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Predicting cardiovascular disease after preeclampsia: Emerging tools and early detection approaches
Chiara Alfaré1, Emma M Giesen2, Evelyn A Huhn2
1Department of Obstetrics and Fetal Medicine, University Medical Center Hamburg-Eppendorf, Hamburg, Germany; Department of Medicine and Surgery, University of Parma, Italy.
Insights
Preeclampsia history increases long-term cardiovascular disease (CVD) risk. This review explores biomarkers and imaging like GLS and USCOM for early CVD detection and risk stratification in women post-preeclampsia.
Area of Science:
- Cardiovascular Medicine
- Obstetrics
- Biomarkers
Background:
- Preeclampsia (PE) is a significant risk factor for long-term cardiovascular disease (CVD).
- Guidelines for cardiovascular follow-up after PE are lacking.
- Early detection of CVD in women with a history of PE is crucial due to the high burden of cardiovascular morbidity.
Purpose of the Study:
- To review current evidence on predictive tools and strategies for CVD prediction and early diagnosis in women with a history of PE.
- To summarize the role of circulating biomarkers and advanced imaging techniques in cardiovascular risk assessment post-PE.
Main Methods:
- Literature review of studies on CVD prediction and diagnosis after PE.
- Analysis of circulating biomarkers (e.g., sFlt1, sEng, IL-6, activin A).
- Evaluation of imaging techniques (e.g., Global Longitudinal Strain - GLS, Ultrasonic Cardiac Output Monitor - USCOM).
Main Results:
- Elevated antiangiogenic markers (sFlt1, sEng) and sFlt1/PlGF ratio correlate with subclinical myocardial dysfunction and postpartum hypertension.
- Increased IL-6 suggests persistent inflammation, and elevated activin A indicates cardiac stress years after hypertensive disorders of pregnancy (HDP).
- GLS is a sensitive parameter for early myocardial impairment, and USCOM shows potential for hemodynamic monitoring and therapy tailoring in HDP.
Conclusions:
- Circulating biomarkers, advanced echocardiography (GLS), and non-invasive hemodynamic monitoring (USCOM) can refine cardiovascular risk stratification after PE.
- These tools support the potential for targeted surveillance and preventive strategies for women at long-term CVD risk.
- Further research is needed to validate these tools and establish definitive management guidelines.
Abstract:
Preeclampsia (PE) in a previous pregnancy is a recognized risk factor for the development of long-term cardiovascular disease (CVD). However, evidence-based guidelines for cardiovascular follow-up in women with a history of PE are lacking. Given the substantial burden of CVD on individual health and society, the identification of predictive tools and strategies for its early detection in this population is crucial. The aim of this review is to summarize current evidence regarding available approaches for CVD prediction and early diagnosis following PE. Circulating biomarkers have emerged as potential tools. Elevated levels of antiangiogenic markers, such as sFlt1 (soluble vascular endothelial growth factor receptor 1) and sEng (soluble endoglin), and the sFlt1/PlGF ratio during pregnancy, have been correlated with subclinical myocardial dysfunction during the third trimester and with postpartum hypertension. Increased IL-6 several years after hypertensive disorders of pregnancy (HDP) suggests persistent systemic inflammation, while elevated activin A indicates ongoing cardiac stress. Imaging techniques also provide valuable insights. Global longitudinal strain (GLS) has emerged as a sensitive echocardiographic parameter for detecting early myocardial impairment and predicting future cardiovascular risk. Additionally, the Ultrasonic Cardiac Output Monitor (USCOM), a non-invasive hemodynamic tool, has been proposed for tailoring antihypertensive therapy in HDP and may hold potential for postpartum cardiovascular surveillance. Together, these findings support the role of circulating biomarkers, advanced echocardiography and non-invasive hemodynamic monitoring in refining cardiovascular risk stratification after PE. Further research is warranted to validate these tools and establish targeted surveillance and preventive strategies for women at long-term risk of CVD.
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