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Identifying novel genetic risk loci for lacunar stroke

机译:鉴定腔隙性卒中的新遗传风险位点

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摘要

In The Lancet Neurology, Matthew Traylor and colleagues report the results of the largest pooled analysis of risk genes for lacunar stroke published to date. The authors included morethan 7000 patients with lacunar stroke and 250000 controls. In almost 3000 cases, MRI confirmed the presence of lacunar stroke. Patients were recruited from the UK DNA Lacunar Stroke studies 1 and 2 and by the collaborators of the International Stroke Genetics Consortium. The authors did a genome-wide association study (GWAS) for lacunar stroke alone, as well as a multi-trait approach with a phenotype including both lacunar strokes and white matter hyperintensities. They also did a transcriptome-wide association study, which identified transcribed genes related to lacunar stroke.
机译:在《柳叶刀神经病学》杂志上,Matthew Taylor及其同事报告了迄今为止发表的对腔隙性中风风险基因的最大汇总分析的结果。作者纳入了7000多名腔隙性卒中患者和250000名对照组。在近 3000 例病例中,MRI 证实了腔隙性卒中的存在。患者是从英国 DNA 腔隙性卒中研究 1 和 2 以及国际卒中遗传学联盟的合作者中招募的。作者仅对腔隙性卒中进行了全基因组关联研究(GWAS),以及具有包括腔隙性卒中和白质高信号在内的表型的多性状方法。他们还进行了一项转录组范围的关联研究,该研究确定了与腔隙性中风相关的转录基因。

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