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Sex steroids and glucose metabolism

Testosterone levels are lower in men with metabolic syndrome and type 2 diabetes mellitus (T2DM) and also predict the onset of these adverse metabolic states. Body composition (body mass index, waist circumference) is an important mediator of this relationship. Sex hormone binding globulin is also i...

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Autor principal: Allan, Carolyn A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3955332/
https://www.ncbi.nlm.nih.gov/pubmed/24457840
http://dx.doi.org/10.4103/1008-682X.122589
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author Allan, Carolyn A
author_facet Allan, Carolyn A
author_sort Allan, Carolyn A
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description Testosterone levels are lower in men with metabolic syndrome and type 2 diabetes mellitus (T2DM) and also predict the onset of these adverse metabolic states. Body composition (body mass index, waist circumference) is an important mediator of this relationship. Sex hormone binding globulin is also inversely associated with insulin resistance and T2DM but the data regarding estrogen are inconsistent. Clinical models of androgen deficiency including Klinefelter's syndrome and androgen deprivation therapy in the treatment of advanced prostate cancer confirm the association between androgens and glucose status. Experimental manipulation of the insulin/glucose milieu and suppression of endogenous testicular function suggests the relationship between androgens and insulin sensitivity is bidirectional. Androgen therapy in men without diabetes is not able to differentiate the effect on insulin resistance from that on fat mass, in particular visceral adiposity. Similarly, several small clinical studies have examined the efficacy of exogenous testosterone in men with T2DM, however, the role of androgens, independent of body composition, in modifying insulin resistance is uncertain.
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spelling pubmed-39553322014-03-25 Sex steroids and glucose metabolism Allan, Carolyn A Asian J Androl Invited Review Testosterone levels are lower in men with metabolic syndrome and type 2 diabetes mellitus (T2DM) and also predict the onset of these adverse metabolic states. Body composition (body mass index, waist circumference) is an important mediator of this relationship. Sex hormone binding globulin is also inversely associated with insulin resistance and T2DM but the data regarding estrogen are inconsistent. Clinical models of androgen deficiency including Klinefelter's syndrome and androgen deprivation therapy in the treatment of advanced prostate cancer confirm the association between androgens and glucose status. Experimental manipulation of the insulin/glucose milieu and suppression of endogenous testicular function suggests the relationship between androgens and insulin sensitivity is bidirectional. Androgen therapy in men without diabetes is not able to differentiate the effect on insulin resistance from that on fat mass, in particular visceral adiposity. Similarly, several small clinical studies have examined the efficacy of exogenous testosterone in men with T2DM, however, the role of androgens, independent of body composition, in modifying insulin resistance is uncertain. Medknow Publications & Media Pvt Ltd 2014 2014-01-24 /pmc/articles/PMC3955332/ /pubmed/24457840 http://dx.doi.org/10.4103/1008-682X.122589 Text en Copyright: © Asian Journal of Andrology http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Invited Review
Allan, Carolyn A
Sex steroids and glucose metabolism
title Sex steroids and glucose metabolism
title_full Sex steroids and glucose metabolism
title_fullStr Sex steroids and glucose metabolism
title_full_unstemmed Sex steroids and glucose metabolism
title_short Sex steroids and glucose metabolism
title_sort sex steroids and glucose metabolism
topic Invited Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3955332/
https://www.ncbi.nlm.nih.gov/pubmed/24457840
http://dx.doi.org/10.4103/1008-682X.122589
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