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The rise and fall of HbA(1c) as a risk marker for diabetes complications
1Department of Clinical Biochemistry, Hull Royal Infirmary, Anlaby Road, Hull, HU3 2JZ, UK. Eric.Kilpatrick@hey.nhs.uk.
Insights
Glycemic variability, specifically HbA1c fluctuations, predicts microvascular complications in type 2 diabetes. Reducing these glucose swings may prevent vascular disease without increasing hypoglycemia risk.
Area of Science:
- Endocrinology
- Metabolic Diseases
- Diabetes Research
Background:
- Short-term glycemic variability's role in diabetes complications remains unclear.
- Longer-term fluctuations in glucose, indicated by HbA1c variability, are increasingly linked to microvascular disease risk.
- Previous studies primarily focused on type 1 diabetes.
Purpose of the Study:
- To investigate if HbA1c variability predicts nephropathy risk in type 2 diabetic patients.
- To explore the potential of managing HbA1c fluctuations for vascular disease prevention.
Main Methods:
- Analysis of data from the Tsukuba Kawai Diabetes Registry in Japan.
- Examining the association between HbA1c variability and the risk of nephropathy.
Main Results:
- HbA1c variability was found to predict the risk of nephropathy in type 2 diabetic patients.
- This finding extends previous observations from type 1 diabetes.
Conclusions:
- HbA1c variability is a significant predictor of microvascular complications, specifically nephropathy, in type 2 diabetes.
- Strategies aimed at reducing HbA1c fluctuations may offer a way to mitigate hyperglycaemia-related vascular disease.
- This approach may reduce the risk of hypoglycemia compared to solely focusing on lowering mean HbA1c.
Abstract:
It is still unclear whether short-term, within-day, variability in glycaemic control is contributory to the development of diabetes micro- or macrovascular complications. However, consistent and compelling data are emerging that longer term fluctuations in glucose, as evidenced by increases in HbA(1c) variability, do indeed add to the mean HbA(1c) value in predicting the risk of microvascular disease. Until now, studies have found this to be the case mainly in type 1 diabetes, but in this issue of Diabetologia (DOI: 10.1007/s00125-012-2572-7 ) an analysis of the Tsukuba Kawai Diabetes Registry in Japan has found that HbA(1c) variability also predicts the risk of nephropathy in type 2 diabetic patients. These observations raise the possibility that reducing rises and falls in HbA(1c) may help avoid hyperglycaemia-related vascular disease without running the same risk of hypoglycaemia that a strategy focusing purely on lower HbA(1c) might incur.
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