ADT-G as a promising biomarker for peripheral hyperandrogenism in adult female acne

Detalhes bibliográficos
Autor(a) principal: Rocha, Marco [UNIFESP]
Data de Publicação: 2017
Outros Autores: Cardozo, Karina H. M., Carvalho, Valdemir M., Bagatin, Edieia [UNIFESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNIFESP
Texto Completo: http://dx.doi.org/10.1080/19381980.2017.1361571
https://repositorio.unifesp.br/handle/11600/57149
Resumo: Acne vulgaris is a chronic inflammatory disease that affects the pilosebaceous unit. Recent studies have shown an increasing number of cases of acne in adult women. These cases are predominantly normoandrogenic and present some clinical differences compared to adolescent acne. Local glandular metabolism turns some weak hormonal precursors into more active substances that increase the production of sebum, leaving these areas more prone to an increasing the colonization by Propionibacterium acnes (P. acnes). Our objective was to evaluate the usefulness of an androgenic metabolite as an adult female acne biomarker. The study population consisted of 38 adult women with acne without any features of hyperandrogenism and a control group. They were recruited from the clinic of Dermatology Hospital Division of Sao Paulo, Federal University of Sao Paulo from January 2012 to September 2014. After the first hormonal dosages, patients with acne were randomized into two different groups: one receiving a combined oral contraceptive (COC) containing 0,02 mg of ethinylestradiol and 3 mg drospirenone in a regimen of 24 days of medication, and the other group was treated with a topical gel containing 15% azelaic acid (AA), twice daily, both for six months. With the end of treatment new dosages were performed. Regarding the hormones, total and free testosterone and dehydroepiandrosterone sultate were quantified. In addition, the detection and quantification of androsterone glucuronate (ADT-G), an androgenic metabolite, has been developed. Only ADT-G was sensitive in detecting differences between the control and acne groups, and presented reduction of their values with systemic treatment. Therefore, only ADT-G was able to analyze the peripheral hyperandrogenism in cases of adult female acne.
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spelling ADT-G as a promising biomarker for peripheral hyperandrogenism in adult female acneAcneadultfemalebiomarkerADT-Gandrosterone glucuronideAcne vulgaris is a chronic inflammatory disease that affects the pilosebaceous unit. Recent studies have shown an increasing number of cases of acne in adult women. These cases are predominantly normoandrogenic and present some clinical differences compared to adolescent acne. Local glandular metabolism turns some weak hormonal precursors into more active substances that increase the production of sebum, leaving these areas more prone to an increasing the colonization by Propionibacterium acnes (P. acnes). Our objective was to evaluate the usefulness of an androgenic metabolite as an adult female acne biomarker. The study population consisted of 38 adult women with acne without any features of hyperandrogenism and a control group. They were recruited from the clinic of Dermatology Hospital Division of Sao Paulo, Federal University of Sao Paulo from January 2012 to September 2014. After the first hormonal dosages, patients with acne were randomized into two different groups: one receiving a combined oral contraceptive (COC) containing 0,02 mg of ethinylestradiol and 3 mg drospirenone in a regimen of 24 days of medication, and the other group was treated with a topical gel containing 15% azelaic acid (AA), twice daily, both for six months. With the end of treatment new dosages were performed. Regarding the hormones, total and free testosterone and dehydroepiandrosterone sultate were quantified. In addition, the detection and quantification of androsterone glucuronate (ADT-G), an androgenic metabolite, has been developed. Only ADT-G was sensitive in detecting differences between the control and acne groups, and presented reduction of their values with systemic treatment. Therefore, only ADT-G was able to analyze the peripheral hyperandrogenism in cases of adult female acne.Univ Fed Sao Paulo, EPM, Sao Paulo, BrazilGrp Fleury Pesquisa & Desenvolvimento, Sao Paulo, BrazilUniv Fed Sao Paulo, Sao Paulo, BrazilUniv Fed Sao Paulo, EPM, Sao Paulo, BrazilUniv Fed Sao Paulo, Sao Paulo, BrazilWeb of ScienceTaylor & Francis Inc2020-08-04T13:39:51Z2020-08-04T13:39:51Z2017info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttp://dx.doi.org/10.1080/19381980.2017.1361571Dermato-Endocrinology. Philadelphia, v. 9, n. 1, p. -, 2017.10.1080/19381980.2017.1361571WOS000428315900001.pdf1938-1972https://repositorio.unifesp.br/handle/11600/57149WOS:000428315900001engDermato-EndocrinologyPhiladelphiainfo:eu-repo/semantics/openAccessRocha, Marco [UNIFESP]Cardozo, Karina H. M.Carvalho, Valdemir M.Bagatin, Edieia [UNIFESP]reponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2024-08-04T09:38:36Zoai:repositorio.unifesp.br/:11600/57149Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652024-08-04T09:38:36Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false
dc.title.none.fl_str_mv ADT-G as a promising biomarker for peripheral hyperandrogenism in adult female acne
title ADT-G as a promising biomarker for peripheral hyperandrogenism in adult female acne
spellingShingle ADT-G as a promising biomarker for peripheral hyperandrogenism in adult female acne
Rocha, Marco [UNIFESP]
Acne
adult
female
biomarker
ADT-G
androsterone glucuronide
title_short ADT-G as a promising biomarker for peripheral hyperandrogenism in adult female acne
title_full ADT-G as a promising biomarker for peripheral hyperandrogenism in adult female acne
title_fullStr ADT-G as a promising biomarker for peripheral hyperandrogenism in adult female acne
title_full_unstemmed ADT-G as a promising biomarker for peripheral hyperandrogenism in adult female acne
title_sort ADT-G as a promising biomarker for peripheral hyperandrogenism in adult female acne
author Rocha, Marco [UNIFESP]
author_facet Rocha, Marco [UNIFESP]
Cardozo, Karina H. M.
Carvalho, Valdemir M.
Bagatin, Edieia [UNIFESP]
author_role author
author2 Cardozo, Karina H. M.
Carvalho, Valdemir M.
Bagatin, Edieia [UNIFESP]
author2_role author
author
author
dc.contributor.author.fl_str_mv Rocha, Marco [UNIFESP]
Cardozo, Karina H. M.
Carvalho, Valdemir M.
Bagatin, Edieia [UNIFESP]
dc.subject.por.fl_str_mv Acne
adult
female
biomarker
ADT-G
androsterone glucuronide
topic Acne
adult
female
biomarker
ADT-G
androsterone glucuronide
description Acne vulgaris is a chronic inflammatory disease that affects the pilosebaceous unit. Recent studies have shown an increasing number of cases of acne in adult women. These cases are predominantly normoandrogenic and present some clinical differences compared to adolescent acne. Local glandular metabolism turns some weak hormonal precursors into more active substances that increase the production of sebum, leaving these areas more prone to an increasing the colonization by Propionibacterium acnes (P. acnes). Our objective was to evaluate the usefulness of an androgenic metabolite as an adult female acne biomarker. The study population consisted of 38 adult women with acne without any features of hyperandrogenism and a control group. They were recruited from the clinic of Dermatology Hospital Division of Sao Paulo, Federal University of Sao Paulo from January 2012 to September 2014. After the first hormonal dosages, patients with acne were randomized into two different groups: one receiving a combined oral contraceptive (COC) containing 0,02 mg of ethinylestradiol and 3 mg drospirenone in a regimen of 24 days of medication, and the other group was treated with a topical gel containing 15% azelaic acid (AA), twice daily, both for six months. With the end of treatment new dosages were performed. Regarding the hormones, total and free testosterone and dehydroepiandrosterone sultate were quantified. In addition, the detection and quantification of androsterone glucuronate (ADT-G), an androgenic metabolite, has been developed. Only ADT-G was sensitive in detecting differences between the control and acne groups, and presented reduction of their values with systemic treatment. Therefore, only ADT-G was able to analyze the peripheral hyperandrogenism in cases of adult female acne.
publishDate 2017
dc.date.none.fl_str_mv 2017
2020-08-04T13:39:51Z
2020-08-04T13:39:51Z
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://dx.doi.org/10.1080/19381980.2017.1361571
Dermato-Endocrinology. Philadelphia, v. 9, n. 1, p. -, 2017.
10.1080/19381980.2017.1361571
WOS000428315900001.pdf
1938-1972
https://repositorio.unifesp.br/handle/11600/57149
WOS:000428315900001
url http://dx.doi.org/10.1080/19381980.2017.1361571
https://repositorio.unifesp.br/handle/11600/57149
identifier_str_mv Dermato-Endocrinology. Philadelphia, v. 9, n. 1, p. -, 2017.
10.1080/19381980.2017.1361571
WOS000428315900001.pdf
1938-1972
WOS:000428315900001
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Dermato-Endocrinology
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.coverage.none.fl_str_mv Philadelphia
dc.publisher.none.fl_str_mv Taylor & Francis Inc
publisher.none.fl_str_mv Taylor & Francis Inc
dc.source.none.fl_str_mv reponame:Repositório Institucional da UNIFESP
instname:Universidade Federal de São Paulo (UNIFESP)
instacron:UNIFESP
instname_str Universidade Federal de São Paulo (UNIFESP)
instacron_str UNIFESP
institution UNIFESP
reponame_str Repositório Institucional da UNIFESP
collection Repositório Institucional da UNIFESP
repository.name.fl_str_mv Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)
repository.mail.fl_str_mv biblioteca.csp@unifesp.br
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