Evidence on potential pathophysiologic mechanisms including shared genetic, epigenetic programming and persistent immune dysregulation that contribute to the CV risk is reviewed and recommendations on surveillance strategies in mothers and their offspring are made.
Abstract
Hypertensive disorders of pregnancy (HDP) affect 5–10% of pregnancies globally and are a leading cause of maternal and fetal morbidity and mortality. Beyond their acute obstetrics impact, HDP unmask a lifelong cardiovascular (CV) vulnerability in affected women and confer intergenerational risk to their offspring. In this review, we discuss the latest evidence regarding the CV risk profiles following HDP in the mothers and their offspring. In mothers, HDP is associated with a 7.29-fold increased risk of new chronic hypertension (HTN) within 24 months postpartum and long-term risks of heart failure, coronary heart disease and stroke. Offspring exposed carry a 1.5-fold increased risk for adult HTN and increased risks for ischemic heart disease and stroke. We review evidence on potential pathophysiologic mechanisms including shared genetic, epigenetic programming and persistent immune dysregulation that contribute to the CV risk. We make recommendations on surveillance strategies in mothers and their offspring beginning in the immediate postpartum period and for lifelong follow-up. Management strategies of the CV risk factors, using latest guidelines are discussed. We suggest future directions for research and intervention. Integrated maternal-offspring CV care, women-specific risk prediction tools and equity focused research are needed to reduce the intergenerational burden of HDP.
Hypertensive disorders of pregnancy (HDP) are heterogeneous maternal-placental syndromes and continue to be a major cause of maternal and perinatal morbidity and mortality worldwide. Their clinical spectrum ranges from gestational and chronic hypertension to preeclampsia, eclampsia and HELLP syndrome with markedly diff...
Sanjay Gupte, Manjusha G. Deulkar, Divya R. Chatla et al.· International Journal of Rep...· 0 citations
This final Review in the Series extends the focus from cardiovascular disease during pregnancy and HDP to the long-term cardiovascular implications of APOs after delivery, synthesising epidemiological data quantifying cardiovascular risk across major APO phenotypes and emerging evidence linking maternal APO history wit...
M. A. Pabón, Graeme N. Smith, Garima Sharma et al.· The Lancet· 2 citations
Hypertensive disorders of pregnancy (HDP) affect approximately 1 in 7 pregnancies in the United States and are increasingly recognized as early and independent markers of lifetime cardiovascular disease. This review provides an update of the evidence for classification, pathophysiology, and management of HDP with an em...
Jessica Gottula, Tiffany Corlin, M. Burn et al.· Current Cardiovascular Risk...· 0 citations
Abstract Introduction Hypertensive disorders of pregnancy (HDP) complicate 5%–10% of pregancies, to maternal morbidity and mortality. HDP increases the risk of cardiovascular events later in life, but whether repeated HDP episodes confer cumulative risk remains unclear. We aimed to assess the association between recurr...
D. Wilson, J. Mateus, J. Pittman et al.· Pregnancy· 0 citations
Pregnancy represents a critical period during which the maternal cardiovascular system adapts to profound haemodynamic and metabolic demands. When these adaptive mechanisms are impaired, adverse pregnancy outcomes (APOs)-including hypertensive disorders of pregnancy, gestational diabetes, pre-term birth, small-for-gest...
V. Giorgione, N. Parikh, D. Pedicino et al.· European Heart Journal· 0 citations
Objectives: To investigate whether genetic predisposition to hypertensive disorders of pregnancy (HDP), measured using polygenic risk scores (PRS), is associated with subsequent cardiovascular disease (CVD) outcomes in analyses stratified by HDP history. Study design and main outcome measures: This population-based coh...
G. Krishnamurthy, J. A. Temple, M. A. Ahmed et al.· medRxiv· 0 citations
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