Evidence map›Paper›PMID 36219136›Full record

ReviewAmerican journal of physiology. Lung cellular and molecular physiology2022

Understanding the role of placental pathophysiology in the development of bronchopulmonary dysplasia.

Andrew Parsons, Adom Netsanet, Gregory Seedorf, Steven H Abman, Elizabeth S Taglauer

Abstract readReview
In one paragraph

Review in American journal of physiology. Lung cellular and molecular physiology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 2 pooled it
–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

17 citing papers in PubMed, 2 syntheses or guidelines pooled it.

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  15. PlacingChildren (Basel, Switzerland) · 2023
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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

5 authors.

Andrew ParsonsBoston Combined Residency Program, Boston Children's Hospital, Boston, Massachusetts.
Adom NetsanetUniversity of Colorado School of Medicine, Aurora, Colorado.
Gregory SeedorfPediatric Heart Lung Center, Department of Pediatrics, University of Colorado School of Medicine, Aurora, Colorado.
Steven H AbmanPediatric Heart Lung Center, Department of Pediatrics, University of Colorado School of Medicine, Aurora, Colorado.ORCID 0000-0002-7292-2085
Elizabeth S TaglauerDepartment of Pediatrics, Boston Medical Center, Boston University School of Medicine, Boston, Massachusetts.ORCID 0000-0001-5163-2436

Funding

Project-005UL1TR001430 · NCATS · BOSTON UNIVERSITY MEDICAL CAMPUS · PI BAIR-MERRITT, MEGAN H, CENTER, DAVID M. · 2015 to 2024
$52.3M
Role of VEGF in Perinatal Pulmonary HypertensionR01HL068702 · NHLBI · UNIVERSITY OF COLORADO DENVER · PI ABMAN, STEVEN HERBERT, SHEPHERD, DOUGLAS · 2001 to 2021
$6.7M
Neonatal Research Training ProgramT32HD098061 · NICHD · BOSTON CHILDREN'S HOSPITAL · PI Stella Kourembanas, Martha C. Sola-Visner · 2019 to 2026
$4.0M
CCDC92 and Cardiovascular DiseaseR01HL167024 · NHLBI · UNIVERSITY OF CINCINNATI · PI Yanbo Fan · 2023 to 2026
$2.5M
NCATS NIH HHS UL1 TR001430NHLBI NIH HHS R01 HL068702NHLBI NIH HHS R01 HL167024NICHD NIH HHS T32 HD098061
6 · The paper itself

Abstract

The associations between bronchopulmonary dysplasia (BPD) and the gestational pathologies of chorioamnionitis (CA) and hypertensive disorders of pregnancy (HDP) have become increasingly well recognized. However, the mechanisms through which these antenatal conditions cause increased risk of BPD remain less well characterized. The objective of this review is to discuss the role of the placenta in BPD predisposition as a primary driver of intrauterine alterations adversely impacting fetal lung development. We hypothesize that due to similarities in structure and function, placental disorders during pregnancy can uniquely impact the developing fetal lung, creating a unique placental-pulmonary connection. In the current review, we explore this hypothesis through analysis of clinical literature and preclinical model systems evaluating BPD predisposition, discussion of BPD phenotypes, and an overview on strategies to incorporate placental investigation into research on fetal lung development. We also discuss important concepts learned from research on antenatal steroids as a modulator fetal lung development. Finally, we propose that the appropriate selection of animal models and establishment of in vitro lung developmental model systems incorporating primary human placental components are key in continuing to understand and address antenatal predisposition to BPD.

Indexed as

Bronchopulmonary DysplasiaChorioamnionitisAnimalsFemaleFetal DevelopmentHumansInfant, NewbornLungPlacentaPregnancybronchopulmonary dysplasiachorioamnionitisfetal lungplacentapreeclampsia

Identifiers

PMID36219136
PMCPMC9722259

What Socratic holds

Textmetadata
Read underepoch 390

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 Socratic graph.