Related Experiment Video
Updated: May 6, 2026

Assessing Endothelial Vasodilator Function with the Endo-PAT 2000
Published on: October 16, 2010
Endothelial dysfunction and increased arterial intima-media thickness in children with type 1 diabetes
Mikko J Järvisalo1, Maria Raitakari, Jyri O Toikka
1Department of Clinical Physiology, University of Turku, Turku, Finland. mikko.jarvisalo@utu.fi
Insights
Children with type 1 diabetes often show impaired endothelial function, indicated by reduced flow-mediated dilation (FMD). This dysfunction is linked to early signs of atherosclerosis, specifically increased carotid artery intima-media thickness (IMT).
Area of Science:
- Pediatric Endocrinology
- Cardiovascular Research
- Diabetes Mellitus
Background:
- Endothelial dysfunction is implicated in atherosclerosis development in type 1 diabetes.
- Early detection of vascular changes in diabetic children is crucial.
Purpose of the Study:
- To investigate vascular endothelial function in children with type 1 diabetes.
- To determine if endothelial dysfunction correlates with early atherosclerotic changes.
Main Methods:
- Utilized noninvasive ultrasound to assess brachial artery flow-mediated dilation (FMD) and carotid artery intima-media thickness (IMT).
- Studied 75 children: 45 with type 1 diabetes and 30 healthy controls.
Main Results:
- Children with type 1 diabetes exhibited significantly lower FMD and increased IMT compared to controls.
- Endothelial dysfunction (low FMD) in diabetic children was associated with higher carotid IMT and elevated LDL cholesterol.
- Multivariate analysis identified diabetes, low FMD, and high LDL cholesterol as correlates of increased IMT.
Conclusions:
- Impaired FMD is a common finding in children with type 1 diabetes.
- Endothelial dysfunction is associated with increased carotid artery IMT in this population.
- These findings suggest a predisposition to early atherosclerosis in children with type 1 diabetes due to endothelial dysfunction.
Background:
Endothelial dysfunction may play a pathophysiological role in the development of atherosclerosis in subjects with type 1 diabetes. We examined whether alterations in vascular endothelial function exist in children with type 1 diabetes and tested the hypothesis that endothelial dysfunction is associated with early structural atherosclerotic vascular changes in these children.
Methods And Results:
Noninvasive ultrasound was used to measure brachial artery flow-mediated dilation (FMD) responses and carotid artery intima-media thickness (IMT) in 75 children (mean age 11+/-2 years), 45 with type 1 diabetes (diabetes duration 4.4+/-2.9 years) and 30 healthy control children. Children with diabetes had lower peak FMD response (4.4+/-3.4% versus 8.7+/-3.6%, P<0.001) and increased IMT (P<0.001) compared with controls. Sixteen children with diabetes (36%) had endothelial dysfunction defined as total FMD response in the lowest decile for normal children. These children had increased carotid IMT (0.58+/-0.05 versus 0.54+/-0.04 mm, P=0.01) and higher LDL cholesterol concentration (2.63+/-0.76 versus 2.16+/-0.60 mmol/L, P=0.03) compared with diabetic children without endothelial dysfunction. Multivariate correlates of increased IMT included diabetes group (P=0.03), low FMD (P=0.03), and high LDL cholesterol (P=0.08).
Conclusions:
Impaired FMD response is a common manifestation in children with type 1 diabetes and is associated with increased carotid artery IMT. These data suggest that endothelial dysfunction in children with type 1 diabetes may predispose them to the development of early atherosclerosis.
More Related Videos
09:33A Methodological Approach to Non-invasive Assessments of Vascular Function and Morphology
Published on: February 7, 2015
08:22Combined Intravital Microscopy and Contrast-enhanced Ultrasonography of the Mouse Hindlimb to Study Insulin-induced Vasodilation and Muscle Perfusion
Published on: March 20, 2017
Related Concept Videos
Peripheral Artery Disease I: Introduction
Type I Diabetes I: Introduction
Type I Diabetes II: Pathophysiology
Type II Diabetes II: Pathophysiology
Diabetic Retinopathy
Diabetic Nephropathy