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Updated: May 18, 2026

Fetal Mouse Cardiovascular Imaging Using a High-frequency Ultrasound (30/45MHZ) System
Published on: May 5, 2018
[Fetal programming of cardiovascular disease: new causes and underlying mechanisms]
C Sartori1, E Rexhaj, S F Rimoldi
1Département de médecine interne CHUV, Lausanne. claudio.sartori@chuv.ch
Insights
Early life health events, like perinatal hypoxemia and preeclampsia, are linked to adult cardiovascular disease. Assisted reproductive technologies may also increase risks for vascular dysfunction and early arteriosclerosis.
Area of Science:
- Cardiovascular Science
- Developmental Biology
- Reproductive Medicine
Background:
- Early life pathologic events are associated with adult cardiovascular disease.
- Conditions like perinatal hypoxemia and preeclampsia can lead to long-term endothelial dysfunction.
- Offspring of assisted reproductive technologies exhibit vascular dysfunction and early arteriosclerosis.
Purpose of the Study:
- To explore the link between early life events and adult cardiovascular disease.
- To investigate the role of assisted reproductive technologies in fetal programming of cardiovascular disease.
- To understand the pathophysiological mechanisms, including oxidative stress and epigenetic alterations.
Main Methods:
- Review of existing literature on perinatal conditions and cardiovascular outcomes.
- Analysis of studies on offspring of assisted reproductive technologies.
- Examination of animal models investigating oxidative stress and epigenetic factors.
Main Results:
- Transient perinatal hypoxemia can cause exaggerated hypoxic pulmonary hypertension.
- Preeclampsia predisposes offspring to pulmonary and systemic endothelial dysfunction.
- Assisted reproductive technologies are associated with generalized vascular dysfunction and early arteriosclerosis.
Conclusions:
- Early life insults can program cardiovascular disease development later in life.
- Oxidative stress and epigenetic alterations are implicated in fetal programming of cardiovascular disease.
- Further research is needed to mitigate these risks.
Abstract:
There exists an association between pathologic events occurring during early life and the development of cardiovascular disease in adulthood. For example, transient perinatal hypoxemia predisposes to exaggerated hypoxic pulmonary hypertension and preeclampsia predisposes the offspring to pulmonary and systemic endothelial dysfunction later in life. The latter finding offers a scientific basis for observations demonstrating an increased risk for premature cardiovascular morbidity in this population. Very recently, we showed that offspring of assisted reproductive technologies also display generalized vascular dysfunction and early arteriosclerosis. Studies in animal models have provided evidence that oxidative stress and/or epigenetic alterations play an important pathophysiological role in the fetal programming of cardiovascular disease.
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