Association of Chlamydia trachomatis, C. pneumoniae, and IL-6 and IL-8 Gene alterations with heart diseases

Detalhes bibliográficos
Autor(a) principal: Almeida, Núbia Caroline Costa de
Data de Publicação: 2019
Outros Autores: Queiroz, Maria Alice Freitas, Lima, Sandra Souza, Costa, Igor Brasil, Fossa, Marco Antonio Ayin, Vallinoto, Antonio Carlos Rosário, Ishak, Marluísa de Oliveira Guimarães, Ishak, Ricardo
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Digital do Instituto Evandro Chagas (Patuá)
Texto Completo: https://patua.iec.gov.br/handle/iec/3594
Resumo: Atherosclerosis is a progressive disease characterized by chronic inflammation of the arterial walls, associated with genetic and infectious factors. The present study investigated the involvement of Chlamydia trachomatis and Chlamydia pneumoniae infections and immunological markers (C-reactive protein, CRP, TNF-alpha, IL-6, IL-8, and IL-10) in the process of atherosclerosis. The evaluation included 159 patients for surgical revascularization (CAD) and 71 patients for surgical heart valve disease (HVD) at three hospitals in Belem, Brazil. The control group (CG) comprised 300 healthy individuals. Blood samples collected before surgery were used for antibodies detection (enzyme immunoassay), CRP (immunoturbidimetry) and IL-6 levels (enzyme immunoassay). Tissue fragments (atheroma plaque, heart valve and ascending aorta) were collected during surgery and subjected to qPCR for detection of bacterial DNA. Promoter region polymorphisms of eachmarker and relative quantification of TNF-alpha, IL-8, and IL-10 gene expression were performed. Demography and social information were similar to the general population involved with both diseases. Antibody prevalence to C. trachomatis was 30.6, 20.3, and 36.7% (in the CAD, HVD, and CG, respectively) and to C. pneumoniae was 83.6, 84.5, and 80.3% (in the CAD, HVD, and CG, respectively). C. trachomatis cryptic plasmid DNA was detected in 7.4% of the samples. Frequency of IL6-174G > C polymorphism was higher in CAD and HVD than in CG regardless of previous exposure to Chlamydia. Previous C. trachomatis infection showed involvement in HVD and CAD. Significant association between disease and previous C. pneumoniae infection was found only among HVD. GG genotype of IL6-174G > C is apparently a risk factor for heart disease, whereas AT genotype of IL8-251A > T was mainly involved in valvulopathies, including patients with prior exposure to C. pneumoniae.
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spelling Almeida, Núbia Caroline Costa deQueiroz, Maria Alice FreitasLima, Sandra SouzaCosta, Igor BrasilFossa, Marco Antonio AyinVallinoto, Antonio Carlos RosárioIshak, Marluísa de Oliveira GuimarãesIshak, Ricardo2019-02-18T18:03:47Z2019-02-18T18:03:47Z2019ALMEIDA, Nubia Caroline Costa et al. Association of Chlamydia trachomatis, C. pneumoniae, and IL-6 and IL-8 Gene alterations with heart diseases. Frontiers in Immunology, v. 10 n. 87, Feb. 2019.1664-3224https://patua.iec.gov.br/handle/iec/359410.3389/fimmu.2019.00087Atherosclerosis is a progressive disease characterized by chronic inflammation of the arterial walls, associated with genetic and infectious factors. The present study investigated the involvement of Chlamydia trachomatis and Chlamydia pneumoniae infections and immunological markers (C-reactive protein, CRP, TNF-alpha, IL-6, IL-8, and IL-10) in the process of atherosclerosis. The evaluation included 159 patients for surgical revascularization (CAD) and 71 patients for surgical heart valve disease (HVD) at three hospitals in Belem, Brazil. The control group (CG) comprised 300 healthy individuals. Blood samples collected before surgery were used for antibodies detection (enzyme immunoassay), CRP (immunoturbidimetry) and IL-6 levels (enzyme immunoassay). Tissue fragments (atheroma plaque, heart valve and ascending aorta) were collected during surgery and subjected to qPCR for detection of bacterial DNA. Promoter region polymorphisms of eachmarker and relative quantification of TNF-alpha, IL-8, and IL-10 gene expression were performed. Demography and social information were similar to the general population involved with both diseases. Antibody prevalence to C. trachomatis was 30.6, 20.3, and 36.7% (in the CAD, HVD, and CG, respectively) and to C. pneumoniae was 83.6, 84.5, and 80.3% (in the CAD, HVD, and CG, respectively). C. trachomatis cryptic plasmid DNA was detected in 7.4% of the samples. Frequency of IL6-174G > C polymorphism was higher in CAD and HVD than in CG regardless of previous exposure to Chlamydia. Previous C. trachomatis infection showed involvement in HVD and CAD. Significant association between disease and previous C. pneumoniae infection was found only among HVD. GG genotype of IL6-174G > C is apparently a risk factor for heart disease, whereas AT genotype of IL8-251A > T was mainly involved in valvulopathies, including patients with prior exposure to C. pneumoniae.Conselho Nacional de Desenvolvimento Cientifico e Tecnologico/Programa de Apoio a Nucleos de Excelencia/Fundacao Amazonia de Amparo a Estudos e Pesquisas do Para (CNPq/PRONEX/FAPESPA) ICAAF092/2010; Pro-reitoria de Pesquisa e Pos-Graduacao-PROPESP/UFPA (PAPQ-2018)Federal University of Pará. Institute of Biological Sciences. Virus Laboratory. Belém, PA, Brazil.Federal University of Pará. Institute of Biological Sciences. Virus Laboratory. Belém, PA, Brazil.Federal University of Pará. Institute of Biological Sciences. Virus Laboratory. Belém, PA, Brazil.Ministério da Saúde. Secretaria de Vigilância em Saúde. Instituto Evandro Chagas. Ananindeua, PA, Brasil.Portuguese Beneficent Hospital. Cardiology Unit. Belém, PA, Brazil.Federal University of Pará. Institute of Biological Sciences. Virus Laboratory. Belém, PA, Brazil.Federal University of Pará. Institute of Biological Sciences. Virus Laboratory. Belém, PA, Brazil.engFrontiers MediaAssociation of Chlamydia trachomatis, C. pneumoniae, and IL-6 and IL-8 Gene alterations with heart diseasesinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleSistema CardiovascularAteroscleroseVasos Coronários / anatomia & histologiaValva Aórtica / anatomia & histologiaChlamydia trachomatis / patogenicidadeChlamydophila pneumoniae / patogenicidadeBiomarcadores / análiseInfecções por Chlamydia / patogenicidadeinfo:eu-repo/semantics/openAccessreponame:Repositório Digital do Instituto Evandro Chagas (Patuá)instname:Instituto Evandro Chagas (IEC)instacron:IECORIGINALAssociation of Chlamydia trachomatis, C. pneumoniae, and IL-6 and IL-8 Gene alterations with heart diseases.pdfAssociation of Chlamydia trachomatis, C. pneumoniae, and IL-6 and IL-8 Gene alterations with heart diseases.pdfapplication/pdf1719953https://patua.iec.gov.br/bitstreams/2c1619e1-f7ee-4a40-af59-f755e9a97870/downloadc0dd173e79b10abd15e4a4d3a0bf56a1MD51LICENSElicense.txtlicense.txttext/plain; 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dc.title.pt_BR.fl_str_mv Association of Chlamydia trachomatis, C. pneumoniae, and IL-6 and IL-8 Gene alterations with heart diseases
title Association of Chlamydia trachomatis, C. pneumoniae, and IL-6 and IL-8 Gene alterations with heart diseases
spellingShingle Association of Chlamydia trachomatis, C. pneumoniae, and IL-6 and IL-8 Gene alterations with heart diseases
Almeida, Núbia Caroline Costa de
Sistema Cardiovascular
Aterosclerose
Vasos Coronários / anatomia & histologia
Valva Aórtica / anatomia & histologia
Chlamydia trachomatis / patogenicidade
Chlamydophila pneumoniae / patogenicidade
Biomarcadores / análise
Infecções por Chlamydia / patogenicidade
title_short Association of Chlamydia trachomatis, C. pneumoniae, and IL-6 and IL-8 Gene alterations with heart diseases
title_full Association of Chlamydia trachomatis, C. pneumoniae, and IL-6 and IL-8 Gene alterations with heart diseases
title_fullStr Association of Chlamydia trachomatis, C. pneumoniae, and IL-6 and IL-8 Gene alterations with heart diseases
title_full_unstemmed Association of Chlamydia trachomatis, C. pneumoniae, and IL-6 and IL-8 Gene alterations with heart diseases
title_sort Association of Chlamydia trachomatis, C. pneumoniae, and IL-6 and IL-8 Gene alterations with heart diseases
author Almeida, Núbia Caroline Costa de
author_facet Almeida, Núbia Caroline Costa de
Queiroz, Maria Alice Freitas
Lima, Sandra Souza
Costa, Igor Brasil
Fossa, Marco Antonio Ayin
Vallinoto, Antonio Carlos Rosário
Ishak, Marluísa de Oliveira Guimarães
Ishak, Ricardo
author_role author
author2 Queiroz, Maria Alice Freitas
Lima, Sandra Souza
Costa, Igor Brasil
Fossa, Marco Antonio Ayin
Vallinoto, Antonio Carlos Rosário
Ishak, Marluísa de Oliveira Guimarães
Ishak, Ricardo
author2_role author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Almeida, Núbia Caroline Costa de
Queiroz, Maria Alice Freitas
Lima, Sandra Souza
Costa, Igor Brasil
Fossa, Marco Antonio Ayin
Vallinoto, Antonio Carlos Rosário
Ishak, Marluísa de Oliveira Guimarães
Ishak, Ricardo
dc.subject.decsPrimary.pt_BR.fl_str_mv Sistema Cardiovascular
Aterosclerose
Vasos Coronários / anatomia & histologia
Valva Aórtica / anatomia & histologia
Chlamydia trachomatis / patogenicidade
Chlamydophila pneumoniae / patogenicidade
Biomarcadores / análise
Infecções por Chlamydia / patogenicidade
topic Sistema Cardiovascular
Aterosclerose
Vasos Coronários / anatomia & histologia
Valva Aórtica / anatomia & histologia
Chlamydia trachomatis / patogenicidade
Chlamydophila pneumoniae / patogenicidade
Biomarcadores / análise
Infecções por Chlamydia / patogenicidade
description Atherosclerosis is a progressive disease characterized by chronic inflammation of the arterial walls, associated with genetic and infectious factors. The present study investigated the involvement of Chlamydia trachomatis and Chlamydia pneumoniae infections and immunological markers (C-reactive protein, CRP, TNF-alpha, IL-6, IL-8, and IL-10) in the process of atherosclerosis. The evaluation included 159 patients for surgical revascularization (CAD) and 71 patients for surgical heart valve disease (HVD) at three hospitals in Belem, Brazil. The control group (CG) comprised 300 healthy individuals. Blood samples collected before surgery were used for antibodies detection (enzyme immunoassay), CRP (immunoturbidimetry) and IL-6 levels (enzyme immunoassay). Tissue fragments (atheroma plaque, heart valve and ascending aorta) were collected during surgery and subjected to qPCR for detection of bacterial DNA. Promoter region polymorphisms of eachmarker and relative quantification of TNF-alpha, IL-8, and IL-10 gene expression were performed. Demography and social information were similar to the general population involved with both diseases. Antibody prevalence to C. trachomatis was 30.6, 20.3, and 36.7% (in the CAD, HVD, and CG, respectively) and to C. pneumoniae was 83.6, 84.5, and 80.3% (in the CAD, HVD, and CG, respectively). C. trachomatis cryptic plasmid DNA was detected in 7.4% of the samples. Frequency of IL6-174G > C polymorphism was higher in CAD and HVD than in CG regardless of previous exposure to Chlamydia. Previous C. trachomatis infection showed involvement in HVD and CAD. Significant association between disease and previous C. pneumoniae infection was found only among HVD. GG genotype of IL6-174G > C is apparently a risk factor for heart disease, whereas AT genotype of IL8-251A > T was mainly involved in valvulopathies, including patients with prior exposure to C. pneumoniae.
publishDate 2019
dc.date.accessioned.fl_str_mv 2019-02-18T18:03:47Z
dc.date.available.fl_str_mv 2019-02-18T18:03:47Z
dc.date.issued.fl_str_mv 2019
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.citation.fl_str_mv ALMEIDA, Nubia Caroline Costa et al. Association of Chlamydia trachomatis, C. pneumoniae, and IL-6 and IL-8 Gene alterations with heart diseases. Frontiers in Immunology, v. 10 n. 87, Feb. 2019.
dc.identifier.uri.fl_str_mv https://patua.iec.gov.br/handle/iec/3594
dc.identifier.issn.-.fl_str_mv 1664-3224
dc.identifier.doi.-.fl_str_mv 10.3389/fimmu.2019.00087
identifier_str_mv ALMEIDA, Nubia Caroline Costa et al. Association of Chlamydia trachomatis, C. pneumoniae, and IL-6 and IL-8 Gene alterations with heart diseases. Frontiers in Immunology, v. 10 n. 87, Feb. 2019.
1664-3224
10.3389/fimmu.2019.00087
url https://patua.iec.gov.br/handle/iec/3594
dc.language.iso.fl_str_mv eng
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dc.publisher.none.fl_str_mv Frontiers Media
publisher.none.fl_str_mv Frontiers Media
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instacron:IEC
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