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Cardiac dysfunction and remodeling regulated by anti-angiogenic environment in patients with preeclampsia: the
Johana Ullmo1,2, Monica Cruz-Lemini1,2,3, Olga Sánchez-García2,3
1Obstetrics and Gynecology Department, Santa Creu i Sant Pau University Hospital & Universitat Autònoma, Barcelona, Spain.
Insights
This study investigates the link between angiogenic factors, preeclampsia (PE), and maternal cardiovascular (CV) complications. Findings aim to improve CV health for women with PE, reducing future disease risk.
Area of Science:
- Obstetrics and Gynecology
- Cardiology
- Perinatology
Background:
- Cardiovascular diseases (CVD) remain a leading cause of mortality despite advances in diagnosis and treatment.
- Pregnancy significantly impacts the maternal cardiovascular system, with preeclampsia (PE) increasing long-term CVD risk up to fourfold.
- An anti-angiogenic environment is implicated in PE, but its connection to maternal cardiovascular complications requires further research.
Purpose of the Study:
- To investigate the association between angiogenic factors and maternal cardiac dysfunction or remodeling in women with preeclampsia.
- To determine if novel cardiac biomarkers and echocardiography can detect these changes.
- To evaluate the long-term cardiovascular impact of PE on maternal health.
Main Methods:
- A prospective cohort study involving 440 high-risk pregnant women, women with diagnosed PE, and healthy controls.
- Assessment of placental biochemical and biophysical cardiovascular markers in the first and third trimesters.
- Maternal and fetal echocardiography in the third trimester, with maternal cardiac function reassessed 12 months postpartum.
Main Results:
- The study is designed to characterize the relationship between anti-angiogenic factors and maternal cardiovascular dysfunction during and after pregnancy.
- It will correlate angiogenic markers and echocardiographic findings with PE status and long-term cardiovascular risk.
- Fetal cardiac function will be evaluated and correlated with maternal variables.
Conclusions:
- This research will elucidate the link between an anti-angiogenic state and maternal cardiovascular complications in PE.
- The findings are expected to enhance the understanding of future CVD risk in women with a history of PE.
- The ultimate goal is to improve cardiovascular health outcomes for women affected by PE, thereby reducing disease burden.
Background:
Cardiovascular diseases (CVD) are cause of increased morbidity and mortality in spite of advances for diagnosis and treatment. Changes during pregnancy affect importantly the maternal CV system. Pregnant women that develop preeclampsia (PE) have higher risk (up to 4 times) of clinical CVD in the short- and long-term. Predominance of an anti-angiogenic environment during pregnancy is known as main cause of PE, but its relationship with CV complications is still under research. We hypothesize that angiogenic factors are associated to maternal cardiac dysfunction/remodeling and that these may be detected by new cardiac biomarkers and maternal echocardiography.
Methods:
Prospective cohort study of pregnant women with high-risk of PE in first trimester screening, established diagnosis of PE during gestation, and healthy pregnant women (total intended sample size n = 440). Placental biochemical and biophysical cardiovascular markers will be assessed in the first and third trimesters of pregnancy, along with maternal echocardiographic parameters. Fetal cardiac function at third trimester of pregnancy will be also evaluated and correlated with maternal variables. Maternal cardiac function assessment will be determined 12 months after delivery, and correlation with CV and PE risk variables obtained during pregnancy will be evaluated.
Discussion:
The study will contribute to characterize the relationship between anti-angiogenic environment and maternal CV dysfunction/remodeling, during and after pregnancy, as well as its impact on future CVD risk in patients with PE. The ultimate goal is to improve CV health of women with high-risk or previous PE, and thus, reduce the burden of the disease.
Trial Registration:
NCT04162236.
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