Evidence map›Paper›PMID 28473324›Full record

ArticleAmerican journal of physiology. Lung cellular and molecular physiology2017

miR-29b supplementation decreases expression of matrix proteins and improves alveolarization in mice exposed to maternal inflammation and neonatal hyperoxia.

Shaheen Durrani-Kolarik, Caylie A Pool, Ashley Gray, Kathryn M Heyob, Mary J Cismowski, Gloria Pryhuber, L James Lee, Zhaogang Yang, Trent E Tipple, Lynette K Rogers

Open access · bronzeAbstract read
In one paragraph

Article in American journal of physiology. Lung cellular and molecular physiology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
5.3field-weighted citation impact, top 4% 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

38 citing papers in PubMed, 71 citations in OpenAlex.

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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

10 authors at 4 institutions in 1 country.

Shaheen Durrani-KolarikCenter for Perinatal Research, The Research Institute at Nationwide Children's Hospital, Columbus, Ohio.
Caylie A PoolCenter for Perinatal Research, The Research Institute at Nationwide Children's Hospital, Columbus, Ohio.
Ashley GrayCenter for Perinatal Research, The Research Institute at Nationwide Children's Hospital, Columbus, Ohio.
Kathryn M HeyobCenter for Perinatal Research, The Research Institute at Nationwide Children's Hospital, Columbus, Ohio.
Mary J CismowskiCenter for Cardiovascular Research, The Research Institute at Nationwide Children's Hospital, Columbus, Ohio.
Gloria PryhuberDepartment of Pediatrics, University of Rochester Medical Center, Rochester, New York.
L James LeeThe Center for Affordable Nanoengineering of Polymeric Biomedical Devices, The Ohio State University, Columbus, Ohio.
Zhaogang YangThe Center for Affordable Nanoengineering of Polymeric Biomedical Devices, The Ohio State University, Columbus, Ohio.
Trent E TippleDivision of Neonatology, Department of Pediatrics, University of Alabama at Birmingham, Birmingham, Alabama; and.
Lynette K RogersCenter for Perinatal Research, The Research Institute at Nationwide Children's Hospital, Columbus, Ohio; lynette.rogers@nationwidechildrens.org.
Nationwide Children's Hospital · USThe Ohio State University · USUniversity of Alabama at Birmingham · USUniversity of Rochester Medical Center · US

Funding

Targeting Thioredoxin Reductase-1 to Prevent Bronchopulmonary DysplasiaR01HL119280 · NHLBI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI TIPPLE, TRENT · 2014 to 2018
$2.0M
DHA attenuates Inflammatory Responses Through Altering RAGE SignalingR01AT006880 · NCCIH · RESEARCH INST NATIONWIDE CHILDREN'S HOSP · PI ROGERS, LYNETTE KAY · 2011 to 2015
$1.8M
Optimizing Therapeutic delivery of MicroRNAs to prevent chronic lung disease in Preterm infants.R01HD088033 · NICHD · RESEARCH INST NATIONWIDE CHILDREN'S HOSP · PI ROGERS, LYNETTE KAY · 2017 to 2021
$1.6M
NCCIH NIH HHS R01 AT006880NHLBI NIH HHS R01 HL119280NICHD NIH HHS R01 HD088033
6 · The paper itself

Abstract

Even with advances in the care of preterm infants, chronic lung disease or bronchopulmonary dysplasia (BPD) continues to be a significant pulmonary complication. Among those diagnosed with BPD, a subset of infants develop severe BPD with disproportionate pulmonary morbidities. In addition to decreased alveolarization, these infants develop obstructive and/or restrictive lung function due to increases in or dysregulation of extracellular matrix proteins. Analyses of plasma obtained from preterm infants during the first week of life indicate that circulating miR-29b is suppressed in infants that subsequently develop BPD and that decreased circulating miR-29b is inversely correlated with BPD severity. Our mouse model mimics the pathophysiology observed in infants with severe BPD, and we have previously reported decreased pulmonary miR-29b expression in this model. The current studies tested the hypothesis that adeno-associated 9 (AAV9)-mediated restoration of miR-29b in the developing lung will improve lung alveolarization and minimize the deleterious changes in matrix deposition. Pregnant C3H/HeN mice received an intraperitoneal LPS injection on embryonic

Indexed as

AnimalsAnimals, NewbornDisease Models, AnimalExtracellular Matrix ProteinsHumansHyperoxiaInfant, NewbornInflammationLungMiceMice, Inbred C3HMicroRNAsOxygenExtracellular Matrix ProteinsMicroRNAsMIRN29 microRNA, mouseOxygenadeno-associated virusbronchopulmonary dysplasiafibrosishyperoxiamaternal inflammationmicroRNA

Identifiers

PMID28473324
PMCPMC5582933
OpenAlexW2611772469

What OpenQuestion 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 OpenQuestion graph.