# Refractory Dysmenorrhea Managed With a Glucagon-Like Peptide-1 Agonist: A Case Report

**Authors:** Mary Tran, Nicholas Swartz, Sabine D Elisèe

PMC · DOI: 10.7759/cureus.77387 · Cureus · 2025-01-13

## TL;DR

A patient with severe dysmenorrhea found symptom relief using semaglutide, a GLP-1 agonist, suggesting potential new treatment options.

## Contribution

This case report explores the novel use of a GLP-1 agonist for managing refractory dysmenorrhea.

## Key findings

- Semaglutide reduced dysmenorrhea symptoms without lifestyle changes or additional medications.
- The patient experienced minimal side effects and no weight changes during treatment.
- The case suggests GLP-1 agonists may have anti-inflammatory and anti-estrogenic properties.

## Abstract

Dysmenorrhea includes symptoms such as abdominal pain, nausea, and vomiting. It is a clinical diagnosis with typical treatment involving the use of non-steroidal anti-inflammatory drugs (NSAIDs) and hormonal therapy. Even with conventional treatment, many women deal with dysmenorrhea refractory to treatment. They are often subject to dealing with the adverse effects of those treatments, such as peptic ulcer disease. We present a case of a patient with severe refractory dysmenorrhea who was able to minimize symptoms with the use of semaglutide, a glucagon-like peptide-1 (GLP-1) agonist. With no changes in the patient’s lifestyle and no additional medications added, the semaglutide therapy was able to minimize the patient’s symptoms to where she was able to continue activities of daily living and minimize the use of NSAID therapy. Moreover, the patient experienced no changes in weight and only transient loss of appetite while on semaglutide. We hypothesize that anti-estrogenic and anti-inflammatory properties are potential mechanisms of action in this case. This case brings to light the possible multifaceted applications of GLP-1 agonists beyond weight control and diabetes. The outcome of this case suggests that a controlled trial of GLP-1 agonist therapy is warranted to determine its potential for the management of dysmenorrhea.

## Linked entities

- **Chemicals:** semaglutide (PubChem CID 56843331)
- **Diseases:** dysmenorrhea (MONDO:1060205), peptic ulcer disease (MONDO:0004247)

## Full-text entities

- **Genes:** GCG (glucagon) [NCBI Gene 2641] {aka GLP-1, GLP1, GLP2, GRPP}
- **Diseases:** inflammatory (MESH:D007249), estrogenic (MESH:D056828), abdominal pain (MESH:D015746), nausea (MESH:D009325), peptic ulcer disease (MESH:D010437), loss of appetite (MESH:D001068), vomiting (MESH:D014839), Dysmenorrhea (MESH:D004412), diabetes (MESH:D003920)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## References

20 references — full list in the complete paper: https://tomesphere.com/paper/PMC11821293/full.md

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Source: https://tomesphere.com/paper/PMC11821293