Department of Biostatistics, Epidemiology and Informatics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
AMIA Annu Symp Proc. 2022 Feb 21;2021:601-610. eCollection 2021.
Sex-specific differences have been noted among people with chronic obstructive pulmonary disease (COPD), but whether these differences are attributable to genetic variation is poorly understood. The availability of large biobanks with deeply phenotyped subjects such as the UK Biobank enables the investigation of sex-specific genetic associations that may provide new insights into COPD risk factors. We performed sex-stratified genome-wide association studies (GWAS) of COPD (male: 12,958 cases and 95,631 controls; female: 11,311 cases and 123,714 controls) and found that while most associations were shared between sexes, several regions had sex-specific contributions, including respiratory viral infection-related loci in/near C5orf56 and PELI1. Using the newly developed R package 'snpsettest', we performed gene-based association tests and identified gene-level sex-specific associations, including C5orf56 on 5q31.1, CFDP1/TMEM170A/CHST6 on 16q23.1 and ASTN2/TRIM32 on 9q33.1. Our results identified promising genes to pursue in functional studies to better understand sexual dimorphism in COPD.
性别特异性差异在慢性阻塞性肺疾病(COPD)患者中已经被注意到,但这些差异是否归因于遗传变异尚不清楚。英国生物库等具有深度表型的大型生物库的出现,使得能够研究可能为 COPD 风险因素提供新见解的性别特异性遗传关联。我们对 COPD 进行了性别分层的全基因组关联研究(GWAS)(男性:12958 例病例和 95631 例对照;女性:11311 例病例和 123714 例对照),发现尽管大多数关联在性别间是共享的,但有几个区域存在性别特异性贡献,包括 C5orf56 内/附近的与呼吸道病毒感染相关的位点和 PELI1。使用新开发的 R 包“snpsettest”,我们进行了基于基因的关联测试,并确定了基因水平的性别特异性关联,包括 5q31.1 上的 C5orf56、16q23.1 上的 CFDP1/TMEM170A/CHST6 和 9q33.1 上的 ASTN2/TRIM32。我们的结果确定了有前途的基因,以在功能研究中进一步探索 COPD 的性别二态性。