TY - JOUR
T1 - Risk prediction models for mortality in patients with cardiovascular disease
T2 - The BioBank Japan project
AU - Biobank Japan Cooperative Hospital Group
AU - Hata, Jun
AU - Nagai, Akiko
AU - Hirata, Makoto
AU - Kamatani, Yoichiro
AU - Tamakoshi, Akiko
AU - Yamagata, Zentaro
AU - Muto, Kaori
AU - Matsuda, Koichi
AU - Kubo, Michiaki
AU - Nakamura, Yusuke
AU - Kiyohara, Yutaka
AU - Ninomiya, Toshiharu
AU - Saito, Shigeru
AU - Shimomura, Hideki
AU - Higashiue, Sinichi
AU - Misumi, Kazuo
AU - Minami, Shiro
AU - Yasutake, Masahiro
AU - Takano, Hitoshi
AU - Shimada, Kazunori
AU - Konishi, Hakuoh
AU - Miyamoto, Nobukazu
AU - Asai, Satoshi
AU - Moriyama, Mitsuhiko
AU - Takahashi, Yasuo
AU - Fujioka, Tomoaki
AU - Obara, Wataru
AU - Mori, Seijiro
AU - Ito, Hideki
AU - Nagayama, Satoshi
AU - Miki, Yoshio
AU - Masumoto, Akihide
AU - Yamada, Akira
AU - Nishizawa, Yasuko
AU - Kodama, Ken
AU - Sugimoto, Yoshihisa
AU - Ashihara, Takashi
AU - Koretsune, Yukihiro
AU - Ikeda, Sachiko
AU - Yano, Ryozo
N1 - Funding Information:
This study was supported by the funding from the Ministry of Education, Culture, Sports, Science, and Technology (from 2003 to March 2015) and the Japan Agency for Medical Research and Development, AMED (since April 2015).
Publisher Copyright:
© 2017 The Authors.
PY - 2017
Y1 - 2017
N2 - 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.
AB - 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.
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U2 - 10.1016/j.je.2016.10.007
DO - 10.1016/j.je.2016.10.007
M3 - Article
C2 - 28142037
AN - SCOPUS:85016436378
SN - 0917-5040
VL - 27
SP - S71-S76
JO - Journal of epidemiology
JF - Journal of epidemiology
IS - 3
ER -