Evidence map›Paper›PMID 40953476›Full record

ReviewThe Journal of physiology2025

Compromised cardiopulmonary transition in fetal growth restricted and small for gestational age neonates.

Zahrah Azman, Arvind Sehgal, Suzanne L Miller, Kristen J Bubb, Graeme R Polglase, Beth J Allison

Abstract readReview
In one paragraph

Review in The Journal of physiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Observational
  2. Review
  3. Review
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.

Zahrah AzmanThe Ritchie Centre, Hudson Institute of Medical Research, Clayton, Victoria, Australia.ORCID 0000-0002-4627-0095
Arvind SehgalMonash Newborn, Monash Medical Centre, Clayton, Victoria, Australia.ORCID 0000-0003-2600-7529
Suzanne L MillerThe Ritchie Centre, Hudson Institute of Medical Research, Clayton, Victoria, Australia.ORCID 0000-0002-0451-8304
Kristen J BubbBiomedicine Discovery Institute, Monash University, Clayton, Victoria, Australia.ORCID 0000-0002-3846-1414
Graeme R PolglaseThe Ritchie Centre, Hudson Institute of Medical Research, Clayton, Victoria, Australia.ORCID 0000-0002-8906-614X
Beth J AllisonThe Ritchie Centre, Hudson Institute of Medical Research, Clayton, Victoria, Australia.ORCID 0000-0002-1060-513X

Funding

Federal Government | DHAC | National Health and Medical Research Council (NHMRC) 1173731Federal Government | DHAC | National Health and Medical Research Council (NHMRC) 1175843
6 · The paper itself

Abstract

The cardiopulmonary transition at birth is a critical physiological process requiring coordinated cardiovascular adaptation to meet the increased circulatory demands of extrauterine life. This transition may be compromised in infants affected by suboptimal fetal growth, such as in infants born small for gestational age (SGA) or classified with fetal growth restriction (FGR). Suboptimal fetal growth often arises from reduced oxygen and nutrient supply, leading to prioritised perfusion of crucial organs and subsequent cardiac and arterial remodelling. These cardiovascular adaptations, while necessary for fetal survival, may persist postnatally and increase the risk of an impaired cardiovascular transition at birth. Altered echocardiographic function and cardiac injury biomarkers are often detectable in this population during the early postnatal period, indicating underlying myocardial stress and a predisposition to an impaired transition. FGR and/or SGA neonates often exhibit impaired diastolic function, reflecting impaired myocardial relaxation and reduced compliance, and systolic dysfunction, including a reduced capacity to increase left ventricular output over time. Additionally, elevated pulmonary vascular resistance contributes to an increased risk of respiratory morbidity. Emerging preclinical data suggest that these adaptations may impede the neonate's ability to respond to perinatal stressors, thus increasing the risk of adverse outcomes. Understanding the multifaceted nature of cardiovascular dysfunction in FGR and/or SGA infants during the perinatal period is essential to improving their long-term outcomes, thus reducing the risk of cardiovascular disease later in life.

Indexed as

Fetal Growth RetardationHeartInfant, Small for Gestational AgeAnimalsFemaleHumansInfant, NewbornPregnancybirthcardiopulmonary transitioncardiovascularfetal growth restrictionsmall for gestational age

Identifiers

PMID40953476
PMCPMC12645549

What OpenQuestion holds

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Registered trials

None linked

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.