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Review
. 2024 May 25;316(6):248.
doi: 10.1007/s00403-024-02969-3.

Rare cutaneous adverse reactions associated with GLP-1 agonists: a review of the published literature

Affiliations
Review

Rare cutaneous adverse reactions associated with GLP-1 agonists: a review of the published literature

Carlos E Salazar et al. Arch Dermatol Res. .

Abstract

Glucagon-like-peptide-1 (GLP-1) agonists are an emerging class of medications used to manage type 2 diabetes mellitus (T2DM) and weight loss, with demonstrated efficacy in reducing hemoglobin A1c levels, body mass index, and adverse cardiovascular events. While previous studies have reviewed notable cutaneous adverse effects with other antidiabetic medications, little is known about GLP-1 agonist-induced cutaneous reactions. Nevertheless, rare but significant cutaneous adverse reactions have been reported, including but not limited to dermal hypersensitivity reactions, eosinophilic panniculitis, bullous pemphigoid, and morbilliform drug eruptions. As GLP-1 induced cutaneous reactions are diverse, diagnosis requires clinical suspicion, thorough history-taking, and supportive histopathological findings when available. Management involves cessation of the offending agent with a tailored regimen to address inflammatory and/or immunogenic etiologies as well as irritative symptoms. This review aims to consolidate available information from case reports and case series regarding rare skin-related adverse outcomes due to GLP-1 use, aiming to provide a comprehensive overview of the presentation, pathogenesis, and management for dermatologists and other clinicians.

Keywords: Cutaneous adverse effects; Dulaglutide; Exenatide; GLP-1 agonists; Glucagon-like-peptide-1; Hemoglobin A1c; Liraglutide; Lixisenatide; Semaglutide; Tirzepatide; Type 2 diabetes mellitus; Weight loss.

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References

    1. Nauck MA, Quast DR, Wefers J, Meier JJ (2021) GLP-1 receptor agonists in the treatment of type 2 diabetes—state-of-the-art. Mol Metab. 46:101102. https://doi.org/10.1016/j.molmet.2020.101102 . (Epub 2020 Oct 14. PMID: 33068776; PMCID: PMC8085572) - DOI - PubMed
    1. Trujillo JM, Nuffer W, Smith BA (2021) GLP-1 receptor agonists: an updated review of head-to-head clinical studies. Ther Adv Endocrinol Metab 9(12):2042018821997320. https://doi.org/10.1177/2042018821997320 . (PMID: 33767808; PMCID: PMC7953228) - DOI
    1. Madsbad S (2019) Liraglutide for the prevention of major adverse cardiovascular events in diabetic patients. Expert Rev Cardiovasc Ther 17(5):377–387. https://doi.org/10.1080/14779072.2019.1615444 . (Epub 2019 May 17. PMID: 31055989) - DOI - PubMed
    1. Boyle JG, Livingstone R, Petrie JR (2018) Cardiovascular benefits of GLP-1 agonists in type 2 diabetes: a comparative review. Clin Sci (Lond) 132(15):1699–1709. https://doi.org/10.1042/CS20171299 . (PMID: 30115742) - DOI - PubMed
    1. Trujillo J (2020) Safety and tolerability of once-weekly GLP-1 receptor agonists in type 2 diabetes. J Clin Pharm Ther 45(Suppl 1):43–60. https://doi.org/10.1111/jcpt.13225 . (PMID: 32910487; PMCID: PMC7540535) - DOI - PubMed - PMC

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