Evidence map›Paper›PMID 30650073›Full record

ArticlePLoS neglected tropical diseases2019

Association study between CCR2-CCR5 genes polymorphisms and chronic Chagas heart disease in Wichi and in admixed populations from Argentina.

Natalia Anahí Juiz, Elkyn Estupiñán, Daniel Hernández, Alejandra Garcilazo, Raúl Chadi, Gisela Morales Sanfurgo, Alejandro Gabriel Schijman, Silvia Andrea Longhi, Clara Isabel González

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In one paragraph

Article in PLoS neglected tropical diseases, 2019. 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
0.5field-weighted citation impact, top 34% 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, 8 citations in OpenAlex.

  1. Pooled it
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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

9 authors at 4 institutions in 2 countries.

Natalia Anahí JuizINGEBI-CONICET, Buenos Aires, Argentina.ORCID 0000-0003-3330-4425
Elkyn EstupiñánGIEM, Universidad Industrial de Santander, Bucaramanga, Colombia.
Daniel HernándezFacultad de Medicina, Universidad Nacional del Nordeste, Corrientes, Argentina.
Alejandra GarcilazoServicio de Cardiología, Hospital Pirovano, Buenos Aires, Argentina.
Raúl ChadiServicio de Cardiología, Hospital Pirovano, Buenos Aires, Argentina.
Gisela Morales SanfurgoServicio de Cardiología, Hospital Ramos Mejía, Buenos Aires, Argentina.
Alejandro Gabriel SchijmanINGEBI-CONICET, Buenos Aires, Argentina.
Silvia Andrea LonghiINGEBI-CONICET, Buenos Aires, Argentina.ORCID 0000-0001-5036-8717
Clara Isabel GonzálezGIEM, Universidad Industrial de Santander, Bucaramanga, Colombia.
Consejo Nacional de Investigaciones Científicas y Técnicas · ARIndustrial University of Santander · COHospital Ramos Mejía · ARNational University of the Northeast · AR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Several studies have proposed different genetic markers of susceptibility to develop chronic Chagas cardiomyopathy (CCC). Many genes may be involved, each one making a small contribution. For this reason, an appropriate approach for this problematic is to study a large number of single nucleotide polymorphisms (SNPs) in individuals sharing a genetic background. Our aim was to analyze two CCR2 and seven CCR5 SNPs and their association to CCC in Argentina. A case-control study was carried out in 480 T. cruzi seropositive adults from Argentinean Gran Chaco endemic region (Wichi and Creole) and patients from Buenos Aires health centres. They were classified according to the Consensus on Chagas-Mazza Disease as non-demonstrated (non-DC group) or demonstrated (DC group) cardiomyopathy, i.e. asymptomatic or with CCC patients, respectively. Since, after allelic analysis, 2 out of 9 studied SNPs did not fit Hardy-Weinberg equilibrium in the unaffected non-DC group from Wichi patients, we analyzed them as a separate population. Only rs1800024T and rs41469351T in CCR5 gene showed significant differences within non-Wichi population (Creole + patients from Buenos Aires centres), being the former associated to protection, and the latter to risk of CCC. No evidence of association was observed between any of the analyzed CCR2-CCR5 gene polymorphisms and the development of CCC; however, the HHE haplotype was associated with protection in Wichi population. Our findings support the hypothesis that CCR2-CCR5 genes and their haplotypes are associated with CCC; however, depending on the population studied, different associations can be found. Therefore, the evolutionary context, in which the genes or haplotypes are associated with diseases, acquires special relevance.

Indexed as

Genetic Predisposition to DiseaseAdolescentAdultAgedAged, 80 and overArgentinaCase-Control StudiesChagas CardiomyopathyFemaleHaplotypesHumansMaleMiddle AgedPolymorphism, Single NucleotideReceptors, CCR2Receptors, CCR5CCR2 protein, humanCCR5 protein, humanReceptors, CCR2Receptors, CCR5

Identifiers

PMID30650073
PMCPMC6334923
OpenAlexW2909815477

What OpenQuestion holds

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LicenceCC BY
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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.