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Published on: January 26, 2024
Novel Cardiovascular Biomarkers Associated with Increased Cardiovascular Risk in Women With Prior Preeclampsia/HELLP
Esmee Me Bovee1, Martha Gulati2, Angela Hem Maas3
1Radboud University Nijmegen, the Netherlands.
Insights
Women with a history of preeclampsia or haemolysis, elevated liver enzymes and low platelets (HELLP) syndrome face higher cardiovascular disease risk. Promising biomarkers like soluble fms-like tyrosine kinase-1 and interleukins may aid in early risk stratification.
Area of Science:
- Cardiovascular Disease Research
- Reproductive Health Biomarkers
Background:
- Preeclampsia and HELLP syndrome significantly increase long-term cardiovascular disease (CVD) risk in women.
- Current guidelines for post-pregnancy CVD screening and management in these women are undefined.
- Identifying novel cardiovascular biomarkers is crucial for predicting high-risk individuals.
Purpose of the Study:
- To review current literature on circulating cardiovascular biomarkers associated with increased CVD risk in women with a history of preeclampsia/HELLP syndrome.
- To identify promising biomarkers for cardiovascular risk stratification in this population.
Main Methods:
- A narrative review of 56 studies examining 53 different biomarkers.
- Synthesis of evidence on circulating biomarkers linked to cardiovascular risk post-preeclampsia/HELLP syndrome.
Main Results:
- Several biomarkers demonstrated potential, including soluble fms-like tyrosine kinase-1, placental growth factor, interleukin-6 (IL-6), IL-6/IL-10 ratio, high-sensitivity cardiac troponin I, activin A, soluble human leukocyte antigen G, pregnancy-associated plasma protein A, and norepinephrine.
- These biomarkers may be valuable for cardiovascular risk stratification.
- Further exploration of these candidates is warranted.
Conclusions:
- Circulating biomarkers show promise for identifying women at elevated cardiovascular risk after preeclampsia/HELLP syndrome.
- These biomarkers could inform the development of targeted prevention strategies for hypertension and adverse events.
- Personalized cardiovascular risk assessment may be improved through these novel markers.
Abstract:
Evidence has shown that women with a history of preeclampsia or haemolysis, elevated liver enzymes and low platelets (HELLP) syndrome have an increased risk of cardiovascular disease later in life. Recommendations for screening, prevention and management after such pregnancies are not yet defined. The identification of promising non-traditional cardiovascular biomarkers might be useful to predict which women are at greatest risk. Many studies are inconsistent and an overview of the most promising biomarkers is currently lacking. This narrative review provides an update of the current literature on circulating cardiovascular biomarkers that may be associated with an increased cardiovascular disease risk in women after previous preeclampsia/HELLP syndrome. Fifty-six studies on 53 biomarkers were included. From the summary of evidence, soluble fms-like tyrosine kinase-1, placental growth factor, interleukin (IL)-6, IL-6/IL-10 ratio, high-sensitivity cardiac troponin I, activin A, soluble human leukocyte antigen G, pregnancy-associated plasma protein A and norepinephrine show potential and are interesting candidate biomarkers to further explore. These biomarkers might be potentially eligible for cardiovascular risk stratification after preeclampsia/HELLP syndrome and may contribute to the development of adequate strategies for prevention of hypertension and adverse events in this population.
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