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Effects of Newer Antidiabetic Drugs on Endothelial Function and Arterial Stiffness: A Systematic Review and Meta-Analysis

Authors :
Konstantinos Batzias
Alexios S. Antonopoulos
Evangelos Oikonomou
Gerasimos Siasos
Evanthia Bletsa
Panagiota K. Stampouloglou
Chara-Vasiliki Mistakidi
Marina Noutsou
Niki Katsiki
Periklis Karopoulos
Georgios Charalambous
Anastasia Thanopoulou
Nicholas Tentolouris
Dimitris Tousoulis
Source :
Journal of Diabetes Research, Vol 2018 (2018)
Publication Year :
2018
Publisher :
Hindawi Limited, 2018.

Abstract

Background. Newer antidiabetic drugs, i.e., dipeptidyl peptidase-4 (DPP-4) inhibitors, sodium-glucose cotransporter-2 (SGLT-2) inhibitors, and glucagon-like peptide-1 receptor agonists (GLP-1 RAs) may exert distinct cardiovascular effects. We sought to explore their impact on vascular function. Methods. Published literature was systematically searched up to January 2018 for clinical studies assessing the effects of DPP-4 inhibitors, GLP-1 RAs, and SGLT-2 inhibitors on endothelial function and arterial stiffness, assessed by flow-mediated dilation (FMD) of the brachial artery and pulse wave velocity (PWV), respectively. For each eligible study, we used the mean difference (MD) with 95% confidence intervals (CIs) for FMD and PWV. The pooled MD for FMD and PWV were calculated by using a random-effect model. The presence of heterogeneity among studies was evaluated by the I2 statistic. Results. A total of 26 eligible studies (n=668 patients) were included in the present meta-analysis. Among newer antidiabetic drugs, only SGLT-2 inhibitors significantly improved FMD (pooled MD 1.14%, 95% CI: 0.18 to 1.73, p=0.016), but not DPP-4 inhibitors (pooled MD = 0.86%, 95% CI: -0.15 to 1.86, p=0.095) or GLP-1 RA (pooled MD = 2.37%, 95% CI: -0.51 to 5.25, p=0.107). Both GLP-1 RA (pooled MD = −1.97, 95% CI: -2.65 to -1.30, p

Details

Language :
English
ISSN :
23146745 and 23146753
Volume :
2018
Database :
Directory of Open Access Journals
Journal :
Journal of Diabetes Research
Publication Type :
Academic Journal
Accession number :
edsdoj.59915ba8f68d4c7ca716dea1126b1f68
Document Type :
article
Full Text :
https://doi.org/10.1155/2018/1232583