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Published on: February 28, 2013
Diabetes and cardiovascular disease: the role of glycemic control
Alice Y Y Cheng1, Lawrence A Leiter
1St. Michael's Hospital, 6121-61 Queen Street East, Toronto, Ontario M5C 2T2, Canada.
Insights
Intensive glycemic control (HbA1c < 6%) does not reduce cardiovascular risk in high-risk type 2 diabetes patients. Early intervention may offer long-term benefits, supporting an HbA1c target of < 7%.
Area of Science:
- Endocrinology
- Cardiovascular Medicine
- Diabetes Research
Background:
- Recent clinical guidelines recommended lower glycemic targets for type 2 diabetes.
- Intensive glycemic control aims to reduce diabetes-related complications.
Purpose of the Study:
- To evaluate the cardiovascular risk associated with intensive glycemic targets in type 2 diabetes.
- To determine optimal hemoglobin A1c targets for managing type 2 diabetes.
Main Methods:
- Analysis of recent randomized controlled trials (ACCORD, ADVANCE, VADT) and UKPDS post-trial monitoring.
- Assessment of cardiovascular outcomes in relation to glycemic control strategies.
Main Results:
- Intensive glycemic targets (HbA1c < 6%) did not reduce cardiovascular risk in high-risk individuals over 3.5-5 years.
- UKPDS showed long-term cardiovascular benefits from early intensive glycemic control (median 17 years).
Conclusions:
- A hemoglobin A1c target below 6% is not recommended for high-risk type 2 diabetes patients.
- An HbA1c target below 7% is supported for reducing microvascular and potentially macrovascular complications, especially with early intervention.
Abstract:
Over the past decade, clinical practice guidelines have lowered their glycemic targets for people with type 2 diabetes. However, recent randomized controlled trials (ACCORD, ADVANCE, and VADT) demonstrate that intensive glycemic targets do not reduce cardiovascular risk among higher-risk individuals over a period of 3.5 to 5 years. Thus, targeting a hemoglobin A(1c) below 6% among high-risk patients should not be recommended. However, the 10-year post-trial monitoring of the UKPDS demonstrated cardiovascular benefit of intensive glycemic control among those with newly diagnosed type 2 diabetes over a median follow-up of 17 years. This raises the possibility that cardiovascular benefits of glycemic control require many years to manifest and early intervention may carry greater benefit. Therefore, these recent trials continue to support the recommended hemoglobin A(1c) target of below 7% to reduce microvascular complications in type 2 diabetes and perhaps macrovascular complications in those with newly diagnosed diabetes.
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