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Tirzepatide

Mounjaro, Zepbound, LY3298176

Quick Stats
Studies 183
Trials 100
Score 4
2025 pubmed 1 citations

GLP-1R Agonists for Weight Loss in Psychiatric Disorders: A Systematic Review and Meta-analysis.

Müller Alves. Klara K; Teixeira da Silva. Manoela M; Kramer. Caroline Kaercher CK; Viana. Luciana Verçoza LV

Key Findings

  • Average weight loss of about 5 kg compared with placebo.
  • BMI dropped by roughly 1.6 kg/m² and waist circumference shrank by ~3.4 cm.
  • Fasting glucose fell modestly (≈0.3 mmol/L) and total cholesterol improved.
  • Gastro‑intestinal side effects were common but mild and rarely caused people to stop the drug.

Practical Outcomes

  • For biohackers dealing with medication‑induced weight gain, GLP‑1R agonists are a proven, relatively safe tool to shed pounds and improve metabolic markers. Start with a low dose, titrate slowly, and watch for nausea or diarrhea. While tirzepatide looks promising, it hasn't been tested in this specific group yet, so stick with the already‑studied agents until more data appear.

Summary

A review of 10 clinical trials shows that drugs that activate the GLP‑1 receptor (like semaglutide and liraglutide) reliably cut weight, belly size, and blood sugar in people with mental‑health conditions who are also overweight, and they do so with only mild stomach upset.

Abstract

Individuals with psychiatric disorders have a higher prevalence of obesity, partly because of the use of psychotropic medications. Safe and effective pharmacological interventions for weight management in this population are needed. To assess the efficacy and safety of glucagon-like peptide-1 receptor agonists (GLP-1Ras) in individuals with psychiatric disorders and obesity/overweight through a systematic review and meta-analysis, focusing on weight and metabolic outcomes. We searched PubMed, Embase, Cochrane CENTRAL, and ClinicalTrials.gov until May 2025 for observational studies that evaluated GLP-1RAs in this population. Studies including adults with psychiatric disorders and obesity treated with GLP-1RAs were eligible; 10 randomized controlled trials met the inclusion criteria. Two reviewers independently extracted the data and assessed the risk of bias using the Cochrane RoB 2 tool. Outcomes included weight, body mass index (BMI), waist circumference, glucose level, systolic blood pressure, total cholesterol, high-density lipoprotein cholesterol, triglycerides, and adverse events. GLP-1RAs significantly reduced body weight [mean difference (MD) -5.03 kg; 95% confidence interval (CI): -6.04 to -4.01)], BMI (MD -1.59 kg/m²; 95% CI: -2 to -1.18), waist circumference (MD -3.4 cm 95% CI: -4.83 to-1.97), and fasting glucose (MD -0.29 mmol/L; 95% CI: -0.53 to -0.05) compared to controls. Gastrointestinal side effects were more frequent but generally mild and did not increase discontinuation rates. GLP-1RAs are effective and well-tolerated for managing obesity in psychiatric populations, offering significant weight and metabolic benefits. Further studies are needed to evaluate newer agents, such as semaglutide and tirzepatide, particularly in longer trials with standardized protocols.

Study Information

Provider

pubmed

Year

2025

Date

2025-11-11T00:00:00.000Z

DOI

10.1210/jendso/bvaf150

Citations

1

References

63