Evidence map›Paper›PMID 32983159›Full record

ArticleFrontiers in immunology2020

RvE1 Attenuates Polymicrobial Sepsis-Induced Cardiac Dysfunction and Enhances Bacterial Clearance.

Jianmin Chen, Gareth S D Purvis, Debora Collotta, Sura Al Zoubi, Michelle A Sugimoto, Antonino Cacace, Lukas Martin, Roman A Colas, Massimo Collino, Jesmond Dalli and 1 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
3.3field-weighted citation impact, top 7% 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

20 citing papers in PubMed, 36 citations in OpenAlex.

  1. Defective efferocytosis in diabetes: molecular mechanisms and emerging therapeutic strategies.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2026
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  11. Lipoxin AFASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2023
    Article
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  13. Article
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  15. Protective Potential of Maresins in Cardiovascular Diseases.Frontiers in cardiovascular medicine · 2022
    Review
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  17. Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 4 institutions in 5 countries.

Jianmin ChenBarts and the London School of Medicine and Dentistry, William Harvey Research Institute, Queen Mary University of London, London, United Kingdom.
Gareth S D PurvisSir William Dunn School of Pathology, University of Oxford, Oxford, United Kingdom.
Debora CollottaDepartment of Drug Science and Technology, University of Turin, Turin, Italy.
Sura Al ZoubiBarts and the London School of Medicine and Dentistry, William Harvey Research Institute, Queen Mary University of London, London, United Kingdom.
Michelle A SugimotoBarts and the London School of Medicine and Dentistry, William Harvey Research Institute, Queen Mary University of London, London, United Kingdom.
Antonino CacaceBarts and the London School of Medicine and Dentistry, William Harvey Research Institute, Queen Mary University of London, London, United Kingdom.
Lukas MartinBarts and the London School of Medicine and Dentistry, William Harvey Research Institute, Queen Mary University of London, London, United Kingdom.
Roman A ColasBarts and the London School of Medicine and Dentistry, William Harvey Research Institute, Queen Mary University of London, London, United Kingdom.
Massimo CollinoDepartment of Drug Science and Technology, University of Turin, Turin, Italy.
Jesmond DalliBarts and the London School of Medicine and Dentistry, William Harvey Research Institute, Queen Mary University of London, London, United Kingdom.
Christoph ThiemermannBarts and the London School of Medicine and Dentistry, William Harvey Research Institute, Queen Mary University of London, London, United Kingdom.
William Harvey Research Institute · GBQueen Mary University of London · GBUniversity of Turin · ITUniversity of Oxford · GB

Funding

Wellcome TrustWellcome Trust 107613/Z/15/Z
6 · The paper itself

Abstract

The development of cardiac dysfunction caused by microbial infection predicts high mortality in sepsis patients. Specialized pro-resolving mediators (SPMs) mediate resolution of inflammation in many inflammatory diseases, and are differentially expressed in plasma of sepsis patients. Here, we investigated whether the levels of SPMs are altered in the murine septic heart following polymicrobial sepsis-induced cardiac dysfunction. Ten weeks-old male C57BL/6 mice were subjected to polymicrobial sepsis induced by cecal ligation and puncture (CLP), which is a clinically relevant sepsis model receiving analgesics, antibiotics, and fluid resuscitation. CLP caused a significant systolic dysfunction assessed by echocardiography. The hearts were subjected to LC-MS/MS based lipid mediator profiling. Many SPMs were significantly reduced in septic hearts, among which RvE1 had a ~93-fold reduction. Treatment of CLP mice with synthetic RvE1 (1 μg/mouse

Indexed as

AnimalsBacterial LoadBiomarkersDisease Models, AnimalEchocardiographyEicosapentaenoic AcidFlow CytometryGene Expression RegulationHeart DiseasesHeart Function TestsImmunityInflammation MediatorsLipid MetabolismMacrophagesMiceModels, Biological5S,12R,18R-trihydroxy-6Z,8E,10E,14Z,16E-eicosapentaenoic acidBiomarkersEicosapentaenoic AcidInflammation Mediatorsbacterial clearancecardiomyopathyimmune responsepolymicrobial sepsisresolvin E1

Identifiers

PMID32983159
PMCPMC7492649
OpenAlexW3082082167

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.