The retrospective cohort study, presented by Mr Yagiz Akiska (George Washington University, Washington D.C., USA), analysed data from the TriNetX US Collaborative Network (2014–2024), encompassing 67 healthcare organisations [1]. Adults aged 18–89 years with ≥2 GLP-1RA prescriptions (liraglutide, semaglutide, dulaglutide, exenatide, lixisenatide, or tirzepatide) were compared with propensity-matched controls without GLP-1RA exposure. Exclusion criteria included prior hair loss, thyroid disease, malnutrition, chemotherapy, and other confounding factors.
At 12 months, GLP-1RA use was significantly associated with telogen effluvium (adjusted odds ratio (aOR) 1.76; 95% CI 1.34–2.32; P <0.001) and AGA (aOR 1.64; 95% CI 1.35–1.99; P<0.001), while no significant increase in alopecia areata was detected. Overall, nonscarring hair loss was also more likely (aOR 1.40; 95% CI 1.31–1.49; P<0.001). These associations were already apparent by 6 months for AGA and overall nonscarring hair loss, with statistical significance achieved at P <0.001 in both cases.
Longitudinal data from 2014 to 2024 demonstrated a marked rise in the incidence of nonscarring hair loss among GLP-1RA users, particularly telogen effluvium and AGA. This trend highlights the need for clinical vigilance, especially in patients experiencing rapid weight loss, a known precipitant of telogen effluvium.
The authors recommend proactive counselling for patients initiating GLP-1RA therapy about potential hair loss risks. Nutritional monitoring and multidisciplinary management may help mitigate this adverse effect and support treatment adherence.
Recognising and addressing the dermatological impact of GLP-1RAs is essential for maintaining quality-of-life and treatment continuation.
- Akiska Y, et al. Increased incidence and risk of hair loss with GLP-1 agonists: A real-world multicenter cohort study. EPS04.04, EADV Congress 2025, 17–20 September, Paris, France.
Medical writing support was provided by Dr Susanne Kammerer and Karin Drooff
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