Evidence map›Paper›PMID 41543275›Full record

ArticleJournal of clinical hypertension (Greenwich, Conn.)2026

Elevated Blood Pressure in Newborns From Hypertensive Disorders of Pregnancy During the Immediate Postnatal Period.

Colman I Freel, Audrey E Bavari, Teri J Mauch, Corrine K Hanson, Paras Kumar Mishra, Ann L Anderson-Berry

Abstract read
In one paragraph

Article in Journal of clinical hypertension (Greenwich, Conn.), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Colman I FreelDepartment of Cellular and Integrative Physiology, University of Nebraska Medical Center, Omaha, Nebraska, USA.
Audrey E BavariDivision of Newborn Medicine, Department of Pediatrics, University of Nebraska Medical Center, Omaha, Nebraska, USA.
Teri J MauchPediatric Nephrology, University of Nebraska Medical Center, Omaha, Nebraska, USA.
Corrine K HansonCollege of Allied Health Professions, University of Nebraska Medical Center, Omaha, Nebraska, USA.
Paras Kumar MishraDepartment of Cellular and Integrative Physiology, University of Nebraska Medical Center, Omaha, Nebraska, USA.
Ann L Anderson-BerryDivision of Newborn Medicine, Department of Pediatrics, University of Nebraska Medical Center, Omaha, Nebraska, USA.

Funding

Tracking and Evaluation CoreU54GM115458 · NIGMS · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI PHILIBERT, INGRID · 2016 to 2025
$42.8M
The role of hemoglobin alpha in diabetes-related vascular dysfunctionR01HL155618 · NHLBI · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI BAGHER, POONEH · 2021 to 2025
$2.5M
Mechanism of metabolic remodeling in the diabetic heartR56HL156806 · NHLBI · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI MISHRA, PARAS KUMAR · 2022 to 2022
$400k
NHLBI NIH HHS R01 HL155618NHLBI NIH HHS R56 HL156806NIGMS NIH HHS U54 GM115458NIH HHS R01HL155618NIH HHS R56HL156806
6 · The paper itself

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.

Indexed as

Blood PressureHypertensionHypertension, Pregnancy-InducedPre-EclampsiaAdultDevelopmental Origins of Health and DiseaseFemaleHeart RateHumansInfant, NewbornMalePostpartum PeriodPregnancyRetrospective StudiesRisk Factorscardiovascular diseasedevelopmental programminghypertensive disorders of pregnancynewborn healthpregnancy

Identifiers

PMID41543275
PMCPMC12810192

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LicenceCC BY-NC-ND
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.