Evidence map›Paper›PMID 27182885›Full record

ArticlePLoS neglected tropical diseases2016

Genomic African and Native American Ancestry and Chagas Disease: The Bambui (Brazil) Epigen Cohort Study of Aging.

M Fernanda Lima-Costa, James Macinko, Juliana Vaz de Mello Mambrini, Sérgio Viana Peixoto, Alexandre Costa Pereira, Eduardo Tarazona-Santos, Antonio Luiz Pinho Ribeiro

Abstract read
In one paragraph

Article in PLoS neglected tropical diseases, 2016. 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
–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

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

  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

7 authors.

M Fernanda Lima-CostaFundação Oswaldo Cruz, Instituto de Pesquisas René Rachou, Belo Horizonte, Brazil.
James MacinkoUniversity of California, Fielding School of Public Health, Departments of Health Policy and Management and Community Health Sciences, Los Angeles, California, United States of America.
Juliana Vaz de Mello MambriniFundação Oswaldo Cruz, Instituto de Pesquisas René Rachou, Belo Horizonte, Brazil.
Sérgio Viana PeixotoFundação Oswaldo Cruz, Instituto de Pesquisas René Rachou, Belo Horizonte, Brazil.
Alexandre Costa PereiraUniversidade de São Paulo, Instituto do Coração, São Paulo, Brazil.
Eduardo Tarazona-SantosUniversidade Federal de Minas Gerais, Instituto de Ciências Biológicas, Departamento de Biologia Geral, Belo Horizonte, Brazil.
Antonio Luiz Pinho RibeiroUniversidade Federal de Minas Gerais, Hospital das Clínicas e Faculdade de Medicina, Belo Horizonte, Brazil.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe influence of genetic ancestry on Trypanosoma cruzi infection and Chagas disease outcomes is unknown. METHODOLOGY/PRINCIPAL

findingsWe used 370,539 Single Nucleotide Polymorphisms (SNPs) to examine the association between individual proportions of African, European and Native American genomic ancestry with T. cruzi infection and related outcomes in 1,341 participants (aged ≥ 60 years) of the Bambui (Brazil) population-based cohort study of aging. Potential confounding variables included sociodemographic characteristics and an array of health measures. The prevalence of T. cruzi infection was 37.5% and 56.3% of those infected had a major ECG abnormality. Baseline T. cruzi infection was correlated with higher levels of African and Native American ancestry, which in turn were strongly associated with poor socioeconomic circumstances. Cardiomyopathy in infected persons was not significantly associated with African or Native American ancestry levels. Infected persons with a major ECG abnormality were at increased risk of 15-year mortality relative to their counterparts with no such abnormalities (adjusted hazard ratio = 1.80; 95% 1.41, 2.32). African and Native American ancestry levels had no significant effect modifying this association. CONCLUSIONS/SIGNIFICANCE: Our findings indicate that African and Native American ancestry have no influence on the presence of major ECG abnormalities and had no influence on the ability of an ECG abnormality to predict mortality in older people infected with T. cruzi. In contrast, our results revealed a strong and independent association between prevalent T. cruzi infection and higher levels of African and Native American ancestry. Whether this association is a consequence of genetic background or differential exposure to infection remains to be determined.

Indexed as

Genetic Predisposition to DiseaseAgingBlack PeopleBrazilChagas CardiomyopathyChagas DiseaseCohort StudiesElectrocardiographyGenomicsHumansIndians, North AmericanPolymorphism, Single NucleotidePrevalenceProportional Hazards ModelsSocial ClassTrypanosoma cruzi

Identifiers

PMID27182885
PMCPMC4868305

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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.