# The Impact of Glucagon-Like Peptide-1 (GLP-1) Agonists on Acne, Hidradenitis, and Sebaceous Activity

**Authors:** Azra Jabin, Shahab Khan, Hammad Khan, Zain Ullah Durrani, Khizer Hamza, Faiza Gul, Sana Atta Ullah, Fahad Dayam, Muhammad Yaseen, Saleem Shah

PMC · DOI: 10.7759/cureus.101212 · Cureus · 2026-01-10

## TL;DR

This study shows that semaglutide, a diabetes drug, can improve acne, hidradenitis, and sebaceous activity while also improving metabolic markers.

## Contribution

The study demonstrates a novel dermatologic benefit of GLP-1 agonists, linking skin condition improvements to metabolic changes.

## Key findings

- Acne severity decreased significantly over 24 months of semaglutide therapy.
- Hidradenitis suppurativa activity and sebaceous gland function also improved significantly.
- Metabolic improvements were independently correlated with dermatologic benefits.

## Abstract

Background and objective

Glucagon-like peptide-1 receptor agonists (GLP-1 RAs), especially semaglutide, are commonly used to treat obesity and diabetes. They may influence sebaceous gland activity, hidradenitis suppurativa (HS), and acne via metabolic and anti-inflammatory pathways. This study aimed to assess the effects of semaglutide on acne severity, HS activity, and sebaceous gland function, and to evaluate associations with metabolic improvements.

Materials and methods

This prospective, observational, single-arm study was conducted at the Department of Dermatology, Hayatabad Medical Complex, Peshawar, from January 2023 to December 2024. Adults with acne, HS, or increased sebaceous gland activity who initiated semaglutide therapy between the ages of 18 and 65 years were included. Sebumetry, HS severity using the Hidradenitis Suppurativa Area and Severity Index - Revised (HASI-R), and acne grading using the Investigator’s Global Assessment (IGA) were evaluated at baseline and at three, six, 12, 18, and 24 months. Concurrent measurements of metabolic markers, including BMI, HbA1c, fasting glucose, and insulin, were also obtained. Statistical analyses included Pearson and Spearman correlations, multivariate regression to adjust for confounders, and paired t-tests for pre- and post-treatment comparisons. P-values below 0.05 were considered statistically significant.

Results

Of the 120 enrolled participants, 110 completed the follow-up (91.7%). Over 24 months, acne severity decreased from 1.92 ± 0.78 to 1.21 ± 0.63, HS activity declined from 11.34 ± 4.56 to 7.45 ± 3.21, and sebaceous gland activity was reduced from 186.45 ± 52.34 to 138.56 ± 42.78 µg/cm². Improvements in BMI, HbA1c, fasting glucose, and insulin were significantly associated with dermatologic improvement (p < 0.05). Adverse events were mild and transient and occurred in 17 participants (15.45%).

Conclusions

Semaglutide therapy was significantly associated with improvement in acne, HS activity, and sebaceous gland function, independently correlated with metabolic enhancements. These findings indicate a potential dermatologic benefit of GLP-1 agonists, supporting the need for further controlled studies.

## Linked entities

- **Proteins:** GCG (glucagon)
- **Chemicals:** semaglutide (PubChem CID 56843331)
- **Diseases:** acne (MONDO:0011438), hidradenitis suppurativa (MONDO:0006559), obesity (MONDO:0011122), diabetes (MONDO:0005015)

## Full-text entities

- **Genes:** GCG (glucagon) [NCBI Gene 2641] {aka GLP-1, GLP1, GLP2, GRPP}, INS (insulin) [NCBI Gene 3630] {aka IDDM, IDDM1, IDDM2, ILPR, IRDN, MODY10}, GLP1R (glucagon like peptide 1 receptor) [NCBI Gene 2740] {aka GLP-1, GLP-1-R, GLP-1R}
- **Diseases:** inflammatory (MESH:D007249), HS (MESH:D017497), diabetes (MESH:D003920), Acne (MESH:D000152), Hidradenitis (MESH:D016575), obesity (MESH:D009765)
- **Chemicals:** glucose (MESH:D005947)

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12884193/full.md

## References

21 references — full list in the complete paper: https://tomesphere.com/paper/PMC12884193/full.md

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Source: https://tomesphere.com/paper/PMC12884193