Treatment of anabolic-androgenic steroid dependence: Emerging evidence and its implications

被引:73
作者
Kanayama, Gen [1 ,2 ]
Brower, Kirk J. [3 ]
Wood, Ruth I. [4 ]
Hudson, James I. [1 ,2 ]
Pope, Harrison G., Jr. [1 ,2 ]
机构
[1] McLean Hosp, Biol Psychiat Lab, Belmont, MA 02178 USA
[2] Harvard Univ, Sch Med, Dept Psychiat, Boston, MA 02478 USA
[3] Univ Michigan, Addict Res Ctr, Ann Arbor, MI 48109 USA
[4] Univ So Calif, Keck Sch Med, Dept Cell & Neurobiol, Los Angeles, CA 90033 USA
关键词
Anabolic-androgenic steroids; Androgens; Testosterone; Substance dependence; Treatment; Men; BODY DYSMORPHIC DISORDER; NALBUPHINE HYDROCHLORIDE DEPENDENCE; PERFORMANCE ENHANCING SUBSTANCES; REWARDING AFFECTIVE PROPERTIES; MUSCLE DYSMORPHIA; RISK-FACTORS; OPEN-LABEL; CONTINGENCY MANAGEMENT; INDUCED HYPOGONADISM; TESTOSTERONE LEVELS;
D O I
10.1016/j.drugalcdep.2010.01.011
中图分类号
R194 [卫生标准、卫生检查、医药管理];
学科分类号
摘要
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. (C) 2010 Elsevier Ireland Ltd. All rights reserved.
引用
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页码:6 / 13
页数:8
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