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ATP结合盒亚家族A成员1基因的R219K多态性与中国人群缺血性脑卒中易感性

The R219K Polymorphism of the ATP Binding Cassette Subfamily a Member 1 Gene and Susceptibility to Ischemic Stroke in Chinese Population.

作者信息

Li Jianmin, Wen Ming, Zhang Zhiping, Qiu Zhihua, Sun Yiming

机构信息

Department of Pharmacy, Karamay Central Hospital of Xinjiang, MM, Karamay City, Xinjiang Province, China, 834000.

Department of Neurosurgery, Wuhan Wuchang Hospital, MM, Wuhan City, Hubei Province, China, 430063.

出版信息

Open Med (Wars). 2020 Apr 6;15:274-282. doi: 10.1515/med-2020-0039. eCollection 2020.

Abstract

Stroke is the major cause of death and disability worldwide. ABCA1 R219K has been suggested as a risk factor for ischemic stroke, but the results remain inconclusive in the Chinese population. This study aimed to assess the association between ABCA1 R219K and ischemic stroke using meta-analysis. A systematic literature search was conducted to select eligible studies and the pooled odds ratio (OR) with 95% confidence interval (CI) was used to evaluate the strength of association. Fourteen studies containing 2865 cases and 3227 controls were included in the meta-analysis and the results suggested that there is a strong association between ABCA1 R219K and the ischemic stroke risks (K vs. R: OR = 0.837, 95% CI: 0.735- 0.954, p=0.008; KK vs. RR: OR = 0.689, 95% CI: 0.520-0.912, p=0.009; KK+RK vs. RR: OR = 0.782, 95% CI: 0.691-0.885, p<0.001). Subgroup analysis revealed that significant association was found for the 4 genetic models (p<0.05) in the Southern population, while in the northern population significant association was only found under the dominant model (KK+RK vs. RR: OR = 0.744, 95% CI: 0.583- 0.949, p<0.017). This meta-analysis suggested that ABCA1 R219K polymorphism might be a protective factor against developing IS, indicating this SNP may contribute to the pathogenesis of ischemic stroke and might be potentially used as a biomarker to predict the susceptibility to ischemic stroke.

摘要

中风是全球范围内死亡和残疾的主要原因。ABCA1 R219K已被认为是缺血性中风的一个风险因素,但在中国人群中的结果仍无定论。本研究旨在通过荟萃分析评估ABCA1 R219K与缺血性中风之间的关联。进行了系统的文献检索以选择符合条件的研究,并使用合并优势比(OR)和95%置信区间(CI)来评估关联强度。荟萃分析纳入了14项研究,共2865例病例和3227例对照,结果表明ABCA1 R219K与缺血性中风风险之间存在强关联(K与R:OR = 0.837,95% CI:0.735 - 0.954,p = 0.008;KK与RR:OR = 0.689,95% CI:0.520 - 0.912,p = 0.009;KK + RK与RR:OR = 0.782,95% CI:0.691 - 0.885,p < 0.001)。亚组分析显示,在南方人群中,4种遗传模型均存在显著关联(p < 0.05),而在北方人群中,仅在显性模型下发现显著关联(KK + RK与RR:OR = 0.744,95% CI:0.583 - 0.949,p < 0.017)。这项荟萃分析表明,ABCA1 R219K多态性可能是预防缺血性中风的一个保护因素,表明该单核苷酸多态性可能参与缺血性中风的发病机制,并且可能潜在地用作预测缺血性中风易感性的生物标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2d7e/7147290/d4297bd77b19/med-15-274-g001.jpg

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