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Gene-based pleiotropy across migraine with aura and migraine without aura patient groups

机译:带有先兆的偏头痛和没有先兆的偏头痛患者群体的基因多效性

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摘要

Introduction It is unclear whether patients diagnosed according to International Classification of Headache Disorders criteria for migraine with aura (MA) and migraine without aura (MO) experience distinct disorders or whether their migraine subtypes are genetically related. Aim Using a novel gene-based (statistical) approach, we aimed to identify individual genes and pathways associated both with MA and MO. Methods Gene-based tests were performed using genome-wide association summary statistic results from the most recent International Headache Genetics Consortium study comparing 4505 MA cases with 34,813 controls and 4038 MO cases with 40,294 controls. After accounting for non-independence of gene-based test results, we examined the significance of the proportion of shared genes associated with MA and MO. Results We found a significant overlap in genes associated with MA and MO. Of the total 1514 genes with a nominally significant gene-based p value (p
机译:引言目前尚不清楚根据国际头痛分类标准对先兆偏头痛(MA)和无先兆偏头痛(MO)进行诊断的患者是否患有明显的疾病,或者他们的偏头痛亚型是否与遗传相关。目的我们使用一种新颖的基于基因的(统计)方法,旨在鉴定与MA和MO相关的单个基因和途径。方法使用国际头痛遗传学协会最新研究的全基因组关联汇总统计结果进行基于基因的测试,比较4505例MA病例和34,813例对照以及4038例MO患者和40,294例对照。在考虑了基于基因的测试结果的非独立性之后,我们检查了与MA和MO相关的共享基因比例的重要性。结果我们发现与MA和MO相关的基因存在明显的重叠。在总共1514个基因中,具有基于基因的显着性p值(p

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