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Development and Validation of a Polygenic Risk Score for Stroke in the Chinese Population

医学 危险系数 冲程(发动机) 多基因风险评分 比例危险模型 人口 内科学 弗雷明翰风险评分 前瞻性队列研究 风险评估 人口学 置信区间 环境卫生 生物 遗传学 疾病 单核苷酸多态性 基因型 社会学 计算机安全 计算机科学 工程类 基因 机械工程
作者
Xiangfeng Lu,Xiaoge Niu,Chong Shen,Fangchao Liu,Zhongying Liu,Keyong Huang,Laiyuan Wang,Jianxin Li,Dongsheng Hu,Yingxin Zhao,Xueli Yang,Fanghong Lu,Xiaoqing Liu,Jie Cao,Shufeng Chen,Hongfan Li,Wuzhuang Tang,Zhanyun Ren,Ling Yu,Xianping Wu
出处
期刊:Neurology [Ovid Technologies (Wolters Kluwer)]
卷期号:97 (6) 被引量:40
标识
DOI:10.1212/wnl.0000000000012263
摘要

Objective

To construct a polygenic risk score (PRS) for stroke and evaluate its utility in risk stratification and primary prevention for stroke.

Methods

Using a meta-analytic approach and large genome-wide association results for stroke and stroke-related traits in East Asians, we generated a combined PRS (metaPRS) by incorporating 534 genetic variants in a training set of 2,872 patients with stroke and 2,494 controls. We then validated its association with incident stroke using Cox regression models in large Chinese population-based prospective cohorts comprising 41,006 individuals.

Results

During a total of 367,750 person-years (mean follow-up 9.0 years), 1,227 participants developed stroke before age 80 years. Individuals with high polygenic risk had an about 2-fold higher risk of incident stroke compared with those with low polygenic risk (hazard ratio [HR] 1.99, 95% confidence interval [CI] 1.66–2.38), with the lifetime risk of stroke being 25.2% (95% CI 22.5%–27.7%) and 13.6% (95% CI 11.6%–15.5%), respectively. Individuals with both high polygenic risk and family history displayed lifetime risk as high as 41.1% (95% CI 31.4%–49.5%). Individuals with high polygenic risk achieved greater benefits in terms of absolute risk reductions from adherence to ideal fasting blood glucose and total cholesterol than those with low polygenic risk. Maintaining favorable cardiovascular health (CVH) profile could substantially mitigate the increased risk conferred by high polygenic risk to the level of low polygenic risk (from 34.6% to 13.2%).

Conclusions

Our metaPRS has great potential for risk stratification of stroke and identification of individuals who may benefit more from maintaining ideal CVH.

Classification of Evidence

This study provides Class I evidence that metaPRS is predictive of stroke risk.
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