Efficacy and Safety of Topical or Oral Hydrolyzed Collagen in Women with Dermatoporosis: A Randomized, Double-Blind, Factorial Design Study

Detalhes bibliográficos
Autor(a) principal: Guadanhim, Lilia R. S.
Data de Publicação: 2023
Outros Autores: Miot, Hélio A. [UNESP], Soares, Juliana L. M., Silva, Silas A. M., Leonardi, Gislaine R., Lopes, Renato D., Bagatin, Ediléia
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1007/s13555-022-00859-y
http://hdl.handle.net/11449/248079
Resumo: Background: Dermatoporosis defines the progressive chronic cutaneous insufficiency syndrome. Stage I is characterized by cutaneous atrophy, senile purpura, and stellate pseudoscars. Objective: To assess clinical, histologic, quality of life, and biophysical effects of oral and/or topical hydrolyzed collagen (HC) on forearm skin of postmenopausal women with Dermatoporosis stage I. Methods: Double-blind randomized placebo-controlled factorial design study. Two groups of menopausal women with stage I dermatoporosis on forearms were randomized to oral HC 5 g/day or matching placebo, and also to topical serum 2.5% HC or matching placebo once a day, for 6 months. Results: A total of 56 women, age range 60–93 years (mean 69.5 ± 7.3 years) were included. Comparing data from baseline and after 6 months, no significant difference was observed for each intervention nor their comparison, for all efficacy parameters: clinical and quality of life scores, dermal elasticity, thickness and echogenicity, and histologic and immunohistochemical markers (p > 0.1). Limitations: Larger studies to confirm our findings are warranted. Conclusions: In menopausal women with stage I dermatoporosis, oral or topical collagen peptides used alone or in combination do not have benefits on forearm skin after 6 months of intervention, and therefore should not be used routinely in this population. Graphical Abstract: CONSORT flow chart [Figure not available: see fulltext.].
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spelling Efficacy and Safety of Topical or Oral Hydrolyzed Collagen in Women with Dermatoporosis: A Randomized, Double-Blind, Factorial Design StudyCollagen peptidesCutaneous atrophyDermatoporosisHydrolyzed collagenPhotoagingSenile purpuraBackground: Dermatoporosis defines the progressive chronic cutaneous insufficiency syndrome. Stage I is characterized by cutaneous atrophy, senile purpura, and stellate pseudoscars. Objective: To assess clinical, histologic, quality of life, and biophysical effects of oral and/or topical hydrolyzed collagen (HC) on forearm skin of postmenopausal women with Dermatoporosis stage I. Methods: Double-blind randomized placebo-controlled factorial design study. Two groups of menopausal women with stage I dermatoporosis on forearms were randomized to oral HC 5 g/day or matching placebo, and also to topical serum 2.5% HC or matching placebo once a day, for 6 months. Results: A total of 56 women, age range 60–93 years (mean 69.5 ± 7.3 years) were included. Comparing data from baseline and after 6 months, no significant difference was observed for each intervention nor their comparison, for all efficacy parameters: clinical and quality of life scores, dermal elasticity, thickness and echogenicity, and histologic and immunohistochemical markers (p > 0.1). Limitations: Larger studies to confirm our findings are warranted. Conclusions: In menopausal women with stage I dermatoporosis, oral or topical collagen peptides used alone or in combination do not have benefits on forearm skin after 6 months of intervention, and therefore should not be used routinely in this population. Graphical Abstract: CONSORT flow chart [Figure not available: see fulltext.].Universidade Federal de São PauloDepartment of Dermatology Universidade Federal de São Paulo/UNIFESP, Rua Botucatu, 821 - 5o andarDepartment of Dermatology Universidade Estadual de São Paulo/UNESPFaculty of Pharmaceutical Sciences Universidade Estadual de Campinas/UNICAMPDivision of Cardiology Duke University Medical CenterDepartment of Dermatology Universidade Estadual de São Paulo/UNESPUniversidade Federal de São Paulo (UNIFESP)Universidade Estadual Paulista (UNESP)Universidade Estadual de Campinas (UNICAMP)Duke University Medical CenterGuadanhim, Lilia R. S.Miot, Hélio A. [UNESP]Soares, Juliana L. M.Silva, Silas A. M.Leonardi, Gislaine R.Lopes, Renato D.Bagatin, Ediléia2023-07-29T13:33:57Z2023-07-29T13:33:57Z2023-02-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article523-534http://dx.doi.org/10.1007/s13555-022-00859-yDermatology and Therapy, v. 13, n. 2, p. 523-534, 2023.2190-91722193-8210http://hdl.handle.net/11449/24807910.1007/s13555-022-00859-y2-s2.0-85144646223Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengDermatology and Therapyinfo:eu-repo/semantics/openAccess2024-08-14T18:46:09Zoai:repositorio.unesp.br:11449/248079Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-14T18:46:09Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Efficacy and Safety of Topical or Oral Hydrolyzed Collagen in Women with Dermatoporosis: A Randomized, Double-Blind, Factorial Design Study
title Efficacy and Safety of Topical or Oral Hydrolyzed Collagen in Women with Dermatoporosis: A Randomized, Double-Blind, Factorial Design Study
spellingShingle Efficacy and Safety of Topical or Oral Hydrolyzed Collagen in Women with Dermatoporosis: A Randomized, Double-Blind, Factorial Design Study
Guadanhim, Lilia R. S.
Collagen peptides
Cutaneous atrophy
Dermatoporosis
Hydrolyzed collagen
Photoaging
Senile purpura
title_short Efficacy and Safety of Topical or Oral Hydrolyzed Collagen in Women with Dermatoporosis: A Randomized, Double-Blind, Factorial Design Study
title_full Efficacy and Safety of Topical or Oral Hydrolyzed Collagen in Women with Dermatoporosis: A Randomized, Double-Blind, Factorial Design Study
title_fullStr Efficacy and Safety of Topical or Oral Hydrolyzed Collagen in Women with Dermatoporosis: A Randomized, Double-Blind, Factorial Design Study
title_full_unstemmed Efficacy and Safety of Topical or Oral Hydrolyzed Collagen in Women with Dermatoporosis: A Randomized, Double-Blind, Factorial Design Study
title_sort Efficacy and Safety of Topical or Oral Hydrolyzed Collagen in Women with Dermatoporosis: A Randomized, Double-Blind, Factorial Design Study
author Guadanhim, Lilia R. S.
author_facet Guadanhim, Lilia R. S.
Miot, Hélio A. [UNESP]
Soares, Juliana L. M.
Silva, Silas A. M.
Leonardi, Gislaine R.
Lopes, Renato D.
Bagatin, Ediléia
author_role author
author2 Miot, Hélio A. [UNESP]
Soares, Juliana L. M.
Silva, Silas A. M.
Leonardi, Gislaine R.
Lopes, Renato D.
Bagatin, Ediléia
author2_role author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade Federal de São Paulo (UNIFESP)
Universidade Estadual Paulista (UNESP)
Universidade Estadual de Campinas (UNICAMP)
Duke University Medical Center
dc.contributor.author.fl_str_mv Guadanhim, Lilia R. S.
Miot, Hélio A. [UNESP]
Soares, Juliana L. M.
Silva, Silas A. M.
Leonardi, Gislaine R.
Lopes, Renato D.
Bagatin, Ediléia
dc.subject.por.fl_str_mv Collagen peptides
Cutaneous atrophy
Dermatoporosis
Hydrolyzed collagen
Photoaging
Senile purpura
topic Collagen peptides
Cutaneous atrophy
Dermatoporosis
Hydrolyzed collagen
Photoaging
Senile purpura
description Background: Dermatoporosis defines the progressive chronic cutaneous insufficiency syndrome. Stage I is characterized by cutaneous atrophy, senile purpura, and stellate pseudoscars. Objective: To assess clinical, histologic, quality of life, and biophysical effects of oral and/or topical hydrolyzed collagen (HC) on forearm skin of postmenopausal women with Dermatoporosis stage I. Methods: Double-blind randomized placebo-controlled factorial design study. Two groups of menopausal women with stage I dermatoporosis on forearms were randomized to oral HC 5 g/day or matching placebo, and also to topical serum 2.5% HC or matching placebo once a day, for 6 months. Results: A total of 56 women, age range 60–93 years (mean 69.5 ± 7.3 years) were included. Comparing data from baseline and after 6 months, no significant difference was observed for each intervention nor their comparison, for all efficacy parameters: clinical and quality of life scores, dermal elasticity, thickness and echogenicity, and histologic and immunohistochemical markers (p > 0.1). Limitations: Larger studies to confirm our findings are warranted. Conclusions: In menopausal women with stage I dermatoporosis, oral or topical collagen peptides used alone or in combination do not have benefits on forearm skin after 6 months of intervention, and therefore should not be used routinely in this population. Graphical Abstract: CONSORT flow chart [Figure not available: see fulltext.].
publishDate 2023
dc.date.none.fl_str_mv 2023-07-29T13:33:57Z
2023-07-29T13:33:57Z
2023-02-01
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.1007/s13555-022-00859-y
Dermatology and Therapy, v. 13, n. 2, p. 523-534, 2023.
2190-9172
2193-8210
http://hdl.handle.net/11449/248079
10.1007/s13555-022-00859-y
2-s2.0-85144646223
url http://dx.doi.org/10.1007/s13555-022-00859-y
http://hdl.handle.net/11449/248079
identifier_str_mv Dermatology and Therapy, v. 13, n. 2, p. 523-534, 2023.
2190-9172
2193-8210
10.1007/s13555-022-00859-y
2-s2.0-85144646223
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Dermatology and Therapy
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 523-534
dc.source.none.fl_str_mv Scopus
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
reponame_str Repositório Institucional da UNESP
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
repository.mail.fl_str_mv
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