Meta-analyses of the effects of DPP-4 inhibitors, SGLT2 inhibitors and GLP1 receptor analogues on cardiovascular death, myocardial infarction, stroke and hospitalization for heart failure.
Cardiovascular Diseases
/ chemically induced
Diabetes Mellitus, Type 2
/ drug therapy
Dipeptidyl-Peptidase IV Inhibitors
/ pharmacology
Glucagon-Like Peptide 1
/ agonists
Heart Failure
/ chemically induced
Hospitalization
/ statistics & numerical data
Humans
Hypoglycemic Agents
/ pharmacology
Incidence
Myocardial Infarction
Sodium-Glucose Transporter 2 Inhibitors
/ pharmacology
Stroke
/ chemically induced
Cardiovascular death
Cardiovascular outcomes trial
Dipeptidyl peptidase 4 inhibitor (DPP-4i)
Heart failure
Meta-analysis
Myocardial infarction
Sodium glucose linked transporter inhibitor (SGLT2-i) and glucagon like peptide 1 receptor analogues
Stroke
Type 2 diabetes
Journal
Diabetes research and clinical practice
ISSN: 1872-8227
Titre abrégé: Diabetes Res Clin Pract
Pays: Ireland
ID NLM: 8508335
Informations de publication
Date de publication:
Apr 2019
Apr 2019
Historique:
received:
25
12
2018
revised:
17
01
2019
accepted:
15
02
2019
pubmed:
23
2
2019
medline:
10
7
2019
entrez:
23
2
2019
Statut:
ppublish
Résumé
To assess the effects DPP-4i; SGLT2-i & GLP1-RA on CV death, MI, stroke and hHF. This is probably the first meta-analysis to assess the effects of these drugs on MI and stroke in totality, including non-fatal & fatal MI and stroke. Scientific databases were searched for RCTs with pre-specified inclusion criteria and each end-point from the selected 13 studies was reported as an effect size (M H odds ratio) with a 95% confidence interval P value. The pooled analysis of all the 5 available CVOT with DPP-4i resulted in a neutral effect on MI, stroke, the combined end points of MI & Stroke, CV death and hHF. The pooled analysis of all the 5 available CVOTs with GLP1-RA resulted in a neutral effect on MI. However, there was a statistically significant 12% reduction in CV death (P = 0.01), 13% reduction in stroke (P = 0.02) and 11% reduction the combined end points of MI & Stroke (P = 0.001). The impact of GLP1-RA inhibitors on hHF was neutral. The pooled analysis of all the 3 available CVOTs with SGLT2-i resulted in a neutral effect on MI, stroke, the combined end points of MI & Stroke and CV death. There was however a statistically significant 28% reduction in hHF (P < 0.001). DPP-4i & SGLT-2i are neutral as far as all aspects of CV outcomes are concerned except for hHF which is significantly reduced by the latter. GLP1-RA as a class reduce risk of ASCVD showing a significant reduction in MI and stroke.
Identifiants
pubmed: 30794833
pii: S0168-8227(18)31933-8
doi: 10.1016/j.diabres.2019.02.014
pii:
doi:
Substances chimiques
Dipeptidyl-Peptidase IV Inhibitors
0
Hypoglycemic Agents
0
Sodium-Glucose Transporter 2 Inhibitors
0
Glucagon-Like Peptide 1
89750-14-1
Types de publication
Journal Article
Meta-Analysis
Langues
eng
Sous-ensembles de citation
IM
Pagination
8-16Informations de copyright
Copyright © 2019 Elsevier B.V. All rights reserved.