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Elevated Blood Pressure in Newborns From Hypertensive Disorders of Pregnancy During the Immediate Postnatal Period
Colman I Freel1,2, Audrey E Bavari2, Teri J Mauch3
1Department of Cellular and Integrative Physiology, University of Nebraska Medical Center, Omaha, Nebraska, USA.
Insights
Hypertensive disorders of pregnancy (HDP) are linked to higher newborn blood pressure and heart rate variability. These findings suggest early cardiovascular changes at birth, supporting the developmental origins of health and disease theory.
Area of Science:
- Obstetrics and Gynecology
- Neonatology
- Cardiovascular Research
Background:
- Hypertensive disorders of pregnancy (HDP) affect up to 22% of pregnancies.
- Offspring of mothers with HDP have increased risks for future cardiovascular disease, including elevated blood pressure in childhood.
- Primary vascular endothelial cells from HDP pregnancies show in vitro dysfunction, suggesting impaired long-term vascular function and supporting the developmental origins of health and disease (DOHaD) theory.
Purpose of the Study:
- To determine if cardiovascular function changes associated with HDP are detectable in the immediate postnatal period.
- To investigate the association between HDP and newborn heart rate (HR) and blood pressure (BP) at birth.
Main Methods:
- Retrospective analysis of 1655 maternal-infant dyads.
- Utilized inverse probability weighted regression adjustment to assess associations between HDP and newborn cardiovascular parameters.
- Compared outcomes for gestational hypertension (GH) and preeclampsia (PE) against normotension (NT).
Main Results:
- Gestational hypertension (GH) and preeclampsia (PE) were associated with significantly higher newborn mean arterial and diastolic blood pressure compared to normotension (NT).
- GH was also linked to increased newborn systolic blood pressure and greater variability in newborn heart rate and diastolic blood pressure.
- These findings indicate subtle, measurable cardiovascular alterations present at birth in infants exposed to HDP.
Conclusions:
- Subtle but measurable newborn cardiovascular alterations associated with gestational hypertension and preeclampsia are present at birth.
- These early alterations provide temporal insight into the developmental origins of health and disease in HDP.
- The findings may reflect underlying vascular dysfunction originating during fetal development.
Abstract:
Hypertensive disorders of pregnancy (HDP) impact up to 22% of pregnancies. Offspring from HDP, face an increased risk of future cardiovascular disease, with elevated blood pressure reported as early as childhood. Additionally, primary vascular endothelial cells derived from HDP demonstrate dysfunction in vitro. These data suggest that HDP affect fetal development in ways that impair long-term vascular function, supporting the developmental origins of health and disease (DOHaD) theory that health risks begin before birth. However, it remains unclear at what point these physiological changes first emerge and can be detected systemically. To assess whether changes in cardiovascular function can be detected in the immediate post-natal period, we conducted a retrospective analysis of 1655 maternal-infant dyads delivered between the years 2012 and 2025. Using inverse probability weighted regression adjustment, we assessed associations between HDP and newborn heart rate (HR) and blood pressure (BP). Gestational hypertension (GH) and preeclampsia (PE) were associated with higher newborn mean arterial (+2.1 mmHg, p = 0.02; +2.9 mmHg, p = 0.04) and diastolic BP (+2.0 mmHg, p = 0.02; +2.6 mmHg, p = 0.04) compared to normotension (NT). GH was also associated with increased newborn systolic blood pressure (+2.3 mmHg, p = 0.04) and increased variability of newborn HR and diastolic BP (+1 bpm, p = 0.009; +1.4 mmHg, p = 0.001) compared to normotension. These findings suggest that subtle but measurable newborn cardiovascular alterations associated with GH and PE are present at birth. While the mechanisms remain to be elucidated, these early alterations provide additional temporal insight into the DOHaD in HDP and may reflect underlying vascular dysfunction.
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