Risks of alopecia areata in long COVID: Binational population‐based cohort studies from South Korea and Japan

Author:

Kyung Seoyeon12,Son Yejun13,Kim Minji12,Kang Jiseung45,Smith Lee6,Lee Hayeon17,Yon Dong Keon1238ORCID

Affiliation:

1. Center for Digital Health, Medical Science Research Institute, Kyung Hee University Medical Center Kyung Hee University College of Medicine Seoul South Korea

2. Department of Regulatory Science Kyung Hee University Seoul South Korea

3. Department of Precision Medicine Kyung Hee University College of Medicine Seoul South Korea

4. Harvard Medical School Division of Sleep Medicine Boston Massachusetts USA

5. Department of Anesthesia, Critical Care and Pain Medicine Massachusetts General Hospital Boston Massachusetts USA

6. Centre for Health, Performance and Wellbeing Anglia Ruskin University Cambridge UK

7. Department of Biomedical Engineering Kyung Hee University Yongin South Korea

8. Department of Pediatrics, Kyung Hee University Medical Center Kyung Hee University College of Medicine Seoul South Korea

Abstract

AbstractPrevious studies have proposed alopecia areata (AA) as a potential outcome of COVID‐19 infection among autoimmune diseases, yet the findings might be inconclusive and difficult to generalize due to limited sample sizes and evidence levels. Thus, we aimed to investigate in detail the long‐term risk of AA following SARS‐CoV‐2 infection based on large, binational, general population‐based cohort studies. Our study investigated the long‐term AA risk after SARS‐CoV‐2 infection by analyzing bi‐national, claim‐based cohorts in South Korea and Japan: a Korean nationwide cohort (K‐COV‐N cohort; discovery cohort; total n = 10 027 506) and a Japanese claims‐based cohort (JMDC cohort; validation cohort; total n = 12 218 680). AA was identified based on the international classification of diseases 10th revision code (L63) requiring at least three claims within 1 year. After exposure‐driven propensity score matching, SARS‐CoV‐2 infection was associated with an increased risk of incident AA (aHR, 1.66; 95% CI, 1.38–1.99). This increased risk was observed and persisted for up to 6 months. A similar pattern was observed in the validation cohort. As modifiable factors, severe COVID‐19 increased the risk of AA, whereas receiving two or more doses of the COVID‐19 vaccine before infection decreased the risk of AA. Through a bi‐national cohort study in South Korea and Japan, SARS‐CoV‐2 infection was associated with an elevated risk for incident AA in the aspect of long COVID.

Publisher

Wiley

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