Evidence map›Paper›PMID 29166391›Full record

ArticlePloS one2017

Early kinetics of serum Interleukine-17A and infarct size in patients with reperfused acute ST-elevated myocardial infarction.

Thomas Bochaton, Nathan Mewton, NDieme Thiam, Fabien Lavocat, Delphine Baetz, Nathalie Dufay, Cyril Prieur, Eric Bonnefoy-Cudraz, Pierre Miossec, Michel Ovize

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.2field-weighted citation impact, top 18% 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

12 citing papers in PubMed, 16 citations in OpenAlex.

  1. Trial
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  9. Article
  10. Systemic effects of IL-17 in inflammatory arthritis.Nature reviews. Rheumatology · 2019
    Review
  11. Article
  12. Dynamic Profile of CD4Mediators of inflammation · 2019
    Article
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

10 authors at 3 institutions in 1 country.

Thomas BochatonINSERM U1060, CarMeN laboratory, Université de Lyon, Groupement Hospitalier Est, Bron, France.ORCID http://orcid.org/0000-0002-5889-7506
Nathan MewtonService d'explorations fonctionnelles Cardiovasculaires, Hôpital Louis Pradel, Hospices Civils de Lyon, Lyon, France.
NDieme ThiamImmunogénomique et Inflammation, Hôpital Edouard Herriot Pavillon P, Lyon, France.
Fabien LavocatImmunogénomique et Inflammation, Hôpital Edouard Herriot Pavillon P, Lyon, France.
Delphine BaetzINSERM U1060, CarMeN laboratory, Université de Lyon, Groupement Hospitalier Est, Bron, France.
Nathalie DufayNeuroBioTec, Groupement Hospitalier Est, Hôpital Neurologique Pierre Wertheimer, Lyon, France.
Cyril PrieurUnité de Soins Intensifs Cardiologiques, Hôpital Louis Pradel, Hospices Civils de Lyon, Lyon, France.
Eric Bonnefoy-CudrazINSERM U1060, CarMeN laboratory, Université de Lyon, Groupement Hospitalier Est, Bron, France.
Pierre MiossecImmunogénomique et Inflammation, Hôpital Edouard Herriot Pavillon P, Lyon, France.
Michel OvizeINSERM U1060, CarMeN laboratory, Université de Lyon, Groupement Hospitalier Est, Bron, France.
Hospices Civils de Lyon · FRUniversité Claude Bernard Lyon 1 · FRHôpital Louis Pradel · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundRecently, it was shown that interleukin-17A (IL-17A) is involved in the pathophysiology of reperfusion injury and associated with infarct size (IS) in experimental models of myocardial infarction. Our aim was to evaluate whether the IL-17A serum level and the IL-17A active fraction was correlated with IS in humans.

methods101 patients presenting with a ST-elevated Myocardial Infarction (STEMI) referred for primary percutaneous coronary intervention (PPCI) and 10 healthy controls were included. For each participant, blood samples at admission (H0) and 4 hours after admission (H4) were collected. IL-17A serum levels were assessed using ELISA and the active fraction was assessed with a functional test. IS was determined by peak troponin and peak CK levels for every patient and by contrast-enhanced cardiac magnetic resonance (ce-CMR) for 20 patients.

resultsThe IL-17A serum level was significantly increased in STEMI patients compared to healthy controls, (0.9 pg/mL IQR [0.0-3.2] at H0 and 1.0 pg/mL IQR [0.2-2.8] at H4 versus 0.2 pg/mL IQR [0.0-0.7] for healthy controls; p<0.005). At either time points, IL-17A levels did not correlate with IS as measured by peak troponin, peak CK pr ce-CMR. Also, no correlation was found between the active fraction of IL-17A and IS.

conclusionSerum IL-17A level is significantly increased in patients at the early phase of acute MI compared to healthy controls. However, the level of IL-17A in the early hours after reperfusion does not correlate with IS.

Indexed as

Myocardial ReperfusionBiomarkersCase-Control StudiesCohort StudiesFemaleHospitalizationHumansHuman Umbilical Vein Endothelial CellsInflammationInterleukin-17KineticsMaleMiddle AgedNeutrophilsST Elevation Myocardial InfarctionBiomarkersIL17A protein, humanInterleukin-17

Identifiers

PMID29166391
PMCPMC5699816
OpenAlexW2770346493

What OpenQuestion holds

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Registered trials

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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.