Evidence map›Paper›PMID 32321279›Full record

ArticleAmerican journal of physiology. Lung cellular and molecular physiology2020

Circulating miRNA 887 is differentially expressed in ARDS and modulates endothelial function.

Andrew J Goodwin, Pengfei Li, Perry V Halushka, James A Cook, Aman S Sumal, Hongkuan Fan

Open access · bronzeAbstract read
In one paragraph

Article in American journal of physiology. Lung cellular and molecular physiology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.9field-weighted citation impact, top 13% 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

15 citing papers in PubMed, 30 citations in OpenAlex.

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  15. The future of sepsis research: time to think differently?American journal of physiology. Lung cellular and molecular physiology · 2020
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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

6 authors at 1 institution in 1 country.

Andrew J GoodwinDivision of Pulmonary, Critical Care, Allergy, and Sleep Medicine, Department of Medicine, Medical University of South Carolina, Charleston, South Carolina.
Pengfei LiDepartment of Pathology and Laboratory Medicine, Medical University of South Carolina, Charleston, South Carolina.
Perry V HalushkaDepartment of Medicine, Medical University of South Carolina, Charleston, South Carolina.
James A CookDepartment of Neurosciences, Medical University of South Carolina, Charleston, South Carolina.
Aman S SumalDepartment of Pathology and Laboratory Medicine, Medical University of South Carolina, Charleston, South Carolina.
Hongkuan FanDepartment of Pathology and Laboratory Medicine, Medical University of South Carolina, Charleston, South Carolina.
Medical University of South Carolina · US

Funding

The Beneficial Effects of Endothelial Progenitor Cells in the Vascular Dysfunction of SepsisR01GM113995 · NIGMS · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI FAN, HONGKUAN · 2015 to 2019
$1.9M
The Role of Pericytes in the Vascular Dysfunction of SepsisR01GM130653 · NIGMS · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI FAN, HONGKUAN · 2018 to 2021
$1.3M
University of Pittsburgh Clinical and Translational Science InstituteTL1TR000145 · NCATS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI REIS, STEVEN E · 2012 to 2015
$872k
The Role of Circulating Micro RNAs in ARDS Pathogenesis and OutcomesK23HL135263 · NHLBI · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI GOODWIN, ANDREW J · 2017 to 2019
$537k
NCATS NIH HHS TL1 TR000145NHLBI NIH HHS K23 HL135263NIGMS NIH HHS R01 GM113995NIGMS NIH HHS R01 GM130653NIH/NCATS UL1 TR00145
6 · The paper itself

Abstract

Circulating microRNAs (miRNAs) can be taken up by recipient cells and have been recently associated with the acute respiratory distress syndrome (ARDS). Their role in host predisposition to the syndrome is unknown. The objective of the study was to identify circulating miRNAs associated with the development of sepsis-related ARDS and examine their impact on endothelial cell gene expression and function. We determined miRNA levels in plasma collected from subjects during the first 24 h of admission to a tertiary intensive care unit for sepsis. A miRNA that was differentially expressed between subjects who did and did not develop ARDS was identified and was transfected into human pulmonary microvascular endothelial cells (HPMECs). RNA sequencing, in silico analysis, cytokine expression, and leukocyte migration assays were used to determine the impact of this miRNA on gene expression and cell function. In two cohorts, circulating miR-887-3p levels were elevated in septic patients who developed ARDS compared with those who did not. Transfection of miR-887-3p into HPMECs altered gene expression, including the upregulation of several genes previously associated with ARDS (e.g.,

Indexed as

Gene Expression RegulationCell MovementChemokinesCirculating MicroRNACohort StudiesEndothelial CellsFemaleHumansLungMaleMicroRNAsMicrovesselsMiddle AgedNeutrophilsRespiratory Distress SyndromeChemokinesCirculating MicroRNAMicroRNAsMIRN887 microRNA, humanacute respiratory distress syndromechemokinesleukocytesmicroRNAssepsis

Identifiers

PMID32321279
PMCPMC7347270
OpenAlexW3019826795

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.