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Intrapersonal HbA(1c) variability and the risk of progression of nephropathy in patients with Type 2 diabetes
S Rodríguez-Segade1, J Rodríguez, J M García López
1Department of Biochemistry and Molecular Biology, The University Hospital, Santiago de Compostela, Spain. ssegade@telefonica.net
Insights
High HbA1c variability, not just the average, significantly increases nephropathy progression risk in Type 2 diabetes patients. This finding highlights the importance of stable blood sugar control for kidney health.
Area of Science:
- Nephrology
- Endocrinology
- Diabetology
Background:
- Diabetic nephropathy is a major complication of Type 2 diabetes.
- Glycemic control, particularly HbA1c levels, is crucial for managing diabetic complications.
- The impact of HbA1c variability on nephropathy progression requires further investigation.
Purpose of the Study:
- To examine the association between HbA1c variability and the risk of nephropathy progression in Type 2 diabetes patients.
- To determine if HbA1c variability independently predicts nephropathy progression.
Main Methods:
- A cohort of 2103 Type 2 diabetes patients was followed for a mean of 6.6 years.
- Albumin excretion rate and HbA1c measurements were used to assess nephropathy and glycemic variability.
- Multivariate Cox regression analysis was employed to evaluate the risk of nephropathy progression, adjusting for numerous confounding factors.
Main Results:
- Nephropathy progressed in 18.3% of the study participants.
- Patients with progressing nephropathy exhibited significantly higher HbA1c variability compared to non-progressors.
- HbA1c variability emerged as a significant independent predictor of nephropathy progression (HR 1.37, 95% CI 1.12-1.69).
Conclusions:
- Increased HbA1c variability is a significant risk factor for nephropathy progression in Type 2 diabetes.
- This association persists independently of the updated mean HbA1c.
- Managing glycemic variability is essential for preventing diabetic kidney disease progression.
Aim:
To investigate the association between nephropathy and HbA(1c) variability (assessed as the standard deviation of each patient's HbA(1c) measurements) among patients with Type 2 diabetes.
Methods:
Albumin excretion rate and HbA(1c) were measured in 2103 patients followed up for a mean 6.6 years. Multivariate Cox regression analysis was used to determine the influence of HbA(1c) variability on the risk of progression of nephropathy after adjustment for age, sex, duration of diabetes, baseline condition (two cohorts defined by duration of diabetes, retinopathy and albumin excretion rate), baseline HbA(1c) , insulin use, BMI, use of anti-hypertensive agents, smoking, lipid status, retinopathy, updated mean HbA(1c) and number of HbA(1c) measurements.
Results:
Nephropathy progressed in 18.3% of subjects. HbA(1c) variability was significantly greater among progressors than among non-progressors (12 vs. 10 mmol/mol; 1.12 vs. 0.90%; P < 0.0001) and was a significant predictor of progression of nephropathy even after adjustment for updated mean HbA(1c) and other risk factors (hazard ratio 1.37, 95% CI 1.12-1.69).
Conclusion:
In patients with Type 2 diabetes, the risk of progression of nephropathy increases significantly with HbA(1c) variability, independently of the influence of updated mean HbA(1c) .
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