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Published on: February 28, 2013
Lifetime glycaemic exposure predicts reduced coronary vasoreactivity in Type 1 diabetic subjects
J Sundell1, T Janatuinen, T Rönnemaa
1Turku PET Centre, University of Turku, FIN-2052 Turku, Finland. jan.sundell@utu.fi
Insights
Lifetime glycemic exposure, measured by glycosylated hemoglobin A1c (HbA1c) over months, significantly impacts coronary vasoreactivity in Type 1 diabetes. Poor long-term glycemic control is linked to reduced myocardial blood flow, an early sign of coronary artery disease.
Area of Science:
- Cardiology
- Endocrinology
- Metabolic Diseases
Background:
- Type 1 diabetes is associated with impaired coronary vasoreactivity.
- The specific impact of long-term glycemic control on myocardial perfusion in Type 1 diabetes remains unclear.
Purpose of the Study:
- To investigate the effect of lifetime glycemic exposure on coronary vasoreactivity in Type 1 diabetic individuals.
- To differentiate the impact of long-term versus recent glycemic control on myocardial blood flow.
Main Methods:
- Positron emission tomography (PET) with (15)O-water was used to measure myocardial blood flow.
- Coronary vasoreactivity was assessed during pharmacologically induced hyperemia in fasting and hyperinsulinemic clamp states.
- Lifetime glycemic exposure was quantified using glycosylated hemoglobin A1c (HbA1c) over months.
Main Results:
- Hyperemic myocardial blood flow showed a significant inverse correlation with log HbA1c (lifetime glycemic exposure) in both fasting (r = -0.72, P < 0.01) and clamp states (r = -0.35, P < 0.05).
- These correlations persisted after adjusting for cardiovascular risk factors including lipids, blood pressure, BMI, and age.
- No significant association was found between hyperemic flow and recent HbA1c or plasma glucose levels.
Conclusions:
- Lifetime glycemic exposure is a stronger predictor of reduced coronary vasoreactivity than recent glycemic control in Type 1 diabetes.
- Diminished coronary vasoreactivity in Type 1 diabetics with poor glycemic control may indicate early coronary artery disease development.
Aims:
Subjects with Type 1 diabetes have impaired coronary vasoreactivity but the independent role of glycaemic control on myocardial perfusion is less clear. We examined the effect of lifetime glycaemic exposure on coronary vasoreactivity in 43 otherwise healthy Type 1 diabetic subjects.
Methods:
Myocardial blood flow was calculated basally and during pharmacologically induced hyperaemia in the fasting state and during euglycaemic hyperinsulinaemic clamp (at an insulin infusion rate of 1 mU/kg per min for 60 min) using positron emission tomography and (15)O-water. Glycaemic exposure was estimated as glycosylated haemoglobin A(1c) (HbA(1c)) months.
Results:
Hyperaemic myocardial blood flow was inversely associated with log HbA(1c) months in the fasting state (r = -0.72, P < 0.01) and during clamp (r = -0.35, P < 0.05). These correlations remained significant after adjustment for lipid values, blood pressures, sex, smoking, body mass index (BMI) and age (r = -0.70, P < 0.05 and r = -0.35, P < 0.05, respectively). No significant correlation was detected between hyperaemic flow and HbA(1c) or plasma glucose values measured immediately preceding the PET study.
Conclusions:
The present study demonstrates that the lifetime glycaemic exposure appears to be a better predictor of reduced coronary vasoreactivity than recent glycaemic control in Type 1 diabetic subjects. Reduced coronary vasoreactivity in diabetic subjects with poor glycaemic control and/or long duration of diabetes may represent an early precursor of coronary artery disease.
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