Impact of dipeptidyl peptidase-4 inhibitors on glucose-dependent insulinotropic polypeptide in type 2 diabetes mellitus: a systematic review and meta-analysis.

dipeptidyl peptidase-4 inhibitor glucose-dependent insulinotropic polypeptide meta-analysis metabolism randomized controlled trials

Journal

Frontiers in endocrinology
ISSN: 1664-2392
Titre abrégé: Front Endocrinol (Lausanne)
Pays: Switzerland
ID NLM: 101555782

Informations de publication

Date de publication:
2023
Historique:
received: 10 04 2023
accepted: 24 07 2023
medline: 29 8 2023
pubmed: 28 8 2023
entrez: 28 8 2023
Statut: epublish

Résumé

Glucose-dependent insulinotropic polypeptide (GIP) confers a variety of metabolic benefits in type 2 diabetes mellitus (T2DM). This meta-analysis was conducted to investigate the impact of dipeptidyl peptidase 4 (DPP4) inhibitors on GIP levels in T2DM patients. Medline (PubMed), CENTER (Cochrane Library), and Embase (Ovid) were searched and randomized controlled trials (RCTs) evaluating the impact of DPP4 inhibitors on fasting and postprandial GIP levels were obtained. For postprandial GIP, only studies with the data of GIP changes reported as the total area under the curve (AUC Overall, 14 RCTs with 541 T2DM patients were included. Compared to placebo/no treatment, the use of DPP4 inhibitors significantly increased the fasting GIP level (standard mean difference [SMD]: 0.77, 95% confidence interval [CI]: 0.48-1.05, The use of DPP4 inhibitors effectively increases the fasting and postprandial GIP concentrations in T2DM patients. https://www.crd.york.ac.uk/prospero/, identifier CRD42022356716.

Identifiants

pubmed: 37635974
doi: 10.3389/fendo.2023.1203187
pmc: PMC10450336
doi:

Substances chimiques

Dipeptidyl-Peptidase IV Inhibitors 0
Gastric Inhibitory Polypeptide 59392-49-3
Glucose IY9XDZ35W2

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

1203187

Informations de copyright

Copyright © 2023 Chai, Zhang, Carr, Deacon, Zheng, Rajpathak, Chen and Yu.

Déclaration de conflit d'intérêts

SC, RZ, YZ and JC are employees of MSD China; SR is employee of Merck Sharp & Dohme LLC., a subsidiary of Merck & Co., Inc., Rahway, NJ, USA. The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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Auteurs

Shangyu Chai (S)

Merck Research Laboratories (MRL) Global Medical Affairs, Merck Sharp & Dohme (MSD) China, Shanghai, China.

Ruya Zhang (R)

Merck Research Laboratories (MRL) Global Medical Affairs, Merck Sharp & Dohme (MSD) China, Shanghai, China.

Richard David Carr (RD)

Hatter Cardiovascular Institute, University College London, London, United Kingdom.
School of Biomedical Sciences, Ulster University, Coleraine, United Kingdom.

Carolyn F Deacon (CF)

School of Biomedical Sciences, Ulster University, Coleraine, United Kingdom.
Department of Biomedical Sciences, University of Copenhagen, Copenhagen, Denmark.

Yiman Zheng (Y)

Merck Research Laboratories (MRL) Global Medical Affairs, Merck Sharp & Dohme (MSD) China, Shanghai, China.

Swapnil Rajpathak (S)

Merck Research Laboratories, Merck & Co., Inc., Rahway, NJ, United States.

Jingya Chen (J)

Merck Research Laboratories (MRL) Global Medical Affairs, Merck Sharp & Dohme (MSD) China, Shanghai, China.

Miao Yu (M)

Department of Endocrinology, Key Laboratory of Endocrinology, National Health Commission, Peking Union Medical College Hospital, Peking Union Medical College and Chinese Academy of Medical Sciences, Beijing, China.

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