Department of Neurology, Neurological Institute, Taipei Veterans General Hospital, No. 201, Sec. 2, Shih-Pai Road, Taipei, 112, Taiwan.
Brain Research Center, National Yang Ming Chiao Tung University, Taipei, Taiwan.
J Headache Pain. 2022 Nov 21;23(1):147. doi: 10.1186/s10194-022-01517-6.
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.
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.
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), rs10188640 in MERTK (odds ratio = 1.52, 95% CI 1.33‒1.73, p = 8.58 × 10), and rs13028839 in STAB2 (odds ratio = 0.63, 95% CI 0.52‒0.78, p = 2.81 × 10), 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.
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.
丛集性头痛是一种具有高度致残性的神经障碍,存在显著的种族间差异。全基因组关联研究(GWAS)最近在欧洲人中发现了可复制的丛集性头痛基因组位点,但亚洲人群中丛集性头痛的遗传基础仍不清楚。本研究旨在探讨中国台湾汉族人群丛集性头痛的遗传结构和易感基因位点。
我们对 2007 年至 2022 年期间招募的台湾队列进行了两阶段全基因组关联研究,以鉴定与丛集性头痛相关的遗传变异。使用国际头痛疾病分类第三版(ICHD-3)的标准对丛集性头痛进行回顾性诊断。对照人群来自台湾生物银行。使用 Axiom 全基因组芯片 TWB 进行基因分型,然后进行全基因组 imputation。通过多基因风险评分来区分患者和对照。进行了下游分析,包括基因集和组织富集、连锁不平衡评分回归以及通路分析。
我们纳入了 734 例丛集性头痛患者和 9846 名基于人群的对照。我们鉴定出了三个可重复的位点,其中主要的 SNP 是 CAPN2 中的 rs1556780(比值比=1.59,95%CI 1.42-1.78,p=7.61×10)、MERTK 中的 rs10188640(比值比=1.52,95%CI 1.33-1.73,p=8.58×10)和 STAB2 中的 rs13028839(比值比=0.63,95%CI 0.52-0.78,p=2.81×10),后两者在欧洲人群中也有重复。几个先前报道的基因在我们的样本中也与丛集性头痛有显著关联。多基因风险评分可通过受试者工作特征曲线下面积 0.77 区分患者和对照。下游分析提示昼夜节律调节和免疫过程与丛集性头痛的发病机制有关。
本研究揭示了中国台湾汉族人群丛集性头痛的遗传结构和新的易感基因位点。我们的发现支持了不同种族间丛集性头痛的共同遗传贡献,并为丛集性头痛的发病机制提供了新的机制见解。