Article Publish Status: FREE
Abstract Title:

Medications affecting the biochemical conversion to type 2 diabetes: A systematic review and meta-analysis.

Abstract Source:

J Clin Endocrinol Metab. 2019 Jul 31. Epub 2019 Jul 31. PMID: 31365088

Abstract Author(s):

Juan Pablo Domecq, Gabriela Prutsky, Tarig Elraiyah, Zhen Wang, Karen F Mauck, Juan Pablo Brito, Chaitanya Undavalli, Vishnu Sundaresh, Larry J Prokop, Victor M Montori, Mohammad H Murad

Article Affiliation:

Juan Pablo Domecq


BACKGROUND: The extent to which some pharmacological interventions reduce or increase the risk of biochemical conversion to T2DM in at-risk individuals is unclear.

METHODS: We searched MEDLINE, EMBASE, Cochrane Central Register of Controlled Trials, Cochrane Database of Systematic Reviews and Scopus through August 24, 2017, for randomized controlled trials evaluating the effect of drugs suspected to modify the risk of biochemical conversion to T2DM.

RESULTS: We included 43 trials with 192,156 subjects (mean age 60 years; 56% men; mean BMI 30.4 kg/m2). Alpha-glucosidase inhibitors, angiotensin-converting enzyme inhibitors, angiotensin II receptor blockers, metformin, orlistat, phentermine-topiramate and pioglitazone significantly reduced the risk of biochemical conversion to T2DM, whereas statins and nateglinide increased the risk. There was insufficient direct evidence regarding the effects of sulfonylureas, glucagon-like peptide-1 receptor agonists, dipeptidyl peptidase-4 inhibitors and sodium-glucose cotransporter-2 inhibitors. Most trials were brief and evaluated this outcome during treatment without a withdrawal or washout period.

CONCLUSIONS: Several drugs modify the risk of biochemical conversation to T2DM, although whether this effect is persistent and clinically relevant is unclear. Future studies need to focus on cardiovascular disease prevention, mortality and patient-important outcomes instead of biochemical conversion to T2DM.

Study Type : Meta Analysis, Review

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Sayer Ji
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