Genetic predisposition to coronary artery disease is predictive of recurrent events: a Chinese prospective cohort study

被引:8
|
作者
Jiang, Jie [1 ]
Zheng, Qiwen [2 ]
Han, Yaling [3 ]
Qiao, Shubin [4 ]
Chen, Jiyan [5 ]
Yuan, Zuyi [6 ]
Yu, Bo [7 ]
Ge, Lei [8 ]
Jia, Jia [1 ]
Gong, Yanjun [1 ]
Wang, Zhi [1 ]
Chen, Dafang [2 ]
Zhang, Yan [1 ]
Huo, Yong [1 ]
机构
[1] Peking Univ, Dept Cardiol, Hosp 1, 8 Xishiku St, Beijing 100034, Peoples R China
[2] Peking Univ, Sch Publ Hlth, Dept Epidemiol & Biostat, Beijing 100191, Peoples R China
[3] Gen Hosp Northern Theater Command, Dept Cardiol, Shenyang 110016, Peoples R China
[4] Fuwai Hosp, Dept Cardiol, Beijing 100037, Peoples R China
[5] Guangdong Prov Peoples Hosp, Dept Cardiol, Guangzhou 510080, Peoples R China
[6] Xi An Jiao Tong Univ, Dept Cardiol, Affiliated Hosp 1, Xian 710061, Peoples R China
[7] Harbin Med Univ, Dept Cardiol, Affiliated Hosp 2, Harbin 150001, Peoples R China
[8] Fudan Univ, Zhongshan Hosp, Dept Cardiol, Shanghai 200032, Peoples R China
关键词
RISK SCORE; MYOCARDIAL-INFARCTION; CARDIOVASCULAR-DISEASE; INCREMENTAL VALUE; CARDIAC DEATH; LOCI; ASSOCIATION; 9P21; MI;
D O I
10.1093/hmg/ddaa025
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Evidence of the effects of genetic risk score (GRS) on secondary prevention is scarce and mixed. We investigated whether coronary artery disease (CAD) susceptible loci can be used to predict the risk of major adverse cardiovascular events (MACEs) in a cohort with acute coronary syndromes (ACSs). A total of 1667 patients hospitalized with ACS were enrolled and prospectively followed for a median of 2 years. We constructed a weighted GRS comprising 79 CAD risk variants and investigated the association between GRS and MACE using a multivariable cox proportional hazard regression model. The incremental value of adding GRS into the prediction model was assessed by integrated discrimination improvement (IDI) and decision curve analysis (DCA). In the age- and sex-adjusted model, each increase in standard deviation in the GRS was associated with a 33% increased risk of MACE (hazard ratio: 1.33; 95% confidence interval: 1.10-1.61; P = 0.003), with this association not attenuating after further adjustment for traditional cardiovascular risk factors. The addition of GRS to a prediction model of seven clinical risk factors and EPICOR prognostic model slightly improved risk stratification for MACE as calculated by IDI (+1.7%, P = 0.006; +0.3%, P = 0.024, respectively). DCA demonstrated positive net benefits by adding GRS to other models. GRS was associated with MACE after multivariable adjustment in a cohort comprising Chinese ACS patients. Future studies are needed to validate our results and further evaluate the predictive value of GRS in secondary prevention.
引用
收藏
页码:1044 / 1053
页数:10
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