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ABSTRACT: Introduction
The physical impact of alopecia areata (AA) is visible, but the psychological and social consequences and emotional burden are often underrecognized.Methods
In this cross-sectional study, 547 participants recruited via the National Alopecia Areata Foundation completed a survey encompassing demographics; AA illness characteristics; and five patient-reported outcome measures on anxiety and depression, perceived stress, psychological illness impact, stigma, and quality of life (QoL). Differences in disease severity subgroups were assessed via analysis of variance (ANOVA) and t tests.Results
Mean age was 44.6 years, and 76.6% were female. Participants with more severe hair loss tended to report longer duration of experiencing AA symptoms (P < 0.001). Overal
SUBMITTER: Mesinkovska N
PROVIDER: S-EPMC10307747 | biostudies-literature | 2023 Jul
REPOSITORIES: biostudies-literature