Genome-wide analyses identify novel risk loci for cluster headache in Han Chinese residing in Taiwan

• Published in: Journal of headache and pain Vol. 23; no. 1; p. 147
• Main Authors: Chen, Shih-Pin, Hsu, Chia-Lin, Wang, Yen-Feng, Yang, Fu-Chi, Chen, Ting-Huei, Huang, Jia-Hsin, Pan, Li-Ling Hope, Fuh, Jong-Ling, Chang, Hsueh-Chen, Lee, Yi-Lun, Chang, Hung-Ching, Lee, Ko-Han, Chang, Yu-Chuan, Fann, Cathy Shen-Jang, Wang, Shuu-Jiun
• Format: Journal Article
• Language: English
• Published: Milan Springer Milan 21.11.2022; Springer Nature B.V; BMC
• Subjects: Asian People - genetics; CAPN2; China; Circadian rhythm; Circadian rhythms; Cluster headache; Cluster Headache - genetics; Gene loci; Genetic diversity; Genetic Predisposition to Disease; Genome-wide association studies; Genome-Wide Association Study; Genomes; Genotyping; Headache; Headaches; Humans; Internal Medicine; Linkage disequilibrium; Medicine; Medicine & Public Health; MERTK; Neurology; Pain Medicine; Pathogenesis; Retrospective Studies; Single-nucleotide polymorphism; STAB2; Taiwan; China; Taiwan; Genome-wide association study; Cluster headache; CAPN2; STAB2; MERTK
• ISSN: 1129-2369; 1129-2377
• DOI: 10.1186/s10194-022-01517-6

Background Cluster headache is a highly debilitating neurological disorder with considerable inter-ethnic differences. Genome-wide association studies (GWAS) recently identified replicable genomic loci for cluster headache in Europeans, but the genetic underpinnings for cluster headache in Asians remain unclear. The objective of this study is to investigate the genetic architecture and susceptibility loci of cluster headache in Han Chinese resided in Taiwan. Methods We conducted a two-stage genome-wide association study in a Taiwanese cohort enrolled from 2007 through 2022 to identify the genetic variants associated with cluster headache. Diagnosis of cluster headache was retrospectively ascertained with the criteria of International Classification of Headache Disorders, third edition. Control subjects were enrolled from the Taiwan Biobank. Genotyping was conducted with the Axiom Genome-Wide Array TWB chip, followed by whole genome imputation. A polygenic risk score was developed to differentiate patients from controls. Downstream analyses including gene-set and tissue enrichment, linkage disequilibrium score regression, and pathway analyses were performed. Results We enrolled 734 patients with cluster headache and 9,846 population-based controls. We identified three replicable loci, with the lead SNPs being rs1556780 in CAPN2 (odds ratio = 1.59, 95% CI 1.42‒1.78, p  = 7.61 × 10 –16 ), rs10188640 in MERTK (odds ratio = 1.52, 95% CI 1.33‒1.73, p  = 8.58 × 10 –13 ), and rs13028839 in STAB2 (odds ratio = 0.63, 95% CI 0.52‒0.78, p  = 2.81 × 10 –8 ), with the latter two replicating the findings in European populations. Several previously reported genes also showed significant associations with cluster headache in our samples. Polygenic risk score differentiated patients from controls with an area under the receiver operating characteristic curve of 0.77. Downstream analyses implicated circadian regulation and immunological processes in the pathogenesis of cluster headache. Conclusions This study revealed the genetic architecture and novel susceptible loci of cluster headache in Han Chinese residing in Taiwan. Our findings support the common genetic contributions of cluster headache across ethnicities and provide novel mechanistic insights into the pathogenesis of cluster headache.