Modeling biological age using blood biomarkers and physical measurements in Chinese adults

被引:42
作者
Chen, Lu [1 ]
Zhang, Yiqian [1 ]
Yu, Canqing [1 ,2 ]
Guo, Yu [3 ]
Sun, Dianjianyi [1 ,2 ]
Pang, Yuanjie [1 ]
Pei, Pei [2 ]
Yang, Ling [4 ,5 ,6 ]
Millwood, Iona Y. [4 ,5 ,6 ]
Walters, Robin G. [4 ,5 ,6 ]
Chen, Yiping [4 ,5 ,6 ]
Du, Huaidong [4 ,5 ,6 ]
Liu, Yongmei [7 ]
Burgess, Sushila [5 ,6 ]
Stevens, Rebecca [5 ,6 ]
Chen, Junshi [8 ]
Chen, Zhengming [5 ,6 ]
Li, Liming [1 ,2 ]
Lv, Jun [1 ,2 ,9 ]
机构
[1] Peking Univ, Sch Publ Hlth, Dept Epidemiol & Biostat, Beijing 100191, Peoples R China
[2] Peking Univ, Ctr Publ Hlth & Epidem Preparedness & Response, Beijing 100191, Peoples R China
[3] Chinese Acad Med Sci, Fuwai Hosp, Beijing, Peoples R China
[4] Univ Oxford, Med Res Council, Populat Hlth Res Unit, Oxford, England
[5] Univ Oxford, Clin Trial Serv Unit, Oxford, England
[6] Univ Oxford, Nuffield Dept Populat Hlth, Epidemiol Studies Unit, Oxford, England
[7] Qingdao Ctr Dis Control & Prevent CDC, Qingdao, Peoples R China
[8] China Natl Ctr Food Safety Risk Assessment, Beijing, Peoples R China
[9] Peking Univ, Dept Epidemiol & Biostat, Hlth Sci Ctr, 38 Xueyuan Rd, Beijing 100191, Peoples R China
基金
中国国家自然科学基金; 国家重点研发计划; 英国惠康基金; 英国医学研究理事会;
关键词
Biological age; Blood biomarkers; Physical measurements; Mortality; Cardiovascular health; MORTALITY; KADOORIE; BIOBANK;
D O I
10.1016/j.ebiom.2023.104458
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background This study aimed to: 1) assess the associations of biological age acceleration based on Klemera and Doubal's method (KDM-AA) with long-term risk of all-cause mortality; and 2) compare the association of KDM-AA with all-cause mortality among participants potentially at different stages of the cardiovascular disease (CVD) continuum. Methods The present study was based on a subpopulation of the China Kadoorie Biobank, with baseline survey during 2004-08. A total of 12,377 participants free of ischemic heart disease, stroke, or cancer at baseline were included, in which 8180 participants were identified to develop major coronary event (MCE), ischemic stroke (IS), intracerebral hemorrhage (ICH) or subarachnoid hemorrhage (SAH), and 4197 remained free of these cardiovascular diseases before 1 January 2014. These participants were followed up until 1 Jan 2018. KDM-AA was calculated by regressing biological age measurement, which was constructed based on baseline 16 physical and 9 biochemical markers using Klemera and Doubal's method, on chronological age. We estimated the associations of KDM-AA with the mortality risk using the hazard ratio (HR) and 95% confidence interval (CI) from Cox proportional hazard models. We assessed discrimination performance by Harrell's C-index and net reclassification index (NRI). Findings The participants who developed MCE (mean KDM-AA = 0.1 year, standard deviation [SD] = 1.6 years) or ICH/SAH (0.3 +/- 1.5 years) during subsequent follow-up showed accelerated aging at baseline compared to those of IS (0.0 +/- 1.2 years) and control (-0.3 +/- 1.3 years) groups. The KDM-AA was positively associated with long-term risk of all-cause mortality (HR = 1.20; 95% CI: 1.17, 1.23), and the association was robust for participants potentially at different stages of the CVD continuum. Adding KDM-AA improved mortality prediction compared to the model only with sociodemographic and lifestyle factors in whole participants, with the Harrell's C-index increasing from 0.813 (0.807, 0.819) to 0.821 (0.815, 0.826) (NRI = 0.011; 95% CI: 0.003, 0.019). Interpretation In this middle-aged and elderly Chinese population, the KDM-AA is a promising measurement for biological age, and can capture the difference in cardiovascular health and predict the risk of all-cause mortality over a decade. Copyright (c) 2023 The Author(s). Published by Elsevier B.V.
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页数:10
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