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GLP-1 receptor agonists and pancreatic beta cell apoptosis in diabetes mellitus: a systematic review and meta-analysis of preclinical studies.

Meta AnalysisLow Moderate evidence

This record provides bibliographic details and links to the original research. An editorial study breakdown is not available.

What the researchers found

GLP-1 receptor agonists reduced pancreatic beta cell death by about 10 percentage points in preclinical models, supporting the idea that these drugs help preserve insulin-producing cells.

Why it matters

Diabetes involves the gradual loss of beta cells that make insulin. If GLP-1 drugs can slow this loss, they may do more than just control blood sugar. They could help protect the pancreas itself.

The numbers in context

Pooled mean difference in apoptosis: -0.10 (95% CI -0.15 to -0.05, p = 0.0003). 5 studies included. I-squared = 100% (extreme heterogeneity). Egger's test p = 0.80 (no publication bias detected).

How the study worked

Systematic review and meta-analysis following PRISMA guidelines. Searched Scopus, PubMed, Embase, and Google Scholar. Included preclinical studies of GLP-1 RA effects on human beta cell apoptosis. Random-effects model.

Who was studied

Human pancreatic beta cells in laboratory culture (preclinical)

What this study cannot tell us

Only five studies met criteria. Extreme heterogeneity (I-squared = 100%) limits confidence in the pooled estimate. All preclinical data from cell cultures. No human clinical evidence. Long-term effects on beta cell function unknown.

Read the original research

GLP-1 receptor agonists and pancreatic beta cell apoptosis in diabetes mellitus: a systematic review and meta-analysis of preclinical studies.

Frontiers in clinical diabetes and healthcare, 6, 1579961

Citation

Rea, Nicolas; Ramdass, Prakash V A K. (2025). GLP-1 receptor agonists and pancreatic beta cell apoptosis in diabetes mellitus: a systematic review and meta-analysis of preclinical studies.. Frontiers in clinical diabetes and healthcare, 6, 1579961. https://doi.org/10.3389/fcdhc.2025.1579961