Prognostic value of lipoprotein-associated phospholipase A2 mass for all-cause mortality and vascular events within one year after acute ischemic stroke

四分位数 医学 危险系数 内科学 比例危险模型 脂蛋白相关磷脂酶A2 冲程(发动机) 置信区间 体质指数 脂蛋白 心脏病学 胆固醇 机械工程 工程类
作者
Liyuan Han,Chongke Zhong,Xiaoqing Bu,Tan Xu,Aili Wang,Yanbo Peng,Tian Xu,Jinchao Wang,Hao Peng,Qunwei Li,Zhong Ju,Deqing Geng,Yonghong Zhang,Jiang He
出处
期刊:Atherosclerosis [Elsevier BV]
卷期号:266: 1-7 被引量:27
标识
DOI:10.1016/j.atherosclerosis.2017.09.013
摘要

Background and aims We performed a prospective investigation of the longer-term prognostic value of lipoprotein-associated phospholipase A2 (Lp-PLA2) mass for all-cause mortality and vascular events within one year after acute ischemic stroke. Methods We examined the Lp-PLA2 mass among 3401 participants enrolled in the China Antihypertensive Trial in Acute Ischemic Stroke. The primary outcome was all-cause mortality. Cox proportional hazard ratios (HRs) and 95% confidence intervals (95% CIs) were constructed to assess the independent associations between the baseline Lp-PLA2 mass and the outcomes after adjustment for variables in models 1, 2, and 3 [further adjusted for low-density lipoprotein cholesterol (LDL-C)]. Results Overall, 3278 patients completed the follow-up, during which, 188 all-cause death events occurred. The Kaplan-Meier survival curve showed that the cumulative incidence rate of all-cause mortality increased across quartiles of Lp-PLA2 mass (log-rank p = 0.018). Compared with the lowest quartile of Lp-PLA2, the HRs (95% CIs) for the highest quartile of Lp-PLA2 were 1.89 (1.22–2.91), 2.16 (1.31–3.55), and 2.17 (1.32–3.58) for all-cause mortality after adjusting for the covariables in models 1, 2, and 3, respectively. In addition, patients in the highest quartile of Lp-PLA2 mass coupled with higher LDL-C had significantly highest risk of all-cause mortality (HR, 1.81; 95% CI, 1.05 to 3.11; p = 0.032). Conclusions The elevated Lp-PLA2 mass was associated with all cause-death independently of other risk factors within one year after acute ischemic stroke.
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