiro Koretsune, Mitsumasa Ogawara, and Kazunari Yamana
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Stage ,Adult ,Male ,medicine.medical_specialty ,Lung Neoplasms ,Epidemiology ,Histological type ,Young Adult ,03 medical and health sciences ,0302 clinical medicine ,Japan ,Risk Factors ,Internal medicine ,medicine ,Humans ,030212 general & internal medicine ,Mortality ,Intensive care medicine ,Lung cancer ,Life Style ,Biological Specimen Banks ,lcsh:R5-920 ,business.industry ,Smoking ,Cancer ,General Medicine ,Middle Aged ,Prognosis ,medicine.disease ,Biobank ,030220 oncology & carcinogenesis ,Original Article ,Female ,lcsh:Medicine (General) ,business ,Follow-Up Studies - Abstract
Background In Japanese males and females, lung cancer is currently the second and fourth most common type of cancer, and the first and second leading cause of cancer-related deaths, respectively. Methods Of all Japanese male and female lung cancer patients aged ≥20 years whom the BioBank Japan Project originally enrolled between 2003 and 2008, 764 males and 415 females were registered within 90 days after their diagnosis. We described the lifestyle and clinical characteristics of these patients at study entry. Furthermore, we examined the effect of these characteristics on all-cause mortality. Results In the lung cancer patients registered within 90 days, the frequencies of occult or stage 0, stage I, II, III and IV were 0.4%, 55.8%, 10.8%, 22.0% and 11.0% for males and 0.3%, 62.4%, 9.9%, 17.1% and 10.2% for females, respectively. The proportions of histological types in males and females were 56.3% and 82.4% for adenocarcinoma, 26.9% and 8.2% for squamous cell carcinoma, 4.5% and 1.5% for large cell carcinoma, 7.7% and 4.1% for small cell carcinoma and 4.6% and 3.8% for others, respectively. Among 1120 participants who registered within 90 days, 572 participants died during 5811 person-years of follow-up. Low body mass index, ever smoker, more advanced stage, squamous cell or small cell carcinoma and high serum carcinoembryonic antigen level at study entry were crudely associated with an increased risk of all-cause mortality after adjustment for age. Conclusions This study showed the association of several lifestyle and clinical characteristics with all-cause mortality in lung cancer patients., Highlights • Nearly one-tenth of Japanese lung cancer patients were diagnosed as stage IV. • Adenocarcinoma was the most common histological type in both males and females. • Some characteristics would affect all-cause mortality in lung cancer patients.
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- 2017
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8. Risk prediction models for mortality in patients with cardiovascular disease: The BioBank Japan project
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Jun Hata, Akiko Nagai, Makoto Hirata, Yoichiro Kamatani, Akiko Tamakoshi, Zentaro Yamagata, Kaori Muto, Koichi Matsuda, Michiaki Kubo, Yusuke Nakamura, Yutaka Kiyohara, Toshiharu Ninomiya, Shigeru Saito, Hideki Shimomura, Sinichi Higashiue, Kazuo Misumi, Shiro Minami, Masahiro Yasutake, Hitoshi Takano, Kazunori Shimada, Hakuoh Konishi, Nobukazu Miyamoto, Satoshi Asai, Mitsuhiko Moriyama, Yasuo Takahashi, Tomoaki Fujioka, Wataru Obara, Seijiro Mori, Hideki Ito, Satoshi Nagayama, Yoshio Miki, Akihide Masumoto, Akira Yamada, Yasuko Nishizawa, Ken Kodama, Yoshihisa Sugimoto, Takashi Ashihara, Yukihiro Koretsune, Sachiko Ikeda, and Ryozo Yano
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Adult ,Male ,medicine.medical_specialty ,All-cause death ,Epidemiology ,Disease ,030204 cardiovascular system & hematology ,Risk Assessment ,03 medical and health sciences ,0302 clinical medicine ,Japan ,Cause of Death ,Internal medicine ,Diabetes mellitus ,medicine ,Risk of mortality ,Humans ,Myocardial infarction ,Intensive care medicine ,Stroke ,Aged ,Biological Specimen Banks ,Cause of death ,Aged, 80 and over ,lcsh:R5-920 ,Models, Statistical ,Ischemic stroke ,business.industry ,General Medicine ,Middle Aged ,medicine.disease ,Biobank ,Cardiovascular Diseases ,Cardiovascular death ,Female ,Original Article ,lcsh:Medicine (General) ,business ,Body mass index ,030217 neurology & neurosurgery ,Follow-Up Studies ,Risk prediction model - Abstract
Background Cardiovascular disease (CVD) is a leading cause of death in Japan. The present study aimed to develop new risk prediction models for long-term risks of all-cause and cardiovascular death in patients with chronic phase CVD. Methods Among the subjects registered in the BioBank Japan database, 15,058 patients aged ≥40 years with chronic ischemic CVD (ischemic stroke or myocardial infarction) were divided randomly into a derivation cohort (n = 10,039) and validation cohort (n = 5019). These subjects were followed up for 8.55 years in median. Risk prediction models for all-cause and cardiovascular death were developed using the derivation cohort by Cox proportional hazards regression. Their prediction performances for 5-year risk of mortality were evaluated in the validation cohort. Results During the follow-up, all-cause and cardiovascular death events were observed in 2962 and 962 patients from the derivation cohort and 1536 and 481 from the validation cohort, respectively. Risk prediction models for all-cause and cardiovascular death were developed from the derivation cohort using ten traditional cardiovascular risk factors, namely, age, sex, CVD subtype, hypertension, diabetes, total cholesterol, body mass index, current smoking, current drinking, and physical activity. These models demonstrated modest discrimination (c-statistics, 0.703 for all-cause death; 0.685 for cardiovascular death) and good calibration (Hosmer-Lemeshow χ2-test, P = 0.17 and 0.15, respectively) in the validation cohort. Conclusions We developed and validated risk prediction models of all-cause and cardiovascular death for patients with chronic ischemic CVD. These models would be useful for estimating the long-term risk of mortality in chronic phase CVD., Highlights • We developed risk prediction models for death after cardiovascular disease (CVD). • Performances of these models were validated in an independent cohort. • Our models may be used to estimate mortality risk in chronic CVD patients.
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- 2016
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