Biomarkers in atopic dermatitis-a review on behalf of the International Eczema Council

Yael Renert-Yuval, Jacob P. Thyssen, Robert Bissonnette, Thomas Bieber, Kenji Kabashima, Dirk Jan Hijnen, Emma Guttman-Yassky*

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

214 Citations (Scopus)
159 Downloads (Pure)

Abstract

Atopic dermatitis (AD) is a common yet complex skin disease, posing a therapeutic challenge with increasingly recognized different phenotypes among variable patient populations. Because therapeutic response may vary on the basis of heterogeneous clinical and molecular phenotypes, a shift toward precision medicine approaches may improve AD management. Herein, we will consider biomarkers as potential instruments in the toolbox of precision medicine in AD and will review the process of biomarker development and validation, the opinion of AD experts on the use of biomarkers, types of biomarkers, encompassing biomarkers that may improve AD diagnosis, biomarkers reflecting disease severity, and those potentially predicting AD development, concomitant atopic diseases, or therapeutic response, and current practice of biomarkers in AD. We found that chemokine C-C motif ligand 17/thymus and activation-regulated chemokine, a chemoattractant of T(H)2 cells, has currently the greatest evidence for robust correlation with AD clinical severity, at both baseline and during therapy, by using the recommendations, assessment, development, and evaluation approach. Although the potential of biomarkers in AD is yet to be fully elucidated, due to the complexity of the disease, a comprehensive approach taking into account both clinical and reliable, AD-specific biomarker evaluations would further facilitate AD research and improve patient management.
Original languageEnglish
Pages (from-to)1174-1190.e1
Number of pages18
JournalJournal of Allergy and Clinical Immunology
Volume147
Issue number4
Early online dateApr 2021
DOIs
Publication statusPublished - Apr 2021

Bibliographical note

Funding Information:
Y.R.-Y. was supported in part by the National Center for Advancing Translational Sciences , National Institutes of Health , through Rockefeller University (grant no. UL1TR001866 ).

Publisher Copyright: © 2021 The Authors

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