Evidence map›Paper›PMID 32876202›Full record

ArticleArquivos brasileiros de cardiologia2020

Early Changes in Circulating Interleukins and Residual Inflammatory Risk After Acute Myocardial Infarction.

Maria E R Coste, Carolina N França, Maria Cristina Izar, Daniela Teixeira, Mayari E Ishimura, Ieda Longo-Maugeri, Amanda S Bacchin, Henrique Tria Bianco, Flavio T Moreira, Ibraim Masciarelli Pinto and 5 more

Abstract read
In one paragraph

Article in Arquivos brasileiros de cardiologia, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
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

7 citing papers in PubMed.

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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

15 authors.

Maria E R CosteUniversidade Federal de São Paulo, São Paulo, SP - Brasil.
Carolina N FrançaUniversidade de Santo Amaro, São Paulo, SP - Brasil.
Maria Cristina IzarUniversidade Federal de São Paulo, São Paulo, SP - Brasil.ORCID 0000-0002-5738-2623
Daniela TeixeiraUniversidade Federal de São Paulo, São Paulo, SP - Brasil.
Mayari E IshimuraUniversidade Federal de São Paulo, São Paulo, SP - Brasil.
Ieda Longo-MaugeriUniversidade Federal de São Paulo, São Paulo, SP - Brasil.
Amanda S BacchinUniversidade Federal de São Paulo, São Paulo, SP - Brasil.
Henrique Tria BiancoUniversidade Federal de São Paulo, São Paulo, SP - Brasil.ORCID 0000-0001-6746-8327
Flavio T MoreiraUniversidade Federal de São Paulo, São Paulo, SP - Brasil.
Ibraim Masciarelli PintoInstituto Dante Pazzanese de Cardiologia, São Paulo, SP - Brasil.
Gilberto SzarfUniversidade Federal de São Paulo, São Paulo, SP - Brasil.
Adriano Mendes CaixetaUniversidade Federal de São Paulo, São Paulo, SP - Brasil.
Otavio BerwangerHospital Israelita Albert Einstein, São Paulo, SP - Brasil.
Iran GonçalvesUniversidade Federal de São Paulo, São Paulo, SP - Brasil.
Francisco A H FonsecaUniversidade Federal de São Paulo, São Paulo, SP - Brasil.ORCID 0000-0002-9911-4598

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPatients with acute myocardial infarction may have a large infarcted area and ventricular dysfunction despite early thrombolysis and revascularization.

objectiveTo investigate the behavior of circulating cytokines in patients with ST-segment elevation myocardial infarction (STEMI) and their relationship with ventricular function.

methodsIn the BATTLE-AMI (B and T Types of Lymphocytes Evaluation in Acute Myocardial Infarction) trial, patients with STEMI were treated with a pharmacoinvasive strategy. The plasma levels of cytokines (IL-1 β , IL-4, IL-6, IL-10, and IL-18) were tested using enzyme-linked immunosorbent assay (ELISA) at baseline and after 30 days. Infarcted mass and left ventricular ejection fraction (LVEF) were examined by 3-T cardiac magnetic resonance imaging. All p-values < 0.05 were considered statistically significant.

resultsCompared to baseline, lower levels were detected for IL-1 β (p = 0.028) and IL-18 (p < 0.0001) 30 days after STEMI, whereas higher levels were observed for IL-4 (p = 0.001) and IL-10 (p < 0.0001) at that time point. Conversely, no changes were detected for IL-6 levels (p = 0.63). The levels of high-sensitivity C-reactive protein and IL-6 correlated at baseline (rho = 0.45, p < 0.0001) and 30 days after STEMI (rho = 0.29, p = 0.009). At baseline, correlation between IL-6 levels and LVEF was also observed (rho = -0.50, p = 0.004).

conclusionsDuring the first month post-MI, we observed a marked improvement in the balance of pro- and anti-inflammatory cytokines, except for IL-6. These findings suggest residual inflammatory risk. (Arq Bras Cardiol. 2020; [online].ahead print, PP.0-0).

Indexed as

Myocardial InfarctionST Elevation Myocardial InfarctionBiomarkersHumansInterleukinsStroke VolumeVentricular Function, LeftBiomarkersInterleukins

Identifiers

PMID32876202
PMCPMC8133737

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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.