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Assessment of Maternal Vascular Remodeling During Pregnancy in the Mouse Uterus
Published on: December 5, 2015
Association of Hypertensive Disorders of Pregnancy With Coronary Microvascular Dysfunction 8 to 10 Years After
Malamo E Countouris1, Janet M Catov2,3, Jianhui Zhu1
1Division of Cardiology, Department of Medicine, University of Pittsburgh Medical Center, PA (M.E.C., J.Z., X.C., K.L.B., A.C.S., F.S.V.).
Insights
History of hypertensive disorders of pregnancy (HDP) is linked to coronary microvascular dysfunction a decade later. This dysfunction may contribute to cardiovascular disease, potentially influenced by metabolic factors like obesity and diabetes.
Area of Science:
- Cardiology
- Obstetrics
- Vascular Biology
Background:
- Hypertensive disorders of pregnancy (HDP) are linked to later cardiac issues.
- The role of myocardial microvascular disease in HDP-associated cardiac remodeling and cardiovascular disease (CVD) is unclear.
- Investigating microvascular dysfunction as a potential link between HDP and CVD is crucial.
Purpose of the Study:
- To determine if HDP history correlates with coronary microvascular dysfunction (CMD) 8-10 years post-delivery.
- To assess if CMD correlates with left ventricular (LV) remodeling in women with HDP history.
- To explore the association between CMD, HDP, and cardiometabolic factors.
Main Methods:
- Utilized myocardial contrast echocardiography to assess coronary flow reserve (CFR) in women post-delivery.
- Quantified myocardial perfusion at rest and during dobutamine stress.
- Calculated CFR as the ratio of stress to rest myocardial blood flow.
Main Results:
- Individuals with CMD (CFR < 2.0) had a higher prevalence of HDP history (46.2% vs. 16.7%).
- The association between CFR and HDP was attenuated after adjusting for cardiometabolic factors.
- Exploratory analysis revealed higher CMD in women with both HDP history and LV remodeling (41.7%).
Conclusions:
- A history of HDP is associated with coronary microvascular dysfunction up to a decade postpartum.
- Metabolic factors like obesity and diabetes may partly drive this association.
- Coronary microvascular dysfunction may be a key mechanism contributing to cardiovascular disease risk in women with HDP history.
Background:
Hypertensive disorders of pregnancy (HDP) are associated with subsequent adverse cardiac remodeling and cardiovascular disease. The role of myocardial microvascular disease among individuals with HDP and left ventricular (LV) remodeling as a potential link to cardiovascular disease is unknown. We aimed to determine whether individuals with HDP history have coronary microvascular dysfunction measured by coronary flow reserve 8 to 10 years after delivery and whether microvascular dysfunction correlates with LV remodeling.
Methods:
Individuals with pregnancies delivered from 2008 to 2010 underwent burst-replenishment myocardial contrast echocardiography (2017-2020) to quantify myocardial perfusion at rest and during dobutamine stress. Video intensity versus time data were used to derive β, the rate of rise of video intensity, a correlate for myocardial blood flow. Coronary flow reserve was calculated as the ratio of β at peak stress to β at rest, averaged across LV myocardial regions of interest.
Results:
We studied 91 individuals (aged 38±6 and 9.1±0.9 years postdelivery) and 19 with a history of HDP. Individuals with coronary microvascular dysfunction (coronary flow reserve <2.0; n=13) had a higher proportion of HDP (46.2% versus 16.7%; P=0.026) and higher prepregnancy body mass index, baseline heart rate, and hemoglobin A1c compared with those without microvascular dysfunction. The association of coronary flow reserve and HDP was attenuated after adjusting for cardiometabolic factors (P=0.133). In exploratory subgroup analyses, individuals with both LV remodeling (relative wall thickness >0.42) and HDP (n=12) had the highest proportion of microvascular dysfunction (41.7% versus +HDP-LV remodeling [n=7] 14.3%; -HDP+LV remodeling [n=26] 7.7%; P=0.0498).
Conclusions:
In this small study, HDP history is associated with coronary microvascular dysfunction 1 decade after delivery, findings that may, in part, be driven by metabolic factors including obesity and diabetes. Microvascular dysfunction may contribute to cardiovascular disease among individuals with a history of HDP.
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