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The Influence of OLR1 and PCSK9 Gene Polymorphisms on Ischemic Stroke: Evidence from a Meta-Analysis

机译:OLR1和PCSK9基因多态性对缺血性卒中的影响:荟萃分析的证据。

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摘要

Both OLR1 and PCSK9 genes are associated with atherosclerosis, cardiovascular disease and ischemic stroke. The overall prevalence of PCSK9 rs505151 and OLR1 rs11053646 variants in ischemic stroke were 0.005 and 0.116, respectively. However, to date, association between these polymorphisms and ischemic stroke remains inconclusive. Therefore, this first meta-analysis was carried out to clarify the presumed influence of these polymorphisms on ischemic stroke. All eligible case-control and cohort studies that met the search terms were retrieved in multiple databases. Demographic and genotyping data were extracted from each study, and the meta-analysis was performed using RevMan 5.3 and Metafor R 3.2.1. The pooled odd ratios (ORs) and 95% confidence intervals (CIs) were calculated using both fixed- and random-effect models. Seven case-control studies encompassing 1897 cases and 2119 controls were critically evaluated. Pooled results from the genetic models indicated that OLR1 rs11053646 dominant (OR = 1.33, 95%  CI:1.11–1.58) and co-dominant models (OR = 1.24, 95%  CI:1.02–1.51) were significantly associated with ischemic stroke. For the PCSK9 rs505151 polymorphism, the OR of co-dominant model (OR = 1.36, 95%  CI:1.01–1.58) was found to be higher among ischemic stroke patients. In conclusion, the current meta-analysis highlighted that variant allele of OLR1 rs11053646 G > C and PCSK9 rs505151 A > G may contribute to the susceptibility risk of ischemic stroke.
机译:OLR1和PCSK9基因均与动脉粥样硬化,心血管疾病和缺血性中风有关。在缺血性卒中中PCSK9 rs505151和OLR1 rs11053646变体的总体患病率分别为0.005和0.116。然而,迄今为止,这些多态性与缺血性中风之间的关联仍不确定。因此,进行该首次荟萃分析以阐明这些多态性对缺血性卒中的推测影响。所有符合条件的病例对照研究和队列研究均符合检索条件,并在多个数据库中进行了检索。从每个研究中提取人口统计学和基因分型数据,并使用RevMan 5.3和Metafor R 3.2.1进行荟萃分析。使用固定效应模型和随机效应模型计算合并的奇数比(OR)和95%置信区间(CI)。对包括1897个病例和2119个对照的7个病例对照研究进行了严格评估。遗传模型的汇总结果表明,OLR1 rs11053646优势型(OR = 1.33,95%CI:1.11-1.58)和共主导模型(OR = 1.24,95%CI:1.02-1.51)与缺血性卒中显着相关。对于PCSK9 rs505151多态性,在缺血性卒中患者中,共显性模型的OR(OR = 1.36,95%CI:1.01-1.58)更高。总之,当前的荟萃分析突出表明,OLR1 rs11053646 G646> C和PCSK9 rs505151 A> G的变异等位基因可能会导致缺血性中风的易感性风险。

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