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Skin disease related to metabolic syndrome in women [Image: see text] ()()

Sex hormones are involved in pathways of metabolic syndrome (MetS), an observation supported by animal studies. The relationships of sex hormones with components of MetS, such as insulin resistance and dyslipidemia, have been studied in pre- and postmenopausal women. High testosterone, low sex hormo...

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Detalles Bibliográficos
Autores principales: Misitzis, Angelica, Cunha, Paulo R., Kroumpouzos, George
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6831757/
https://www.ncbi.nlm.nih.gov/pubmed/31700973
http://dx.doi.org/10.1016/j.ijwd.2019.06.030
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author Misitzis, Angelica
Cunha, Paulo R.
Kroumpouzos, George
author_facet Misitzis, Angelica
Cunha, Paulo R.
Kroumpouzos, George
author_sort Misitzis, Angelica
collection PubMed
description Sex hormones are involved in pathways of metabolic syndrome (MetS), an observation supported by animal studies. The relationships of sex hormones with components of MetS, such as insulin resistance and dyslipidemia, have been studied in pre- and postmenopausal women. High testosterone, low sex hormone-binding globulin, and low estrogen levels increase the risks of MetS and type 2 diabetes in women. Cutaneous diseases that are sex hormone mediated, such as polycystic ovary syndrome, acanthosis nigricans, acne vulgaris, and pattern alopecia, have been associated with insulin resistance and increased risk for MetS. Furthermore, inflammatory skin conditions, such as hidradenitis suppurativa and psoriasis, increase the risk for MetS. Patients with such skin conditions should be followed for metabolic complications, and early lifestyle interventions toward these populations may be warranted.
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spelling pubmed-68317572019-11-07 Skin disease related to metabolic syndrome in women [Image: see text] ()() Misitzis, Angelica Cunha, Paulo R. Kroumpouzos, George Int J Womens Dermatol Article Sex hormones are involved in pathways of metabolic syndrome (MetS), an observation supported by animal studies. The relationships of sex hormones with components of MetS, such as insulin resistance and dyslipidemia, have been studied in pre- and postmenopausal women. High testosterone, low sex hormone-binding globulin, and low estrogen levels increase the risks of MetS and type 2 diabetes in women. Cutaneous diseases that are sex hormone mediated, such as polycystic ovary syndrome, acanthosis nigricans, acne vulgaris, and pattern alopecia, have been associated with insulin resistance and increased risk for MetS. Furthermore, inflammatory skin conditions, such as hidradenitis suppurativa and psoriasis, increase the risk for MetS. Patients with such skin conditions should be followed for metabolic complications, and early lifestyle interventions toward these populations may be warranted. Elsevier 2019-07-04 /pmc/articles/PMC6831757/ /pubmed/31700973 http://dx.doi.org/10.1016/j.ijwd.2019.06.030 Text en © 2019 Published by Elsevier Inc. on behalf of Women's Dermatologic Society. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Misitzis, Angelica
Cunha, Paulo R.
Kroumpouzos, George
Skin disease related to metabolic syndrome in women [Image: see text] ()()
title Skin disease related to metabolic syndrome in women [Image: see text] ()()
title_full Skin disease related to metabolic syndrome in women [Image: see text] ()()
title_fullStr Skin disease related to metabolic syndrome in women [Image: see text] ()()
title_full_unstemmed Skin disease related to metabolic syndrome in women [Image: see text] ()()
title_short Skin disease related to metabolic syndrome in women [Image: see text] ()()
title_sort skin disease related to metabolic syndrome in women [image: see text] ()()
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6831757/
https://www.ncbi.nlm.nih.gov/pubmed/31700973
http://dx.doi.org/10.1016/j.ijwd.2019.06.030
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