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Peripheral arterial function in infants and young children with one-ventricle physiology and hypoxemia
Shobha Natarajan1, Christian Heiss, Yerem Yeghiazarians
1Division of Pediatric Cardiology, University of California San Francisco, San Francisco, CA, USA. natarajans@email.chop.edu
Insights
Infants with single-ventricle (1V) physiology and hypoxemia show impaired brachial artery flow-mediated dilation (FMD) and elevated endothelin-1 (ET-1) levels before the Fontan procedure, indicating early peripheral arterial dysfunction.
Area of Science:
- Cardiovascular Research
- Pediatric Cardiology
- Vascular Biology
Background:
- Single-ventricle (1V) physiology poses risks for peripheral arterial dysfunction in young patients.
- Early identification of vascular issues is crucial for long-term outcomes in 1V patients.
Purpose of the Study:
- To assess peripheral arterial dysfunction in infants and young children with 1V physiology and hypoxemia before the Fontan operation.
- To compare vascular parameters between 1V patients and healthy controls.
Main Methods:
- Measured flow-mediated dilation (FMD) of the brachial artery using high-resolution ultrasound.
- Quantified serum levels of endothelin-1 (ET-1) and nitric oxide metabolites.
- Assessed arterial stiffness via pulse-wave velocity (PWV) in the aorta.
Main Results:
- Patients with 1V physiology exhibited significantly lower FMD (2.4% vs. 11.3%, p <0.0005).
- Elevated ET-1 levels were observed in 1V patients compared to controls (35.5% vs. 24.1%, p = 0.003).
- No significant differences in nitric oxide levels or PWV were found between groups.
Conclusions:
- Infants and young children with 1V physiology and hypoxemia demonstrate blunted FMD and increased ET-1 levels pre-Fontan operation.
- These findings suggest peripheral arterial dysfunction is present early in 1V physiology.
- Further research into hypoxemia, low cardiac index, and ET-1's role may guide targeted therapies for improved survival in 1V patients.
Abstract:
Patients with 1-ventricle (1V) physiology may be at risk for peripheral arterial dysfunction at a young age. To determine whether infants and young children with 1V physiology and hypoxemia have peripheral arterial dysfunction before undergoing the Fontan operation, we measured (1) flow-mediated vasodilation (FMD) in the brachial artery, (2) serum levels of vasoactive mediators endothelin-1 (ET-1) and metabolites of nitric oxide, and (3) arterial stiffness with pulse-wave velocity (PWV) in the aorta. Eighteen patients with 1V physiology before the Fontan procedure and hypoxemia and 19 patients with normoxemia and 2-ventricle (2V) physiology were studied. Measurements were collected during cardiac catheterization. FMD in the brachial artery was the diameter gain after 4.5 minutes of forearm occlusion measured with high-resolution ultrasound and edge-detection software. Nitric oxide and ET-1 levels were measured in venous blood. PWV between the left carotid and femoral arteries was measured using pulse Doppler ultrasound. FMD was lower (2.4 +/- 3.7% vs 11.3 +/- 6%, p <0.0005) and ET-1 levels were higher (35.5 +/- 11.3% vs 24.1 +/- 9.7%, p = 0.003) in subjects with 1V physiology versus those with 2V physiology, respectively. There were no differences in nitric oxide levels or PWV. In conclusion, infants and young children with 1V physiology and hypoxemia have blunted FMD and higher ET-1 levels before undergoing the Fontan operation compared with normoxemic subjects with 2V physiology. A further understanding of pathophysiologic mechanisms underlying peripheral arterial dysfunction, including the roles of hypoxemia, low cardiac index, and ET-1, may lead to targeted therapies and improve the long-term survival of patients with 1V physiology.
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