Predicting heart failure events in patients with coronary heart disease and impaired glucose tolerance: Insights from the Acarbose Cardiovascular Evaluation (ACE) trial.
Acarbose
/ therapeutic use
Aged
Coronary Disease
/ epidemiology
Creatinine
/ blood
Diabetes Mellitus, Type 2
/ blood
Double-Blind Method
Female
Glucose Intolerance
/ epidemiology
Glycoside Hydrolase Inhibitors
/ therapeutic use
Heart Failure
/ epidemiology
Humans
Incidence
Male
Middle Aged
Myocardial Infarction
/ epidemiology
Proportional Hazards Models
Risk Factors
Treatment Outcome
Acarbose
Coronary heart disease
Diabetes
Heart failure
Impaired glucose tolerance (IGT)
Randomised controlled trial
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:
Dec 2020
Dec 2020
Historique:
received:
04
08
2020
revised:
24
09
2020
accepted:
25
09
2020
pubmed:
10
10
2020
medline:
12
1
2021
entrez:
9
10
2020
Statut:
ppublish
Résumé
Heart failure is a fatal complication of type 2 diabetes but little is known about its incidence in people with impaired glucose tolerance (IGT). We used Acarbose Cardiovascular Evaluation (ACE) trial data to identify predictors of hospitalisation for heart failure (hHF) or cardiovascular (CV) death in patients with coronary heart disease (CHD) and IGT randomised to acarbose or placebo. Independent hHF/CV death risk factors were determined using Cox proportional hazards models, with participants censored at first hHF event, CV death, or end of follow-up. During median 5-year follow-up, the composite outcome of hHF/CV death occurred in 393 (6.0%) participants. Significant hHF/CV death multivariate predictors were higher age and plasma creatinine, and prior heart failure (HF), myocardial infarction (MI), atrial fibrillation (AF) and stroke. Acarbose, compared with placebo, did not reduce hHF/CV death (hazard ratio [HR] 0.89, 95% CI 0.64-1.24, P = 0.48) or hHF (HR 0.90, 95% CI 0.74-1.10, P = 0.32). Patients with CHD and IGT at greater risk of hHF/CV death were older with higher plasma creatinine, prior HF, MI, AF or stroke. Addition of acarbose to optimised CV therapy to reduce post-prandial glucose excursions did not reduce the risk of hHF/CV death or hHF. ClinicalTrials.gov, number NCT00829660, and the International Standard Randomised Controlled Trial Number registry, number ISRCTN91899513.
Identifiants
pubmed: 33035598
pii: S0168-8227(20)30741-5
doi: 10.1016/j.diabres.2020.108488
pii:
doi:
Substances chimiques
Glycoside Hydrolase Inhibitors
0
Creatinine
AYI8EX34EU
Acarbose
T58MSI464G
Banques de données
ClinicalTrials.gov
['NCT00829660']
Types de publication
Journal Article
Multicenter Study
Randomized Controlled Trial
Langues
eng
Sous-ensembles de citation
IM
Pagination
108488Informations de copyright
Copyright © 2020 Elsevier B.V. All rights reserved.
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.