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.
Abstract

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