Abstract

AimsHeart 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. MethodsIndependent 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. ResultsDuring 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). ConclusionsPatients 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. Clinical Trial RegistrationClinicalTrials.gov, number NCT00829660, and the International Standard Randomised Controlled Trial Number registry, number ISRCTN91899513.

Highlights

  • Heart failure is a fatal complication of type 2 diabetes but little is known about its incidence in patients with impaired glucose tolerance (IGT)

  • Patients with coronary heart disease (CHD) and IGT at greater risk of hospitalisation for heart failure (hHF)/CV death were older with higher plasma creatinine, and had prior heart failure (HF), myocardial infarction (MI), atrial fibrillation (AF) or stroke

  • Addition of acarbose to optimized CV therapy did not reduce the risk of hHF/CV death or hHF

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Summary

Introduction

Heart failure is a fatal complication of type 2 diabetes but little is known about its incidence in patients 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 randomized to acarbose 50mg TID or placebo. Using ACE data, we aimed to identify independent baseline predictors for a composite endpoint of incident hospitalisation for heart failure (hHF), or incident hHF or cardiovascular (CV) death in this population, and to assess the impact of post-prandial glucose lowering with acarbose on this outcome, compared with placebo. We investigated the cumulative risk of hHF, recurrent hHF (given the competing risk of death), and death following hHF, to determine the total burden of hHF in this population

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