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首页> 外文期刊>European Neurology >Ischaemic Stroke Subtypes and Their Genetic Basis: A Comprehensive Meta-Analysis of Small and Large Vessel Stroke
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Ischaemic Stroke Subtypes and Their Genetic Basis: A Comprehensive Meta-Analysis of Small and Large Vessel Stroke

机译:缺血性卒中亚型及其遗传基础:大小血管卒中的综合Meta分析

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Background: The extent to which genetic effects on the different subtypes of small (SVD) and large vessel disease (LVD) ischaemic stroke differ remains controversial. Methods: A comprehensive genetic meta-analysis of all genes investigated by ischaemic stroke subtype was conducted. Odds ratio (OR) and 95% confidence intervals (CI) were determined for each gene disease association. Results: From the initial search of 526 manuscripts, 5 candidate genes were studied comprising 7,533 cases (LVD 4,181, SVD 3,352) and 9,835 control subjects. There was a preferential association for SVD compared to LVD with ACE/DD (SVD: OR 1.31, 95% CI 0.96-1.79; LVD: OR 1.02, 95% CI 0.82-1.26) and eNOS intron 4 ab polymorphism (SVD: OR 1.41, 95% CI 0.94-2.11; LVD: OR 1.07, 95% CI 0.77-1.49), although statistical significance was not reached. No such preference was observed for MTHFR C677T, ApoE/ε4 or PAI-1 4G/5G polymorphism. The overall number of studies and the number of subjects recruited per study in whom stroke subtype was classified were small when compared to previous published work without such phenotype classification. Conclusion: Our findings suggest that genetic effects may differ between small and large vessel subtypes, although the evidence base is small.
机译:背景:对小(SVD)和大血管疾病(LVD)缺血性中风的不同亚型的遗传效应差异仍存在争议。方法:对缺血性卒中亚型调查的所有基因进行了全面的遗传荟萃分析。确定每种基因疾病关联的赔率(OR)和95%置信区间(CI)。结果:从最初的526篇文献中,研究了5个候选基因,包括7,533例(LVD 4,181,SVD 3,352)和9,835例对照受试者。与具有ACE / DD的LVD(SVD:OR 1.31,95%CI 0.96-1.79; LVD:OR 1.02,95%CI 0.82-1.26)和eNOS内含子4 ab多态性(SVD:OR 1.41)相比,SVD存在优先关联,95%CI 0.94-2.11; LVD:OR 1.07,95%CI 0.77-1.49),但未达到统计学显着性。对于MTHFR C677T,ApoE /ε4或PAI-1 4G / 5G多态性未观察到这样的偏爱。与之前没有这种表型分类的已发表研究相比,研究的总数和每项研究中分类为卒中亚型的研究对象的数量都很少。结论:我们的发现表明,尽管证据基础很小,小血管和大血管亚型之间的遗传效应也可能不同。

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