Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine
03 medical and health sciences
0302 clinical medicine
3. Good health
DOI:
10.1101/030288
Publication Date:
2015-11-04T06:12:14Z
AUTHORS (104)
ABSTRACT
Abstract Migraine is a debilitating neurological disorder affecting around 1 in 7 people worldwide, but its molecular mechanisms remain poorly understood. Some debate exists over whether migraine disease of vascular dysfunction, or result neuronal dysfunction with secondary changes. Genome-wide association (GWA) studies have thus far identified 13 independent loci associated migraine. To identify new susceptibility loci, we performed the largest genetic study to date, comprising 59,674 cases and 316,078 controls from 22 GWA studies. We 45 single nucleotide polymorphisms (SNPs) significantly risk ( P < 5 × 10 −8 ) that map 38 distinct genomic including 28 not previously reported first locus on chromosome X. Furthermore, subset analysis for without aura (MO) seven same as full sample, whereas no reached genome-wide significance (MA) subset. In subsequent computational analyzes, showed enrichment genes expressed smooth muscle tissues, consistent predominant theory highlights etiologies.
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