Genome-wide association study reveals susceptibility loci for self-reported headache in a large community-based Asian population

Cephalalgia. 2022 Mar;42(3):229-238. doi: 10.1177/03331024211037269. Epub 2021 Aug 18.

Abstract

Background: The genetic substrate for headache in the general population has not been identified in Asians. We investigated susceptible genetic variants for self-reported headache in a large community-based Asian population.

Methods: We conducted a genome-wide association study in participants recruited from a community-based cohort to identify the genetic variants associated with headache in Taiwanese. All participants received a structured questionnaire for self-reported headache. A total of 2084 patients with "self-reported headache" and 11,822 age- and sex-matched controls were enrolled. Gene enrichment analysis using the Genotype-Tissue Expression version 6 database was performed to explore the potential function of the identified variants.

Results: We identified two novel loci, rs10493859 in TGFBR3 and rs13312779 in FGF23, that are functionally relevant to vascular function and migraine to be significantly associated with self-reported headache after adjusting age, sex and top 10 principal components (p = 8.53 × 10-11 and p = 1.07 × 10-8, respectively). Gene enrichment analysis for genes with GWAS suggestive significance (p < 10-6) demonstrated that the expression of these genes was significantly enriched in the artery (p = 8.18 × 10-4) and adipose tissue (p = 8.95 × 10-4).

Conclusion: Our results suggest that vascular dysfunction might play important roles in the pathogenesis of self-reported headache in Asian populations.

Keywords: FGF23; Headache; TGFBR3; genome-wide association; tissue expression.

MeSH terms

  • Asian People / genetics
  • Case-Control Studies
  • Genetic Predisposition to Disease* / genetics
  • Genome-Wide Association Study* / methods
  • Genotype
  • Headache
  • Humans
  • Polymorphism, Single Nucleotide / genetics
  • Self Report