Department of Internal Medicine, Division of Pulmonary and Critical Care, Lahey Hospital and Medical Center, Burlington, Mass.
Department of Internal Medicine, Wake Forest School of Medicine, Winston-Salem, NC.
J Allergy Clin Immunol. 2019 Dec;144(6):1524-1533. doi: 10.1016/j.jaci.2019.08.033. Epub 2019 Sep 11.
Minority groups of African descent experience disproportionately greater asthma morbidity compared with other racial groups, suggesting that genetic variation from a common ancestry could influence exacerbation risk.
We evaluated clinical trial measures in the context of self-reported race and genetic ancestry to identify risk factors for asthma exacerbations.
One thousand eight hundred forty multiethnic subjects from 12 Asthma Clinical Research Network and AsthmaNet trials were analyzed for incident asthma exacerbations with Poisson regression models that included clinical measures, self-reported race (black, non-Hispanic white, and other), and estimates of global genetic African ancestry in a subgroup (n = 760).
Twenty-four percent of 1840 subjects self-identified as black. Black and white subjects had common risk factors for exacerbations, including a history of 2 or more exacerbations in the previous year and FEV percent predicted values, whereas chronic sinusitis, allergic rhinitis, and gastroesophageal reflux disease were only associated with increased exacerbation risk in black subjects. In the combined multiethnic cohort, neither race (P = .30) nor percentage of genetic African ancestry as a continuous variable associated with exacerbation risk (adjusted rate ratio [RR], 1.26 [95% CI, 0.94-1.70; P = .13]; RR per 1-SD change [32% ancestry], 0.97 [95% CI, 0.78-1.19; P = .74]). However, in 161 black subjects with genetic data, those with African ancestry greater than the median (≥82%) had a significantly greater risk of exacerbation (RR, 3.06 [95% CI, 1.09-8.6; P = .03]).
Black subjects have unique risk factors for asthma exacerbations, of which global African genetic ancestry had the strongest effect.
非洲裔少数群体经历的哮喘发病率不成比例地高于其他种族群体,这表明来自共同祖先的遗传变异可能会影响恶化风险。
我们评估了临床试验措施在自我报告的种族和遗传祖先背景下,以确定哮喘恶化的危险因素。
对来自 12 个哮喘临床研究网络和哮喘网络试验的 1840 名多种族受试者进行分析,采用泊松回归模型评估哮喘恶化的发生率,该模型包括临床指标、自我报告的种族(黑人、非西班牙裔白人和其他)和亚组中全球遗传非洲祖先的估计(n=760)。
1840 名受试者中有 24%自我认定为黑人。黑人和白人受试者有共同的恶化危险因素,包括前一年有 2 次或更多次恶化史和 FEV%预测值,而慢性鼻窦炎、过敏性鼻炎和胃食管反流病仅与黑人受试者的恶化风险增加相关。在联合多民族队列中,种族(P=0.30)或遗传非洲祖先的百分比作为连续变量均与恶化风险无关(调整后的发病比[RR],1.26[95%CI,0.94-1.70;P=0.13];每 1-SD 变化[32%祖先]的 RR,0.97[95%CI,0.78-1.19;P=0.74])。然而,在 161 名具有遗传数据的黑人受试者中,具有高于中位数(≥82%)的非洲祖先的个体哮喘恶化的风险显著增加(RR,3.06[95%CI,1.09-8.6;P=0.03])。
黑人受试者有独特的哮喘恶化危险因素,其中全球非洲遗传祖先是最强的影响因素。