Abstract | BACKGROUND: METHODS: We analyzed data from randomized controlled trials with a minimum duration of 24 weeks that assessed the incidence of neoplasms in type 2 diabetes patients receiving GLP-1 receptor agonists compared with placebo or other hypoglycemic drugs. We searched the MEDLINE, Embase, and Cochrane databases with a language restriction of English through October 1, 2018, and carried out a meta-analysis of the available trial data using a fixed effects model to calculate odds ratios ( ORs) for neoplasia. RESULTS: Thirty-four relevant articles, providing data for 50452 patients, were included in the meta-analysis. Compared with the incidence of malignant neoplasia with placebo or other interventions, no increase in malignant neoplasm formation was observed with the use of GLP-1 receptor agonists (OR 1.04, 95% confidence interval (CI) 0.94-1.15; p = 0.46), liraglutide (OR 1.08, 95% CI 0.91-1.27; p = 0.38), exenatide (OR 1.00, 95% CI 0.86-1.16; p = 1.00), semaglutide (OR 0.89, 95% CI 0.35-2.22; p = 0.80), or albiglutide (OR 1.07, 95% CI 0.23-4.88; p = 0.93). A subanalysis of trials lasting longer than 3 years also showed no increase in the neoplasia risk with GLP-1 receptor agonist use (OR 1.03, 95% CI 0.92-1.15; p = 0.60). Between-trial statistical heterogeneity was low for all comparisons. CONCLUSION:
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Authors | Yufang Liu, Xiaomei Zhang, Sanbao Chai, Xin Zhao, Linong Ji |
Journal | Journal of diabetes research
(J Diabetes Res)
Vol. 2019
Pg. 1534365
( 2019)
ISSN: 2314-6753 [Electronic] England |
PMID | 31396537
(Publication Type: Journal Article, Meta-Analysis, Systematic Review)
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Chemical References |
- Glucagon-Like Peptide-1 Receptor
- Hypoglycemic Agents
- semaglutide
- rGLP-1 protein
- Glucagon-Like Peptides
- Liraglutide
- Glucagon-Like Peptide 1
- Exenatide
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Topics |
- Diabetes Mellitus, Type 2
(drug therapy, epidemiology)
- Exenatide
(therapeutic use)
- Glucagon-Like Peptide 1
(analogs & derivatives, therapeutic use)
- Glucagon-Like Peptide-1 Receptor
(agonists)
- Glucagon-Like Peptides
(therapeutic use)
- Humans
- Hypoglycemic Agents
(therapeutic use)
- Incidence
- Liraglutide
(therapeutic use)
- Neoplasms
(chemically induced, epidemiology)
- Risk Factors
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