Evidence map›Paper›PMID 39819570›Full record

ArticleThe European respiratory journal2025

Nasal CPAP increases alveolar number in a rhesus monkey model of moderate prematurity.

Cindy T McEvoy, Kelvin D MacDonald, Lyndsey E Shorey-Kendrick, Michael H Davies, Kelli C Lund, Ryan Lam, Brandy L Dozier, Lauren Drew Martin, Fiona Corcoran, Robert L Schelonka and 2 more

Abstract read
In one paragraph

Article in The European respiratory journal, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Trial
  2. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors.

Cindy T McEvoyDepartment of Pediatrics, Oregon Health and Science University, Portland, OR, USA.
Kelvin D MacDonaldDepartment of Pediatrics, Oregon Health and Science University, Portland, OR, USA.
Lyndsey E Shorey-KendrickDivision of Neuroscience, Oregon National Primate Research Center, Beaverton, OR, USA.
Michael H DaviesDivision of Neuroscience, Oregon National Primate Research Center, Beaverton, OR, USA.
Kelli C LundDepartment of Pediatrics, University of Utah Health, Salt Lake City, UT, USA.
Ryan LamDepartment of Neonatology, Salem Hospital, Salem, OR, USA.
Brandy L DozierDivision of Comparative Medicine, Oregon National Primate Research Center, Beaverton, OR, USA.
Lauren Drew MartinDivision of Comparative Medicine, Oregon National Primate Research Center, Beaverton, OR, USA.
Fiona CorcoranDivision of Neuroscience, Oregon National Primate Research Center, Beaverton, OR, USA.
Robert L SchelonkaDepartment of Pediatrics, Oregon Health and Science University, Portland, OR, USA.
Robert S TepperDepartment of Pediatrics, H.B. Wells Center for Pediatric Research, Indiana University School of Medicine, Indianapolis, IN, USA.
Eliot R SpindelDivision of Neuroscience, Oregon National Primate Research Center, Beaverton, OR, USA spindele@ohsu.edu.

Funding

Upgrade of confocal microscopy at the Oregon National Primate Research CenterP51OD011092 · OD · OREGON HEALTH & SCIENCE UNIVERSITY · PI Bonnie J. Nagel · 2012 to 2026
$203.9M
CPAP Drives Lung Growth and Pulmonary Function in Moderately Preterm PrimatesR01HL129060 · NHLBI · OREGON HEALTH & SCIENCE UNIVERSITY · PI MCEVOY, CYNTHIA T, SPINDEL, ELIOT R · 2015 to 2019
$3.9M
NHLBI NIH HHS R01 HL129060NIH HHS P51 OD011092
6 · The paper itself

Abstract

backgroundMost premature human infants are born in the moderate to late preterm (MLP) range, ≥30 to <37 weeks gestation, and demonstrate increased incidence of wheeze and respiratory illness as they age. Animal models suggest that mechanical lung distention stimulates lung growth and alveolar development. To determine if nasal continuous positive airway pressure (nCPAP) influences MLP infant lung development, we developed a rhesus monkey model of moderate prematurity, randomised to 9 days of nCPAP or sham nCPAP.

methodsTimed-pregnant fetuses were delivered by elective hysterotomy at gestational age (GA) 140±1 days (85% gestation; term=165 days; human equivalent of 32-34 weeks) or at GA-149±1 days as a relative gestational age reference (GA-control). The day after delivery, the GA-140 animals were treated with nCPAP or sham nCPAP for 9 days, 12 consecutive hours each day. Pulmonary function testing followed by necropsy for analysis of lung structure and gene expression was performed on the equivalent of GA-150 for all animals.

resultsThe nCPAP and sham groups were clinically similar but distinct from the GA-control group. Stereological analysis of lung structure showed significantly increased numbers of alveoli in the nCPAP group compared to the sham group. Other functional and anatomical changes were consistent with increased alveolarisation. Gene expression between the nCPAP and sham groups remained highly similar and distinct from GA-control animals.

conclusionsWe show that nCPAP in MLP infants stimulates alveolarisation with relatively few other changes. How this may benefit subsequent infant respiratory health requires further study.

Indexed as

Continuous Positive Airway PressurePulmonary AlveoliAnimalsAnimals, NewbornDisease Models, AnimalFemaleGestational AgeHumansInfant, NewbornInfant, PrematureLungMacaca mulattaPregnancyRespiratory Function Tests

Identifiers

PMID39819570
PMCPMC12330955

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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.