Evidence map›Paper›PMID 42295024›Full record

ArticlePediatric pulmonology2026

Respiratory Outcomes in Children With Neonatal Respiratory Distress Syndrome and Monoallelic ABCA3 Variants.

Velda Ocasio Ramírez, Jennifer A Wambach, Rebekah J Nevel, Laura Voss, Daniel Craven, Alicia Casey, Devaney Camburn, Steven K Brennan, Whitney Bour Eldridge, F Sessions Cole and 5 more

Abstract read
In one paragraph

Article in Pediatric pulmonology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

15 authors.

Velda Ocasio RamírezEudowood Division of Pediatric Respiratory Sciences, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.ORCID https://orcid.org/0000-0001-5134-3845
Jennifer A WambachEdward Mallinckrodt Department of Pediatrics, Washington University School of Medicine, St. Louis Children's Hospital, Saint Louis, Missouri, USA.
Rebekah J NevelChild Health, Division of Pediatric Pulmonary Medicine, University of Missouri, Columbia, Missouri, USA.
Laura VossDepartment of Pediatrics, Division of Pulmonary and Sleep Medicine, Children's Hospital of Philadelphia, University of Pennsylvania Perelman School of Medicine, Philadelphia, Pennsylvania, USA.
Daniel CravenPediatric Pulmonology, Rainbow Babies and Children's Hospital, Cleveland, Ohio, USA.ORCID https://orcid.org/0009-0009-0194-3207
Alicia CaseyDivision of Pulmonary Medicine, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts, USA.
Devaney CamburnDepartment of Pediatrics, Division of Pulmonary and Sleep Medicine, Children's Hospital of Philadelphia, University of Pennsylvania Perelman School of Medicine, Philadelphia, Pennsylvania, USA.
Steven K BrennanEdward Mallinckrodt Department of Pediatrics, Washington University School of Medicine, St. Louis Children's Hospital, Saint Louis, Missouri, USA.
Whitney Bour EldridgeEdward Mallinckrodt Department of Pediatrics, Washington University School of Medicine, St. Louis Children's Hospital, Saint Louis, Missouri, USA.
F Sessions ColeEdward Mallinckrodt Department of Pediatrics, Washington University School of Medicine, St. Louis Children's Hospital, Saint Louis, Missouri, USA.
Gail H DeutschPathology, Seattle Children's Hospital, Seattle, Washington, USA.
Michael W KuzniewiczDivision of Research, Kaiser Permanente Northern California, Oakland, California, USA.
Lisa R YoungDepartment of Pediatrics, Division of Pulmonary and Sleep Medicine, Children's Hospital of Philadelphia, University of Pennsylvania Perelman School of Medicine, Philadelphia, Pennsylvania, USA.ORCID https://orcid.org/0000-0003-3297-8532
Lawrence NogeeEudowood Neonatal Pulmonary Division, Department of Pediatrics, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.ORCID https://orcid.org/0000-0003-0540-8083
S Christy SadreameliEudowood Division of Pediatric Respiratory Sciences, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.ORCID https://orcid.org/0000-0001-9167-6994

Funding

Functional Characterization of ABCA3 Genomic VariantsR01HL149853 · NHLBI · WASHINGTON UNIVERSITY · PI Jennifer Wambach · 2020 to 2026
$3.9M
High-Content Analysis to Accelerate Mechanistic and Therapeutic Identification for ABCA3 DeficiencyR03TR004845 · NCATS · WASHINGTON UNIVERSITY · PI WAMBACH, JENNIFER · 2025 to 2025
$156k
NCATS NIH HHS R03 TR004845NHLBI NIH HHS R01 HL149853
6 · The paper itself

Abstract

introductionLung disease due to ABCA3 variants and resultant surfactant dysfunction is an autosomal recessive disease. However, monoallelic ABCA3 variants are overrepresented in term or late-preterm infants with non-fatal neonatal respiratory distress syndrome (RDS). The childhood respiratory outcomes of infants with monoallelic ABCA3 variants who present with neonatal RDS are unknown. In this study, we report the respiratory outcomes beyond neonatal hospitalization (median follow-up 1 year [range 1-9.4 years]) for infants with monoallelic ABCA3 variants and neonatal RDS.

methodsParticipants with monoallelic ABCA3 variants classified as pathogenic, likely pathogenic, or of uncertain significance with neonatal RDS identified in 3 cohorts (ChILD Registry n = 9, disease-based cohort n = 19, and nested case-control n = 20) were included in this retrospective, descriptive study. The primary outcome was duration of supplemental oxygen use. Secondary outcomes included respiratory morbidities after NICU discharge.

resultsOf 48 infants who met inclusion criteria, 8 (17%) were discharged home on supplemental oxygen, including two who required home invasive mechanical ventilation. The ABCA3 pathogenic variant p.Glu292Val was the most common variant identified in the infants who required oxygen beyond NICU discharge (6 of 8). Oxygen was discontinued by 10 months of age in 50% of infants discharged from birth hospitalization on oxygen. Respiratory morbidities, including hospitalizations (62% vs. 8%, p = 0.005) and emergency department (ED) visits (71% vs. 35%, p < 0.01), were more common among participants discharged home on oxygen compared to those discharged home without oxygen.

conclusionsThese findings suggest that infants with monoallelic ABCA3 variants and neonatal RDS may require prolonged home oxygen or mechanical ventilation and experience increased risk for respiratory morbidities, including subsequent hospitalization and ED visits.

Indexed as

ATP-Binding Cassette TransportersRespiratory Distress Syndrome, NewbornCase-Control StudiesChildFemaleFollow-Up StudiesHumansInfantInfant, NewbornMaleOxygen Inhalation TherapyRespiration, ArtificialRetrospective StudiesABCA3 protein, humanATP-Binding Cassette Transporters

Identifiers

PMID42295024
PMCPMC13380821

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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.