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Derm TherObservational study

Dermatologists' Perspectives and Real-World Assessment of Alopecia Areata Severity, Burden, and Healthcare Resource Utilization in Adults in the Kingdom of Saudi Arabia.

Al Ajlan MAF, Alenzi KA, Al-Haddab MA, AlHarbi I, Alturaiki A, Arsalan MS, Behiry A, Kurosky SK, Encinas GA, Anderson P, Cha-Silva AS, Vaghela S, Canosa JM

Dermatology and TherapyIn the feed 14 Aug 2026, published online 14 Aug 2026, issue 2026 Oct, added to PubMed 14 Aug 2026

Topics: Hair

Abstract

INTRODUCTIONAlopecia areata (AA), an autoimmune disease, causes hair loss on the scalp, face, and body, with a prevalence of approximately 2% in the Middle East. AA is associated with significant impacts to patient quality of life (QoL). This study described dermatologist perceptions and experiences treating AA in the Kingdom of Saudi Arabia (KSA) while new treatments were introduced, and examined patient disease burden and unmet treatment need.

METHODSData were analyzed from the Adelphi Real World AA Disease Specific Programme™, conducted September 2022-March 2023. Dermatologists rated their agreement with statements on diagnosing/managing AA and provided clinical and treatment information for four patients (mild/moderate AA: one each; severe/very severe AA: two). A subset of these patients completed the SKINDEX-16, Hospital Anxiety and Depression Scale (HADS), and the Work Productivity and Activity Impairment-AA (WPAI-AA) questionnaires. Analyses were stratified by percent scalp hair loss (SHL).

RESULTSA total of 50 dermatologists and 185 patients were included. Most dermatologists reported severe AA was difficult to treat owing to lack of effective therapies. A median of 51.5% SHL was reported as typical of severe AA. Impact of AA on patient QoL was the most frequently reported factor informing disease severity. Overall, 52.4% of patients had severe or very severe AA (as assessed by their physician). Approximately one-third of patients had abnormal anxiety and depression scores as measured by HADS. Patients with ≤ 20% SHL generally had lower mean Skindex-16 scores (impact of AA on QoL). Patients with ≥ 50% SHL reported greater work and activity impacts on the WPAI-AA. Most patients were receiving their first AA treatment, with the most common treatments differing by SHL category. Healthcare resource utilization and costs were greater among patients with ≥ 50% SHL.

CONCLUSIONSIn the KSA, the burden of AA extends beyond SHL to include both mental health and economic burdens, highlighting the need for effective treatments.

Abstract from PubMed

PMID 42601567 · DOI 10.1007/s13555-026-01873-0