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Cardiovascular Risk Assessment in Young Women After Index Pregnancy With and Without Placental Complications

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About this study

In this project, the investigators aim to study how all these factors determine the cardiovascular status of a total of 1,800 mothers, 3 to 6 years after delivery. In addition, the investigators want to assess whether lifestyle and living conditions after childbirth may improve or worsen this imprint, since women often prioritize their families over themselves, making it more difficult to maintain a healthy lifestyle that could reduce their cardiovascular risk. Furthermore, the investigators will evaluate how environmental exposures influence their health, as well as explore potential strategies for prediction and prevention. The goal is to develop an easy-to-use algorithm or test that allows women and their physicians to assess this risk, ideally in the form of a mobile app. Although predictive algorithms for cardiovascular health already exist, most have been developed using predominantly male or older populations, and none have taken into account pregnancy-related events or environmental exposure - both of which are key determinants of women's cardiovascular health.

Condition
Cardiovascular (CV) Risk, Preeclampsia (PE), Fetal Weight
Sponsor
Fundació Institut de Recerca de l'Hospital de la Santa Creu i Sant Pau

Who can join

Age
18 years and older
Sex
Female only
Healthy volunteers
Accepted

Inclusion 7

  • Minimum age: 18 years
  • Eligible sex: Female
  • Study condition: Cardiovascular (CV) Risk, Preeclampsia (PE), Fetal Weight
  • Patients who participated in the BiSC (Barcelona Life Study Cohort), EuroPE (Randomized open-label control trial to evaluate if the incorporation of sFlt1/PlGF ratio in the diagnosis and classification of PE improves maternal and perinatal outcomes in women with suspicion of the disease;
  • PI16/00375) and AngioCor (Cardiac dysfunction and remodeling in patients with preeclampsia regulated by antiangiogenic environment: clinical and experimental approach, PI19/00702) cohort studies
  • Who have delivered within the previous 3-6 years.
  • Give written consent when invited to participate in this study protocol.

Exclusion 2

  • Unwillingness to participate in this study
  • Probability of loss to follow-up.

Where

1 site, 1 recruiting

Hospital de la Santa Creu i de Sant Pau

Barcelona, Spain

Recruiting

Contact

Potential match only. Final eligibility is determined by the study team.