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Tirzepatide

Mounjaro, Zepbound, LY3298176

Quick Stats
Studies 183
Trials 100
Score 3
2025 pubmed

Effect of Glucagon-Like Peptide 1 Receptor Agonists on Patients With Rheumatoid Arthritis.

Kellner. David A DA; Dente. Elizabeth E; Tran. Vincent V; Welsh. Travis T; Tran. Victor V; Saha. Angshuman A; Baker. Joshua F JF; Elashoff. David A DA; Ranganath. Veena K VK

Key Findings

  • GLP‑1RA users had bigger drops in RA disease activity scores and pain than non‑users.
  • Significant reductions were seen in weight, total cholesterol, LDL, triglycerides, HbA1c, ESR, and CRP.
  • Around 33% discontinued tirzepatide or semaglutide, mainly due to gastrointestinal side effects.

Practical Outcomes

  • For biohackers with RA or chronic inflammation, tirzepatide may offer dual benefits: weight loss/metabolic improvement and reduced joint inflammation. However, the risk of GI upset and the need for a prescription mean it’s not a universal hack. Consider it if you already qualify for GLP‑1 therapy and can monitor inflammatory markers.

Summary

A review of medical records found that people with rheumatoid arthritis who took GLP‑1 drugs like tirzepatide lost weight, had lower blood sugar and cholesterol, and also showed less joint inflammation and pain compared to similar patients who didn’t take the drug. About one‑third stopped the medication because of stomach upset.

Abstract

Glucagon-like peptide 1 receptor agonists (GLP-1RAs) are approved for weight loss, diabetes, and cardiovascular risk reduction. Despite widespread use, GLP-1RAs have not been well studied in patients with rheumatoid arthritis (RA). We examined the effects of GLP-1RAs on RA disease activity and cardiovascular risk profile in patients with RA and overweight or obesity. We conducted a retrospective chart review study of patients with RA with a body mass index of ≥27 who were prescribed a GLP-1RA (semaglutide or tirzepatide). Between 2018 and 2024, 173 patients with RA were identified in the treatment group (prescribed and took a GLP-1RA), and 42 patients with RA were identified in the control group (prescribed but did not take GLP-1RA). Patients were assessed at three-month intervals for up to one year after prescription. Outcome measures included RA disease activity, cardiovascular risk markers, and patient-reported outcomes. Changes in outcome measures within and between groups were assessed with linear mixed effect models, with adjustments for baseline characteristics that differed significantly between groups. GLP-1RA-treated patients experienced significantly greater reductions in RA disease activity, pain, body weight, total cholesterol, and glycosylated hemoglobin than controls (P < 0.05). Within the treatment group, there were also significant reductions in erythrocyte sedimentation rate, C-reactive protein values, low-density lipoprotein cholesterol values, and triglyceride values (P < 0.05). Nearly one-third of the treatment group discontinued the GLP-1RA during the study period, with the most common adverse effect being gastrointestinal issues. This study suggests that the use of GLP-1RAs can improve RA disease activity and cardiovascular risk profile. Although further research is needed, this novel finding has significant clinical implications because it suggests that anti-obesity medications may improve both cardiovascular and RA outcomes.

Study Information

Provider

pubmed

Year

2025

Date

2025-09-01T00:00:00.000Z

DOI

10.1002/acr2.70103

References

15