Predicting heart failure events in patients with coronary heart disease and impaired glucose tolerance: Insights from the Acarbose Cardiovascular Evaluation (ACE) 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
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

108488

Informations 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.

Auteurs

Malgorzata Wamil (M)

Diabetes Trials Unit, Radcliffe Department of Medicine, University of Oxford, Oxford, UK.

John J V McMurray (JJV)

Institute of Cardiovascular & Medical Sciences, University of Glasgow, Glasgow, UK.

Charles A B Scott (CAB)

Diabetes Trials Unit, Radcliffe Department of Medicine, University of Oxford, Oxford, UK.

Ruth L Coleman (RL)

Diabetes Trials Unit, Radcliffe Department of Medicine, University of Oxford, Oxford, UK.

Yihong Sun (Y)

China-Japan Friendship Hospital, Beijing, China.

Eberhard Standl (E)

Diabetes Research Group eV at Munich Helmholtz Centre, Munich, Germany.

Lars Rydén (L)

Department of Medicine K2, Karolinska Institute, Stockholm, Sweden.

Rury R Holman (RR)

Diabetes Trials Unit, Radcliffe Department of Medicine, University of Oxford, Oxford, UK. Electronic address: rury.holman@dtu.ox.ac.uk.

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Classifications MeSH