Evidence map›Paper›PMID 30135517›Full record

ArticleScientific reports2018

Plasma proteomics reveals gestational age-specific responses to mechanical ventilation and identifies the mechanistic pathways that initiate preterm lung injury.

Prue M Pereira-Fantini, Sean G Byars, Karen E McCall, Elizabeth J Perkins, Regina B Oakley, R L Dellacà, Peter A Dargaville, Peter G Davis, Vera Ignjatovic, David G Tingay

Abstract read
In one paragraph

Article in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

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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.

Prue M Pereira-FantiniNeonatal Research, Murdoch Childrens Research Institute, Parkville, Australia. prue.pereira@mcri.edu.au.
Sean G ByarsDepartment of Pathology, University of Melbourne, Parkville, Australia.
Karen E McCallNeonatal Research, Murdoch Childrens Research Institute, Parkville, Australia.
Elizabeth J PerkinsNeonatal Research, Murdoch Childrens Research Institute, Parkville, Australia.
Regina B OakleyNeonatal Research, Murdoch Childrens Research Institute, Parkville, Australia.
R L DellacàLaboratorio di Tecnologie Biomediche, Dipartimento di Elettronica, Informazione e Ingegneria Biomedica-DEIB, Politecnico di Milano University, Milano, Italy.ORCID 0000-0002-3672-4591
Peter A DargavilleMenzies Institute for Medical Research, University of Tasmania, Hobart, Australia.
Peter G DavisNeonatal Research, Murdoch Childrens Research Institute, Parkville, Australia.ORCID 0000-0001-6742-7314
Vera IgnjatovicDepartment of Paediatrics, University of Melbourne, Parkville, Australia.
David G TingayNeonatal Research, Murdoch Childrens Research Institute, Parkville, Australia.ORCID 0000-0003-1522-4691

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The preterm lung is particularly vulnerable to ventilator-induced lung injury (VILI) as a result of mechanical ventilation. However the developmental and pathological cellular mechanisms influencing the changing patterns of VILI have not been comprehensively delineated, preventing the advancement of targeted lung protective therapies. This study aimed to use SWATH-MS to comprehensively map the plasma proteome alterations associated with the initiation of VILI following 60 minutes of standardized mechanical ventilation from birth in three distinctly different developmental lung states; the extremely preterm, preterm and term lung using the ventilated lamb model. Across these gestations, 34 proteins were differentially altered in matched plasma samples taken at birth and 60 minutes. Multivariate analysis of the plasma proteomes confirmed a gestation-specific response to mechanical ventilation with 79% of differentially-expressed proteins altered in a single gestation group only. Six cellular and molecular functions and two physiological functions were uniquely enriched in either the extremely preterm or preterm group. Correlation analysis supported gestation-specific protein-function associations within each group. In identifying the gestation-specific proteome and functional responses to ventilation we provide the founding evidence required for the potential development of individualized respiratory support approaches tailored to both the developmental and pathological state of the lung.

Indexed as

AnimalsAnimals, NewbornDisease Models, AnimalGestational AgeLungMass SpectrometryPlasmaPremature BirthProteomeProteomicsRespiration, ArtificialSheep, DomesticVentilator-Induced Lung InjuryProteome

Identifiers

PMID30135517
PMCPMC6105628

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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.