Malassezia specific IgE in head and neck dermatitis of eczema: A systematic review & meta‐analysis

Author:

See Tow Hui Xin1ORCID,Yew Yik Weng23ORCID

Affiliation:

1. Yong Loo Lin School of Medicine National University of Singapore Singapore City Singapore

2. National Skin Centre Singapore City Singapore

3. Lee Kong Chian School of Medicine, Nanyang Technological University Singapore City Singapore

Abstract

AbstractHead and neck atopic dermatitis (HNAD) is a subtype of atopic dermatitis (AD), a common inflammatory skin condition with a distinctive clinical appearance. Malassezia spp., a predominant skin yeast, is considered to exacerbate HNAD. In this study, we investigate the prevalence of Malassezia‐specific IgE among HNAD patients. A comprehensive search was performed for observational studies analysing the association between Malassezia‐specific IgE and HNAD. This study was performed according to the Preferred Reporting Items for Systematic reviews and Meta‐Analyses 2020 checklist and quality was assessed via the Newcastle‐Ottawa Quality Assessment Scale (NOS). Fourteen observational studies (840 patients) were included in the analysis. 58% of HNAD patients were male (95% CI: 45.2–69.7). Overall prevalence of Malassezia‐specific IgE among HNAD patients was 79.3% (95% CI: 57.5–91.5). Prevalence of Malassezia‐specific IgE among HNAD patients varied significantly between geographical regions (p = 0.0441), with 88% in non‐Asian regions (95% CI: 61.06–97.17) and 54.73% in Asian regions (95% CI: 34.36–73.63). Malassezia‐specific IgE prevalence among HNAD patients varied significantly among studies of higher and lower NOS quality score (p = 0.0386), with 95.42% in studies with NOS ≥7 (95% CI: 63.54–99.60) and 58.05% in studies with NOS <7 (95% CI: 41.44–73.01). Malassezia‐specific IgE prevalence among HNAD patients did not vary significantly between more and less predominant Malassezia species (p = 0.1048). Malassezia spp. plays a crucial role in the pathogenesis of HNAD, and IgE anti‐Malassezia antibodies appeared to be a common marker for HNAD. Understanding the pathophysiology of Malassezia in HNAD can help develop more targeted therapeutic approaches in managing AD.

Publisher

Wiley

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