Key result
A history of pre-eclampsia was independently associated with a higher risk of subclinical myocardial dysfunction at six years postpartum (HR 4.01; 95% CI 1.05-15.3; p=0.03).
Why the study?
Echocardiographic studies evaluating myocardial strain after hypertensive disorders of pregnancy (HDP) have yielded inconsistent findings, and none had comprehensively evaluated deformation indices across all biventricular and biatrial chambers.
Does a history of hypertensive disorders of pregnancy increase the risk of subclinical myocardial dysfunction and early carotid atherosclerosis at six years postpartum?
Cohort (n=61)
Does a history of hypertensive disorders of pregnancy increase the risk of subclinical myocardial dysfunction and early carotid atherosclerosis at six years postpartum?
Hazard Ratio: 4.01 (95% CI 1.05–15.3)
p-value: p=0.03
Women with a history of pre-eclampsia have a significantly higher risk of subclinical myocardial dysfunction and early carotid atherosclerosis at six years postpartum, highlighting the need for long-term cardiovascular monitoring.
Post-HDP strain changes need outcome validation; extends inconsistent data but leaves clinical utility open.
Background: Over the past decade, few echocardiographic investigations have assessed myocardial strain parameters in women with a history of hypertensive disorders of pregnancy (HDP), and their findings have been inconsistent. Moreover, no study has comprehensively evaluated deformation indices of all biventricular and biatrial chambers in women post-HDP. This study aimed to examine the structural and functional myocardial properties of all cardiac chambers in a cohort of women with prior HDP at six years after delivery. Methods: We analyzed a consecutive cohort of women with previous HDP and compared them with a control group of normotensive healthy women matched for age and body mass index (BMI). Both groups underwent standard transthoracic echocardiography (TTE) supplemented by a detailed speckle tracking echocardiography (STE) evaluation of biventricular and biatrial myocardial deformation, along with carotid ultrasound, at six years postpartum. The primary endpoint was subclinical myocardial dysfunction, defined by impaired left ventricular global longitudinal strain (LV-GLS < 20%), while the secondary endpoint was early carotid atherosclerosis, defined by common carotid artery intima-media thickness (CCA-IMT) ≥ 0.7 mm. Results: The study included 31 women with previous HDP (mean age 42.3 ± 5.9 years) and 30 matched controls without HDP history (mean age 40.8 ± 5.0 years). The average follow-up duration was 6.1 ± 1.3 years postpartum. Despite preserved and comparable systolic function on conventional TTE, most myocardial strain and strain rate measures in both ventricles and atria were significantly reduced in the HDP group compared to controls. Subclinical myocardial dysfunction was detected in 58.1% of women with prior HDP, and 67.7% exhibited increased CCA-IMT (≥0.7 mm). A history of pre-eclampsia (PE) was independently associated with subclinical myocardial dysfunction (HR 4.01, 95% CI 1.05–15.3, p = 0.03). Both third-trimester BMI (HR 1.21, 95% CI 1.07–1.38, p = 0.003) and PE (HR 6.38, 95% CI 1.50–27.2, p = 0.01) independently predicted early carotid atherosclerosis. Notably, a third-trimester BMI above 27 kg/m2 showed optimal sensitivity and specificity for identifying the secondary outcome. Conclusions: A history of PE is independently associated with a higher risk of subclinical myocardial dysfunction and early carotid atherosclerosis at six years postpartum.
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Sonaglioni et al. (2025) conducted a cohort in Hypertensive disorders of pregnancy (n=61). History of hypertensive disorders of pregnancy (HDP) / pre-eclampsia vs. Normotensive healthy women matched for age and BMI was evaluated on Subclinical myocardial dysfunction (impaired left ventricular global longitudinal strain < 20%) (HR 4.01, 95% CI 1.05-15.3, p=0.03). A history of pre-eclampsia was independently associated with a higher risk of subclinical myocardial dysfunction at six years postpartum (HR 4.01; 95% CI 1.05-15.3; p=0.03).
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