FAS gene polymorphisms (rs3740286 and rs4064) were not associated with pre-eclampsia risk
Autor(a) principal: | |
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Data de Publicação: | 2020 |
Outros Autores: | , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Anais da Academia Brasileira de Ciências (Online) |
Texto Completo: | http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0001-37652020000700927 |
Resumo: | Abstract Pre-eclampsia results in real risk and significant impact on indicators related to maternal and child health. The only known treatment is delivery of the fetus and placenta. Despite intensive research, the causes of PE remain to be elucidated. It is suggested that pre-eclampsia is caused by a global maternal inflammatory response to a damaged placenta. Besides inflammation, cytotoxic and apoptotic mechanisms are also implicated in the pathogenesis of pre-eclampsia. Considering the importance of apoptosis to pre-eclampsia genesis, the aim of this study was to determine the frequencies of the genotypes for FAS gene polymorphisms (rs3740286 and rs4064) and to associate these with pre-eclampsia development. Women with and without pre-eclampsia were investigated. Accordingly, peripheral blood was collected, and DNA extracted, followed by genotyping using Real-time PCR with hydrolysis probe. The results showed no association between genotypes and pre-eclampsia development for both polymorphisms studied (χ2=3.39; p=.177, for rs3740286 and χ2=0.119; p=.94 for rs4064). Women with familiar history of pre-eclampsia and primiparity showed more probability to develop the condition, by multiple logistic regression analysis (OR=8.61, CI=3.39-21.86, p<0.0001; OR=6.64. CI=2.94-14.99, p<0.0001, respectively). It seems that FAS gene polymorphisms (rs3740286 and rs4064) might not be important candidates for the development of pre-eclampsia. |
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FAS gene polymorphisms (rs3740286 and rs4064) were not associated with pre-eclampsia riskApoptosisFas ReceptorPolymorphismGeneticPre-EclampsiaWomen’s HealthAbstract Pre-eclampsia results in real risk and significant impact on indicators related to maternal and child health. The only known treatment is delivery of the fetus and placenta. Despite intensive research, the causes of PE remain to be elucidated. It is suggested that pre-eclampsia is caused by a global maternal inflammatory response to a damaged placenta. Besides inflammation, cytotoxic and apoptotic mechanisms are also implicated in the pathogenesis of pre-eclampsia. Considering the importance of apoptosis to pre-eclampsia genesis, the aim of this study was to determine the frequencies of the genotypes for FAS gene polymorphisms (rs3740286 and rs4064) and to associate these with pre-eclampsia development. Women with and without pre-eclampsia were investigated. Accordingly, peripheral blood was collected, and DNA extracted, followed by genotyping using Real-time PCR with hydrolysis probe. The results showed no association between genotypes and pre-eclampsia development for both polymorphisms studied (χ2=3.39; p=.177, for rs3740286 and χ2=0.119; p=.94 for rs4064). Women with familiar history of pre-eclampsia and primiparity showed more probability to develop the condition, by multiple logistic regression analysis (OR=8.61, CI=3.39-21.86, p<0.0001; OR=6.64. CI=2.94-14.99, p<0.0001, respectively). It seems that FAS gene polymorphisms (rs3740286 and rs4064) might not be important candidates for the development of pre-eclampsia.Academia Brasileira de Ciências2020-01-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0001-37652020000700927Anais da Academia Brasileira de Ciências v.92 n.4 2020reponame:Anais da Academia Brasileira de Ciências (Online)instname:Academia Brasileira de Ciências (ABC)instacron:ABC10.1590/0001-3765202020200355info:eu-repo/semantics/openAccessTANAKA,SARAH C.S.V.ORLANDO JÚNIOR,IVANIR C.HORTOLANI,ANDREZZA C.C.CINTRA,MARIÂNGELA T.R.BALARIN,MARLY A.S.SILVA,SUELI R. DAPISSETTI,CRISTINA W.eng2020-12-03T00:00:00Zoai:scielo:S0001-37652020000700927Revistahttp://www.scielo.br/aabchttps://old.scielo.br/oai/scielo-oai.php||aabc@abc.org.br1678-26900001-3765opendoar:2020-12-03T00:00Anais da Academia Brasileira de Ciências (Online) - Academia Brasileira de Ciências (ABC)false |
dc.title.none.fl_str_mv |
FAS gene polymorphisms (rs3740286 and rs4064) were not associated with pre-eclampsia risk |
title |
FAS gene polymorphisms (rs3740286 and rs4064) were not associated with pre-eclampsia risk |
spellingShingle |
FAS gene polymorphisms (rs3740286 and rs4064) were not associated with pre-eclampsia risk TANAKA,SARAH C.S.V. Apoptosis Fas Receptor Polymorphism Genetic Pre-Eclampsia Women’s Health |
title_short |
FAS gene polymorphisms (rs3740286 and rs4064) were not associated with pre-eclampsia risk |
title_full |
FAS gene polymorphisms (rs3740286 and rs4064) were not associated with pre-eclampsia risk |
title_fullStr |
FAS gene polymorphisms (rs3740286 and rs4064) were not associated with pre-eclampsia risk |
title_full_unstemmed |
FAS gene polymorphisms (rs3740286 and rs4064) were not associated with pre-eclampsia risk |
title_sort |
FAS gene polymorphisms (rs3740286 and rs4064) were not associated with pre-eclampsia risk |
author |
TANAKA,SARAH C.S.V. |
author_facet |
TANAKA,SARAH C.S.V. ORLANDO JÚNIOR,IVANIR C. HORTOLANI,ANDREZZA C.C. CINTRA,MARIÂNGELA T.R. BALARIN,MARLY A.S. SILVA,SUELI R. DA PISSETTI,CRISTINA W. |
author_role |
author |
author2 |
ORLANDO JÚNIOR,IVANIR C. HORTOLANI,ANDREZZA C.C. CINTRA,MARIÂNGELA T.R. BALARIN,MARLY A.S. SILVA,SUELI R. DA PISSETTI,CRISTINA W. |
author2_role |
author author author author author author |
dc.contributor.author.fl_str_mv |
TANAKA,SARAH C.S.V. ORLANDO JÚNIOR,IVANIR C. HORTOLANI,ANDREZZA C.C. CINTRA,MARIÂNGELA T.R. BALARIN,MARLY A.S. SILVA,SUELI R. DA PISSETTI,CRISTINA W. |
dc.subject.por.fl_str_mv |
Apoptosis Fas Receptor Polymorphism Genetic Pre-Eclampsia Women’s Health |
topic |
Apoptosis Fas Receptor Polymorphism Genetic Pre-Eclampsia Women’s Health |
description |
Abstract Pre-eclampsia results in real risk and significant impact on indicators related to maternal and child health. The only known treatment is delivery of the fetus and placenta. Despite intensive research, the causes of PE remain to be elucidated. It is suggested that pre-eclampsia is caused by a global maternal inflammatory response to a damaged placenta. Besides inflammation, cytotoxic and apoptotic mechanisms are also implicated in the pathogenesis of pre-eclampsia. Considering the importance of apoptosis to pre-eclampsia genesis, the aim of this study was to determine the frequencies of the genotypes for FAS gene polymorphisms (rs3740286 and rs4064) and to associate these with pre-eclampsia development. Women with and without pre-eclampsia were investigated. Accordingly, peripheral blood was collected, and DNA extracted, followed by genotyping using Real-time PCR with hydrolysis probe. The results showed no association between genotypes and pre-eclampsia development for both polymorphisms studied (χ2=3.39; p=.177, for rs3740286 and χ2=0.119; p=.94 for rs4064). Women with familiar history of pre-eclampsia and primiparity showed more probability to develop the condition, by multiple logistic regression analysis (OR=8.61, CI=3.39-21.86, p<0.0001; OR=6.64. CI=2.94-14.99, p<0.0001, respectively). It seems that FAS gene polymorphisms (rs3740286 and rs4064) might not be important candidates for the development of pre-eclampsia. |
publishDate |
2020 |
dc.date.none.fl_str_mv |
2020-01-01 |
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=S0001-37652020000700927 |
url |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0001-37652020000700927 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
10.1590/0001-3765202020200355 |
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 |
Academia Brasileira de Ciências |
publisher.none.fl_str_mv |
Academia Brasileira de Ciências |
dc.source.none.fl_str_mv |
Anais da Academia Brasileira de Ciências v.92 n.4 2020 reponame:Anais da Academia Brasileira de Ciências (Online) instname:Academia Brasileira de Ciências (ABC) instacron:ABC |
instname_str |
Academia Brasileira de Ciências (ABC) |
instacron_str |
ABC |
institution |
ABC |
reponame_str |
Anais da Academia Brasileira de Ciências (Online) |
collection |
Anais da Academia Brasileira de Ciências (Online) |
repository.name.fl_str_mv |
Anais da Academia Brasileira de Ciências (Online) - Academia Brasileira de Ciências (ABC) |
repository.mail.fl_str_mv |
||aabc@abc.org.br |
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1754302869658402816 |