Evidence map›Paper›PMID 32393333›Full record

ArticleInfectious diseases of poverty2020

CXCL9 and CXCL10 display an age-dependent profile in Chagas patients: a cohort study of aging in Bambui, Brazil.

Fernanda Fortes de Araújo, Karen Cecília Lima Torres, Sérgio Viana Peixoto, Antonio Luiz Pinho Ribeiro, Juliana Vaz Melo Mambrini, Vitor Bortolo Rezende, Maria Luiza Lima Silva, Antônio Ignácio Loyola Filho, Andréa Teixeira-Carvalho, Maria Fernanda Lima-Costa and 1 more

Open access · goldAbstract read
In one paragraph

Article in Infectious diseases of poverty, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

15 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
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  3. Toxoplasma gondii IgG Serointensity Is Positively Associated With Frailty.The journals of gerontology. Series A, Biological sciences and medical sciences · 2024
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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

11 authors at 3 institutions in 1 country.

Fernanda Fortes de AraújoIntegrated Research Group in Biomarkers, Rene Rachou Institute, Oswaldo Cruz Foundation, Avenida Augusto de Lima, 1715 - Barro Preto -, Belo Horizonte, Minas Gerais, 30190-002, Brazil.
Karen Cecília Lima TorresIntegrated Research Group in Biomarkers, Rene Rachou Institute, Oswaldo Cruz Foundation, Avenida Augusto de Lima, 1715 - Barro Preto -, Belo Horizonte, Minas Gerais, 30190-002, Brazil.
Sérgio Viana PeixotoCenter for Studies in Public Health and Aging, Rene Rachou Institute, Oswaldo Cruz Foundation, Belo Horizonte, Brazil.
Antonio Luiz Pinho RibeiroClinical Hospital and Faculty of Medicine, Federal University of Minas Gerais, Belo Horizonte, Brazil.
Juliana Vaz Melo MambriniCenter for Studies in Public Health and Aging, Rene Rachou Institute, Oswaldo Cruz Foundation, Belo Horizonte, Brazil.
Vitor Bortolo RezendeIntegrated Research Group in Biomarkers, Rene Rachou Institute, Oswaldo Cruz Foundation, Avenida Augusto de Lima, 1715 - Barro Preto -, Belo Horizonte, Minas Gerais, 30190-002, Brazil.
Maria Luiza Lima SilvaCenter for Studies in Public Health and Aging, Rene Rachou Institute, Oswaldo Cruz Foundation, Belo Horizonte, Brazil.
Antônio Ignácio Loyola FilhoCenter for Studies in Public Health and Aging, Rene Rachou Institute, Oswaldo Cruz Foundation, Belo Horizonte, Brazil.
Andréa Teixeira-CarvalhoIntegrated Research Group in Biomarkers, Rene Rachou Institute, Oswaldo Cruz Foundation, Avenida Augusto de Lima, 1715 - Barro Preto -, Belo Horizonte, Minas Gerais, 30190-002, Brazil.
Maria Fernanda Lima-CostaCenter for Studies in Public Health and Aging, Rene Rachou Institute, Oswaldo Cruz Foundation, Belo Horizonte, Brazil.
Olindo Assis Martins-FilhoIntegrated Research Group in Biomarkers, Rene Rachou Institute, Oswaldo Cruz Foundation, Avenida Augusto de Lima, 1715 - Barro Preto -, Belo Horizonte, Minas Gerais, 30190-002, Brazil. oamfilho@gmail.com.
Fundação Oswaldo Cruz · BRUniversidade Federal de Minas Gerais · BRUniversidade José do Rosário Vellano · BR

Funding

Fundação de Amparo à Pesquisa do Estado de Minas Gerais PP-SUS CDS - APQ-03590-13
6 · The paper itself

Abstract

backgroundChagas disease is endemic in Latin America and still represents an important public health problem in the region. Chronic cardiomyopathy is the most significant chronic form due to its association with morbidity and mortality. The last decade has seen increasing evidence that inflammatory cytokines and chemokines are responsible for the generation of inflammatory infiltrate and tissue damage, with chronic chagasic cardiomyopathy patients presenting a pro-inflammatory immune response. Although studies have evaluated the role of chemokines in experimental T. cruzi infection, few have addressed their systemic profile, especially for human infection and in aging populations. The present work aimed to use the data from a large population based study of older adults, conducted in an endemic area for Chagas disease, to examine the association between serum levels of cytokines and chemokines, T. cruzi infection and electrocardiogram (ECG) abnormality.

methodsThe present work evaluated serum levels of CCL2, CXCL9, CXCL10, CCL5, CXCL8, IL-1β, IL-6, TNF, IL-12 and IL-10 by Flow Cytometric Bead Array assay (CBA) and the results expressed in pg/ml. The baseline survey started in January 1st 1997, with 1284 participants of an aged population-based cohort. Participants signed an informed consent at baseline and at each subsequent visit and authorized death certificate and medical records verification.

resultsOur results demonstrated that Chagas disease patients had higher serum levels of CXCL9, CXCL10 and IL-1β and lower serum levels of CCL5 than non-infected subjects. Moreover, our data demonstrated that CXCL9 and CXCL10 increased in an age-dependent profile in Chagas disease patients.

conclusionTogether, this study provided evidences that serum biomarkers increase along the age continuum and may have potential implications for establishing clinical management protocols and therapeutic intervention in Chagas disease patients.

Indexed as

AgingAgedAged, 80 and overBiomarkersBrazilChagas DiseaseChemokine CXCL10Chemokine CXCL9Cohort StudiesElectrocardiographyFemaleHumansMaleMiddle AgedTrypanosoma cruziBiomarkersChemokine CXCL10Chemokine CXCL9CXCL10 protein, humanCXCL9 protein, humanChagas diseaseChemokinesCohortCytokinesImmune biomarkers

Identifiers

PMID32393333
PMCPMC7216412
OpenAlexW3027453330

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.