Semaglutide Use and Clinical Experience: Editorial Letter

Authors

  • Mert Adnan Derviş Defne Satate Hospital

DOI:

https://doi.org/10.5281/zenodo.17591229

Keywords:

Semaglutide, diabetes, Clinical Experience

Abstract

Semaglutide has emerged in recent years as a prominent pharmaceutical agent used to treat Type 2 diabetes. Its mechanism of action is based on its role as a glucagon-like peptide-1 receptor agonist. A multicenter phase three study was conducted, in which 1,197 participants were observed over a period of 240 weeks. As indicated by the findings of the study, there was a substantial decline in the identification of steatohepatitis, concurrent with a notable decrease in body mass index among obese patients (1, 2).

Semaglutide has been associated with a variety of adverse effects, including gastrointestinal complaints, renal and biliary problems. Gastrointestinal adverse effects encompass a range of symptoms, including but not limited to: nausea, vomiting, abdominal pain, diarrhea, and constipation (3). In biliary pathologies, cholelithiasis and cholecystitis have been reported, and cases of pancreatitis are documented in the literature (4).

Dear Editor,It is worth noting that analogous observations have been made in the patients under our supervision. In the subsequent follow-up of patients using semaglutide, a reduction in weight was observed, and the conditions of hepatosteatosis and steatohepatitis demonstrated regression. In addition to the observed decrease in body weight, it was noted that patients frequently exhibited gastrointestinal symptoms, particularly during the medication adaptation process. Conversely, no significant adverse effects have been observed in patients exhibiting dyspeptic abdominal pain. However, subsequent patient monitoring has demonstrated that these adverse effects can lead to a decline in medication adherence and the cessation of weight loss after a certain duration. It is imperative that patients receive comprehensive information regarding any findings pertaining to the gastrointestinal system during subsequent follow-up appointments. In cases where such symptoms are present, it is imperative to provide supportive treatment and symptomatic relief.

References

1. Sanyal AJ, Newsome PN, Kliers I, Østergaard LH, Long MT, Kjær MS, Cali AMG, Bugianesi E, Rinella ME, Roden M, Ratziu V; ESSENCE Study Group. Phase 3 Trial of Semaglutide in Metabolic Dysfunction-Associated Steatohepatitis. N Engl J Med. 2025 Jun 5;392(21):2089-2099. doi: 10.1056/NEJMoa2413258. Epub 2025 Apr 30. PMID: 40305708.

2. Wilding JPH, Batterham RL, Calanna S, Davies M, Van Gaal LF, Lingvay I, McGowan BM, Rosenstock J, Tran MTD, Wadden TA, Wharton S, Yokote K, Zeuthen N, Kushner RF; STEP 1 Study Group. Once-Weekly Semaglutide in Adults with Overweight or Obesity. N Engl J Med. 2021 Mar 18;384(11):989-1002. doi: 10.1056/NEJMoa2032183. Epub 2021 Feb 10. PMID: 33567185.

3. Htike ZZ, Zaccardi F, Papamargaritis D, Webb DR, Khunti K, Davies MJ. Efficacy and safety of glucagon-like peptide-1 receptor agonists in type 2 diabetes: A systematic review and mixed-treatment comparison analysis. Diabetes Obes Metab. 2017 Apr;19(4):524-536. doi: 10.1111/dom.12849. Epub 2017 Feb 17. PMID: 27981757.

4. Marso SP, Bain SC, Consoli A, Eliaschewitz FG, Jódar E, Leiter LA, Lingvay I, Rosenstock J, Seufert J, Warren ML, Woo V, Hansen O, Holst AG, Pettersson J, Vilsbøll T; SUSTAIN-6 Investigators. Semaglutide and Cardiovascular Outcomes in Patients with Type 2 Diabetes. N Engl J Med. 2016 Nov 10;375(19):1834-1844. doi: 10.1056/NEJMoa1607141. Epub 2016 Sep 15. PMID: 27633186.

Published

2025-11-15

How to Cite

Derviş, M. A. (2025). Semaglutide Use and Clinical Experience: Editorial Letter. Acta Medica Young Doctors, 1(3), 1–2. https://doi.org/10.5281/zenodo.17591229

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