The response to testosterone undecanoate in men with type 2 diabetes is dependent on achieving threshold serum levels (the BLAST study)

Summary Background The association between testosterone deficiency and insulin resistance in men with type 2 diabetes is well established. Current Endocrine Society and European Association of Urology guidelines recommend the measurement of testosterone levels in all men with type 2 diabetes and in...

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Veröffentlicht in:International journal of clinical practice (Esher) 2014-02, Vol.68 (2), p.203-215
Hauptverfasser: Hackett, G., Cole, N., Bhartia, M., Kennedy, D., Raju, J., Wilkinson, P., Saghir, A.
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container_issue 2
container_start_page 203
container_title International journal of clinical practice (Esher)
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creator Hackett, G.
Cole, N.
Bhartia, M.
Kennedy, D.
Raju, J.
Wilkinson, P.
Saghir, A.
description Summary Background The association between testosterone deficiency and insulin resistance in men with type 2 diabetes is well established. Current Endocrine Society and European Association of Urology guidelines recommend the measurement of testosterone levels in all men with type 2 diabetes and in men suffering from erectile dysfunction. It is recognised that a range of physical symptoms appear as the testosterone level falls but few studies have addressed the threshold at which symptoms improve with physiological replacement. We report the first double‐blind placebo‐controlled study conducted exclusively in a male type 2 diabetes population to assess the metabolic changes with testosterone replacement. Methods The type 2 diabetes registers of seven general practices were screened to establish the prevalence of low testosterone and the associations with diabetes control. Of 550 eligible patients approached, 488 men (mean age 62.6) consented to take part in screening with a morning testosterone level, assessed between 8 and 11 am. This identified 211 patients for a double‐blind placebo‐controlled study of long acting testosterone undecanoate (TU) 1000 mg lasting 30 weeks followed by 52 weeks of open label use. The population was divided into a SEVERE group with either total testosterone (TT) of 8 nmol/l or less or free testosterone (FT) 180 pmol/l or less or a MILD group with TT 8.1–12 nmol/l or FT 181–250 pmol/l. Results Men in the SEVERE group increased mean through TT from 7.73 nmol/l at baseline to 9.93 at 30 weeks and the MILD group from 10.47 to 11.94. The SEVERE group showed marked improvement in sexual function, but no significant improvement in metabolic parameters. The MILD group showed no improvement in sexual function, but significant improvement in weight, body mass index, waist circumference and Hospital Anxiety and Depression Scale. Improvement was seen in all parameters during 52 weeks open label treatment where trough TT levels approached 15 nmol/l. Baseline prostate‐specific antigen (PSA) was lower in the SEVERE group and increased with TU for 30 weeks and then stabilised. There was no increase in PSA with treatment in the MILD group. Conclusions Testosterone undecanoate significantly improves sexual parameters and Ageing Male Symptom Score, but not metabolic factors at 30 weeks in men with SEVERE testosterone deficiency syndrome (TDS). In men with MILD TDS, significant improvements in metabolic but not sexual parameters were seen, sugges
doi_str_mv 10.1111/ijcp.12235
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Current Endocrine Society and European Association of Urology guidelines recommend the measurement of testosterone levels in all men with type 2 diabetes and in men suffering from erectile dysfunction. It is recognised that a range of physical symptoms appear as the testosterone level falls but few studies have addressed the threshold at which symptoms improve with physiological replacement. We report the first double‐blind placebo‐controlled study conducted exclusively in a male type 2 diabetes population to assess the metabolic changes with testosterone replacement. Methods The type 2 diabetes registers of seven general practices were screened to establish the prevalence of low testosterone and the associations with diabetes control. Of 550 eligible patients approached, 488 men (mean age 62.6) consented to take part in screening with a morning testosterone level, assessed between 8 and 11 am. This identified 211 patients for a double‐blind placebo‐controlled study of long acting testosterone undecanoate (TU) 1000 mg lasting 30 weeks followed by 52 weeks of open label use. The population was divided into a SEVERE group with either total testosterone (TT) of 8 nmol/l or less or free testosterone (FT) 180 pmol/l or less or a MILD group with TT 8.1–12 nmol/l or FT 181–250 pmol/l. Results Men in the SEVERE group increased mean through TT from 7.73 nmol/l at baseline to 9.93 at 30 weeks and the MILD group from 10.47 to 11.94. The SEVERE group showed marked improvement in sexual function, but no significant improvement in metabolic parameters. The MILD group showed no improvement in sexual function, but significant improvement in weight, body mass index, waist circumference and Hospital Anxiety and Depression Scale. Improvement was seen in all parameters during 52 weeks open label treatment where trough TT levels approached 15 nmol/l. Baseline prostate‐specific antigen (PSA) was lower in the SEVERE group and increased with TU for 30 weeks and then stabilised. There was no increase in PSA with treatment in the MILD group. Conclusions Testosterone undecanoate significantly improves sexual parameters and Ageing Male Symptom Score, but not metabolic factors at 30 weeks in men with SEVERE testosterone deficiency syndrome (TDS). In men with MILD TDS, significant improvements in metabolic but not sexual parameters were seen, suggesting that there are threshold levels for response to testosterone replacement therapy and that trials of therapy need to achieve sustained therapeutic levels to be effective. PSA showed minor rises, but only for 30 weeks in the SEVERE group.</description><identifier>ISSN: 1368-5031</identifier><identifier>EISSN: 1742-1241</identifier><identifier>DOI: 10.1111/ijcp.12235</identifier><identifier>PMID: 24355040</identifier><language>eng</language><publisher>England: Blackwell Publishing Ltd</publisher><subject>Adult ; Aged ; Aged, 80 and over ; Androgens - administration &amp; dosage ; Androgens - adverse effects ; Antigens ; Clinical medicine ; Diabetes ; Diabetes Mellitus, Type 2 - complications ; Diabetes Mellitus, Type 2 - drug therapy ; Double-Blind Method ; Drug Administration Schedule ; Drug therapy ; Humans ; Hypoglycemic Agents - therapeutic use ; Hypogonadism - blood ; Hypogonadism - complications ; Hypogonadism - drug therapy ; Injections, Intramuscular ; Insulin resistance ; Male ; Middle Aged ; Patient Satisfaction ; Prospective Studies ; Sexual Dysfunction, Physiological - drug therapy ; Testosterone ; Testosterone - administration &amp; dosage ; Testosterone - adverse effects ; Testosterone - analogs &amp; derivatives ; Testosterone - blood ; Testosterone - deficiency ; Treatment Outcome</subject><ispartof>International journal of clinical practice (Esher), 2014-02, Vol.68 (2), p.203-215</ispartof><rights>2013 John Wiley &amp; Sons Ltd</rights><rights>2013 John Wiley &amp; Sons Ltd.</rights><rights>Copyright © 2014 John Wiley &amp; Sons Ltd</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3955-16e19da994f16bc52005b56ecdf917fb16e6195a8332742f20a820ecc19de3ec3</citedby><cites>FETCH-LOGICAL-c3955-16e19da994f16bc52005b56ecdf917fb16e6195a8332742f20a820ecc19de3ec3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fijcp.12235$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fijcp.12235$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,777,781,1412,27905,27906,45555,45556</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24355040$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hackett, G.</creatorcontrib><creatorcontrib>Cole, N.</creatorcontrib><creatorcontrib>Bhartia, M.</creatorcontrib><creatorcontrib>Kennedy, D.</creatorcontrib><creatorcontrib>Raju, J.</creatorcontrib><creatorcontrib>Wilkinson, P.</creatorcontrib><creatorcontrib>Saghir, A.</creatorcontrib><creatorcontrib>Blast Study Group</creatorcontrib><creatorcontrib>BLAST STUDY GROUP</creatorcontrib><title>The response to testosterone undecanoate in men with type 2 diabetes is dependent on achieving threshold serum levels (the BLAST study)</title><title>International journal of clinical practice (Esher)</title><addtitle>Int J Clin Pract</addtitle><description>Summary Background The association between testosterone deficiency and insulin resistance in men with type 2 diabetes is well established. Current Endocrine Society and European Association of Urology guidelines recommend the measurement of testosterone levels in all men with type 2 diabetes and in men suffering from erectile dysfunction. It is recognised that a range of physical symptoms appear as the testosterone level falls but few studies have addressed the threshold at which symptoms improve with physiological replacement. We report the first double‐blind placebo‐controlled study conducted exclusively in a male type 2 diabetes population to assess the metabolic changes with testosterone replacement. Methods The type 2 diabetes registers of seven general practices were screened to establish the prevalence of low testosterone and the associations with diabetes control. Of 550 eligible patients approached, 488 men (mean age 62.6) consented to take part in screening with a morning testosterone level, assessed between 8 and 11 am. This identified 211 patients for a double‐blind placebo‐controlled study of long acting testosterone undecanoate (TU) 1000 mg lasting 30 weeks followed by 52 weeks of open label use. The population was divided into a SEVERE group with either total testosterone (TT) of 8 nmol/l or less or free testosterone (FT) 180 pmol/l or less or a MILD group with TT 8.1–12 nmol/l or FT 181–250 pmol/l. Results Men in the SEVERE group increased mean through TT from 7.73 nmol/l at baseline to 9.93 at 30 weeks and the MILD group from 10.47 to 11.94. The SEVERE group showed marked improvement in sexual function, but no significant improvement in metabolic parameters. The MILD group showed no improvement in sexual function, but significant improvement in weight, body mass index, waist circumference and Hospital Anxiety and Depression Scale. Improvement was seen in all parameters during 52 weeks open label treatment where trough TT levels approached 15 nmol/l. Baseline prostate‐specific antigen (PSA) was lower in the SEVERE group and increased with TU for 30 weeks and then stabilised. There was no increase in PSA with treatment in the MILD group. Conclusions Testosterone undecanoate significantly improves sexual parameters and Ageing Male Symptom Score, but not metabolic factors at 30 weeks in men with SEVERE testosterone deficiency syndrome (TDS). In men with MILD TDS, significant improvements in metabolic but not sexual parameters were seen, suggesting that there are threshold levels for response to testosterone replacement therapy and that trials of therapy need to achieve sustained therapeutic levels to be effective. PSA showed minor rises, but only for 30 weeks in the SEVERE group.</description><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Androgens - administration &amp; dosage</subject><subject>Androgens - adverse effects</subject><subject>Antigens</subject><subject>Clinical medicine</subject><subject>Diabetes</subject><subject>Diabetes Mellitus, Type 2 - complications</subject><subject>Diabetes Mellitus, Type 2 - drug therapy</subject><subject>Double-Blind Method</subject><subject>Drug Administration Schedule</subject><subject>Drug therapy</subject><subject>Humans</subject><subject>Hypoglycemic Agents - therapeutic use</subject><subject>Hypogonadism - blood</subject><subject>Hypogonadism - complications</subject><subject>Hypogonadism - drug therapy</subject><subject>Injections, Intramuscular</subject><subject>Insulin resistance</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Patient Satisfaction</subject><subject>Prospective Studies</subject><subject>Sexual Dysfunction, Physiological - drug therapy</subject><subject>Testosterone</subject><subject>Testosterone - administration &amp; dosage</subject><subject>Testosterone - adverse effects</subject><subject>Testosterone - analogs &amp; derivatives</subject><subject>Testosterone - blood</subject><subject>Testosterone - deficiency</subject><subject>Treatment Outcome</subject><issn>1368-5031</issn><issn>1742-1241</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kc1u1DAYRSMEoqWw4QHQJ7EpSCn-iTOTZRlBWzQqRQQhsbEc5wvxkNjBdlrmCXhtPEzbBQu8sSWfe_xzs-w5JSc0jTdmo6cTyhgXD7JDuihYTllBH6Y1L5e5IJweZE9C2BDChFiSx9kBK7gQpCCH2e-6R_AYJmcDQnQQMUQXInpnEWbbolbWqYhgLIxo4cbEHuJ2QmDQGtVgCoAJ0OKEibYRnAWle4PXxn6H2Cd574YWAvp5hAGvcQhwHNOxb9enn2sIcW63r55mjzo1BHx2Ox9lX96_q1fn-frj2cXqdJ1rXgmR0xJp1aqqKjpaNlowQkQjStRtV9FF16T9klZCLTln6SM6RtSSEdQ6pZCj5kfZ8d47efdzTm-Vowkah0FZdHOQtKhYWRFa0IS-_AfduNnbdLsdRUtR8uWOer2ntHcheOzk5M2o_FZSInf1yF098m89CX5xq5ybEdt79K6PBNA9cGMG3P5HJS8-rK7upPk-Y1Jtv-4zyv-Q5YIvhPx6eSbP6ytSi8tP8hv_A_gYqeY</recordid><startdate>201402</startdate><enddate>201402</enddate><creator>Hackett, G.</creator><creator>Cole, N.</creator><creator>Bhartia, M.</creator><creator>Kennedy, D.</creator><creator>Raju, J.</creator><creator>Wilkinson, P.</creator><creator>Saghir, A.</creator><general>Blackwell Publishing Ltd</general><general>Hindawi Limited</general><scope>BSCLL</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>7T5</scope><scope>7TK</scope><scope>7TS</scope><scope>7U9</scope><scope>H94</scope><scope>K9.</scope><scope>NAPCQ</scope><scope>7X8</scope></search><sort><creationdate>201402</creationdate><title>The response to testosterone undecanoate in men with type 2 diabetes is dependent on achieving threshold serum levels (the BLAST study)</title><author>Hackett, G. ; 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dosage</topic><topic>Testosterone - adverse effects</topic><topic>Testosterone - analogs &amp; derivatives</topic><topic>Testosterone - blood</topic><topic>Testosterone - deficiency</topic><topic>Treatment Outcome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hackett, G.</creatorcontrib><creatorcontrib>Cole, N.</creatorcontrib><creatorcontrib>Bhartia, M.</creatorcontrib><creatorcontrib>Kennedy, D.</creatorcontrib><creatorcontrib>Raju, J.</creatorcontrib><creatorcontrib>Wilkinson, P.</creatorcontrib><creatorcontrib>Saghir, A.</creatorcontrib><creatorcontrib>Blast Study Group</creatorcontrib><creatorcontrib>BLAST STUDY GROUP</creatorcontrib><collection>Istex</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>Immunology Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Physical Education Index</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Nursing &amp; Allied Health Premium</collection><collection>MEDLINE - Academic</collection><jtitle>International journal of clinical practice (Esher)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hackett, G.</au><au>Cole, N.</au><au>Bhartia, M.</au><au>Kennedy, D.</au><au>Raju, J.</au><au>Wilkinson, P.</au><au>Saghir, A.</au><aucorp>Blast Study Group</aucorp><aucorp>BLAST STUDY GROUP</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The response to testosterone undecanoate in men with type 2 diabetes is dependent on achieving threshold serum levels (the BLAST study)</atitle><jtitle>International journal of clinical practice (Esher)</jtitle><addtitle>Int J Clin Pract</addtitle><date>2014-02</date><risdate>2014</risdate><volume>68</volume><issue>2</issue><spage>203</spage><epage>215</epage><pages>203-215</pages><issn>1368-5031</issn><eissn>1742-1241</eissn><abstract>Summary Background The association between testosterone deficiency and insulin resistance in men with type 2 diabetes is well established. Current Endocrine Society and European Association of Urology guidelines recommend the measurement of testosterone levels in all men with type 2 diabetes and in men suffering from erectile dysfunction. It is recognised that a range of physical symptoms appear as the testosterone level falls but few studies have addressed the threshold at which symptoms improve with physiological replacement. We report the first double‐blind placebo‐controlled study conducted exclusively in a male type 2 diabetes population to assess the metabolic changes with testosterone replacement. Methods The type 2 diabetes registers of seven general practices were screened to establish the prevalence of low testosterone and the associations with diabetes control. Of 550 eligible patients approached, 488 men (mean age 62.6) consented to take part in screening with a morning testosterone level, assessed between 8 and 11 am. This identified 211 patients for a double‐blind placebo‐controlled study of long acting testosterone undecanoate (TU) 1000 mg lasting 30 weeks followed by 52 weeks of open label use. The population was divided into a SEVERE group with either total testosterone (TT) of 8 nmol/l or less or free testosterone (FT) 180 pmol/l or less or a MILD group with TT 8.1–12 nmol/l or FT 181–250 pmol/l. Results Men in the SEVERE group increased mean through TT from 7.73 nmol/l at baseline to 9.93 at 30 weeks and the MILD group from 10.47 to 11.94. The SEVERE group showed marked improvement in sexual function, but no significant improvement in metabolic parameters. The MILD group showed no improvement in sexual function, but significant improvement in weight, body mass index, waist circumference and Hospital Anxiety and Depression Scale. Improvement was seen in all parameters during 52 weeks open label treatment where trough TT levels approached 15 nmol/l. Baseline prostate‐specific antigen (PSA) was lower in the SEVERE group and increased with TU for 30 weeks and then stabilised. There was no increase in PSA with treatment in the MILD group. Conclusions Testosterone undecanoate significantly improves sexual parameters and Ageing Male Symptom Score, but not metabolic factors at 30 weeks in men with SEVERE testosterone deficiency syndrome (TDS). In men with MILD TDS, significant improvements in metabolic but not sexual parameters were seen, suggesting that there are threshold levels for response to testosterone replacement therapy and that trials of therapy need to achieve sustained therapeutic levels to be effective. PSA showed minor rises, but only for 30 weeks in the SEVERE group.</abstract><cop>England</cop><pub>Blackwell Publishing Ltd</pub><pmid>24355040</pmid><doi>10.1111/ijcp.12235</doi><tpages>13</tpages></addata></record>
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source MEDLINE; Wiley Online Library Journals Frontfile Complete
subjects Adult
Aged
Aged, 80 and over
Androgens - administration & dosage
Androgens - adverse effects
Antigens
Clinical medicine
Diabetes
Diabetes Mellitus, Type 2 - complications
Diabetes Mellitus, Type 2 - drug therapy
Double-Blind Method
Drug Administration Schedule
Drug therapy
Humans
Hypoglycemic Agents - therapeutic use
Hypogonadism - blood
Hypogonadism - complications
Hypogonadism - drug therapy
Injections, Intramuscular
Insulin resistance
Male
Middle Aged
Patient Satisfaction
Prospective Studies
Sexual Dysfunction, Physiological - drug therapy
Testosterone
Testosterone - administration & dosage
Testosterone - adverse effects
Testosterone - analogs & derivatives
Testosterone - blood
Testosterone - deficiency
Treatment Outcome
title The response to testosterone undecanoate in men with type 2 diabetes is dependent on achieving threshold serum levels (the BLAST study)
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