Logo

American Heart Association

  33
  0


Final ID: MP2215

Glucagon-Like Peptide-1 Receptor Agonists Show Varied Impact on Venous Thromboembolism Risk: A Comprehensive Bayesian Network Meta-Analysis of Randomized Controlled Trials

Abstract Body (Do not enter title and authors here): Background: Glucagon-like peptide-1 receptor agonists (GLP-1RAs) are increasingly used in diabetes management, but their association with venous thromboembolism (VTE), including deep vein thrombosis (DVT) and pulmonary embolism (PE), remains unclear.
Research Questions: We sought to determine whether glucagon-like peptide-1 receptor agonists (GLP-1RAs) significantly increase venous thromboembolism (VTE) risk compared to placebo or other anti-diabetic drugs.
Methods: A systematic search of PubMed, SCOPUS, and EMBASE was conducted for RCTs comparing GLP-1RAs (dulaglutide, lixisenatide, exenatide, semaglutide, albiglutide, liraglutide) with placebo or other anti-diabetic drugs, reporting DVT and PE outcomes. A Bayesian network meta-analysis was performed to estimate odds ratios (OR) with 95% credible intervals (CrI) using Markov Chain Monte Carlo (MCMC) methods, and convergence was evaluated through the Gelman-Rubin diagnostic. Surface under the cumulative ranking curve (SUCRA) ranked treatments by efficacy.
Results: From 39 RCTs with 70,499 participants, GLP-1RAs showed varied risks. For VTE versus control: dulaglutide (OR: 1.63, 95% CrI: 0.05 to 8.45; SUCRA: 65.23%), lixisenatide (OR: 3.66, 95% CrI: 0.03 to 20.47; SUCRA: 61.02%), exenatide (OR: 5.75, 95% CrI: 0.03 to 30.48; SUCRA: 53.77%), semaglutide (OR: 1.59, 95% CrI: 0.28 to 5.82; SUCRA: 50.51%), albiglutide (OR: 3.48, 95% CrI: 0.19 to 16.31; SUCRA: 33.95%), liraglutide (OR: 6.15, 95% CrI: 0.31 to 34.48; SUCRA: 29.15%), control (SUCRA: 56.38%). For DVT versus control: dulaglutide (OR: 1.24, 95% CrI: 0.02 to 6.82; SUCRA: 79.04%), lixisenatide (OR: 8.08, 95% CrI: 0.05 to 45.38; SUCRA: 49.66%), albiglutide (OR: 5.49, 95% CrI: 0.19 to 29.58; SUCRA: 38.77%), liraglutide (OR: 12.28, 95% CrI: 0.21 to 69.73; SUCRA: 33.24%), semaglutide (OR: 5.11, 95% CrI: 0.41 to 24.78; SUCRA: 33.07%), control (SUCRA: 66.23%). For PE versus control: lixisenatide (OR: 0.94, 95% CrI: 0.03 to 3.15; SUCRA: 82.64%), exenatide (OR: 1.28, 95% CrI: 0.05 to 5.91; SUCRA: 62.62%), semaglutide (OR: 0.88, 95% CrI: 0.28 to 2.15; SUCRA: 60.08%), liraglutide (OR: 1.45, 95% CrI: 0.33 to 5.06; SUCRA: 43.99%), dulaglutide (OR: 1.48, 95% CrI: 0.24 to 5.03; SUCRA: 43.58%), control (SUCRA: 44.71%), albiglutide (OR: 4.10, 95% CrI: 0.57 to 16.20; SUCRA: 12.38%).
Conclusions: GLP-1RAs exhibit varied VTE risks, with liraglutide showing the highest risk for VTE, and albiglutide for PE. Dulaglutide and lixisenatide appear safer for DVT and PE, respectively.
  • Khalil, Ibrahim  ( Dhaka Medical College and Hospital , Dhaka , Bangladesh )
  • Hossain, Md. Imran  ( Manikganj Medical College , Manikganj , Bangladesh )
  • Rahman, Mohd Turzo  ( Flushing Hospital Medical Center , Flushing , New York , United States )
  • Akter, Mst. Mahmuda  ( Manikganj Medical College , Manikganj , Bangladesh )
  • Sayed, Md Abu  ( Chattogram medical college , Chattogam , Bangladesh )
  • Sarker, Pallab  ( Reading hospital , West Reading , Pennsylvania , United States )
  • Author Disclosures:
    Ibrahim Khalil: DO NOT have relevant financial relationships | Md. Imran Hossain: No Answer | Mohd Turzo Rahman: DO NOT have relevant financial relationships | Mst. Mahmuda Akter: No Answer | Md Abu Sayed: DO NOT have relevant financial relationships | Pallab Sarker: DO NOT have relevant financial relationships
Meeting Info:

Scientific Sessions 2025

2025

New Orleans, Louisiana

Session Info:

Optimizing Use of GLP-1 RA for Cardiometabolic Benefit: New Strategies and Applications

Monday, 11/10/2025 , 10:45AM - 12:00PM

Moderated Digital Poster Session

More abstracts on this topic:
Acute and Chronic Phosphorylation of CaMKII on Coronary Microvascular/Endothelial Function

Iddrisu Hanisah, Xing Hang, Shi Guangbin, Liu Yuhong, Feng Jun

Add-on Therapy with Dantrolene, a RyR2 Stabilizer, Terminates Ventricular Tachycardia Storm refractory to Intravenous Amiodarone in Heart Failure.

Nawata Junya, Omuro Ayumi, Fukuda Masakazu, Suetomi Takeshi, Miyazaki Yosuke, Fujimura Tatsuhiro, Mochizuki Mamoru, Sano Motoaki, Kobayashi Shigeki, Ishikawa Maho, Nakata Yuki, Murakawa Kaori, Nakashima Yusuke, Hisaoka Masahiro, Matsuyama Tetsuya, Nakamura Yoshihide

More abstracts from these authors:
You have to be authorized to contact abstract author. Please, Login
Not Available