Atopic Eczema: How Genetic Studies Can Contribute to the Understanding of this Complex Trait

被引:3
|
作者
Brown, Sara J. [1 ,2 ]
机构
[1] Univ Edinburgh, Ctr Genom & Expt Med, Inst Genet & Canc, Edinburgh, Midlothian, Scotland
[2] Natl Hlth Serv NHS Lothian, Dept Dermatol, Edinburgh, Midlothian, Scotland
基金
英国惠康基金;
关键词
GENOME-WIDE ASSOCIATION; OF-FUNCTION MUTATIONS; PREDISPOSING FACTOR; MULTIPLE ALLERGIES; SEVERE DERMATITIS; FILAGGRIN; RISK; BARRIER; SUSCEPTIBILITY; ARCHITECTURE;
D O I
10.1016/j.jid.2021.12.020
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Atopic eczema is an itchy inflammatory skin disease. This complex trait results from multiple genetic and environmental factors, but atopic eczema also shows great complexity in its heterogeneous presentation, clinical signs, and longitudinal trajectory, with or without comorbid conditions. The past 50 years have resulted in substantial improvements in the management of atopic eczema, but many patients still suffer a burden of disease affecting personal, social, and family life. Genetic research refocused interest on skin barrier function, but effective targeting of this central pathomechanism remains elusive. This perspective highlights the progress in understanding the molecular mechanisms and translational opportunities for the future.
引用
收藏
页码:1015 / 1019
页数:5
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