Abstract

BackgroundThe prognostic impact of long-term glycemic variability on clinical outcomes in patients with heart failure (HF) and type 2 diabetes mellitus (T2DM) remains unclear. We determined and compared hemoglobin A1c (HbA1c) variability and clinical outcomes for patients with HF with preserved ejection fraction (HFpEF), HF with mid-range ejection fraction (HFmrEF) and HF with reduced ejection fraction (HFrEF) in a prospective longitudinal study.MethodsPatients with HF and T2DM, undergone 3 or more HbA1c determinations during the first 18 months, were then followed for 42 months. The primary outcome was death from any cause. Secondary outcome was composite endpoints with death and HF hospitalization. Cox proportional hazards models were used to compare outcomes for patients with HFpEF, HFmrEF and HFrEF.ResultsOf 902 patients enrolled, 32.2% had HFpEF, 14.5% HFmrEF, and 53.3% HFrEF. During 42 months of follow-up, 270 (29.9%) patients died and 545 (60.4%) patients experienced composite endpoints of death and HF readmission. The risk of all-cause death or composite endpoints was lower for HFpEF than HFrEF. Moreover, higher HbA1c variability was associated with higher all-cause mortality or composite endpoints and HbA1c variability was an independent predictor of all-cause mortality or composite endpoints, regardless of EF.ConclusionsThis prospective longitudinal study showed that the all-cause death and composite events was lower for HFpEF than HFrEF. HbA1c variability was independently and similarly predictive of death or combined endpoints in the three HF phenotypes.

Highlights

  • Heart failure (HF), including heart failure (HF) with preserved ejection fraction (HFpEF), HF with mid-range ejection fraction (HFmrEF) and HF with reduced ejection fraction (HFrEF), is a progressive disease with high mortality and morbidity, and its prevalence is rising in the aging population [1]

  • HF medications were commonly used at the time of the baseline assessment, with 724 (80.3%) of the whole group receiving an angiotensin converting enzyme inhibitor (ACEI)/angiotensin receptor blocker (ARB) and 683 (75.7%) receiving a beta-blocker, more HFrEF patients received ACEI/ARB (70.3% in HF with preserved ejection fraction (HFpEF), 85.2% in HFrEF) or beta-blocker (69.0% in HFpEF, 81.7% in HFrEF) therapy

  • The clinical characteristics of the patients with HF with midrange ejection fraction (HFmrEF) were similar to the HFpEF group, except for systolic blood pressure (SBP), which was similar to HFrEF (Table 1)

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Summary

Introduction

Heart failure (HF), including HF with preserved ejection fraction (HFpEF), HF with mid-range ejection fraction (HFmrEF) and HF with reduced ejection fraction (HFrEF), is a progressive disease with high mortality and morbidity, and its prevalence is rising in the aging population [1]. Glycemic variability is a general denomination to several measures of short-term or long-term fluctuations in glucose level. Long-term glycemic variability refers to glycemic fluctuations over months to years and is generally measured by visit-to-visit variability in either hemoglobin A1c (HbA1c) or fasting glucose. The prognostic impact of long-term glycemic variability on clinical outcomes in patients with heart failure (HF) and type 2 diabetes mellitus (T2DM) remains unclear. We determined and compared hemoglobin A1c (HbA1c) variability and clinical outcomes for patients with HF with preserved ejection fraction (HFpEF), HF with midrange ejection fraction (HFmrEF) and HF with reduced ejection fraction (HFrEF) in a prospective longitudinal study

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