Key result
Higher HbA1c variability independently predicted an increased risk of all-cause mortality (HR 1.649) in patients with heart failure and type 2 diabetes mellitus, regardless of ejection fraction.
Why the study?
Does higher HbA1c variability predict worse clinical outcomes in patients with heart failure and type 2 diabetes mellitus?
Cohort (n=902)
No
Does higher HbA1c variability predict worse clinical outcomes in patients with heart failure and type 2 diabetes mellitus?
Higher HbA1c variability independently predicts all-cause mortality and composite endpoints of death and HF hospitalization in patients with HF and T2DM across all ejection fraction phenotypes.
Answers are grounded in this paper and cite their sources.
HbA1c variability may aid risk stratification in HF with T2DM; extends observational data but leaves open need for interventional trials.
BACKGROUND: 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 mid-range ejection fraction (HFmrEF) and HF with reduced ejection fraction (HFrEF) in a prospective longitudinal study. METHODS: Patients 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. RESULTS: Of 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. CONCLUSIONS: This 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.
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Gu et al. (2018) conducted a cohort in Heart failure and type 2 diabetes mellitus (n=902). High HbA1c variability vs. Low HbA1c variability was evaluated on All-cause mortality (HR 1.649, 95% CI 1.288-2.110, p=<=0.001). Higher HbA1c variability independently predicted an increased risk of all-cause mortality (HR 1.649) in patients with heart failure and type 2 diabetes mellitus, regardless of ejection fraction.
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