Glucagon-like peptide-1 receptor agonist treatment reduces body weight and improves glycaemic outcomes in patients with concurrent overweight/obesity and type 1 diabetes: A systematic review and meta-analysis.
Purcell. Amanda R AR; Zhen. Xi May XM; Wong. Jencia J; Glastras. Sarah J SJ
Key Findings
- Average weight loss of 4.3â¯kg (â9.5â¯lb)
- HbA1c reduced by 0.25â¯%
- Insulin dose decreased by about 9â¯U per day
- Semaglutide showed the biggest improvements among GLPâ1 drugs
- Hypoglycaemia risk increased (ORâ¯1.34)
- Gastroâintestinal side effects were more common
Practical Outcomes
- Consider using semaglutide as an adjunct to insulin for weightâloss and modest glycaemic benefit in T1D patients with BMIâ¯â¥â¯25â¯kg/m². Start at a low dose, titrate slowly, and monitor glucose closely to catch extra hypoglycaemia. Expect some nausea or vomiting, which usually eases with continued use.
Summary
Adding a GLPâ1 drug like semaglutide to insulin in adults with typeâ1 diabetes who are overweight can help them lose about 4â¯kg, lower their A1c by roughly 0.25â¯%, and cut daily insulin by around 9 units, but it also raises the chance of lowâbloodâsugar episodes and causes stomach upset.
Abstract
This systematic review and meta-analysis evaluated the long-term efficacy and safety of glucagon-like peptide-1 receptor agonists (GLP-1RAs) as adjunctive therapies for individuals with type 1 diabetes (T1D) and overweight or obesity. A literature search was conducted in June 2023 and updated in June 2025. Eligible studies included adults with T1D, body mass index ≥25 kg/m<sup>2</sup>, and GLP-1RA treatment alongside insulin for ≥12 weeks. Changes in body weight, HbA1c, and insulin dose were expressed as mean differences (MDs) with 95% confidence intervals (CIs). Safety outcomes were assessed using odds ratios (ORs) with 95% CIs. Data were pooled using random-effects models. Exactly 13 studies met the inclusion criteria. GLP-1RA treatment was associated with a body weight reduction of 4.31 kg (95% CI: 3.61-5.00 kg) and a HbA1c reduction of 0.25% (95% CI: 0.18-0.32%). Across all studies, insulin dosage was reduced by 9.24 U/day (95% CI: 7.04-11.45 U/day). Subgroup analysis identified that semaglutide achieved the greatest reductions in all outcome measures. Hypoglycaemic episodes were increased (OR = 1.34; 95% CI: 1.02-1.76), while hyperglycaemic episodes decreased (OR: 0.69, 95% CI: 0.56-0.87). Gastrointestinal adverse events, including nausea and vomiting, were significantly more frequent with GLP-1RA treatment, though no increase in serious adverse events was observed. GLP-1RAs are effective for body weight reduction and glycaemic improvement in individuals with T1D and overweight/obesity, with acceptable safety profiles. These findings provide evidence that GLP-1RAs can be effectively and safely used as adjunctive therapy to insulin in people with T1D, but additional robust randomised clinical trials are needed.
Study Information
pubmed
2025
2025-10-20T00:00:00.000Z
10.1111/dom.70188