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DOI 10.1002/edm2.70134

Медицинская библиотека · Endocrinology, diabetes & metabolism · 2025

Efficacy and Safety of Orforglipron in Obese Adults With or Without Diabetes: A Systematic Review and Meta-Analysis.

Pandey Ravi Kumar, Jan Mahnoor, Mohammad Aqsa, Jawaid Khawaja Arham, Naveed Mawra, Abid Muhammad Ali, Amir Abdullah Bin, Ahmed Shafique, Safiullah Muhammad, Bhatti Muhammad Imaz, Iftikhar Sana, Saddique Muhammad Nabeel, Alfalh Widyan, Omar Rihab Mohammed Bin, Abu Dawood Husam

СтатьяСистематический обзорМетаанализПеревод пока не подготовлен

Аннотация

BACKGROUND

Obesity represents a major global health challenge, contributing substantially to cardiovascular disease and metabolic complications. Orforglipron, a novel oral non-peptide GLP-1 receptor agonist, has emerged as a promising therapeutic option for weight management and glycemic control. This meta-analysis evaluated the efficacy and safety of orforglipron in obese patients with or without type 2 diabetes mellitus (T2DM).

METHODS

A comprehensive literature search was conducted across PubMed, Embase, Cochrane Library and ClinicalTrials.gov from inception to October 2025 to identify randomised controlled trials (RCTs) evaluating orforglipron in obese patients. Mean differences (MDs) and risk ratios (RRs) with 95% confidence intervals (CIs) were calculated using random-effects models.

RESULTS

Five RCTs comprising 4410 participants were included. Orforglipron demonstrated dose-dependent reductions in body weight from 2.48% at 3 mg to 9.8% at 45 mg, BMI from 0.89 to 3.62 kg/m2, waist circumference from 1.57 to 6.9 cm, and HbA1c from 0.76% to 1.04% compared with placebo. Favourable lipid changes included reductions in total cholesterol (MD: -4.51% [95% CI: -6.91 to -2.11]), LDL-C (MD: -5.34% [95% CI: -7.10 to -3.58]), and triglycerides (MD: -10.07% [95% CI: -12.33 to -7.80]), with increased HDL-C (MD: 2.94% [95% CI: 1.38 to 4.49]). However, gastrointestinal adverse events were significantly more frequent at doses of 12 mg or higher and treatment discontinuation rates were highest at 24 mg (RR:4.61 [95% CI:1.6 to 13.33]) and 36 mg (RR:3.68 [95% CI:2.48 to 5.44]) doses. Serious adverse events and mortality rates were comparable to those with placebo.

CONCLUSION

Orforglipron significantly improved glycemic and lipid parameters in patients with obesity, demonstrating dose-dependent efficacy with maximal benefits at higher doses. While gastrointestinal tolerability remains a clinically important limitation requiring mitigation strategies, orforglipron represents a promising oral therapeutic option for comprehensive obesity and metabolic management.

Для цитирования: Pandey Ravi Kumar, Jan Mahnoor, Mohammad Aqsa, Jawaid Khawaja Arham, Naveed Mawra, Abid Muhammad Ali, Amir Abdullah Bin, Ahmed Shafique, Safiullah Muhammad, Bhatti Muhammad Imaz, Iftikhar Sana, Saddique Muhammad Nabeel, Alfalh Widyan, Omar Rihab Mohammed Bin, Abu Dawood Husam. Efficacy and Safety of Orforglipron in Obese Adults With or Without Diabetes: A Systematic Review and Meta-Analysis.. Endocrinology, diabetes & metabolism. 2025. DOI: 10.1002/edm2.70134.

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