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Estudo dos polimorfismos GSTP1 (rs1695) e TNF A-308 (rs1800629) em pacientes com COVID-19 hospitalizados e associação com dados clínicos

Detalhes bibliográficos
Ano de defesa: 2024
Autor(a) principal: Vieira, Priscila da Silva Antunes lattes
Orientador(a): Lucio, Léia Carolina lattes
Banca de defesa: Lucio, Léia Carolina lattes, Pascotto, Claudicéia Risso lattes, Ghisi, Nédia de Castilhos lattes
Tipo de documento: Dissertação
Tipo de acesso: Acesso aberto
Idioma: por
Instituição de defesa: Universidade Estadual do Oeste do Paraná
Francisco Beltrão
Programa de Pós-Graduação: Programa de Pós-Graduação em Ciências Aplicadas à Saúde
Departamento: Centro de Ciências da Saúde
País: Brasil
Palavras-chave em Português:
Palavras-chave em Inglês:
Área do conhecimento CNPq:
Link de acesso: https://tede.unioeste.br/handle/tede/7311
Resumo: SARS-CoV-2, the new coronavirus agent of COVID-19, quickly spread throughout the world, progressing with diverse clinical manifestations, from asymptomatic, mild, moderate to severe forms, with a major outcome of death. It is still a challenge to understand the pathophysiology of SARS-CoV-2 for control measures and clinical management of the disease. Among the factors that affect the evolution of COVID-19 are: comorbidities, age, sex and lifestyle habits. Genetic factors are also the subject of investigations and may interfere with the susceptibility and evolution of the disease. The main objective of the study was to determine the allelic and genotypic frequency of GSTP1 (rs1695) and TNF A-308 (rs1800629) in patients hospitalized with COVID 19 and verify the association of polymorphisms with the severity, comorbidity, and outcome of hospitalization of patients in southern Brazil. In total, 236 patients positive for COVID-19 admitted to a reference hospital in southwestern Paraná participated in the research. A blood sample was collected from the individuals for genetic characterization using the techniques T-ARMS-PCR (tetra amplification refractory mutation system by Polymerase Chain Reaction) for rs1695 and ARMS-PCR (amplification refractory mutation system by PCR) for rs1800629. At the same time, a search was carried out in the patients' medical records to collect sociodemographic, clinical and comorbidity data. Subsequently, bivariate and multivariate analyses were conducted, including logistic regression. were Of the population, 58.1% were men and 41.9% were women; 63% were severe cases, and 37% were moderate; the hospital discharge outcome was 64%, and 36% died. The results showed that the ancestral allele was the most frequent in rs1695 (A = 71%) and rs1800629 (G = 61%) and that the genotypes AA (rs1695) and AG (rs1800629) were, respectively, 48.73% and 67.81%. For rs1695, both the A allele (OR = 2.9; 95%CI= 1.093–7.884; p=0.033) and the AG genotype (OR = 3.3; 95%CI= 1.185–9.375; p= 0.022) increase the chances of severity for COVID-19. For the rs1800629 polymorphism, no significant association was observed. Regarding hospital outcome, comorbidities, oxygen saturation and length of hospitalization, no association was observed with the investigated polymorphisms. Therefore, the study concludes that both the A allele and the AG genotype of GSTP1 rs1965 are suggestive markers of COVID-19 severity in the southern Brazilian population. And no relationship can be established for the rs1800629 polymorphism of TNF A-308.
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spelling Lucio, Léia Carolinahttp://lattes.cnpq.br/9357029990194108Treco, Fernando Rodrigohttp://lattes.cnpq.br/0633607976550229Lucio, Léia Carolinahttp://lattes.cnpq.br/9357029990194108Pascotto, Claudicéia Rissohttp://lattes.cnpq.br/9474794343913304Ghisi, Nédia de Castilhoshttp://lattes.cnpq.br/4542801151720873http://lattes.cnpq.br/8105725220202910Vieira, Priscila da Silva Antunes2024-07-22T18:36:48Z2024-05-22VIEIRA, Priscila da Silva Antunes. Estudo dos polimorfismos GSTP1 (rs1695) e TNF A-308 (rs1800629) em pacientes com COVID-19 hospitalizados e associação com dados clínicos. 2024. 55f. Dissertação (Mestrado em Ciências Aplicadas à Saúde) - Universidade Estadual do Oeste do Paraná, Francisco Beltrão, 2024.https://tede.unioeste.br/handle/tede/7311SARS-CoV-2, the new coronavirus agent of COVID-19, quickly spread throughout the world, progressing with diverse clinical manifestations, from asymptomatic, mild, moderate to severe forms, with a major outcome of death. It is still a challenge to understand the pathophysiology of SARS-CoV-2 for control measures and clinical management of the disease. Among the factors that affect the evolution of COVID-19 are: comorbidities, age, sex and lifestyle habits. Genetic factors are also the subject of investigations and may interfere with the susceptibility and evolution of the disease. The main objective of the study was to determine the allelic and genotypic frequency of GSTP1 (rs1695) and TNF A-308 (rs1800629) in patients hospitalized with COVID 19 and verify the association of polymorphisms with the severity, comorbidity, and outcome of hospitalization of patients in southern Brazil. In total, 236 patients positive for COVID-19 admitted to a reference hospital in southwestern Paraná participated in the research. A blood sample was collected from the individuals for genetic characterization using the techniques T-ARMS-PCR (tetra amplification refractory mutation system by Polymerase Chain Reaction) for rs1695 and ARMS-PCR (amplification refractory mutation system by PCR) for rs1800629. At the same time, a search was carried out in the patients' medical records to collect sociodemographic, clinical and comorbidity data. Subsequently, bivariate and multivariate analyses were conducted, including logistic regression. were Of the population, 58.1% were men and 41.9% were women; 63% were severe cases, and 37% were moderate; the hospital discharge outcome was 64%, and 36% died. The results showed that the ancestral allele was the most frequent in rs1695 (A = 71%) and rs1800629 (G = 61%) and that the genotypes AA (rs1695) and AG (rs1800629) were, respectively, 48.73% and 67.81%. For rs1695, both the A allele (OR = 2.9; 95%CI= 1.093–7.884; p=0.033) and the AG genotype (OR = 3.3; 95%CI= 1.185–9.375; p= 0.022) increase the chances of severity for COVID-19. For the rs1800629 polymorphism, no significant association was observed. Regarding hospital outcome, comorbidities, oxygen saturation and length of hospitalization, no association was observed with the investigated polymorphisms. Therefore, the study concludes that both the A allele and the AG genotype of GSTP1 rs1965 are suggestive markers of COVID-19 severity in the southern Brazilian population. And no relationship can be established for the rs1800629 polymorphism of TNF A-308.O SARS-CoV-2, coronavírus agente da COVID-19, rapidamente disseminou se em todo o mundo, progredindo com manifestações clínicas diversas, desde a forma assintomática, leve, moderada à grave, com grande desfecho de óbito. Ainda é um desafio a compreensão da fisiopatologia do SARS-CoV-2 para as medidas de controle e manejo clínico da doença. Dentre os fatores que interferem na evolução da COVID-19, estão idade, sexo, hábitos de vida e presença de comorbidades, além de fatores genéticos que são alvo de investigações e podem interferir na susceptibilidade e evolução da doença. O principal objetivo do estudo foi determinar a frequência alélica e genotípica de GSTP1 (rs1695) e TNF A-308 (rs1800629) nos pacientes hospitalizados com COVID-19 e verificar associação dos polimorfismos com a gravidade, comorbidade e o desfecho da hospitalização dos pacientes do sul do Brasil. A amostra foi composta por 236 pacientes positivos para COVID-19 internados em um hospital de referência do sudoeste paranaense. Foi coletado 5 mL de sangue dos indivíduos para caracterização genética, utilizando as técnicas T-ARMS-PCR (tetra amplification refractory mutation system by Polymerase Chain Reaction) para rs1695 e ARMS-PCR (amplification refractory mutation system by PCR) para rs1800629. Para coleta de dados sociodemográficos, clínicos e das comorbidades foi realizada busca em prontuários médicos dos pacientes. Posteriomente, foram conduzidas análises bivariada e multivariada, incluindo a regressão logística. Os resultados mostraram que 58,1% da amostra eram homens e 41,9% mulheres; 63% eram casos graves e 37% moderados; o desfecho de alta hospitalar foi de 64% e 36% foram a óbito. Em relação ao polimosrfismo genético, o alelo ancestral foi o mais frequente em rs1695 (A = 71%) e rs1800629 (G = 61%) e, que os genótipos AA (rs1695) e AG (rs1800629) foram, respectivamente, 48,73% e 67,81%. Para rs1695 tanto o alelo A (OR = 2,9; IC95%= 1,093–7,884; p=0,033) quanto o genótipo AG (OR = 3,3; IC95%= 1,185–9,375; p= 0,022), ampliam as chances de gravidade para COVID-19. Para o polimorfismo rs1800629 nenhuma associação significativa foi observada. Com relação ao desfecho hospitalar, comorbidades, saturação de oxigênio e tempo de hospitalização nenhuma associação foi observada com os polimorfismos investigados. Logo, o estudo conclui que tanto o alelo A quanto o genótipo AG de rs1965 de GSTP1 são marcadores sugestivos de gravidade da COVID-19 na população sul do Brasil. E nenhuma relação pode ser estabelecida para o polimorfismo rs1800629 de TNF A-308.Submitted by Almir Squinsani (almir.squinsani@unioeste.br) on 2024-07-22T18:36:47Z No. of bitstreams: 1 Priscila_Vieira_2024.pdf: 960910 bytes, checksum: 8ee203bb838bb0e02543b19d610b9c23 (MD5)Made available in DSpace on 2024-07-22T18:36:48Z (GMT). No. of bitstreams: 1 Priscila_Vieira_2024.pdf: 960910 bytes, checksum: 8ee203bb838bb0e02543b19d610b9c23 (MD5) Previous issue date: 2024-05-22application/pdfpor-5356284425524309716500Universidade Estadual do Oeste do ParanáFrancisco BeltrãoPrograma de Pós-Graduação em Ciências Aplicadas à SaúdeUNIOESTEBrasilCentro de Ciências da Saúdehttp://creativecommons.org/licenses/by-nc-nd/4.0/info:eu-repo/semantics/openAccessSARS-CoV-2SNPsGlutationa-S-TransferasecitocinaComorbidadesSARS-CoV-2Single-nucleotide polymorphism;Glutathione-S-transferaseCytokineComorbidityCIÊNCIAS DA SAÚDEEstudo dos polimorfismos GSTP1 (rs1695) e TNF A-308 (rs1800629) em pacientes com COVID-19 hospitalizados e associação com dados clínicosStudy of GSTP1 (rs1695) and TNF A-308 (rs1800629) polymorphisms in hospitalized COVID-19 patients and association with clinical statusinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/masterThesis6290525253230630664600600292441653440865123reponame:Biblioteca Digital de Teses e Dissertações do UNIOESTEinstname:Universidade Estadual do Oeste do Paraná (UNIOESTE)instacron:UNIOESTEORIGINALPriscila_Vieira_2024.pdfPriscila_Vieira_2024.pdfapplication/pdf960910http://tede.unioeste.br:8080/tede/bitstream/tede/7311/2/Priscila_Vieira_2024.pdf8ee203bb838bb0e02543b19d610b9c23MD52LICENSElicense.txtlicense.txttext/plain; charset=utf-82165http://tede.unioeste.br:8080/tede/bitstream/tede/7311/1/license.txtbd3efa91386c1718a7f26a329fdcb468MD51tede/73112024-07-22 15:36:48.308oai:tede.unioeste.br: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Biblioteca Digital de Teses e Dissertaçõeshttp://tede.unioeste.br/PUBhttp://tede.unioeste.br/oai/requestbiblioteca.repositorio@unioeste.bropendoar:2024-07-22T18:36:48Biblioteca Digital de Teses e Dissertações do UNIOESTE - Universidade Estadual do Oeste do Paraná (UNIOESTE)false
dc.title.por.fl_str_mv Estudo dos polimorfismos GSTP1 (rs1695) e TNF A-308 (rs1800629) em pacientes com COVID-19 hospitalizados e associação com dados clínicos
dc.title.alternative.eng.fl_str_mv Study of GSTP1 (rs1695) and TNF A-308 (rs1800629) polymorphisms in hospitalized COVID-19 patients and association with clinical status
title Estudo dos polimorfismos GSTP1 (rs1695) e TNF A-308 (rs1800629) em pacientes com COVID-19 hospitalizados e associação com dados clínicos
spellingShingle Estudo dos polimorfismos GSTP1 (rs1695) e TNF A-308 (rs1800629) em pacientes com COVID-19 hospitalizados e associação com dados clínicos
Vieira, Priscila da Silva Antunes
SARS-CoV-2
SNPs
Glutationa-S-Transferase
citocina
Comorbidades
SARS-CoV-2
Single-nucleotide polymorphism;
Glutathione-S-transferase
Cytokine
Comorbidity
CIÊNCIAS DA SAÚDE
title_short Estudo dos polimorfismos GSTP1 (rs1695) e TNF A-308 (rs1800629) em pacientes com COVID-19 hospitalizados e associação com dados clínicos
title_full Estudo dos polimorfismos GSTP1 (rs1695) e TNF A-308 (rs1800629) em pacientes com COVID-19 hospitalizados e associação com dados clínicos
title_fullStr Estudo dos polimorfismos GSTP1 (rs1695) e TNF A-308 (rs1800629) em pacientes com COVID-19 hospitalizados e associação com dados clínicos
title_full_unstemmed Estudo dos polimorfismos GSTP1 (rs1695) e TNF A-308 (rs1800629) em pacientes com COVID-19 hospitalizados e associação com dados clínicos
title_sort Estudo dos polimorfismos GSTP1 (rs1695) e TNF A-308 (rs1800629) em pacientes com COVID-19 hospitalizados e associação com dados clínicos
author Vieira, Priscila da Silva Antunes
author_facet Vieira, Priscila da Silva Antunes
author_role author
dc.contributor.advisor1.fl_str_mv Lucio, Léia Carolina
dc.contributor.advisor1Lattes.fl_str_mv http://lattes.cnpq.br/9357029990194108
dc.contributor.advisor-co1.fl_str_mv Treco, Fernando Rodrigo
dc.contributor.advisor-co1Lattes.fl_str_mv http://lattes.cnpq.br/0633607976550229
dc.contributor.referee1.fl_str_mv Lucio, Léia Carolina
dc.contributor.referee1Lattes.fl_str_mv http://lattes.cnpq.br/9357029990194108
dc.contributor.referee2.fl_str_mv Pascotto, Claudicéia Risso
dc.contributor.referee2Lattes.fl_str_mv http://lattes.cnpq.br/9474794343913304
dc.contributor.referee3.fl_str_mv Ghisi, Nédia de Castilhos
dc.contributor.referee3Lattes.fl_str_mv http://lattes.cnpq.br/4542801151720873
dc.contributor.authorLattes.fl_str_mv http://lattes.cnpq.br/8105725220202910
dc.contributor.author.fl_str_mv Vieira, Priscila da Silva Antunes
contributor_str_mv Lucio, Léia Carolina
Treco, Fernando Rodrigo
Lucio, Léia Carolina
Pascotto, Claudicéia Risso
Ghisi, Nédia de Castilhos
dc.subject.por.fl_str_mv SARS-CoV-2
SNPs
Glutationa-S-Transferase
citocina
Comorbidades
topic SARS-CoV-2
SNPs
Glutationa-S-Transferase
citocina
Comorbidades
SARS-CoV-2
Single-nucleotide polymorphism;
Glutathione-S-transferase
Cytokine
Comorbidity
CIÊNCIAS DA SAÚDE
dc.subject.eng.fl_str_mv SARS-CoV-2
Single-nucleotide polymorphism;
Glutathione-S-transferase
Cytokine
Comorbidity
dc.subject.cnpq.fl_str_mv CIÊNCIAS DA SAÚDE
description SARS-CoV-2, the new coronavirus agent of COVID-19, quickly spread throughout the world, progressing with diverse clinical manifestations, from asymptomatic, mild, moderate to severe forms, with a major outcome of death. It is still a challenge to understand the pathophysiology of SARS-CoV-2 for control measures and clinical management of the disease. Among the factors that affect the evolution of COVID-19 are: comorbidities, age, sex and lifestyle habits. Genetic factors are also the subject of investigations and may interfere with the susceptibility and evolution of the disease. The main objective of the study was to determine the allelic and genotypic frequency of GSTP1 (rs1695) and TNF A-308 (rs1800629) in patients hospitalized with COVID 19 and verify the association of polymorphisms with the severity, comorbidity, and outcome of hospitalization of patients in southern Brazil. In total, 236 patients positive for COVID-19 admitted to a reference hospital in southwestern Paraná participated in the research. A blood sample was collected from the individuals for genetic characterization using the techniques T-ARMS-PCR (tetra amplification refractory mutation system by Polymerase Chain Reaction) for rs1695 and ARMS-PCR (amplification refractory mutation system by PCR) for rs1800629. At the same time, a search was carried out in the patients' medical records to collect sociodemographic, clinical and comorbidity data. Subsequently, bivariate and multivariate analyses were conducted, including logistic regression. were Of the population, 58.1% were men and 41.9% were women; 63% were severe cases, and 37% were moderate; the hospital discharge outcome was 64%, and 36% died. The results showed that the ancestral allele was the most frequent in rs1695 (A = 71%) and rs1800629 (G = 61%) and that the genotypes AA (rs1695) and AG (rs1800629) were, respectively, 48.73% and 67.81%. For rs1695, both the A allele (OR = 2.9; 95%CI= 1.093–7.884; p=0.033) and the AG genotype (OR = 3.3; 95%CI= 1.185–9.375; p= 0.022) increase the chances of severity for COVID-19. For the rs1800629 polymorphism, no significant association was observed. Regarding hospital outcome, comorbidities, oxygen saturation and length of hospitalization, no association was observed with the investigated polymorphisms. Therefore, the study concludes that both the A allele and the AG genotype of GSTP1 rs1965 are suggestive markers of COVID-19 severity in the southern Brazilian population. And no relationship can be established for the rs1800629 polymorphism of TNF A-308.
publishDate 2024
dc.date.accessioned.fl_str_mv 2024-07-22T18:36:48Z
dc.date.issued.fl_str_mv 2024-05-22
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/masterThesis
format masterThesis
status_str publishedVersion
dc.identifier.citation.fl_str_mv VIEIRA, Priscila da Silva Antunes. Estudo dos polimorfismos GSTP1 (rs1695) e TNF A-308 (rs1800629) em pacientes com COVID-19 hospitalizados e associação com dados clínicos. 2024. 55f. Dissertação (Mestrado em Ciências Aplicadas à Saúde) - Universidade Estadual do Oeste do Paraná, Francisco Beltrão, 2024.
dc.identifier.uri.fl_str_mv https://tede.unioeste.br/handle/tede/7311
identifier_str_mv VIEIRA, Priscila da Silva Antunes. Estudo dos polimorfismos GSTP1 (rs1695) e TNF A-308 (rs1800629) em pacientes com COVID-19 hospitalizados e associação com dados clínicos. 2024. 55f. Dissertação (Mestrado em Ciências Aplicadas à Saúde) - Universidade Estadual do Oeste do Paraná, Francisco Beltrão, 2024.
url https://tede.unioeste.br/handle/tede/7311
dc.language.iso.fl_str_mv por
language por
dc.relation.program.fl_str_mv 6290525253230630664
dc.relation.confidence.fl_str_mv 600
600
dc.relation.department.fl_str_mv 292441653440865123
dc.rights.driver.fl_str_mv http://creativecommons.org/licenses/by-nc-nd/4.0/
info:eu-repo/semantics/openAccess
rights_invalid_str_mv http://creativecommons.org/licenses/by-nc-nd/4.0/
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Universidade Estadual do Oeste do Paraná
Francisco Beltrão
dc.publisher.program.fl_str_mv Programa de Pós-Graduação em Ciências Aplicadas à Saúde
dc.publisher.initials.fl_str_mv UNIOESTE
dc.publisher.country.fl_str_mv Brasil
dc.publisher.department.fl_str_mv Centro de Ciências da Saúde
publisher.none.fl_str_mv Universidade Estadual do Oeste do Paraná
Francisco Beltrão
dc.source.none.fl_str_mv reponame:Biblioteca Digital de Teses e Dissertações do UNIOESTE
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