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Global differences in atopic dermatitis
被引:31
|作者:
Suaini, Noor H. A.
[1
,2
]
Tan, Cheryl P. T.
[3
]
Loo, Evelyn X. L.
[1
,3
]
Tham, Elizabeth Huiwen
[3
,4
]
机构:
[1] ASTAR, Singapore Inst Clin Sci SICS, Singapore, Singapore
[2] Murdoch Childrens Res Inst, Populat Allergy, Parkville, Vic, Australia
[3] Natl Univ Singapore NUS, Yong Loo Lin Sch Med, Dept Paediat, Singapore, Singapore
[4] Natl Univ Hlth Syst NUHS, Khoo Teck Puat Natl Univ, Childrens Med Inst, Singapore, Singapore
基金:
英国医学研究理事会;
关键词:
Asia;
atopic dermatitis;
child;
eczema;
environment;
ethnic diversity;
genetics;
global;
immunophenotypes;
tailored treatment;
D O I:
10.1111/pai.13335
中图分类号:
R392 [医学免疫学];
学科分类号:
100102 ;
摘要:
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.
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页码:23 / 33
页数:11
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