Androgen receptor CAG polymorphism and the risk of benign prostatic hyperplasia in a Brazilian population

Detalhes bibliográficos
Autor(a) principal: Biolchi, Vanderlei
Data de Publicação: 2012
Outros Autores: Silva Neto, Brasil, Koff, Walter Jose, Brum, Ilma Simoni
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UFRGS
Texto Completo: http://hdl.handle.net/10183/119119
Resumo: Benign prostatic hyperplasia (BPH) is a very frequent age-related proliferative abnormality in men. Polymorphic CAG repeat in the androgen receptor (AR) can alter transactivation of androgen-responsive genes and potentially infl uence BPH risk. We investigated the association between CAG repeat length and risk of BPH in a case-control study of a Brazilian population. We evaluated 214 patients; 126 with BPH and 88 healthy controls. DNA was extracted from peripheral leucocytes and the AR gene was analyzed using fragment analysis. Hazard ratio (HR) and 95% confi dence interval were estimated using logistic regression models. Mean CAG length was not different between patients with BPH and controls. The CAG repeat length was examined as a categorical variable (CAG ≤ 21 vs. CAG > 21 and CAG ≤ 22 vs. CAG > 22) and did not differ between the control vs. the BPH group. We found no evidence for an association between AR CAG repeat length in BPH risk in a population-based sample of Brazilians
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spelling Biolchi, VanderleiSilva Neto, BrasilKoff, Walter JoseBrum, Ilma Simoni2015-07-11T02:00:17Z20121677-6119http://hdl.handle.net/10183/119119000964015Benign prostatic hyperplasia (BPH) is a very frequent age-related proliferative abnormality in men. Polymorphic CAG repeat in the androgen receptor (AR) can alter transactivation of androgen-responsive genes and potentially infl uence BPH risk. We investigated the association between CAG repeat length and risk of BPH in a case-control study of a Brazilian population. We evaluated 214 patients; 126 with BPH and 88 healthy controls. DNA was extracted from peripheral leucocytes and the AR gene was analyzed using fragment analysis. Hazard ratio (HR) and 95% confi dence interval were estimated using logistic regression models. Mean CAG length was not different between patients with BPH and controls. The CAG repeat length was examined as a categorical variable (CAG ≤ 21 vs. CAG > 21 and CAG ≤ 22 vs. CAG > 22) and did not differ between the control vs. the BPH group. We found no evidence for an association between AR CAG repeat length in BPH risk in a population-based sample of Braziliansapplication/pdfengInternational brazilian journal of urology. Rio de Janeiro, RJ. Vol. 38, no. 3 (May/June 2012), p. 373-379Receptores androgênicosPolimorfismo genéticoHiperplasia prostáticaAndrogen receptor CAG polymorphism and the risk of benign prostatic hyperplasia in a Brazilian populationinfo:eu-repo/semantics/articleinfo:eu-repo/semantics/otherinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UFRGSinstname:Universidade Federal do Rio Grande do Sul (UFRGS)instacron:UFRGSORIGINAL000964015.pdf000964015.pdfTexto completo (inglês)application/pdf212642http://www.lume.ufrgs.br/bitstream/10183/119119/1/000964015.pdf591afb0ee950f58c8d9937e4bd1f9992MD51TEXT000964015.pdf.txt000964015.pdf.txtExtracted Texttext/plain23441http://www.lume.ufrgs.br/bitstream/10183/119119/2/000964015.pdf.txt00c7ba48a20a75da7f6de5baa54131beMD52THUMBNAIL000964015.pdf.jpg000964015.pdf.jpgGenerated Thumbnailimage/jpeg2052http://www.lume.ufrgs.br/bitstream/10183/119119/3/000964015.pdf.jpg4b2e2c09eb63cd036b8d748938405ab1MD5310183/1191192019-01-11 04:10:40.139938oai:www.lume.ufrgs.br:10183/119119Repositório de PublicaçõesPUBhttps://lume.ufrgs.br/oai/requestopendoar:2019-01-11T06:10:40Repositório Institucional da UFRGS - Universidade Federal do Rio Grande do Sul (UFRGS)false
dc.title.pt_BR.fl_str_mv Androgen receptor CAG polymorphism and the risk of benign prostatic hyperplasia in a Brazilian population
title Androgen receptor CAG polymorphism and the risk of benign prostatic hyperplasia in a Brazilian population
spellingShingle Androgen receptor CAG polymorphism and the risk of benign prostatic hyperplasia in a Brazilian population
Biolchi, Vanderlei
Receptores androgênicos
Polimorfismo genético
Hiperplasia prostática
title_short Androgen receptor CAG polymorphism and the risk of benign prostatic hyperplasia in a Brazilian population
title_full Androgen receptor CAG polymorphism and the risk of benign prostatic hyperplasia in a Brazilian population
title_fullStr Androgen receptor CAG polymorphism and the risk of benign prostatic hyperplasia in a Brazilian population
title_full_unstemmed Androgen receptor CAG polymorphism and the risk of benign prostatic hyperplasia in a Brazilian population
title_sort Androgen receptor CAG polymorphism and the risk of benign prostatic hyperplasia in a Brazilian population
author Biolchi, Vanderlei
author_facet Biolchi, Vanderlei
Silva Neto, Brasil
Koff, Walter Jose
Brum, Ilma Simoni
author_role author
author2 Silva Neto, Brasil
Koff, Walter Jose
Brum, Ilma Simoni
author2_role author
author
author
dc.contributor.author.fl_str_mv Biolchi, Vanderlei
Silva Neto, Brasil
Koff, Walter Jose
Brum, Ilma Simoni
dc.subject.por.fl_str_mv Receptores androgênicos
Polimorfismo genético
Hiperplasia prostática
topic Receptores androgênicos
Polimorfismo genético
Hiperplasia prostática
description Benign prostatic hyperplasia (BPH) is a very frequent age-related proliferative abnormality in men. Polymorphic CAG repeat in the androgen receptor (AR) can alter transactivation of androgen-responsive genes and potentially infl uence BPH risk. We investigated the association between CAG repeat length and risk of BPH in a case-control study of a Brazilian population. We evaluated 214 patients; 126 with BPH and 88 healthy controls. DNA was extracted from peripheral leucocytes and the AR gene was analyzed using fragment analysis. Hazard ratio (HR) and 95% confi dence interval were estimated using logistic regression models. Mean CAG length was not different between patients with BPH and controls. The CAG repeat length was examined as a categorical variable (CAG ≤ 21 vs. CAG > 21 and CAG ≤ 22 vs. CAG > 22) and did not differ between the control vs. the BPH group. We found no evidence for an association between AR CAG repeat length in BPH risk in a population-based sample of Brazilians
publishDate 2012
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dc.relation.ispartof.pt_BR.fl_str_mv International brazilian journal of urology. Rio de Janeiro, RJ. Vol. 38, no. 3 (May/June 2012), p. 373-379
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