Department of Health Sciences, University of Leicester, Leicester, England.
Department of Health Sciences, University of Leicester, Leicester, England.
Chest. 2022 May;161(5):1155-1166. doi: 10.1016/j.chest.2021.12.674. Epub 2022 Jan 31.
Some people have characteristics of both asthma and COPD (asthma-COPD overlap), and evidence suggests they experience worse outcomes than those with either condition alone.
What is the genetic architecture of asthma-COPD overlap, and do the determinants of risk for asthma-COPD overlap differ from those for COPD or asthma?
We conducted a genome-wide association study in 8,068 asthma-COPD overlap case subjects and 40,360 control subjects without asthma or COPD of European ancestry in UK Biobank (stage 1). We followed up promising signals (P < 5 × 10) that remained associated in analyses comparing (1) asthma-COPD overlap vs asthma-only control subjects, and (2) asthma-COPD overlap vs COPD-only control subjects. These variants were analyzed in 12 independent cohorts (stage 2).
We selected 31 independent variants for further investigation in stage 2, and discovered eight novel signals (P < 5 × 10) for asthma-COPD overlap (meta-analysis of stage 1 and 2 studies). These signals suggest a spectrum of shared genetic influences, some predominantly influencing asthma (FAM105A, GLB1, PHB, TSLP), others predominantly influencing fixed airflow obstruction (IL17RD, C5orf56, HLA-DQB1). One intergenic signal on chromosome 5 had not been previously associated with asthma, COPD, or lung function. Subgroup analyses suggested that associations at these eight signals were not driven by smoking or age at asthma diagnosis, and in phenome-wide scans, eosinophil counts, atopy, and asthma traits were prominent.
We identified eight signals for asthma-COPD overlap, which may represent loci that predispose to type 2 inflammation, and serious long-term consequences of asthma.
有些人同时具有哮喘和 COPD(哮喘-COPD 重叠)的特征,有证据表明,他们的预后比单独患有这两种疾病中的任何一种都要差。
哮喘-COPD 重叠的遗传结构是什么?其风险决定因素与 COPD 或哮喘是否不同?
我们在 UK Biobank 中进行了一项全基因组关联研究,纳入了 8068 例哮喘-COPD 重叠病例和 40360 例无哮喘或 COPD 的欧洲血统对照(阶段 1)。我们对在比较(1)哮喘-COPD 重叠与仅哮喘对照和(2)哮喘-COPD 重叠与仅 COPD 对照的分析中仍具有相关性的有希望的信号(P < 5 × 10)进行了随访。这些变体在 12 个独立队列中进行了分析(阶段 2)。
我们在阶段 2 中选择了 31 个独立变体进行进一步研究,发现了 8 个哮喘-COPD 重叠的新信号(阶段 1 和 2 研究的荟萃分析)。这些信号表明存在共享遗传影响的谱,其中一些主要影响哮喘(FAM105A、GLB1、PHB、TSLP),另一些主要影响固定气流阻塞(IL17RD、C5orf56、HLA-DQB1)。染色体 5 上的一个基因间信号以前与哮喘、COPD 或肺功能无关。亚组分析表明,这些八个信号的关联不受吸烟或哮喘诊断时年龄的影响,在表型全扫描中,嗜酸性粒细胞计数、过敏和哮喘特征突出。
我们确定了哮喘-COPD 重叠的 8 个信号,这些信号可能代表易患 2 型炎症和哮喘严重长期后果的位点。