Evidence of Hypothalamic-Pituitary-Adrenal and -Gonadal Dysfunction in Cocaine-Addicted Men
Language English Country Switzerland Media print-electronic
Document type Journal Article, Randomized Controlled Trial
Grant support
MR/J012084/1
Medical Research Council - United Kingdom
PubMed
38219711
DOI
10.1159/000535584
PII: 000535584
Knihovny.cz E-resources
- Keywords
- Adrenocorticotrophic hormone, Cortisol, Hypogonadism, Opioids, Testosterone,
- MeSH
- Adrenocorticotropic Hormone MeSH
- Atomoxetine Hydrochloride pharmacology MeSH
- Hydrocortisone MeSH
- Hypogonadism * MeSH
- Cocaine * MeSH
- Quality of Life MeSH
- Humans MeSH
- Cocaine-Related Disorders * MeSH
- Substance-Related Disorders * MeSH
- Pituitary-Adrenal System MeSH
- Hypothalamo-Hypophyseal System MeSH
- Testosterone MeSH
- Check Tag
- Humans MeSH
- Male MeSH
- Publication type
- Journal Article MeSH
- Randomized Controlled Trial MeSH
- Names of Substances
- Adrenocorticotropic Hormone MeSH
- Atomoxetine Hydrochloride MeSH
- Hydrocortisone MeSH
- Cocaine * MeSH
- Testosterone MeSH
INTRODUCTION: Regular cocaine use has been associated with hormonal dysfunction including hypogonadism, which can lead to fatigue, reduced stamina, sexual dysfunction, and impaired quality of life. However, cocaine's endocrine effects are largely under-reported in the scientific addiction literature and, in many cases, are not addressed within treatment services. The low profile of these adverse effects might be attributable to a lack of awareness and linkage with cocaine use, such that they are recognized only when an acute/emergency problem arises. METHODS: We assessed endocrine diurnal function (adrenocorticotrophic hormone [ACTH], cortisol, and testosterone) in 26 healthy and 27 cocaine-dependent men and examined changes in hormone levels in response to a single 40 mg dose of the noradrenaline re-uptake inhibitor atomoxetine in a double-blind, placebo-controlled experimental medicine study. RESULTS: When compared with healthy controls, diurnal and atomoxetine-induced changes in ACTH and cortisol showed greater variability in cocaine-dependent men. Interestingly, despite an exaggerated rise in ACTH following atomoxetine, an attenuated cortisol response was observed, and one-third of cocaine-dependent men had subnormal testosterone levels. CONCLUSION: Our findings point to a potential disconnection between the pituitary and adrenal responses in cocaine-dependent men, a higher rate of hypogonadism, and a pressing need for more research into the endocrine effects of cocaine and their clinical implications.
Department of Kinanthropology Charles University Prague Czechia
Department of Psychiatry University Hospital of Psychiatry University of Basel Basel Switzerland
Department of Psychiatry University of Cambridge Cambridge UK
Department of Systems Neuroscience University Medical Center Hamburg Eppendorf Hamburg Germany
NIHR Cambridge Biomedical Research Centre Cambridge University Hospitals Cambridge UK
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