Polymorphisms rs2010963 and rs833061 of the VEGF gene in polycystic ovary syndrome

Detalhes bibliográficos
Autor(a) principal: Vicente,Anna Luiza Silva Almeida
Data de Publicação: 2022
Outros Autores: 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
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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spelling 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
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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)
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reponame_str Revista da Associação Médica Brasileira (Online)
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repository.name.fl_str_mv Revista da Associação Médica Brasileira (Online) - Associação Médica Brasileira (AMB)
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