Elevated lipoprotein(a) and lipoprotein-associated phospholipase A2 are associated with unfavorable functional outcomes in patients with ischemic stroke

医学 改良兰金量表 优势比 内科学 置信区间 脂蛋白相关磷脂酶A2 脂蛋白(a) 逻辑回归 冲程(发动机) 脂蛋白 入射(几何) 缺血性中风 物理疗法 胆固醇 缺血 工程类 物理 光学 机械工程
作者
Xue Jiang,Jie Xu,Xiwa Hao,Jing Xue,Ke Li,Aoming Jin,Jinxi Lin,Xia Meng,Lemin Zheng,Yongjun Wang
出处
期刊:Journal of Neuroinflammation [Springer Nature]
卷期号:18 (1) 被引量:12
标识
DOI:10.1186/s12974-021-02359-w
摘要

Abstract Background The association of lipoprotein(a) [Lp(a)] and stroke functional outcomes was conflicting. The aim of the study was to clarify whether high Lp(a) is associated with unfavorable functional outcomes in patients with ischemic stroke. Methods A total of 9709 individuals from the third China National Stroke Registry cohort were recruited. Plasma level of Lp(a) at admission was measured with enzyme-linked immunosorbent assay. The cut-off was set at the median for Lp(a). Functional outcome was assessed using the modified Rankin scale (mRS) at 3 months and 1 year after ischemic stroke. The association between Lp(a) and functional outcomes was evaluated using a logistic regression model. Results The median age was 63.0 years, and 31.1% participants were women. Patients in higher Lp(a) group had higher incidences of unfavorable functional outcomes at 3 months. In logistic regression model, elevated Lp(a) levels were associated with unfavorable functional outcomes at 3 months (Q4 vs. Q1: odds ratio 1.33, 95% confidence interval 1.11–1.61). Subgroup analysis showed that in the lower Lp-PLA 2 group, Lp(a) level was not associated with functional outcomes, but in the higher Lp-PLA 2 group, Lp(a) level was significantly associated with functional outcomes. After grouped by different levels of Lp(a) and Lp-PLA 2 , the Lp(a) high/ Lp-PLA 2 high group showed the highest incidence of unfavorable functional outcomes at 3 months and 1 year. Conclusions Elevated Lp(a) level is associated with unfavorable functional outcomes in patients with ischemic stroke. The increment in both Lp(a) and Lp-PLA 2 are associated with unfavorable functional outcomes at 3 months and 1 year after ischemic stroke.
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