New and sex-specific migraine susceptibility loci identified from a multiethnic genome-wide meta-analysis.
Helene ChoquetJie YinAlice S JacobsonBrandon H HortonThomas J HoffmannEric JorgensenAndrew L AvinsAlice R PressmanPublished in: Communications biology (2021)
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.
Keyphrases
- genome wide
- genome wide association
- systematic review
- dna methylation
- genome wide association study
- healthcare
- emergency department
- type diabetes
- gene expression
- mental health
- copy number
- metabolic syndrome
- insulin resistance
- brain injury
- pregnancy outcomes
- middle aged
- health information
- subarachnoid hemorrhage
- cervical cancer screening
- breast cancer risk