Department of Dermatology, Medical University of Vienna, Vienna, Austria.
Department of Dermatology, Icahn School of Medicine at Mount Sinai, New York, New York.
Ann Allergy Asthma Immunol. 2019 May;122(5):449-455. doi: 10.1016/j.anai.2018.11.015. Epub 2018 Nov 20.
To summarize studies investigating ethnical and racial differences in atopic dermatitis (AD) epidemiology, clinical features, and skin and blood phenotypes.
PubMed literature review (years 2000-2018).
Articles discussing primarily human disease.
Higher overall rates of AD were found in Africa and Oceania as opposed to India and Northern and Eastern Europe. In the United States, AD prevalence was found to be higher in African American (19.3%) compared with European American (16.1%) children. Although several studies have consistently found FLG loss-of-function mutations in up to 50% of European and 27% of Asian patients with AD, FLG mutations were 6 times less common in African American than in European American patients, even in patients with severe AD. Thus, FLG mutations seem to play less a pathogenic role in patients of African origin than in individuals of European or Asian ancestry. The immune phenotype of all ethnic groups was characterized by strong T2 activation, but important differences in immune polarization exist among the different ethnicities. Asian patients with AD had stronger T17/T22 activation than African American and European American patients with AD, whereas African American patients had the highest serum IgE levels among all groups, while largely lacking T1 and T17 activation.
AD is a heterogeneous disease that has differences among various ethnic and racial groups, which might be important for the development of future, targeted treatments and for personalized medicine approaches.
总结人种和种族差异在特应性皮炎(AD)流行病学、临床特征、皮肤和血液表型中的研究。
PubMed 文献回顾(2000 年至 2018 年)。
主要讨论人类疾病的文章。
非洲和大洋洲的 AD 总体发病率高于印度和北欧和东欧。在美国,非洲裔美国人(19.3%)的 AD 患病率高于欧洲裔美国人(16.1%)。尽管几项研究一致发现,FLG 失功能突变在多达 50%的欧洲和 27%的亚洲 AD 患者中,但 FLG 突变在非洲裔美国人中比在欧洲裔美国人中少见 6 倍,即使在严重 AD 患者中也是如此。因此,FLG 突变在非洲裔患者中的致病作用似乎不如在欧洲或亚洲血统的个体中那么重要。所有种族的免疫表型均以强烈的 T2 激活为特征,但不同种族之间存在免疫极化的重要差异。与 AD 非洲裔和欧洲裔美国人患者相比,AD 亚洲患者具有更强的 T17/T22 激活,而非洲裔美国人患者在所有组中具有最高的血清 IgE 水平,而很大程度上缺乏 T1 和 T17 激活。
AD 是一种异质性疾病,在不同种族和种族群体中存在差异,这对于未来有针对性的治疗方法和个体化医学方法的发展可能很重要。