Evidence map›Paper›PMID 33075041›Full record

ArticleArchivos de cardiologia de Mexico2020

Polimorfismo de genes de citocinas: ¿factores de riesgo cardiovascular en la población venezolana?

Mercedes Fernández-Mestre, Eva Salazar-Alcalá, Gelly Matos-González, Ingrid Márquez

Abstract readEnglish Abstract
In one paragraph

Article in Archivos de cardiologia de Mexico, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

4 authors.

Mercedes Fernández-MestreSección Inmunogenética, Laboratorio de Fisiopatología, Centro de Medicina Experimental Miguel Layrisse, Instituto Venezolano de Investigaciones Científicas, Caracas, Venezuela.
Eva Salazar-AlcaláSección Inmunogenética, Laboratorio de Fisiopatología, Centro de Medicina Experimental Miguel Layrisse, Instituto Venezolano de Investigaciones Científicas, Caracas, Venezuela.
Gelly Matos-GonzálezUnidad de Cardiología, Hospital General del Este Dr. Domingo Luciani. Caracas, Venezuela.
Ingrid Márquez>Unidad de Cardiología, Hospital General del Este Dr. Domingo Luciani. Caracas, Venezuela.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: To examine whether the polymorphisms of the IL6, TNFA and IL10 genes represent a risk marker for acute myocardial infarction (AMI) and to analyze their correlation with risk factors, age of occurrence and type of AMI. Method: Association study that included 310 unrelated Venezuelan individuals, grouped in 190 patients with AMI and 120 controls with or without cardiovascular risk factors. The IL6-174 G/C (rs1800795), TNFA -308 G/A (rs1800629), and IL10-1082 A/G (rs1800896), -819 C/T (rs1800871) and -592 C/A (rs1800872) polymorphisms were determined using the polymerase chain reaction technique with sequence-specific primers. Results: Comparison of genotypic and allelic frequencies, using adjusted logistic regression analysis for risk factors, showed a significantly increased frequency of the genotype combination G/G-A/A of TNFA-308 G/A (odds ratio [OR]: 3.8; p = 0.00007), GG/-C/C of IL6-174 G/C (OR: 2.3; p = 0.009), A/G-G/G of IL10-1082 A/G (OR: 3.8; p = 0.00001) and the GCC haplotype of IL10 (OR: 3.71; p = 0.0053) in infarcted patients compared to controls. Interactions between the IL10-1082 A/G and TNFA-308 G/A polymorphisms and hypertension were observed. Conclusions: The association of the variants of the TNFA, IL6 and IL10 genes with AMI suggest that the imbalance in the production of cytokines promotes an exacerbated inflammatory process, supporting the fundamental role of inflammation in all stages of the atherosclerotic process.

Indexed as

Acute coronary syndromeAcute myocardial infarctionCytokinesPolymorphism

Identifiers

PMID33075041
PMCPMC8351660

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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.