Program for Clinical Research, Department of Dermatology, University of California, San Francisco, Calif.
Division of Biostatistics and Epidemiology, University of California, Berkeley, Calif.
J Allergy Clin Immunol. 2020 Jan;145(1):192-198.e11. doi: 10.1016/j.jaci.2019.06.044. Epub 2019 Jul 29.
Atopic dermatitis (AD) is more common among African American children. Whether there are racial/ethnic difference among adults with AD and the causes for those disparities are unclear.
We sought to examine the relationship between self-reported race/ethnicity and AD and determine whether African genetic ancestry is predictive of these outcomes among African American subjects.
We analyzed data from 2 independent multiethnic longitudinal studies: 86,893 subjects aged 18 to 100 years from the Kaiser Permanente Genetic Epidemiology Research on Adult Health and Aging (GERA) cohort and 5467 subjects aged 2 to 26 years from the national Pediatric Eczema Elective Registry (PEER) cohort. The primary outcomes were physician-diagnosed AD in GERA and repeated measures of self-reported disease control among patients with physician-diagnosed AD at 6-month intervals in PEER. We examined whether self-identified African American race/ethnicity was predictive of these outcomes and then tested whether a continuous measure of African genetic ancestry was associated with outcomes within the African American group.
AD was more common among self-identified African American subjects than non-Hispanic white subjects in GERA (4.4% vs 2.1%; odds ratio, 2.06; 95% CI, 1.70-2.48) and less well-controlled in PEER subjects (odds of 1-level worse control, 1.91; 95% CI, 1.64-2.22). However, African genetic ancestry was not associated with AD risk or control among self-identified African American subjects in either cohort, nor did an AD polygenic risk score or genetic skin pigment score explain the AD disparities in patients with AD.
Ancestry-related genetic effects do not explain increased AD prevalence or poorer disease control among African American subjects.
特应性皮炎(AD)在非裔美国儿童中更为常见。AD 患者中是否存在种族/民族差异以及这些差异的原因尚不清楚。
我们旨在研究自我报告的种族/民族与 AD 之间的关系,并确定非裔遗传血统是否可预测非裔美国受试者的这些结局。
我们分析了来自 2 项独立的多民族纵向研究的数据:Kaiser Permanente 成人健康与衰老遗传流行病学研究(GERA)队列中的 86893 名年龄在 18 至 100 岁的受试者和全国儿科特应性皮炎选择性登记(PEER)队列中的 5467 名年龄在 2 至 26 岁的受试者。主要结局为 GERA 中的医生诊断 AD 和在 PEER 中每 6 个月对医生诊断 AD 的患者进行的自我报告疾病控制的重复测量。我们检验了自我认定的非裔美国人种族/民族是否可预测这些结局,然后检验了非裔遗传血统的连续测量值是否与非裔美国人组内的结局相关。
在 GERA 中,自我认定的非裔美国受试者的 AD 比非西班牙裔白人受试者更为常见(4.4%比 2.1%;比值比,2.06;95%CI,1.70-2.48),PEER 受试者的控制较差(控制差 1 级的几率,1.91;95%CI,1.64-2.22)。然而,在两个队列中,非裔遗传血统与自我认定的非裔美国人的 AD 风险或控制均无关联,AD 多基因风险评分或遗传皮肤色素评分也不能解释 AD 患者的 AD 差异。
与遗传有关的遗传效应不能解释非裔美国受试者中 AD 患病率增加或疾病控制较差的原因。