Evidence map›Paper›PMID 26312551›Full record

Observational studyArquivos brasileiros de cardiologia2015

Assessment of Galectin-3 Polymorphism in Subjects with Chronic Chagas Disease.

Gabriela da Silva Cruz, Ana Luiza Dias Angelo, Ticiana Ferreira Larocca, Carolina Thé Macedo, Márcia Noya-Rabelo, Luís Claudio Lemos Correia, Jorge Andion Torreão, Bruno Solano de Freitas Souza, Ricardo Ribeiro Dos Santos, Milena Botelho Pereira Soares

Open access · diamondAbstract readObservational Study
In one paragraph

Observational study in Arquivos brasileiros de cardiologia, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 1 pooled it
0.3field-weighted citation impact, top 40% 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

5 citing papers in PubMed, 1 synthesis or guideline pooled it, 11 citations in OpenAlex.

  1. Galectin-3 and fibrosis intensity in Chronic Chagas Cardiomyopathy: a systematic review.Revista do Instituto de Medicina Tropical de Sao Paulo · 2022
    Pooled it
  2. Review
  3. Article
  4. Review
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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

10 authors at 2 institutions in 1 country.

Gabriela da Silva CruzCentro de Biotecnologia e Terapia Celular, Hospital São Rafael, Salvador, BA, Brazil.
Ana Luiza Dias AngeloCentro de Biotecnologia e Terapia Celular, Hospital São Rafael, Salvador, BA, Brazil.
Ticiana Ferreira LaroccaCentro de Biotecnologia e Terapia Celular, Hospital São Rafael, Salvador, BA, Brazil.
Carolina Thé MacedoCentro de Biotecnologia e Terapia Celular, Hospital São Rafael, Salvador, BA, Brazil.
Márcia Noya-RabeloDepartamento de Cardiologia, Hospital São Rafael, Salvador, BA, Brazil.
Luís Claudio Lemos CorreiaDepartamento de Cardiologia, Hospital São Rafael, Salvador, BA, Brazil.
Jorge Andion TorreãoDepartamento de Cardiologia, Hospital São Rafael, Salvador, BA, Brazil.
Bruno Solano de Freitas SouzaCentro de Biotecnologia e Terapia Celular, Hospital São Rafael, Salvador, BA, Brazil.
Ricardo Ribeiro Dos SantosCentro de Biotecnologia e Terapia Celular, Hospital São Rafael, Salvador, BA, Brazil.
Milena Botelho Pereira SoaresCentro de Biotecnologia e Terapia Celular, Hospital São Rafael, Salvador, BA, Brazil.
Fundação Oswaldo Cruz · BRHospital São Rafael · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundGalectin-3, a β-galactoside binding lectin, has been described as a mediator of cardiac fibrosis in experimental studies and as a risk factor associated with cardiovascular events in subjects with heart failure. Previous studies have evaluated the genetic susceptibility to Chagas disease in humans, including the polymorphisms of cytokine genes, demonstrating correlations between the genetic polymorphism and cardiomyopathy development in the chronic phase. However, the relationship between the galectin-3 single nucleotide polymorphism (SNP) and phenotypic variations in Chagas disease has not been evaluated.

objectiveThe present study aimed to determine whether genetic polymorphisms of galectin-3 may predispose to the development of cardiac forms of Chagas disease.

methodsFifty-five subjects with Chagas disease were enrolled in this observational study. Real-time polymerase chain reaction (PCR) was used for genotyping the variants rs4644 and rs4652 of the galectin-3 gene.

resultsFor the SNP rs4644, the relative risk for the cardiac form was not associated with the genotypes AA (OR = 0.79, p = 0.759), AC (OR = 4.38, p = 0.058), or CC (OR = 0.39, p = 0.127). Similarly, for the SNP rs4652, no association was found between the genotypes AA (OR = 0.64, p = 0.571), AC (OR = 2.85, p = 0.105), or CC (OR = 0.49, p = 0.227) and the cardiac form of the disease.

conclusionOur results showed no association between the different genotypes for both SNPs of the galectin-3 gene and the cardiac form of Chagas disease.

Indexed as

Genetic Association StudiesPolymorphism, Single NucleotideAgedBlood ProteinsChagas DiseaseChronic DiseaseEchocardiography, DopplerFemaleFibrosisGalectin 3GalectinsGene FrequencyGenetic Predisposition to DiseaseHumansMagnetic Resonance ImagingMaleBlood ProteinsGalectin 3GalectinsLGALS3 protein, humanPregnancy Proteins

Identifiers

PMID26312551
PMCPMC4651405
OpenAlexW2278746475

What OpenQuestion holds

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LicenceCC BY-NC
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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.