Polymorphisms rs2010963 and rs833061 of the VEGF gene in polycystic ovary syndrome
Autor(a) principal: | |
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Data de Publicação: | 2022 |
Outros Autores: | , , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Revista da Associação Médica Brasileira (Online) |
Texto Completo: | http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0104-42302022000600785 |
Resumo: | SUMMARY OBJECTIVE: The polycystic ovary syndrome is the most common endocrine disorder, characterized by the dysregulation of ovarian angiogenesis. This alteration can be related to changes in the activities of the vascular endothelial growth factor (VEGF) gene. Single-nucleotide polymorphisms have been observed in the promoter, intronic, and untranslated regions of the VEGF gene, and several studies have suggested that these polymorphisms may be associated with the risk of polycystic ovary syndrome. This study aimed to investigate the association between rs2010963 and rs833061 polymorphisms and haplotypes of VEGF in the etiology of polycystic ovary syndrome. METHODS: A total of 210 women, 102 diagnosed with polycystic ovary syndrome and 108 controls, participated in this study. The genotyping of the samples was performed by PCR-RFLP and real-time PCR for rs2010963 and rs833061 polymorphisms, respectively. The statistical analyses were performed by the chi-square test and logistic regression model. RESULTS: The clinical characteristics of the patients showed that 75.8% of the patients did not become pregnant, 36.3% had a family history of polycystic ovary syndrome, 58.6% were obese, and about 60% had clinical characteristics of hyperandrogenism. There were no associations between the distribution of rs2010963 (OR 1.24; 95%CI 0.60–2.57; p=0.56) and rs833061 (OR 0.78; 95%CI 0.32–1.92; p=0.59) in patients and controls. CONCLUSIONS: The patients with polycystic ovary syndrome have similar rates of VEGF polymorphisms rs2010963 and rs833061 on the general population. |
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Polymorphisms rs2010963 and rs833061 of the VEGF gene in polycystic ovary syndromePolycystic ovary syndromePolymorphism, geneticHaplotypesVascular endothelial growth factor ASUMMARY OBJECTIVE: The polycystic ovary syndrome is the most common endocrine disorder, characterized by the dysregulation of ovarian angiogenesis. This alteration can be related to changes in the activities of the vascular endothelial growth factor (VEGF) gene. Single-nucleotide polymorphisms have been observed in the promoter, intronic, and untranslated regions of the VEGF gene, and several studies have suggested that these polymorphisms may be associated with the risk of polycystic ovary syndrome. This study aimed to investigate the association between rs2010963 and rs833061 polymorphisms and haplotypes of VEGF in the etiology of polycystic ovary syndrome. METHODS: A total of 210 women, 102 diagnosed with polycystic ovary syndrome and 108 controls, participated in this study. The genotyping of the samples was performed by PCR-RFLP and real-time PCR for rs2010963 and rs833061 polymorphisms, respectively. The statistical analyses were performed by the chi-square test and logistic regression model. RESULTS: The clinical characteristics of the patients showed that 75.8% of the patients did not become pregnant, 36.3% had a family history of polycystic ovary syndrome, 58.6% were obese, and about 60% had clinical characteristics of hyperandrogenism. There were no associations between the distribution of rs2010963 (OR 1.24; 95%CI 0.60–2.57; p=0.56) and rs833061 (OR 0.78; 95%CI 0.32–1.92; p=0.59) in patients and controls. CONCLUSIONS: The patients with polycystic ovary syndrome have similar rates of VEGF polymorphisms rs2010963 and rs833061 on the general population.Associação Médica Brasileira2022-06-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0104-42302022000600785Revista da Associação Médica Brasileira v.68 n.6 2022reponame:Revista da Associação Médica Brasileira (Online)instname:Associação Médica Brasileira (AMB)instacron:AMB10.1590/1806-9282.20211345info:eu-repo/semantics/openAccessVicente,Anna Luiza Silva AlmeidaMarqui,Alessandra Bernadete Trovó deGomes,Mariana Kefalas OliveiraAssunção-Luiz,Alan ViniciusBalarin,Marly Aparecida SpadottoTanaka,Sarah Cristina Sato VazResende,Elisabete Aparecida Mantovani Rodrigues deLima,Marco Fábio PrataCintra,Mariangela Torreglosa Ruizeng2022-09-15T00:00:00Zoai:scielo:S0104-42302022000600785Revistahttps://ramb.amb.org.br/ultimas-edicoes/#https://old.scielo.br/oai/scielo-oai.php||ramb@amb.org.br1806-92820104-4230opendoar:2022-09-15T00:00Revista da Associação Médica Brasileira (Online) - Associação Médica Brasileira (AMB)false |
dc.title.none.fl_str_mv |
Polymorphisms rs2010963 and rs833061 of the VEGF gene in polycystic ovary syndrome |
title |
Polymorphisms rs2010963 and rs833061 of the VEGF gene in polycystic ovary syndrome |
spellingShingle |
Polymorphisms rs2010963 and rs833061 of the VEGF gene in polycystic ovary syndrome Vicente,Anna Luiza Silva Almeida Polycystic ovary syndrome Polymorphism, genetic Haplotypes Vascular endothelial growth factor A |
title_short |
Polymorphisms rs2010963 and rs833061 of the VEGF gene in polycystic ovary syndrome |
title_full |
Polymorphisms rs2010963 and rs833061 of the VEGF gene in polycystic ovary syndrome |
title_fullStr |
Polymorphisms rs2010963 and rs833061 of the VEGF gene in polycystic ovary syndrome |
title_full_unstemmed |
Polymorphisms rs2010963 and rs833061 of the VEGF gene in polycystic ovary syndrome |
title_sort |
Polymorphisms rs2010963 and rs833061 of the VEGF gene in polycystic ovary syndrome |
author |
Vicente,Anna Luiza Silva Almeida |
author_facet |
Vicente,Anna Luiza Silva Almeida Marqui,Alessandra Bernadete Trovó de Gomes,Mariana Kefalas Oliveira Assunção-Luiz,Alan Vinicius Balarin,Marly Aparecida Spadotto Tanaka,Sarah Cristina Sato Vaz Resende,Elisabete Aparecida Mantovani Rodrigues de Lima,Marco Fábio Prata Cintra,Mariangela Torreglosa Ruiz |
author_role |
author |
author2 |
Marqui,Alessandra Bernadete Trovó de Gomes,Mariana Kefalas Oliveira Assunção-Luiz,Alan Vinicius Balarin,Marly Aparecida Spadotto Tanaka,Sarah Cristina Sato Vaz Resende,Elisabete Aparecida Mantovani Rodrigues de Lima,Marco Fábio Prata Cintra,Mariangela Torreglosa Ruiz |
author2_role |
author author author author author author author author |
dc.contributor.author.fl_str_mv |
Vicente,Anna Luiza Silva Almeida Marqui,Alessandra Bernadete Trovó de Gomes,Mariana Kefalas Oliveira Assunção-Luiz,Alan Vinicius Balarin,Marly Aparecida Spadotto Tanaka,Sarah Cristina Sato Vaz Resende,Elisabete Aparecida Mantovani Rodrigues de Lima,Marco Fábio Prata Cintra,Mariangela Torreglosa Ruiz |
dc.subject.por.fl_str_mv |
Polycystic ovary syndrome Polymorphism, genetic Haplotypes Vascular endothelial growth factor A |
topic |
Polycystic ovary syndrome Polymorphism, genetic Haplotypes Vascular endothelial growth factor A |
description |
SUMMARY OBJECTIVE: The polycystic ovary syndrome is the most common endocrine disorder, characterized by the dysregulation of ovarian angiogenesis. This alteration can be related to changes in the activities of the vascular endothelial growth factor (VEGF) gene. Single-nucleotide polymorphisms have been observed in the promoter, intronic, and untranslated regions of the VEGF gene, and several studies have suggested that these polymorphisms may be associated with the risk of polycystic ovary syndrome. This study aimed to investigate the association between rs2010963 and rs833061 polymorphisms and haplotypes of VEGF in the etiology of polycystic ovary syndrome. METHODS: A total of 210 women, 102 diagnosed with polycystic ovary syndrome and 108 controls, participated in this study. The genotyping of the samples was performed by PCR-RFLP and real-time PCR for rs2010963 and rs833061 polymorphisms, respectively. The statistical analyses were performed by the chi-square test and logistic regression model. RESULTS: The clinical characteristics of the patients showed that 75.8% of the patients did not become pregnant, 36.3% had a family history of polycystic ovary syndrome, 58.6% were obese, and about 60% had clinical characteristics of hyperandrogenism. There were no associations between the distribution of rs2010963 (OR 1.24; 95%CI 0.60–2.57; p=0.56) and rs833061 (OR 0.78; 95%CI 0.32–1.92; p=0.59) in patients and controls. CONCLUSIONS: The patients with polycystic ovary syndrome have similar rates of VEGF polymorphisms rs2010963 and rs833061 on the general population. |
publishDate |
2022 |
dc.date.none.fl_str_mv |
2022-06-01 |
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=S0104-42302022000600785 |
url |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0104-42302022000600785 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
10.1590/1806-9282.20211345 |
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 |
Associação Médica Brasileira |
publisher.none.fl_str_mv |
Associação Médica Brasileira |
dc.source.none.fl_str_mv |
Revista da Associação Médica Brasileira v.68 n.6 2022 reponame:Revista da Associação Médica Brasileira (Online) instname:Associação Médica Brasileira (AMB) instacron:AMB |
instname_str |
Associação Médica Brasileira (AMB) |
instacron_str |
AMB |
institution |
AMB |
reponame_str |
Revista da Associação Médica Brasileira (Online) |
collection |
Revista da Associação Médica Brasileira (Online) |
repository.name.fl_str_mv |
Revista da Associação Médica Brasileira (Online) - Associação Médica Brasileira (AMB) |
repository.mail.fl_str_mv |
||ramb@amb.org.br |
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1754212837742346240 |