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Association of Mean and Variability of HbA1c with Heart Failure in Patients with Type 2 Diabetes
You-Ting Lin1,2, Wei-Lun Huang1,2, Hung-Pin Wu3,4
1Division of Endocrinology and Metabolism, Department of Medicine, China Medical University Hospital, Taichung 40447, Taiwan.
Insights
Mean HbA1c levels, not variability, independently predict heart failure (HF) risk in type 2 diabetes mellitus (T2DM) patients. Stable HbA1c is crucial, even with good glycemic control, to prevent HF.
Area of Science:
- Cardiology
- Endocrinology
- Diabetes Research
Background:
- Heart failure (HF) is a frequent complication in type 2 diabetes mellitus (T2DM) patients.
- While HbA1c levels are linked to HF, the role of HbA1c variability remains unclear.
Purpose of the Study:
- To investigate the association between mean and variability of HbA1c and the risk of developing HF in T2DM patients.
- To determine if HbA1c variability influences HF risk independently of mean HbA1c levels.
Main Methods:
- Retrospective cohort study using Diabetes Share Care Program data (2001-2018).
- Included T2DM patients with recorded mean HbA1c and HbA1c variability (SD, adjSD) over 12-24 months (2001-2008).
- Cox proportional hazard models analyzed HF risk (2008-2018) based on HbA1c-Mean categories (<7%, 7-7.9%, ≥8%) and HbA1c variability tertiles.
Main Results:
- 3824 T2DM patients were analyzed; 315 developed HF over 11.72 years.
- Initially, both increased HbA1c-Mean and HbA1c variability correlated with higher HF risk.
- After mutual adjustment, only mean HbA1c remained a significant, independent predictor of HF in a dose-response manner.
Conclusions:
- Mean HbA1c level is an independent predictor of heart failure in T2DM patients, irrespective of HbA1c variability.
- Maintaining stable HbA1c levels is vital for HF prevention, particularly in patients achieving good glycemic control (mean HbA1c <7%).
Abstract:
Heart failure (HF) is a common presentation in patients with type 2 diabetes mellitus (T2DM). Previous studies revealed that the HbA1c level is significantly associated with HF. However, little is known about the association between HbA1c variability and HF. We aimed to evaluate the association of mean and variability of HbA1c with HF in patients with T2DM. Using Diabetes Share Care Program data, patients with T2DM who had mean HbA1c (HbA1c-Mean), and HbA1c variability (tertiles of HbA1c-SD and HbA1c-adjSD) within 12-24 months during 2001-2008 were included. The cutoffs of HbA1c-Mean were set at <7%, 7-7.9%, and ≥8%. Hazard ratios (HRs) for HF during 2008-2018 were estimated using Cox proportional hazard models. A total of 3824 patients were included, of whom 315 patients developed HF during the observation period of 11.72 years. The associated risk of HF increased with tertiles of HbA1c variability and cutoffs of HbA1c-Mean. In mutually adjusted models, HbA1c-Mean showed a consistent dose-response association with HF, while the association of HbA1c variability with HF disappeared. Among patients with HbA1c-Mean <7%, the associated risk of HF in patients with HbA1c variability in tertile 3 was comparable to patients with HbA1c-Mean ≥8%. In conclusion, mean HbA1c was an independent predictor of HF and not explained by HbA1c variability. In addition to absolute HbA1c level, targeting on stability of HbA1c in patients with good glycemic control was also important for the development of HF in patients with T2DM.
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