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Developmental programming of cardiovascular disease by prenatal hypoxia
11 Department of Physiology, Development and Neuroscience, University of Cambridge, Cambridge, UK.
Insights
Fetal hypoxia during pregnancy programs adult offspring for cardiovascular disease, including heart injury and metabolic syndrome. Early life interventions may protect against these adverse programming effects.
Area of Science:
- Developmental programming
- Cardiovascular health
- Fetal development
Background:
- The fetal environment significantly impacts long-term cardiovascular health.
- Fetal hypoxia, a common pregnancy complication, is increasingly recognized for its programming effects.
- Research on fetal hypoxia's impact is less extensive than on maternal nutrition or stress.
Purpose of the Study:
- To review evidence on how fetal hypoxia programs offspring cardiovascular health.
- To explore mechanisms underlying adverse programming.
- To identify potential interventions for protection.
Main Methods:
- Literature review of studies on fetal hypoxia and offspring health.
- Analysis of evidence for cardiac susceptibility to ischemia-reperfusion (I/R) injury.
- Examination of endothelial dysfunction and metabolic syndrome indices.
Main Results:
- Growing evidence links hypoxic pregnancy to increased cardiac I/R injury susceptibility in offspring.
- Offspring exhibit endothelial dysfunction in peripheral circulation.
- Indices of metabolic syndrome are observed in adult offspring.
Conclusions:
- Fetal hypoxia adversely programs offspring cardiovascular and metabolic health.
- Understanding mechanisms is key to developing protective strategies.
- Maternal and early life interventions show promise in mitigating risks.
Abstract:
It is now recognized that the quality of the fetal environment during early development is important in programming cardiovascular health and disease in later life. Fetal hypoxia is one of the most common consequences of complicated pregnancies worldwide. However, in contrast to the extensive research effort on pregnancy affected by maternal nutrition or maternal stress, the contribution of pregnancy affected by fetal chronic hypoxia to developmental programming is only recently becoming delineated and established. This review discusses the increasing body of evidence supporting the programming of cardiac susceptibility to ischaemia and reperfusion (I/R) injury, of endothelial dysfunction in peripheral resistance circulations, and of indices of the metabolic syndrome in adult offspring of hypoxic pregnancy. An additional focus of the review is the identification of plausible mechanisms and the implementation of maternal and early life interventions to protect against adverse programming.
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