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Review
. 2022 Jun:7:67-77.
doi: 10.1016/j.jdin.2022.02.006. Epub 2022 Feb 22.

Alopecia in patients with COVID-19: A systematic review and meta-analysis

Affiliations
Review

Alopecia in patients with COVID-19: A systematic review and meta-analysis

Betty Nguyen et al. JAAD Int. 2022 Jun.

Abstract

Background: COVID-19 is associated with androgenetic alopecia (AGA), telogen effluvium (TE), and alopecia areata (AA). No studies have analyzed the aggregate data to date.

Objective: We conducted a systematic review to characterize the types, incidence, timing, and clinical outcomes of COVID-19-associated alopecia.

Methods: We searched PubMed/MEDLINE, Scopus, and Embase for articles published between November 2019 and August 2021 using the key words "alopecia" or "hair" and COVID-19-related search terms, identifying 41 original articles describing patients with alopecia and COVID-19.

Results: The current review included 1826 patients with alopecia and COVID-19 (mean age, 54.5 years; 54.3% male). The most common types of alopecia identified were AGA (30.7%, 86.4% male), TE (19.8%, 19.3% male), and AA (7.8%, 40.0% male). AGA preceded COVID-19 symptoms. TE was usually newly triggered by COVID-19 (93.6%). AA usually occurred in patients with preexisting disease (95.1%).

Limitations: Definitions of COVID-19 onset varied. Studies differed in methodology and were susceptible to reporting and sampling bias. Studies with large sample sizes may exert a disproportionate influence on data.

Conclusion: AGA may be a risk factor for severe COVID-19, whereas TE presents as a sequela of COVID-19. AA generally occurs as a relapse in patients with preexisting alopecia.

Keywords: AA, alopecia areata; ADT, androgen-deprivation therapy; AE, anagen effluvium; AGA, androgenetic alopecia; COVID-19; PA, pressure-induced alopecia; SARS-CoV-2; TE, telogen effluvium; alopecia; alopecia areata; anagen effluvium; androgenetic alopecia; coronavirus disease 2019; hair loss; telogen effluvium.

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Conflict of interest statement

Dr Tosti is a consultant for DS Laboratories, Monat Global, Almirall, Thirty Madison, Eli Lilly, Bristol Myers Squibb, P&G, Pfizer, and Myovant. Author Nguyen has no conflicts of interest to declare.

Figures

Fig 1
Fig 1
Flowchart of study identification via PubMed/MEDLINE, Scopus, and Embase according to the Preferred Reporting Items for Systematic Reviews and Meta-Analyses guidelines.

References

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