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Hypoglycemia, but not glucose variability, relates to vascular function in children with type 1 diabetes
Alexia S Peña1, Jennifer J Couper, Jennifer Harrington
1Department of Endocrinology and Diabetes, Women's and Children's Hospital, North Adelaide, South Australia, Australia. alexia.pena@adelaide.edu.au
Insights
Hypoglycemia, not glucose variability, is linked to impaired vascular function in children with type 1 diabetes. This suggests hypoglycemia may be an early cardiovascular disease risk factor.
Area of Science:
- Pediatric Endocrinology
- Cardiovascular Health
- Diabetes Research
Background:
- Chronic hyperglycemia is a known predictor of vascular disease in diabetes.
- The impact of glucose variability and hypoglycemia on vascular risk in type 1 diabetes is not well understood.
- Vascular dysfunction, a precursor to atherosclerosis, is observed in children with type 1 diabetes.
Purpose of the Study:
- To investigate the relationship between glucose variability and vascular function in children with type 1 diabetes.
- To determine if glucose variability or hypoglycemia is associated with impaired vascular endothelial function.
Main Methods:
- Continuous glucose monitoring data (48 hours) were collected from 52 children with type 1 diabetes.
- Glucose variability (mean amplitude of glycemic excursions [MAGE]) and hypoglycemia indices (glycemic risk assessment diabetes equation [GRADE], Low Blood Glucose Index [LBGI]) were assessed.
- Vascular function was evaluated using flow-mediated dilatation (FMD) and glyceryl trinitrate-mediated dilatation (GTN) in subjects and controls.
Main Results:
- Children with type 1 diabetes exhibited significantly lower FMD and GTN compared to controls.
- Hypoglycemia indices (GRADE and LBGI) were inversely correlated with FMD, indicating poorer vascular function with more hypoglycemia.
- Glucose variability measures (MAGE) did not show a significant relationship with FMD or GTN.
Conclusions:
- Hypoglycemia, specifically, is associated with impaired vascular endothelial function in children with type 1 diabetes.
- Hypoglycemia may represent an additional risk factor for early cardiovascular disease in this population.
- The independent effect of glucose variability on vascular function, separate from glycosylated hemoglobin, requires further investigation.
Background:
Chronic sustained hyperglycemia unequivocally predicts vascular disease in diabetes. However, the vascular risk of glucose variability, including hypoglycemia, is uncertain. Vascular dysfunction is present in children with type 1 diabetes and is a critical precursor of atherosclerosis. We aimed to evaluate the relationship between glucose variability and vascular function in children with type 1 diabetes.
Subjects And Methods:
Fifty-two type 1 diabetes subjects (14 [SD 2.7] years old, 25 males) had continuous glucose monitoring that included 48 h of data used to evaluate glucose variability (mean amplitude of glycemic excursions [MAGE] and other measurements) and hypoglycemia indices (glycemic risk assessment diabetes equation [GRADE] hypoglycemia, Low Blood Glucose Index [LBGI], and observed duration of hypoglycemia). Children with type 1 diabetes and 50 age- and gender-matched controls had assessments of vascular function (flow-mediated dilatation [FMD] and glyceryl trinitrate-mediated dilatation [GTN]).
Results:
Children with type 1 diabetes had lower FMD and GTN than controls (P=0.02 and P<0.001, respectively). GRADE hypoglycemia and LBGI were inversely related to FMD (r=-0.36, P=0.009 and r=-0.302, P=0.03, respectively) but did not relate to GTN. GRADE hypoglycemia was independently related to FMD (regression coefficient=-0.25±0.09, P=0.006). MAGE and other measurements of glucose variability measurements did not relate to FMD or GTN.
Conclusions:
Hypoglycemia, but not glucose variability, during continuous glucose monitoring relates to impaired vascular endothelial function in children with type 1 diabetes. Hypoglycemia may be an additional risk factor for early cardiovascular disease, but the effect of glucose variability, independent of glycosylated hemoglobin, on vascular function remains uncertain.
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