Sodium-Glucose Cotransporter 2 Inhibitors and New-onset Type 2 Diabetes in Adults With Prediabetes: Systematic Review and Meta-analysis of Randomized Controlled Trials.


Journal

The Journal of clinical endocrinology and metabolism
ISSN: 1945-7197
Titre abrégé: J Clin Endocrinol Metab
Pays: United States
ID NLM: 0375362

Informations de publication

Date de publication:
17 12 2022
Historique:
received: 19 07 2022
pubmed: 12 10 2022
medline: 21 12 2022
entrez: 11 10 2022
Statut: ppublish

Résumé

The preventive effect of sodium-glucose cotransporter 2 (SGLT2) inhibitors for new-onset diabetes was investigated in secondary analyses of several randomized controlled trials (RCTs). However, the results were inconsistent. This work aimed to synthesize available evidence and evaluate whether SGLT2 inhibitors are effective in preventing new-onset diabetes. In this systematic review and meta-analysis of RCTs, MEDLINE, EMBASE, and Cochrane Central Register of Controlled Trials were searched through February 11, 2022. Two independent authors screened the search results and extracted summary data from eligible RCTs (including original and post hoc analyses) comparing SGLT2 inhibitors and placebo for the risk of new-onset diabetes among adults with prediabetes. Meta-analysis was conducted using random-effects models to calculate risk ratios and 95% CIs. We included 4 RCTs with 5655 participants who had prediabetes. Based on the random-effects meta-analysis, SGLT2 inhibitors were significantly associated with a lower risk of new-onset diabetes (relative risk, 0.79; 95% CI, 0.68-0.93). The relative risks of new-onset diabetes in dapagliflozin and empagliflozin were 0.68 (95% CI, 0.52-0.89) and 0.87 (95% CI, 0.72-1.04), respectively (P-for-heterogeneity = .14). The frequency of severe hypoglycemia was not elevated in the SGLT2 inhibitors group compared to the placebo group. In this meta-analysis, SGLT2 inhibitors were associated with a reduced risk of new-onset type 2 diabetes among adults with prediabetes and heart failure or chronic kidney disease. These findings indicate the potential usefulness of SGLT2 inhibitors in preventing diabetes among high-risk populations with prediabetes.

Identifiants

pubmed: 36217306
pii: 6755521
doi: 10.1210/clinem/dgac591
doi:

Substances chimiques

Sodium-Glucose Transporter 2 Inhibitors 0
Hypoglycemic Agents 0
Glucose IY9XDZ35W2
Sodium 9NEZ333N27

Types de publication

Meta-Analysis Systematic Review Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

221-231

Informations de copyright

© The Author(s) 2022. Published by Oxford University Press on behalf of the Endocrine Society. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.

Auteurs

Yuichiro Mori (Y)

Department of Human Health Sciences, Graduate School of Medicine, Kyoto University, Kyoto 6068507, Japan.

O Kenrik Duru (OK)

Division of General Internal Medicine and Health Services Research, David Geffen School of Medicine at UCLA, Los Angeles, California 90095, USA.

Katherine R Tuttle (KR)

Division of Nephrology, Kidney Research Institute, University of Washington, Seattle, Washington 98104, USA.
Division of Nephrology, University of Washington, Seattle, Washington 98195, USA.
Providence Medical Research Center, Providence Health Care, Spokane, Washington 99204, USA.

Shingo Fukuma (S)

Department of Human Health Sciences, Graduate School of Medicine, Kyoto University, Kyoto 6068507, Japan.

Daisuke Taura (D)

Department of Diabetes, Endocrinology and Nutrition, Graduate School of Medicine, Kyoto University, Kyoto 6068315, Japan.

Norio Harada (N)

Department of Diabetes, Endocrinology and Nutrition, Graduate School of Medicine, Kyoto University, Kyoto 6068315, Japan.

Nobuya Inagaki (N)

Department of Diabetes, Endocrinology and Nutrition, Graduate School of Medicine, Kyoto University, Kyoto 6068315, Japan.

Kosuke Inoue (K)

Department of Social Epidemiology, Graduate School of Medicine, Kyoto University, Kyoto 6068315, Japan.

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Classifications MeSH