Sex hormone binding globulin and insulin resistance

Summary Sex hormone binding globulin (SHBG) is a glycoprotein composed of two 373‐amino‐acid subunits. The SHBG gene and a promotor region have been identified. The SHBG receptor has yet to be cloned but is known to act through a G‐protein‐linked second‐messenger system following plasma membrane bin...

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Veröffentlicht in:Clinical endocrinology (Oxford) 2013-03, Vol.78 (3), p.321-329
Hauptverfasser: Wallace, Ian R., McKinley, Michelle C., Bell, Patrick M., Hunter, Steven J.
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creator Wallace, Ian R.
McKinley, Michelle C.
Bell, Patrick M.
Hunter, Steven J.
description Summary Sex hormone binding globulin (SHBG) is a glycoprotein composed of two 373‐amino‐acid subunits. The SHBG gene and a promotor region have been identified. The SHBG receptor has yet to be cloned but is known to act through a G‐protein‐linked second‐messenger system following plasma membrane binding. The principal function of SHBG has traditionally been considered to be that of a transport protein for sex steroids, regulating circulating concentrations of free (unbound) hormones and their transport to target tissues. Recent research suggests that SHBG has functions in addition to the binding and transport of sex steroids. Observational studies have associated a low SHBG concentration with an increased incidence of type 2 diabetes mellitus (DM) independent of sex hormone levels in men and women. Genetic studies using Mendelian randomization analysis linking three single nucleotide polymorphisms of the SHBG gene to risk of developing type 2 DM suggest SHBG may have a role in the pathogenesis of type 2 DM. The correlation between SHBG and insulin resistance that is evident in a number of cross‐sectional studies is in keeping with the suggestion that the association between SHBG and incidence of type 2 DM is explained by insulin resistance. Several potential mechanisms may account for this association, including the identification of dietary factors that influence SHBG gene transcription. Further research to characterize the SHBG‐receptor and the SHBG second messenger system is required. An interventional study examining the effects on insulin resistance of altering SHBG concentrations may help in determining whether this association is causal.
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The SHBG gene and a promotor region have been identified. The SHBG receptor has yet to be cloned but is known to act through a G‐protein‐linked second‐messenger system following plasma membrane binding. The principal function of SHBG has traditionally been considered to be that of a transport protein for sex steroids, regulating circulating concentrations of free (unbound) hormones and their transport to target tissues. Recent research suggests that SHBG has functions in addition to the binding and transport of sex steroids. Observational studies have associated a low SHBG concentration with an increased incidence of type 2 diabetes mellitus (DM) independent of sex hormone levels in men and women. Genetic studies using Mendelian randomization analysis linking three single nucleotide polymorphisms of the SHBG gene to risk of developing type 2 DM suggest SHBG may have a role in the pathogenesis of type 2 DM. The correlation between SHBG and insulin resistance that is evident in a number of cross‐sectional studies is in keeping with the suggestion that the association between SHBG and incidence of type 2 DM is explained by insulin resistance. Several potential mechanisms may account for this association, including the identification of dietary factors that influence SHBG gene transcription. Further research to characterize the SHBG‐receptor and the SHBG second messenger system is required. 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The SHBG gene and a promotor region have been identified. The SHBG receptor has yet to be cloned but is known to act through a G‐protein‐linked second‐messenger system following plasma membrane binding. The principal function of SHBG has traditionally been considered to be that of a transport protein for sex steroids, regulating circulating concentrations of free (unbound) hormones and their transport to target tissues. Recent research suggests that SHBG has functions in addition to the binding and transport of sex steroids. Observational studies have associated a low SHBG concentration with an increased incidence of type 2 diabetes mellitus (DM) independent of sex hormone levels in men and women. Genetic studies using Mendelian randomization analysis linking three single nucleotide polymorphisms of the SHBG gene to risk of developing type 2 DM suggest SHBG may have a role in the pathogenesis of type 2 DM. The correlation between SHBG and insulin resistance that is evident in a number of cross‐sectional studies is in keeping with the suggestion that the association between SHBG and incidence of type 2 DM is explained by insulin resistance. Several potential mechanisms may account for this association, including the identification of dietary factors that influence SHBG gene transcription. Further research to characterize the SHBG‐receptor and the SHBG second messenger system is required. An interventional study examining the effects on insulin resistance of altering SHBG concentrations may help in determining whether this association is causal.</description><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Diabetes Mellitus, Type 2 - genetics</subject><subject>Diabetes Mellitus, Type 2 - metabolism</subject><subject>Endocrinopathies</subject><subject>Female</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Humans</subject><subject>Insulin resistance</subject><subject>Insulin Resistance - genetics</subject><subject>Insulin Resistance - physiology</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Men</subject><subject>Sex Hormone-Binding Globulin - genetics</subject><subject>Sex Hormone-Binding Globulin - metabolism</subject><subject>Studies</subject><subject>Vertebrates: endocrinology</subject><issn>0300-0664</issn><issn>1365-2265</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp10M9PFDEUB_DGaGRBDvwDZBJjooeB9_pzejQbXI1kPagh4dJ0Zt9AYbaDLRPhv6eyCyYm9tIePu99my9jBwhHWM5xR_EIOTT6BZuh0KrmXKuXbAYCoAat5Q7bzfkKAFQD5jXb4QI5aslnTHynu-pyTOsxUtWGuArxoroYxnYaQqx8XFUh5sd3ohzyrY8dvWGvej9k2t_ee-znp5Mf88_16bfFl_nH07pT3OhaYtdyDdQDSuG9bYUQSFxY0OiN96pX1GthdSdX2GopUXPV8KaRxnpDVuyx95u9N2n8NVG-deuQOxoGH2mcskPecJBCGiz07T_0apxSLL9zqLhV2krQRX3YqC6NOSfq3U0Ka5_uHYL706QrTbrHJos93G6c2jWtnuVTdQW82wKfOz_0qVQT8l9ngNsSW9zxxv0OA93_P9HNT5ZP0fVmovRNd88TPl07bYRR7my5cPYcz-1ysXBfxQMmKJWT</recordid><startdate>201303</startdate><enddate>201303</enddate><creator>Wallace, Ian R.</creator><creator>McKinley, Michelle C.</creator><creator>Bell, Patrick M.</creator><creator>Hunter, Steven J.</creator><general>Blackwell Publishing Ltd</general><general>Blackwell</general><general>Wiley Subscription Services, Inc</general><scope>BSCLL</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QP</scope><scope>K9.</scope><scope>NAPCQ</scope><scope>7X8</scope></search><sort><creationdate>201303</creationdate><title>Sex hormone binding globulin and insulin resistance</title><author>Wallace, Ian R. ; McKinley, Michelle C. ; Bell, Patrick M. ; Hunter, Steven J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5276-41cb260ef0143aa9b3331e239061a7aa5f5ef6396c4d1b64416258288479a7e93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Diabetes Mellitus, Type 2 - genetics</topic><topic>Diabetes Mellitus, Type 2 - metabolism</topic><topic>Endocrinopathies</topic><topic>Female</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Humans</topic><topic>Insulin resistance</topic><topic>Insulin Resistance - genetics</topic><topic>Insulin Resistance - physiology</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Men</topic><topic>Sex Hormone-Binding Globulin - genetics</topic><topic>Sex Hormone-Binding Globulin - metabolism</topic><topic>Studies</topic><topic>Vertebrates: endocrinology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wallace, Ian R.</creatorcontrib><creatorcontrib>McKinley, Michelle C.</creatorcontrib><creatorcontrib>Bell, Patrick M.</creatorcontrib><creatorcontrib>Hunter, Steven J.</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium &amp; Calcified Tissue Abstracts</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Nursing &amp; Allied Health Premium</collection><collection>MEDLINE - Academic</collection><jtitle>Clinical endocrinology (Oxford)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wallace, Ian R.</au><au>McKinley, Michelle C.</au><au>Bell, Patrick M.</au><au>Hunter, Steven J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Sex hormone binding globulin and insulin resistance</atitle><jtitle>Clinical endocrinology (Oxford)</jtitle><addtitle>Clin Endocrinol</addtitle><date>2013-03</date><risdate>2013</risdate><volume>78</volume><issue>3</issue><spage>321</spage><epage>329</epage><pages>321-329</pages><issn>0300-0664</issn><eissn>1365-2265</eissn><coden>CLECAP</coden><abstract>Summary Sex hormone binding globulin (SHBG) is a glycoprotein composed of two 373‐amino‐acid subunits. 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The correlation between SHBG and insulin resistance that is evident in a number of cross‐sectional studies is in keeping with the suggestion that the association between SHBG and incidence of type 2 DM is explained by insulin resistance. Several potential mechanisms may account for this association, including the identification of dietary factors that influence SHBG gene transcription. Further research to characterize the SHBG‐receptor and the SHBG second messenger system is required. An interventional study examining the effects on insulin resistance of altering SHBG concentrations may help in determining whether this association is causal.</abstract><cop>Oxford</cop><pub>Blackwell Publishing Ltd</pub><pmid>23121642</pmid><doi>10.1111/cen.12086</doi><tpages>9</tpages></addata></record>
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subjects Animals
Biological and medical sciences
Diabetes Mellitus, Type 2 - genetics
Diabetes Mellitus, Type 2 - metabolism
Endocrinopathies
Female
Fundamental and applied biological sciences. Psychology
Humans
Insulin resistance
Insulin Resistance - genetics
Insulin Resistance - physiology
Male
Medical sciences
Men
Sex Hormone-Binding Globulin - genetics
Sex Hormone-Binding Globulin - metabolism
Studies
Vertebrates: endocrinology
title Sex hormone binding globulin and insulin resistance
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