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Published on: May 17, 2024
Antioxidants improve vascular function in children conceived by assisted reproductive technologies: A randomized
Stefano F Rimoldi1, Claudio Sartori2, Emrush Rexhaj3
1Department of Cardiology and Clinical Research, Inselspital, University Hospital, Bern, Switzerland stefano.rimoldi@insel.ch.
Insights
Children conceived via assisted reproductive technology (ART) experience vascular dysfunction. Antioxidant treatment improved nitric oxide (NO) bioavailability and vascular function in these children, suggesting reversibility.
Area of Science:
- Cardiovascular Science
- Pediatric Health
- Reproductive Medicine
Background:
- Children conceived by assisted reproductive technology (ART) exhibit vascular dysfunction.
- The mechanisms, long-term effects, and reversibility of ART-induced vascular dysfunction are not well understood.
- ART in mice is linked to hypertension and reduced lifespan due to decreased nitric oxide (NO) synthesis.
Purpose of the Study:
- To investigate if ART-induced vascular dysfunction in humans involves similar mechanisms as in mice.
- To determine if this vascular dysfunction is potentially reversible.
- To test if antioxidant supplementation can improve endothelial function by enhancing NO bioavailability.
Main Methods:
- Prospective, double-blind, placebo-controlled study involving 21 ART children and 21 controls.
- Four-week oral supplementation with antioxidant vitamins C and E or placebo.
- Assessment of flow-mediated vasodilation (FMD) and pulmonary artery pressure via echocardiography during high-altitude exposure.
Main Results:
- Antioxidant supplementation significantly increased plasma NO levels and FMD in ART children.
- Altitude-induced pulmonary hypertension was attenuated in ART children receiving antioxidants.
- No significant effects were observed in the control group.
Conclusions:
- Antioxidant administration improved NO bioavailability and vascular responsiveness in ART children.
- These findings suggest that ART-induced vascular dysfunction in young individuals is redox-regulated and reversible.
- This highlights a potential therapeutic strategy for managing cardiovascular risk in ART-conceived children.
Aims:
Children conceived by assisted reproductive technology (ART) display vascular dysfunction. Its underlying mechanism, potential reversibility and long-term consequences for cardiovascular risk are unknown. In mice, ART induces arterial hypertension and shortens the life span. These problems are related to decreased vascular endothelial nitric oxide synthase (eNOS) expression and nitric oxide (NO) synthesis. The aim of this study was to determine whether ART-induced vascular dysfunction in humans is related to a similar mechanism and potentially reversible. To this end we tested whether antioxidants improve endothelial function by scavenging free radicals and increasing NO bioavailability.
Methods And Results:
In this prospective double-blind placebo controlled study in 21 ART and 21 control children we assessed the effects of a four-week oral supplementation with antioxidant vitamins C (1 g) and E (400 IU) or placebo (allocation ratio 2:1) on flow-mediated vasodilation (FMD) of the brachial artery and pulmonary artery pressure (echocardiography) during high-altitude exposure (3454 m), a manoeuver known to facilitate the detection of pulmonary vascular dysfunction and to decrease NO bioavailability by stimulating oxidative stress. Antioxidant supplementation significantly increased plasma NO measured by ozone-based chemiluminescence (from 21.7 ± 7.9 to 26.9 ± 7.6 µM, p = 0.04) and FMD (from 7.0 ± 2.1 to 8.7 ± 2.0%, p = 0.004) and attenuated altitude-induced pulmonary hypertension (from 33 ± 8 to 28 ± 6 mm Hg, p = 0.028) in ART children, whereas it had no detectable effect in control children.
Conclusions:
Antioxidant administration to ART children improved NO bioavailability and vascular responsiveness in the systemic and pulmonary circulation. Collectively, these findings indicate that in young individuals ART-induced vascular dysfunction is subject to redox regulation and reversible.
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