Evidence map›Paper›PMID 34031519›Full record

ArticleScientific reports2021

High plasma concentration of non-esterified polyunsaturated fatty acids is a specific feature of severe COVID-19 pneumonia.

Maxime Nguyen, Abderrahmane Bourredjem, Lionel Piroth, Bélaïd Bouhemad, Antoine Jalil, Gaetan Pallot, Naig Le Guern, Charles Thomas, Thomas Pilot, Victoria Bergas and 12 more

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in Scientific reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04435223 (Lipid Metabolism in COVID-19 Severe Pneumonia Compared With Severe Pneumonia Caused by Other Pathogen), which is not on this map. Cited by 25 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed, 1 pooled it
1.4field-weighted citation impact, top 16% 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.

NCT04435223 completednot on this map

Lipid Metabolism in COVID-19 Severe Pneumonia Compared With Severe Pneumonia Caused by Other Pathogen

TypeobservationalSponsorCentre Hospitalier Universitaire DijonRan2020 to 2020Enrolled62ConditionsCOVID-19 Severe Pneumonia, Severe Pneumonia Due to Other PathogeneArmsbiological assays in particular on the lipid metabolism
3 · Its place in the literature

Who cites it

25 citing papers in PubMed, 1 synthesis or guideline pooled it, 29 citations in OpenAlex.

  1. Pooled it
  2. The physiological effects of APOE genotype in healthy young/middle-aged individuals.Biological reviews of the Cambridge Philosophical Society · 2026
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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

22 authors at 3 institutions in 1 country.

Maxime NguyenDepartment of Anesthesiology and Intensive Care, CHU Dijon and University of Burgundy, François Mitterrand University Hospital, LNC UMR1231, 21000, Dijon, France. maxime.nguyensoenen@gmail.com.
Abderrahmane BourredjemInserm, CIC1432, Clinical Epidemiology Unit, Clinical Epidemiology/Clinical Trial Unit, Dijon University Hospital, Dijon, France.
Lionel PirothInserm, CIC1432, Clinical Epidemiology Unit, Clinical Epidemiology/Clinical Trial Unit, Dijon University Hospital, Dijon, France.
Bélaïd BouhemadDepartment of Anesthesiology and Intensive Care, CHU Dijon and University of Burgundy, François Mitterrand University Hospital, LNC UMR1231, 21000, Dijon, France.
Antoine JalilINSERM, LNC UMR1231, 21000, Dijon, France.
Gaetan PallotINSERM, LNC UMR1231, 21000, Dijon, France.
Naig Le GuernINSERM, LNC UMR1231, 21000, Dijon, France.
Charles ThomasUniv. Bourgogne Franche-Comté, LNC UMR1231, 21000, Dijon, France.
Thomas PilotINSERM, LNC UMR1231, 21000, Dijon, France.
Victoria BergasLipidomic Analytic Platform, University of Burgundy, Dijon, France.
Hélène ChoubleyLipidomic Analytic Platform, University of Burgundy, Dijon, France.
Jean-Pierre QuenotUniv. Bourgogne Franche-Comté, LNC UMR1231, 21000, Dijon, France.
Pierre-Emmanuel CharlesUniv. Bourgogne Franche-Comté, LNC UMR1231, 21000, Dijon, France.
Laurent LagrostUniv. Bourgogne Franche-Comté, LNC UMR1231, 21000, Dijon, France.
Valerie DeckertUniv. Bourgogne Franche-Comté, LNC UMR1231, 21000, Dijon, France.
Jean-Paul Pais de BarrosINSERM, LNC UMR1231, 21000, Dijon, France.
Pierre-Grégoire GuinotDepartment of Anesthesiology and Intensive Care, CHU Dijon and University of Burgundy, François Mitterrand University Hospital, LNC UMR1231, 21000, Dijon, France.
David MassonUniv. Bourgogne Franche-Comté, LNC UMR1231, 21000, Dijon, France.
Christine BinquetInserm, CIC1432, Clinical Epidemiology Unit, Clinical Epidemiology/Clinical Trial Unit, Dijon University Hospital, Dijon, France.
Thomas GautierUniv. Bourgogne Franche-Comté, LNC UMR1231, 21000, Dijon, France.
Mathieu BlotUniv. Bourgogne Franche-Comté, LNC UMR1231, 21000, Dijon, France.
Lymphonie study group
Inserm · FRMaison des Sciences sociales et des Humanités de Dijon · FRUniversité de Bourgogne · FR

Funding

Agence Nationale de la Recherche ANR-11 LABX-0021-01Centre Hospitalier Regional Universitaire De Dijon AOIc2020
6 · The paper itself

Abstract

COVID-19 pneumonia has specific features and outcomes that suggests a unique immunopathogenesis. Severe forms of COVID-19 appear to be more frequent in obese patients, but an association with metabolic disorders is not established. Here, we focused on lipoprotein metabolism in patients hospitalized for severe pneumonia, depending on COVID-19 status. Thirty-four non-COVID-19 and 27 COVID-19 patients with severe pneumonia were enrolled. Most of them required intensive care. Plasma lipid levels, lipoprotein metabolism, and clinical and biological (including plasma cytokines) features were assessed. Despite similar initial metabolic comorbidities and respiratory severity, COVID-19 patients displayed a lower acute phase response but higher plasmatic concentrations of non-esterified fatty acids (NEFAs). NEFA profiling was characterised by higher level of polyunsaturated NEFAs (mainly linoleic and arachidonic acids) in COVID-19 patients. Multivariable analysis showed that among severe pneumonia, COVID-19-associated pneumonia was associated with higher NEFAs, lower apolipoprotein E and lower high-density lipoprotein cholesterol concentrations, independently of body mass index, sequential organ failure (SOFA) score, and C-reactive protein levels. NEFAs and PUFAs concentrations were negatively correlated with the number of ventilator-free days. Among hospitalized patients with severe pneumonia, COVID-19 is independently associated with higher NEFAs (mainly linoleic and arachidonic acids) and lower apolipoprotein E and HDL concentrations. These features might act as mediators in COVID-19 pathogenesis and emerge as new therapeutic targets. Further investigations are required to define the role of NEFAs in the pathogenesis and the dysregulated immune response associated with COVID-19.Trial registration: NCT04435223.

Indexed as

AgedApolipoproteins EArachidonic AcidsCholesterol, HDLCOVID-19CytokinesFatty Acids, NonesterifiedFemaleHumansLinoleic AcidsMaleMiddle AgedPrincipal Component AnalysisSARS-CoV-2Severity of Illness IndexApolipoproteins EArachidonic AcidsCholesterol, HDLCytokinesFatty Acids, NonesterifiedLinoleic Acids

Identifiers

PMID34031519
PMCPMC8144366
OpenAlexW3111918376

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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.