Evidence map›Paper›PMID 32620587›Full record

ReviewEuropean respiratory review : an official journal of the European Respiratory Society2020

Therapeutic targeting of metabolic alterations in acute respiratory distress syndrome.

Matthew John Robinson, Anna D Krasnodembskaya

Abstract readReview
In one paragraph

Review in European respiratory review : an official journal of the European Respiratory Society, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 1 pooled it
–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

20 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  16. Multi-omic comparative analysis of COVID-19 and bacterial sepsis-induced ARDS.medRxiv : the preprint server for health sciences · 2022
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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

2 authors.

Matthew John RobinsonWellcome-Wolfson Institute for Experimental Medicine, Queen's University of Belfast, Belfast, UK.
Anna D KrasnodembskayaWellcome-Wolfson Institute for Experimental Medicine, Queen's University of Belfast, Belfast, UK.ORCID https://orcid.org/0000-0002-2380-5069

Funding

Medical Research Council MR/L017229/1Medical Research Council MR/R025096/1Medical Research Council MR/S009426/1
6 · The paper itself

Abstract

Acute respiratory distress syndrome (ARDS) remains a significant source of mortality in critically ill patients. Characterised by acute, widespread alveolar inflammation and pulmonary oedema, its pathophysiological heterogeneity has meant that targeted treatments have remained elusive. Metabolomic analysis has made initial steps in characterising the underlying metabolic derangements of ARDS as an indicator of phenotypical class and has identified mitochondrial dysfunction as a potential therapeutic target. Mesenchymal stem cells and their derived extracellular vesicles have shown significant promise as potential therapies in delivering mitochondria in order to redivert metabolism onto physiological pathways.

Indexed as

Cell- and Tissue-Based TherapyEnergy MetabolismHumansMesenchymal Stem Cell TransplantationMetabolomicsMitochondriaPhenotypeRespiratory Distress Syndrome

Identifiers

PMID32620587
PMCPMC9488567

What OpenQuestion holds

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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.