Treatment of anabolic–androgenic steroid dependence: Emerging evidence and its implications
Abstract Currently, few users of anabolic–androgenic steroids (AAS) seek substance abuse treatment. But this picture may soon change substantially, because illicit AAS use did not become widespread until the 1980s, and consequently the older members of this AAS-using population – those who initiated...
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description | Abstract Currently, few users of anabolic–androgenic steroids (AAS) seek substance abuse treatment. But this picture may soon change substantially, because illicit AAS use did not become widespread until the 1980s, and consequently the older members of this AAS-using population – those who initiated AAS as youths in the 1980s – are only now reaching middle age. Members of this group, especially those who have developed AAS dependence, may therefore be entering the age of risk for cardiac and psychoneuroendocrine complications sufficient to motivate them for substance abuse treatment. We suggest that this treatment should address at least three etiologic mechanisms by which AAS dependence might develop. First, individuals with body image disorders such as “muscle dysmorphia” may become dependent on AAS for their anabolic effects ; these body image disorders may respond to psychological therapies or pharmacological treatments. Second, AAS suppress the male hypothalamic–pituitary–gonadal axis via their androgenic effects, potentially causing hypogonadism during AAS withdrawal. Men experiencing prolonged dysphoric effects or frank major depression from hypogonadism may desire to resume AAS, thus contributing to AAS dependence. AAS-induced hypogonadism may require treatment with human chorionic gonadotropin or clomiphene to reactivate neuroendocrine function, and may necessitate antidepressant treatments in cases of depression inadequately responsive to endocrine therapies alone. Third, human and animal evidence indicates that AAS also possess hedonic effects, which likely promote dependence via mechanisms shared with classical addictive drugs, especially opioids. Indeed, the opioid antagonist naltrexone blocks AAS dependence in animals. By inference, pharmacological and psychosocial treatments for human opioid dependence might also benefit AAS-dependent individuals. |
doi_str_mv | 10.1016/j.drugalcdep.2010.01.011 |
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But this picture may soon change substantially, because illicit AAS use did not become widespread until the 1980s, and consequently the older members of this AAS-using population – those who initiated AAS as youths in the 1980s – are only now reaching middle age. Members of this group, especially those who have developed AAS dependence, may therefore be entering the age of risk for cardiac and psychoneuroendocrine complications sufficient to motivate them for substance abuse treatment. We suggest that this treatment should address at least three etiologic mechanisms by which AAS dependence might develop. First, individuals with body image disorders such as “muscle dysmorphia” may become dependent on AAS for their anabolic effects ; these body image disorders may respond to psychological therapies or pharmacological treatments. Second, AAS suppress the male hypothalamic–pituitary–gonadal axis via their androgenic effects, potentially causing hypogonadism during AAS withdrawal. Men experiencing prolonged dysphoric effects or frank major depression from hypogonadism may desire to resume AAS, thus contributing to AAS dependence. AAS-induced hypogonadism may require treatment with human chorionic gonadotropin or clomiphene to reactivate neuroendocrine function, and may necessitate antidepressant treatments in cases of depression inadequately responsive to endocrine therapies alone. Third, human and animal evidence indicates that AAS also possess hedonic effects, which likely promote dependence via mechanisms shared with classical addictive drugs, especially opioids. Indeed, the opioid antagonist naltrexone blocks AAS dependence in animals. By inference, pharmacological and psychosocial treatments for human opioid dependence might also benefit AAS-dependent individuals.</description><identifier>ISSN: 0376-8716</identifier><identifier>EISSN: 1879-0046</identifier><identifier>DOI: 10.1016/j.drugalcdep.2010.01.011</identifier><identifier>PMID: 20188494</identifier><identifier>CODEN: DADEDV</identifier><language>eng</language><publisher>Shannon: Elsevier Ireland Ltd</publisher><subject>Addictive behaviors ; Adult and adolescent clinical studies ; Anabolic Agents ; Anabolic–androgenic steroids ; Androgens ; Biological and medical sciences ; Body Image ; Drug addiction ; Goals ; Humans ; Medical sciences ; Men ; Opioids ; Patient Acceptance of Health Care ; Psychiatry ; Psychology. Psychoanalysis. Psychiatry ; Psychopathology. Psychiatry ; Steroids ; Substance abuse ; Substance dependence ; Substance-Related Disorders - rehabilitation ; Substance-Related Disorders - therapy ; Testosterone ; Treatment</subject><ispartof>Drug and alcohol dependence, 2010-06, Vol.109 (1), p.6-13</ispartof><rights>Elsevier Ireland Ltd</rights><rights>2010 Elsevier Ireland Ltd</rights><rights>2015 INIST-CNRS</rights><rights>Copyright (c) 2010 Elsevier Ireland Ltd. All rights reserved.</rights><rights>2010 Elsevier Ireland Ltd. All rights reserved. 2010</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c595t-e903a91da3d26e4815cd24bb400372696da09abc946f8119fe7afd6e5993d6d53</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0376871610000384$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>230,314,776,780,881,3536,27903,27904,30979,65309</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=22829515$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20188494$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kanayama, Gen</creatorcontrib><creatorcontrib>Brower, Kirk J</creatorcontrib><creatorcontrib>Wood, Ruth I</creatorcontrib><creatorcontrib>Hudson, James I</creatorcontrib><creatorcontrib>Pope, Harrison G</creatorcontrib><title>Treatment of anabolic–androgenic steroid dependence: Emerging evidence and its implications</title><title>Drug and alcohol dependence</title><addtitle>Drug Alcohol Depend</addtitle><description>Abstract Currently, few users of anabolic–androgenic steroids (AAS) seek substance abuse treatment. But this picture may soon change substantially, because illicit AAS use did not become widespread until the 1980s, and consequently the older members of this AAS-using population – those who initiated AAS as youths in the 1980s – are only now reaching middle age. Members of this group, especially those who have developed AAS dependence, may therefore be entering the age of risk for cardiac and psychoneuroendocrine complications sufficient to motivate them for substance abuse treatment. We suggest that this treatment should address at least three etiologic mechanisms by which AAS dependence might develop. First, individuals with body image disorders such as “muscle dysmorphia” may become dependent on AAS for their anabolic effects ; these body image disorders may respond to psychological therapies or pharmacological treatments. Second, AAS suppress the male hypothalamic–pituitary–gonadal axis via their androgenic effects, potentially causing hypogonadism during AAS withdrawal. Men experiencing prolonged dysphoric effects or frank major depression from hypogonadism may desire to resume AAS, thus contributing to AAS dependence. AAS-induced hypogonadism may require treatment with human chorionic gonadotropin or clomiphene to reactivate neuroendocrine function, and may necessitate antidepressant treatments in cases of depression inadequately responsive to endocrine therapies alone. Third, human and animal evidence indicates that AAS also possess hedonic effects, which likely promote dependence via mechanisms shared with classical addictive drugs, especially opioids. Indeed, the opioid antagonist naltrexone blocks AAS dependence in animals. By inference, pharmacological and psychosocial treatments for human opioid dependence might also benefit AAS-dependent individuals.</description><subject>Addictive behaviors</subject><subject>Adult and adolescent clinical studies</subject><subject>Anabolic Agents</subject><subject>Anabolic–androgenic steroids</subject><subject>Androgens</subject><subject>Biological and medical sciences</subject><subject>Body Image</subject><subject>Drug addiction</subject><subject>Goals</subject><subject>Humans</subject><subject>Medical sciences</subject><subject>Men</subject><subject>Opioids</subject><subject>Patient Acceptance of Health Care</subject><subject>Psychiatry</subject><subject>Psychology. Psychoanalysis. Psychiatry</subject><subject>Psychopathology. Psychiatry</subject><subject>Steroids</subject><subject>Substance abuse</subject><subject>Substance dependence</subject><subject>Substance-Related Disorders - rehabilitation</subject><subject>Substance-Related Disorders - therapy</subject><subject>Testosterone</subject><subject>Treatment</subject><issn>0376-8716</issn><issn>1879-0046</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>7QJ</sourceid><recordid>eNqNUk1v1DAQtRCILoW_gHJBnLLYTuLYHCrRqnxIlThQjsia2JPFS2IvdrJSb_wH_iG_BIddWuCENZKl8XtvZvyGkILRNaNMvNiubZw3MBiLuzWnOU1ZDnaPrJhsVUlpLe6TFa1aUcqWiRPyKKUtzUco-pCcZIqUtapX5NN1RJhG9FMR-gI8dGFw5se37-BtDBv0zhRpwhicLXIx9Ba9wZfF5Yhx4_ymwL37lcpcW7gpFW7cZQWYXPDpMXnQw5DwyfE-JR9fX15fvC2v3r95d_HqqjSNaqYSFa1AMQuV5QJryRpjed11Nc0TcKGEBaqgM6oWvWRM9dhCbwU2SlVW2KY6JWcH3d3cjWhNHifCoHfRjRBvdACn_37x7rPehL3msm2qWmaB50eBGL7OmCY9umRwGMBjmJNua94yLniVkfKANDGkFLG_rcKoXszRW31njl7M0ZTlYJn69M8ub4m_3ciAZ0cAJANDH8Ebl-5wXHLVsGXc8wMO85_uHUadjFtMsC6imbQN7n-6OftHxAwu2w3DF7zBtA1z9NkzzXTimuoPyzItu8SWNapkXf0EHT3Kyg</recordid><startdate>20100601</startdate><enddate>20100601</enddate><creator>Kanayama, Gen</creator><creator>Brower, Kirk J</creator><creator>Wood, Ruth I</creator><creator>Hudson, James I</creator><creator>Pope, Harrison G</creator><general>Elsevier Ireland Ltd</general><general>Elsevier</general><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>7QJ</scope><scope>5PM</scope></search><sort><creationdate>20100601</creationdate><title>Treatment of anabolic–androgenic steroid dependence: Emerging evidence and its implications</title><author>Kanayama, Gen ; Brower, Kirk J ; Wood, Ruth I ; Hudson, James I ; Pope, Harrison G</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c595t-e903a91da3d26e4815cd24bb400372696da09abc946f8119fe7afd6e5993d6d53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Addictive behaviors</topic><topic>Adult and adolescent clinical studies</topic><topic>Anabolic Agents</topic><topic>Anabolic–androgenic steroids</topic><topic>Androgens</topic><topic>Biological and medical sciences</topic><topic>Body Image</topic><topic>Drug addiction</topic><topic>Goals</topic><topic>Humans</topic><topic>Medical sciences</topic><topic>Men</topic><topic>Opioids</topic><topic>Patient Acceptance of Health Care</topic><topic>Psychiatry</topic><topic>Psychology. Psychoanalysis. Psychiatry</topic><topic>Psychopathology. Psychiatry</topic><topic>Steroids</topic><topic>Substance abuse</topic><topic>Substance dependence</topic><topic>Substance-Related Disorders - rehabilitation</topic><topic>Substance-Related Disorders - therapy</topic><topic>Testosterone</topic><topic>Treatment</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kanayama, Gen</creatorcontrib><creatorcontrib>Brower, Kirk J</creatorcontrib><creatorcontrib>Wood, Ruth I</creatorcontrib><creatorcontrib>Hudson, James I</creatorcontrib><creatorcontrib>Pope, Harrison G</creatorcontrib><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>Applied Social Sciences Index & Abstracts (ASSIA)</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Drug and alcohol dependence</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kanayama, Gen</au><au>Brower, Kirk J</au><au>Wood, Ruth I</au><au>Hudson, James I</au><au>Pope, Harrison G</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Treatment of anabolic–androgenic steroid dependence: Emerging evidence and its implications</atitle><jtitle>Drug and alcohol dependence</jtitle><addtitle>Drug Alcohol Depend</addtitle><date>2010-06-01</date><risdate>2010</risdate><volume>109</volume><issue>1</issue><spage>6</spage><epage>13</epage><pages>6-13</pages><issn>0376-8716</issn><eissn>1879-0046</eissn><coden>DADEDV</coden><abstract>Abstract Currently, few users of anabolic–androgenic steroids (AAS) seek substance abuse treatment. But this picture may soon change substantially, because illicit AAS use did not become widespread until the 1980s, and consequently the older members of this AAS-using population – those who initiated AAS as youths in the 1980s – are only now reaching middle age. Members of this group, especially those who have developed AAS dependence, may therefore be entering the age of risk for cardiac and psychoneuroendocrine complications sufficient to motivate them for substance abuse treatment. We suggest that this treatment should address at least three etiologic mechanisms by which AAS dependence might develop. First, individuals with body image disorders such as “muscle dysmorphia” may become dependent on AAS for their anabolic effects ; these body image disorders may respond to psychological therapies or pharmacological treatments. Second, AAS suppress the male hypothalamic–pituitary–gonadal axis via their androgenic effects, potentially causing hypogonadism during AAS withdrawal. Men experiencing prolonged dysphoric effects or frank major depression from hypogonadism may desire to resume AAS, thus contributing to AAS dependence. AAS-induced hypogonadism may require treatment with human chorionic gonadotropin or clomiphene to reactivate neuroendocrine function, and may necessitate antidepressant treatments in cases of depression inadequately responsive to endocrine therapies alone. Third, human and animal evidence indicates that AAS also possess hedonic effects, which likely promote dependence via mechanisms shared with classical addictive drugs, especially opioids. Indeed, the opioid antagonist naltrexone blocks AAS dependence in animals. By inference, pharmacological and psychosocial treatments for human opioid dependence might also benefit AAS-dependent individuals.</abstract><cop>Shannon</cop><pub>Elsevier Ireland Ltd</pub><pmid>20188494</pmid><doi>10.1016/j.drugalcdep.2010.01.011</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Addictive behaviors Adult and adolescent clinical studies Anabolic Agents Anabolic–androgenic steroids Androgens Biological and medical sciences Body Image Drug addiction Goals Humans Medical sciences Men Opioids Patient Acceptance of Health Care Psychiatry Psychology. Psychoanalysis. Psychiatry Psychopathology. Psychiatry Steroids Substance abuse Substance dependence Substance-Related Disorders - rehabilitation Substance-Related Disorders - therapy Testosterone Treatment |
title | Treatment of anabolic–androgenic steroid dependence: Emerging evidence and its implications |
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