Danish Headache Center, Department of Neurology, Rigshospitalet, Copenhagen University Hospital, Glostrup, Denmark.
NeuroGenomic, Translational Research Center, Rigshospitalet, Copenhagen University Hospital, Glostrup, Denmark.
Commun Biol. 2024 May 27;7(1):646. doi: 10.1038/s42003-024-06299-y.
Headache disorders are the most common disorders of the nervous system. The lifetime prevalence of headache disorders show that some individuals never experience headache. The etiology of complete freedom from headache is not known. To assess genetic variants associated with complete freedom from headache, we performed a genome-wide association study of individuals who have never experienced a headache. We included 63,992 individuals (2,998 individuals with complete freedom from headache and 60,994 controls) from the Danish Blood Donor Study Genomic Cohort. Participants were included in two rounds, from 2015 to 2018 and in 2020. We discovered a genome-wide significant association, with the lead variant rs7904615[G] in ADARB2 (EAF = 27%, OR = 1.20 [1.13-1.27], p = 3.92 × 10). The genomic locus was replicated in a non-overlapping cohort of 13,032 individuals (539 individuals with complete freedom from headache and 12,493 controls) from the Danish Blood Donor Study Genomic Cohort (p < 0.05, two-sided). Participants for the replication were included from 2015 to 2020. In conclusion, we show that complete freedom from headache has a genetic component, and we suggest that ADARB2 is involved in complete freedom from headache. The genomic locus was specific for complete freedom from headache and was not associated with any primary headache disorders.
头痛障碍是最常见的神经系统疾病。头痛障碍的终身患病率表明,有些个体从未经历过头痛。完全没有头痛的病因尚不清楚。为了评估与完全没有头痛相关的遗传变异,我们对从未经历过头痛的个体进行了全基因组关联研究。我们纳入了来自丹麦献血者研究基因组队列的 63992 名个体(2998 名个体完全没有头痛,60994 名对照)。参与者分两轮纳入,一轮在 2015 年至 2018 年,另一轮在 2020 年。我们发现了一个全基因组显著关联,主要变异为 ADARB2 中的 rs7904615[G](EAF=27%,OR=1.20[1.13-1.27],p=3.92×10)。该基因组座在来自丹麦献血者研究基因组队列的 13032 名个体(539 名个体完全没有头痛,12493 名对照)的非重叠队列中得到了复制(p<0.05,双侧)。复制队列的参与者于 2015 年至 2020 年期间纳入。总之,我们表明完全没有头痛具有遗传成分,并且我们提示 ADARB2 参与了完全没有头痛。该基因组座专门与完全没有头痛相关,与任何原发性头痛障碍无关。