Comparative effectiveness of GLP-1 receptor agonists on glycaemic control, body weight, and lipid profile for type 2 diabetes: systematic review and network meta-analysis.
Yao. Haiqiang H; Zhang. Anqi A; Li. Delong D; Wu. Yuqi Y; Wang. Chong-Zhi CZ; Wan. Jin-Yi JY; Yuan. Chun-Su CS
Key Findings
- CagriSema (semaglutide + cagrilintide) produced the greatest weight loss (~14 kg) among all GLP‑1RA treatments.
- Tirzepatide was the most effective for lowering HbA1c and fasting glucose, but not as strong for weight loss as CagriSema.
- All GLP‑1RAs lowered HbA1c and fasting glucose; semaglutide also modestly reduced LDL‑C and total cholesterol.
- Higher doses of GLP‑1RAs, including CagriSema, raise the risk of gastrointestinal side effects.
Practical Outcomes
- If you’re looking for maximal weight loss, a semaglutide‑cagrilintide combo appears superior to other GLP‑1 drugs. Start with low doses and titrate slowly to limit nausea, vomiting, or diarrhea. Monitor blood sugar and lipid panels, as the combo also improves glucose control and may modestly lower bad cholesterol.
Summary
A big review of many diabetes drugs shows that the combo of semaglutide plus cagrilintide (called CagriSema) cuts weight the most—about 14 kg on average—while also improving blood sugar. It works better than other GLP‑1 drugs, but high doses can cause stomach upset.
Abstract
To evaluate the comparative efficacy and safety of glucagon-like peptide-1 receptor agonists (GLP-1RAs) on glycaemic control, body weight, and lipid profile in adults with type 2 diabetes. Systematic review and network meta-analysis. PubMed, Web of Science, Cochrane Central Register of Controlled Trials (CENTRAL), and Embase from database inception to 19 August 2023. Eligible randomised controlled trials enrolled adults with type 2 diabetes who received GLP-1RA treatments and compared effects with placebo or any GLP-1RA drug, with a follow-up duration of at least 12 weeks. Trials with a crossover design, non-inferiority studies comparing GLP-1RA and other drug classes without a placebo group, using withdrawn drugs, and non-English studies were deemed ineligible. 76 eligible trials involving 15 GLP-1RA drugs and 39 246 participants were included in this network meta-analysis; all subsequent estimates refer to the comparison with placebo. All 15 GLP-1RAs effectively lowered haemoglobin A<sub>1c</sub> and fasting plasma glucose concentrations. Tirzepatide induced the largest reduction of haemoglobin A<sub>1c</sub> concentrations (mean difference -2.10% (95% confidence interval -2.47% to -1.74%), surface under the cumulative ranking curve 94.2%; high confidence of evidence), and fasting plasma glucose concentrations (-3.12 mmol/L (-3.59 to -2.66), 97.2%; high confidence), and proved the most effective GLP-1RA drug for glycaemic control. Furthermore, GLP-1RAs were shown to have strong benefits to weight management for patients with type 2 diabetes. CagriSema (semaglutide with cagrilintide) resulted in the highest weight loss (mean difference -14.03 kg (95% confidence interval -17.05 to -11.00); high confidence of evidence), followed by tirzepatide (-8.47 kg (-9.68 to -7.26); high confidence). Semaglutide was effective in lowering the concentration of low density lipoprotein (-0.16 mmol/L (-0.30 to -0.02)) and total cholesterol (-0.48 mmol/L (-0.84 to -0.11)). Moreover, this study also raises awareness of gastrointestinal adverse events induced by GLP-1RAs, and concerns about safety are especially warranted for high dose administration. GLP-1RAs are efficacious in treating adults with type 2 diabetes. Compared with the placebo, tirzepatide was the most effective GLP-1RA drug for glycaemic control by reducing haemoglobin A<sub>1c</sub> and fasting plasma glucose concentrations. GLP-1RAs also significantly improved weight management for type 2 diabetes, with CagriSema performing the best for weight loss. The results prompt safety concerns for GLP-1RAs, especially with high dose administration, regarding gastrointestinal adverse events. PROSPERO CRD42022342845.
Study Information
pubmed
2024
2024-01-29T00:00:00.000Z
10.1136/bmj-2023-076410
283
29