Obesity as a modifier of the cardiovascular effectiveness of sodium-glucose cotransporter-2 inhibitors in type 2 diabetes.
Humans
Diabetes Mellitus, Type 2
/ complications
Sodium-Glucose Transporter 2 Inhibitors
/ therapeutic use
Cohort Studies
Cardiovascular Diseases
/ epidemiology
Dipeptidyl-Peptidase IV Inhibitors
/ therapeutic use
Heart Failure
/ etiology
Obesity
/ complications
Glucose
Sodium
Hypoglycemic Agents
/ adverse effects
All-cause mortality
Cardiovascular outcomes
Effect modifier
Hospitalization for heart failure
Major adverse cardiovascular events
Obesity
Sodium-glucose cotransporter-2 inhibitors
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:
Oct 2022
Oct 2022
Historique:
received:
05
08
2022
revised:
09
09
2022
accepted:
20
09
2022
pubmed:
28
9
2022
medline:
2
11
2022
entrez:
27
9
2022
Statut:
ppublish
Résumé
To assess the association between the use of sodium-glucose cotransporter-2 (SGLT2i) and cardiovascular outcomes and death as a function of obesity among patients with type 2 diabetes. This new-user, active-comparator cohort study used U.K.'s Clinical Practice Research Datalink linked to Hospital Episodes Statistics repository and Office for National Statistics. The cohort included 34,128 new-users of SGLT2i matched 1:1 to 34,128 new-users of dipeptidyl peptidase-4 inhibitors (DPP-4i) on body mass index and propensity score. Cox proportional hazards models were used to estimate hazard ratios (HRs) with 95% confidence intervals (CIs) of major adverse cardiovascular events (MACE), overall and in body mass index (BMI) categories (≤24.9 kg/m SGLT2i were associated with a decreased risk of MACE (HR: 0.78, 95 %CI: 0.69-0.88) compared to DPP-4i. This decreased risk was most pronounced among obese and severely obese patients (HR: 0.77, 95 %CI: 0.66-0.91; HR: 0.67, 95% CI: 0.49-0.91, respectively) but not among overweight patients (HR: 0.94, 95 %CI: 0.73-1.22). Similar patterns were observed for cardiovascular mortality, all-cause mortality, and heart failure. Compared with DPP-4i, the cardioprotective effect associated with SGLT2i is stronger among patients with higher BMI.
Identifiants
pubmed: 36167266
pii: S0168-8227(22)00908-1
doi: 10.1016/j.diabres.2022.110094
pii:
doi:
Substances chimiques
Sodium-Glucose Transporter 2 Inhibitors
0
Dipeptidyl-Peptidase IV Inhibitors
0
Glucose
IY9XDZ35W2
Sodium
9NEZ333N27
Hypoglycemic Agents
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
110094Informations de copyright
Copyright © 2022. Published by Elsevier B.V.
Déclaration de conflit d'intérêts
Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.