Polymorphisms in the IL17A gene are not involved in the development of preeclampsia in the Brazilian population
Autor(a) principal: | |
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Data de Publicação: | 2019 |
Outros Autores: | , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Jornal Brasileiro de Patologia e Medicina Laboratorial (Online) |
Texto Completo: | http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1676-24442019000200170 |
Resumo: | ABSTRACT Introduction: Preeclampsia is defined by the development of hypertension associated with proteinuria after the 20th week of gestation in previously normotensive women. IL17A is a potent inducer of tissue inflammation and polymorphisms in the IL17A gene can modulate gene expression and affect the functioning of Th17 cells, strengthening susceptibility to preeclampsia. Objective: To investigate the polymorphisms rs4711998 A>G, rs8193036 C>T and rs2275913 A>G in the IL17A gene in women with preeclampsia. Methods: This is a control case study, composed of 263 women, 89 with preeclampsia and 174 of the control group. The polymorphisms investigated by real time polymerase chain reaction (PCR) allele discrimination technique. The risk of IL17A polymorphisms contributing to preeclampsia was assessed by the inheritance model through logistic regression. Statistical power presented 99.5% for association detection. Statistical significance was defined as p < 0.05. Results: Genotype frequencies as well as multiple logistic regression analysis were not statistically significant for the rs4711998 A>G, rs8193036 C>T and rs2275913 A>G polymorphisms of the IL17A gene. No association was found between any haplotypes of the polymorphisms investigated and the risk of developing PE. Conclusion: There is no association between the allele frequencies, genotype, inheritance models and haplotypes of the rs4711998 A>G, rs8193036 C>T and rs2275913 A>G polymorphisms of the IL17A gene and PE. |
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Jornal Brasileiro de Patologia e Medicina Laboratorial (Online) |
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Polymorphisms in the IL17A gene are not involved in the development of preeclampsia in the Brazilian populationpre-eclampsiagenetic polymorphisminterleukinsABSTRACT Introduction: Preeclampsia is defined by the development of hypertension associated with proteinuria after the 20th week of gestation in previously normotensive women. IL17A is a potent inducer of tissue inflammation and polymorphisms in the IL17A gene can modulate gene expression and affect the functioning of Th17 cells, strengthening susceptibility to preeclampsia. Objective: To investigate the polymorphisms rs4711998 A>G, rs8193036 C>T and rs2275913 A>G in the IL17A gene in women with preeclampsia. Methods: This is a control case study, composed of 263 women, 89 with preeclampsia and 174 of the control group. The polymorphisms investigated by real time polymerase chain reaction (PCR) allele discrimination technique. The risk of IL17A polymorphisms contributing to preeclampsia was assessed by the inheritance model through logistic regression. Statistical power presented 99.5% for association detection. Statistical significance was defined as p < 0.05. Results: Genotype frequencies as well as multiple logistic regression analysis were not statistically significant for the rs4711998 A>G, rs8193036 C>T and rs2275913 A>G polymorphisms of the IL17A gene. No association was found between any haplotypes of the polymorphisms investigated and the risk of developing PE. Conclusion: There is no association between the allele frequencies, genotype, inheritance models and haplotypes of the rs4711998 A>G, rs8193036 C>T and rs2275913 A>G polymorphisms of the IL17A gene and PE.Sociedade Brasileira de Patologia Clínica2019-04-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S1676-24442019000200170Jornal Brasileiro de Patologia e Medicina Laboratorial v.55 n.2 2019reponame:Jornal Brasileiro de Patologia e Medicina Laboratorial (Online)instname:Sociedade Brasileira de Patologia (SBP)instacron:SBP10.5935/1676-2444.20190019info:eu-repo/semantics/openAccessTanaka,Sarah Cristina S. V.Hortolani,Andrezza Cristina C.Pissetti,Cristina W.Paschoini,Marina C.Cintra-Ruiz,Mariangela T.Rodrigues Jr.,VirmondesBalarin,Marly Aparecida S.eng2019-05-21T00:00:00Zoai:scielo:S1676-24442019000200170Revistahttp://www.scielo.br/jbpmlhttps://old.scielo.br/oai/scielo-oai.php||jbpml@sbpc.org.br1678-47741676-2444opendoar:2019-05-21T00:00Jornal Brasileiro de Patologia e Medicina Laboratorial (Online) - Sociedade Brasileira de Patologia (SBP)false |
dc.title.none.fl_str_mv |
Polymorphisms in the IL17A gene are not involved in the development of preeclampsia in the Brazilian population |
title |
Polymorphisms in the IL17A gene are not involved in the development of preeclampsia in the Brazilian population |
spellingShingle |
Polymorphisms in the IL17A gene are not involved in the development of preeclampsia in the Brazilian population Tanaka,Sarah Cristina S. V. pre-eclampsia genetic polymorphism interleukins |
title_short |
Polymorphisms in the IL17A gene are not involved in the development of preeclampsia in the Brazilian population |
title_full |
Polymorphisms in the IL17A gene are not involved in the development of preeclampsia in the Brazilian population |
title_fullStr |
Polymorphisms in the IL17A gene are not involved in the development of preeclampsia in the Brazilian population |
title_full_unstemmed |
Polymorphisms in the IL17A gene are not involved in the development of preeclampsia in the Brazilian population |
title_sort |
Polymorphisms in the IL17A gene are not involved in the development of preeclampsia in the Brazilian population |
author |
Tanaka,Sarah Cristina S. V. |
author_facet |
Tanaka,Sarah Cristina S. V. Hortolani,Andrezza Cristina C. Pissetti,Cristina W. Paschoini,Marina C. Cintra-Ruiz,Mariangela T. Rodrigues Jr.,Virmondes Balarin,Marly Aparecida S. |
author_role |
author |
author2 |
Hortolani,Andrezza Cristina C. Pissetti,Cristina W. Paschoini,Marina C. Cintra-Ruiz,Mariangela T. Rodrigues Jr.,Virmondes Balarin,Marly Aparecida S. |
author2_role |
author author author author author author |
dc.contributor.author.fl_str_mv |
Tanaka,Sarah Cristina S. V. Hortolani,Andrezza Cristina C. Pissetti,Cristina W. Paschoini,Marina C. Cintra-Ruiz,Mariangela T. Rodrigues Jr.,Virmondes Balarin,Marly Aparecida S. |
dc.subject.por.fl_str_mv |
pre-eclampsia genetic polymorphism interleukins |
topic |
pre-eclampsia genetic polymorphism interleukins |
description |
ABSTRACT Introduction: Preeclampsia is defined by the development of hypertension associated with proteinuria after the 20th week of gestation in previously normotensive women. IL17A is a potent inducer of tissue inflammation and polymorphisms in the IL17A gene can modulate gene expression and affect the functioning of Th17 cells, strengthening susceptibility to preeclampsia. Objective: To investigate the polymorphisms rs4711998 A>G, rs8193036 C>T and rs2275913 A>G in the IL17A gene in women with preeclampsia. Methods: This is a control case study, composed of 263 women, 89 with preeclampsia and 174 of the control group. The polymorphisms investigated by real time polymerase chain reaction (PCR) allele discrimination technique. The risk of IL17A polymorphisms contributing to preeclampsia was assessed by the inheritance model through logistic regression. Statistical power presented 99.5% for association detection. Statistical significance was defined as p < 0.05. Results: Genotype frequencies as well as multiple logistic regression analysis were not statistically significant for the rs4711998 A>G, rs8193036 C>T and rs2275913 A>G polymorphisms of the IL17A gene. No association was found between any haplotypes of the polymorphisms investigated and the risk of developing PE. Conclusion: There is no association between the allele frequencies, genotype, inheritance models and haplotypes of the rs4711998 A>G, rs8193036 C>T and rs2275913 A>G polymorphisms of the IL17A gene and PE. |
publishDate |
2019 |
dc.date.none.fl_str_mv |
2019-04-01 |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1676-24442019000200170 |
url |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1676-24442019000200170 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
10.5935/1676-2444.20190019 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
text/html |
dc.publisher.none.fl_str_mv |
Sociedade Brasileira de Patologia Clínica |
publisher.none.fl_str_mv |
Sociedade Brasileira de Patologia Clínica |
dc.source.none.fl_str_mv |
Jornal Brasileiro de Patologia e Medicina Laboratorial v.55 n.2 2019 reponame:Jornal Brasileiro de Patologia e Medicina Laboratorial (Online) instname:Sociedade Brasileira de Patologia (SBP) instacron:SBP |
instname_str |
Sociedade Brasileira de Patologia (SBP) |
instacron_str |
SBP |
institution |
SBP |
reponame_str |
Jornal Brasileiro de Patologia e Medicina Laboratorial (Online) |
collection |
Jornal Brasileiro de Patologia e Medicina Laboratorial (Online) |
repository.name.fl_str_mv |
Jornal Brasileiro de Patologia e Medicina Laboratorial (Online) - Sociedade Brasileira de Patologia (SBP) |
repository.mail.fl_str_mv |
||jbpml@sbpc.org.br |
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1752122297227935744 |