Evidence map›Paper›PMID 30622219›Full record

ArticleClinical science (London, England : 1979)2019

Poldip2 deficiency protects against lung edema and vascular inflammation in a model of acute respiratory distress syndrome.

Steven J Forrester, Qian Xu, Daniel S Kikuchi, Derick Okwan-Duodu, Ana Carolina Campos, Elizabeth A Faidley, Guogang Zhang, Bernard Lassègue, Ruxana T Sadikot, Kathy K Griendling and 1 more

Open access · greenAbstract read
In one paragraph

Article in Clinical science (London, England : 1979), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

17 citing papers in PubMed, 25 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

11 authors at 2 institutions in 3 countries.

Steven J ForresterDivision of Cardiology, Department of Medicine, Emory University, Atlanta, GA 30322, U.S.A.
Qian XuDivision of Cardiology, Department of Medicine, Emory University, Atlanta, GA 30322, U.S.A.
Daniel S KikuchiDivision of Cardiology, Department of Medicine, Emory University, Atlanta, GA 30322, U.S.A.
Derick Okwan-DuoduDivision of Cardiology, Department of Medicine, Emory University, Atlanta, GA 30322, U.S.A.
Ana Carolina CamposDivision of Cardiology, Department of Medicine, Emory University, Atlanta, GA 30322, U.S.A.
Elizabeth A FaidleyDivision of Cardiology, Department of Medicine, Emory University, Atlanta, GA 30322, U.S.A.
Guogang ZhangDepartment of Cardiovascular Medicine, Xiangya Hospital, Central South University, Changsha 410008, China.
Bernard LassègueDivision of Cardiology, Department of Medicine, Emory University, Atlanta, GA 30322, U.S.A.
Ruxana T SadikotDepartment of Veterans Affairs, Atlanta VAMC, Atlanta, GA 30033, U.S.A.
Kathy K GriendlingDivision of Cardiology, Department of Medicine, Emory University, Atlanta, GA 30322, U.S.A.
Marina S HernandesDivision of Cardiology, Department of Medicine, Emory University, Atlanta, GA 30322, U.S.A. mshern2@emory.edu.ORCID 0000-0001-6238-1441
Emory University · USCentral South University · CN

Funding

T cell triggering events and hypertensionP01HL095070 · NHLBI · EMORY UNIVERSITY · PI JO, HANJOONG · 2009 to 2019
$20.5M
Research Trainng in Academic CardiologyT32HL007745 · NHLBI · EMORY UNIVERSITY · PI TAYLOR, WILLIAM ROBERT · 1994 to 2023
$10.6M
BLRD VA I01 BX001786NHLBI NIH HHS P01 HL095070NHLBI NIH HHS T32 HL007745
6 · The paper itself

Abstract

Acute respiratory distress syndrome (ARDS) in a deadly disease that can be brought on by endotoxins such as lipopolysaccharide (LPS). ARDS is characterized by vascular permeability, a severe inflammatory response, lung leukocyte infiltration, and resultant lung edema. Polymerase δ-interacting protein 2 (Poldip2) is a novel regulator of blood-brain barrier permeability; however, its role in regulating lung permeability and vascular inflammation is unknown. Here, the role of Poldip2 in regulating vascular permeability and inflammation in a mouse model of ARDS was assessed. Heterozygous deletion of Poldip2 was found to reduce LPS-induced mortality within 20 h, lung inflammatory signaling, and leukocyte infiltration. Moreover, reduced Poldip2-suppressed LP-induced vascular cell adhesion molecule (VCAM)-1 induction, leukocyte recruitment, and mitochondrial reactive oxygen species (ROS) production

Indexed as

Capillary PermeabilityAnimalsCell AdhesionCoculture TechniquesCytokinesDisease Models, AnimalEndothelial CellsFemaleHumansLeukocytesLungMaleMice, Inbred C57BLMitochondrial ProteinsNuclear ProteinsPulmonary EdemaCytokinesMitochondrial Proteinsmitogenin 1 protein, mouseNuclear ProteinsPOLDIP2 protein, humanReactive Oxygen SpeciesVascular Cell Adhesion Molecule-1acute respiratory distress syndromeinflammationleukocytePoldip2

Identifiers

PMID30622219
PMCPMC7954131
OpenAlexW2909773817

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.