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多民族全基因组荟萃分析鉴定出新的性别特异性偏头痛易感基因座。

New and sex-specific migraine susceptibility loci identified from a multiethnic genome-wide meta-analysis.

机构信息

Division of Research, Kaiser Permanente Northern California (KPNC), Oakland, CA, USA.

Sutter Health, Walnut Creek, CA, USA.

出版信息

Commun Biol. 2021 Jul 22;4(1):864. doi: 10.1038/s42003-021-02356-y.

Abstract

Migraine is a common disabling primary headache disorder that is ranked as the most common neurological cause of disability worldwide. Women present with migraine much more frequently than men, but the reasons for this difference are unknown. Migraine heritability is estimated to up to 57%, yet much of the genetic risk remains unaccounted for, especially in non-European ancestry populations. To elucidate the etiology of this common disorder, we conduct a multiethnic genome-wide association meta-analysis of migraine, combining results from the GERA and UK Biobank cohorts, followed by a European-ancestry meta-analysis using public summary statistics. We report 79 loci associated with migraine, of which 45 were novel. Sex-stratified analyses identify three additional novel loci (CPS1, PBRM1, and SLC25A21) specific to women. This large multiethnic migraine study provides important information that may substantially improve our understanding of the etiology of migraine susceptibility.

摘要

偏头痛是一种常见的致残性原发性头痛疾病,被列为全球最常见的神经功能障碍性疾病。女性偏头痛的发病率明显高于男性,但造成这种差异的原因尚不清楚。偏头痛的遗传率估计高达 57%,但遗传风险的很大一部分仍然无法解释,尤其是在非欧洲血统人群中。为了阐明这种常见疾病的病因,我们对偏头痛进行了一项多民族全基因组关联荟萃分析,结合了 GERA 和 UK Biobank 队列的结果,然后使用公共汇总统计数据进行了欧洲血统荟萃分析。我们报告了 79 个与偏头痛相关的基因座,其中 45 个是新的。性别分层分析确定了三个专门针对女性的新基因座(CPS1、PBRM1 和 SLC25A21)。这项大型多民族偏头痛研究提供了重要信息,可能会极大地提高我们对偏头痛易感性病因的理解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d892/8298472/ffff3cbed33e/42003_2021_2356_Fig1_HTML.jpg

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