Evidence map›Paper›PMID 25462113›Full record

ArticlePediatric pulmonology2015

Lung parenchymal development in premature infants without bronchopulmonary dysplasia.

Santiago J Assaf, Daniel V Chang, Christina J Tiller, Jeffrey A Kisling, Jamie Case, Julie A Mund, James E Slaven, Zhangsheng Yu, Shawn K Ahlfeld, Brenda Poindexter and 3 more

Open access · greenAbstract read
In one paragraph

Article in Pediatric pulmonology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.0field-weighted citation impact, top 23% of its field
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

8 citing papers in PubMed, 15 citations in OpenAlex.

  1. Trial
  2. Trial
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  7. Observational
  8. Former-preterm lambs have persistent alveolar simplification at 2 and 5 months corrected postnatal age.American journal of physiology. Lung cellular and molecular physiology · 2018
    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

13 authors at 3 institutions in 1 country.

Santiago J AssafJames Whitcomb Riley Hospital for Children Department of Pediatrics, Sections of Pulmonology, Indiana University School of Medicine, Indianapolis, Indiana.
Daniel V ChangJames Whitcomb Riley Hospital for Children Department of Pediatrics, Sections of Pulmonology, Indiana University School of Medicine, Indianapolis, Indiana.
Christina J TillerJames Whitcomb Riley Hospital for Children Department of Pediatrics, Sections of Pulmonology, Indiana University School of Medicine, Indianapolis, Indiana.
Jeffrey A KislingJames Whitcomb Riley Hospital for Children Department of Pediatrics, Sections of Pulmonology, Indiana University School of Medicine, Indianapolis, Indiana.
Jamie CaseJames Whitcomb Riley Hospital for Children Department of Pediatrics, Section of Neonatology, Indiana University School of Medicine, Indianapolis, Indiana.
Julie A MundJames Whitcomb Riley Hospital for Children Department of Pediatrics, Section of Neonatology, Indiana University School of Medicine, Indianapolis, Indiana.
James E SlavenDepartment of Biostatistics, Indiana University School of Medicine, Indianapolis, Indiana.
Zhangsheng YuDepartment of Biostatistics, Indiana University School of Medicine, Indianapolis, Indiana.
Shawn K AhlfeldJames Whitcomb Riley Hospital for Children Department of Pediatrics, Section of Neonatology, Indiana University School of Medicine, Indianapolis, Indiana.
Brenda PoindexterJames Whitcomb Riley Hospital for Children Department of Pediatrics, Section of Neonatology, Indiana University School of Medicine, Indianapolis, Indiana.
Laura S HanelineJames Whitcomb Riley Hospital for Children Department of Pediatrics, Section of Neonatology, Indiana University School of Medicine, Indianapolis, Indiana.
David A IngramJames Whitcomb Riley Hospital for Children Department of Pediatrics, Section of Neonatology, Indiana University School of Medicine, Indianapolis, Indiana.
Robert S TepperJames Whitcomb Riley Hospital for Children Department of Pediatrics, Sections of Pulmonology, Indiana University School of Medicine, Indianapolis, Indiana.
Indiana University School of MedicineRiley Hospital for Children · USIndiana University – Purdue University Indianapolis · US

Funding

Quality Assurance and Quality Control Project Management: Improving Submissions and Study Conduct in the Human Subjects Research Prior Approval ProcessUL1TR002529 · NCATS · INDIANA UNIVERSITY INDIANAPOLIS · PI MOE, SHARON M, WIEHE, SARAH ELIZABETH · 2018 to 2022
$27.2M
Indiana Clinical and Translational Sciences InstituteUL1TR001108 · NCATS · INDIANA UNIVERSITY INDIANAPOLIS · PI DENNE, SCOTT C., SHEKHAR, ANANTHA · 2013 to 2017
$23.3M
GROWTH OF AIRWAYS AND LUNG PARENCHYMA IN NORMAL INFANTSR01HL054062 · NHLBI · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI TEPPER, ROBERT S. · 1996 to 2009
$3.1M
NCATS NIH HHS UL1 TR001108NHLBI NIH HHS R01 HL054062
6 · The paper itself

Abstract

rationaleWhile infants who are born extremely premature and develop bronchopulmonary dysplasia (BPD) have impaired alveolar development and decreased pulmonary diffusion (DLCO), it remains unclear whether infants born less premature and do not develop BPD, healthy premature (HP), have impaired parenchymal development. In addition, there is increasing evidence that pro-angiogenic cells are important for vascular development; however, there is little information on the relationship of pro-angiogenic cells to lung growth and development in infants.

objectiveand Methods Determine among healthy premature (HP) and fullterm (FT) infants, whether DLCO and alveolar volume (VA) are related to gestational age at birth (GA), respiratory support during the neonatal period (mechanical ventilation [MV], supplemental oxygen [O2], continuous positive airway pressure [CPAP]), and pro-angiogenic circulating hematopoietic stem/progenitor cells (CHSPCs). We measured DLCO, VA, and CHSPCs in infants between 3-33 months corrected-ages; HP (mean GA = 31.7 wks; N = 48,) and FT (mean GA = 39.3 wks; N =88).

resultDLCO was significantly higher in HP than FT subjects, while there was no difference in VA , after adjusting for body length, gender, and race. DLCO and VA were not associated with GA, MV and O2; however, higher values were associated with higher CHSPCs, as well as treatment with CPAP.

conclusionOur findings suggest that in the absence of extreme premature birth, as well as BPD, prematurity per se, does not impair lung parenchymal development.

Indexed as

Continuous Positive Airway PressureFemaleGestational AgeHematopoietic Stem CellsHumansInfantInfant, NewbornInfant, PrematureLungMaleStem CellsTerm Birthcirculating progenitor cellslung growthlung volumepulmonary diffusion

Identifiers

PMID25462113
PMCPMC4452454
OpenAlexW1756267038

What OpenQuestion holds

Textmetadata
LicenceTDM
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 OpenQuestion graph.