Global differences in atopic dermatitis

Atopic dermatitis (AD) is a chronic inflammatory skin disorder, with a highly variable prevalence worldwide. Recent evidence, however, has shown an increase in prevalence in the Asia Pacific region. Nevertheless, most of the published literature has focused mainly on Western populations, and only fe...

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Published inPediatric allergy and immunology Vol. 32; no. 1; pp. 23 - 33
Main Authors Suaini, Noor H. A., Tan, Cheryl P. T., Loo, Evelyn X. L., Tham, Elizabeth Huiwen, Eigenmann, Philippe
Format Journal Article
LanguageEnglish
Published England Wiley Subscription Services, Inc 01.01.2021
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Summary:Atopic dermatitis (AD) is a chronic inflammatory skin disorder, with a highly variable prevalence worldwide. Recent evidence, however, has shown an increase in prevalence in the Asia Pacific region. Nevertheless, most of the published literature has focused mainly on Western populations, and only few clinical trials have included subgroups of other ethnic populations. Reasons for the observed ethnic and geographical differences in AD are not well established. This calls into question the need for a better understanding of AD pathogenesis and inter‐ethnic differences in clinical and immuno‐phenotypes. These differences may reflect inherent variability in disease mechanisms between populations, which in turn may impact upon treatment responses such as biologics that are currently tailored mainly to a specific immuno‐phenotype (T‐helper type 2 dominant). In this article, we reviewed existing literature on the prevalence of AD globally, highlighting differences, if any, in the clinical and immuno‐phenotypes of AD between different ethnicities. We discussed genetic and environmental factors that affect AD in different populations and therapeutic considerations. Our review highlights AD as a disease with ethnic‐dependent clinical and immunological heterogeneity and calls for greater inclusion of ethnic diversity in future research in order to develop targeted treatments.
Bibliography:Funding information
Tham EH is supported by the National Medical Research Council (NMRC) Transition Award grant [MOH‐TA18nov‐003].
ISSN:0905-6157
1399-3038
DOI:10.1111/pai.13335