Exploring Testosterone as emerging Modulator of Risky choices and Impulsivity in Problem Gambling
Session Title
Session 2-2-A: Behavior and Detection
Presentation Type
Event
Location
Caesars Palace, Las Vegas, Nevada
Start Date
29-5-2019 11:00 AM
End Date
29-5-2019 12:25 PM
Disciplines
Behavior and Behavior Mechanisms | Medicine and Health Sciences | Mental Disorders | Neurosciences
Abstract
Growing evidence supports the mediating role of testosterone in risk taking decision making. Community studies show endogenous testosterone level is linked to high economic risk of stock trading and the Iowa-Gambling-Task performance scores. High testosterone levels in healthy male subjects are linked to increased risk taking under conditions of unknown probabilities. Impulsivity and faculty decision making underlie problem gambling(PG). We hypothesize that opiate substitution treatments in opiate use disorders(OUD) exert differential effects in suppressing testosterone and concurrently modify gambling and substance use craving. In our study, we recruited male OUD subjects maintained on :1)methadone, (MET),the prototypal mu-opiate receptor agonist(n=33);2)buprenorphine (BUP),mixed-mu-opiate agonist/kappa-antagonist,(n=31) attending the community-based OUD rehabilitation program. We compared plasma levels of free and total testosterone, prolactin, FSH and LH between BUP and MET groups and determined the prevalence of DSM V criteria :Gambling Disorder(GD):[SOGS(South Oaks Gambling Screen) >5]and craving measures of gambling, substance abuse craving and psychopathology. We found male subjects, MET suppressed free testosterone to a greater extent than BUP:[12.26 nmol/l vs 16.32 nmol/l). BUP group approached normal testosterone level. Gambling urge, smoking urge and alcohol urge are highly inter-related ( p < 0.05). Gambling urge correlated significantly (P < 0.05) with SCL-90(Symptom-Check-list) score of obsessive-compulsiveness in mixed male/female PG cohort (n=50). The findings of our study implicate that testosterone dysregulation underlies the link of OUD and GD , and explain the efficacy of naltrexone, opiate receptor antagonist, in blocking gambling craving through resetting opiate-testosterone signaling modulating behavioral and cognitive impulsivity ,decision- making and reward-punishment sensitivity in GD.
Keywords
Problem Gambling, testosterone, opiates, impulsivity, methadone, buprenorphine
Funding Sources
The study was funded partly from Lawson Health Research Institute, London ON Canada :seed grant on Gambling Disorder, and from the clnical practice of Dr Simon CHIU
Competing Interests
None of the investigators/co-investigators/collaborators receive any competing funding from pharmaceutical companies deemed as potential conflicts of interest.
Exploring Testosterone as emerging Modulator of Risky choices and Impulsivity in Problem Gambling
Caesars Palace, Las Vegas, Nevada
Growing evidence supports the mediating role of testosterone in risk taking decision making. Community studies show endogenous testosterone level is linked to high economic risk of stock trading and the Iowa-Gambling-Task performance scores. High testosterone levels in healthy male subjects are linked to increased risk taking under conditions of unknown probabilities. Impulsivity and faculty decision making underlie problem gambling(PG). We hypothesize that opiate substitution treatments in opiate use disorders(OUD) exert differential effects in suppressing testosterone and concurrently modify gambling and substance use craving. In our study, we recruited male OUD subjects maintained on :1)methadone, (MET),the prototypal mu-opiate receptor agonist(n=33);2)buprenorphine (BUP),mixed-mu-opiate agonist/kappa-antagonist,(n=31) attending the community-based OUD rehabilitation program. We compared plasma levels of free and total testosterone, prolactin, FSH and LH between BUP and MET groups and determined the prevalence of DSM V criteria :Gambling Disorder(GD):[SOGS(South Oaks Gambling Screen) >5]and craving measures of gambling, substance abuse craving and psychopathology. We found male subjects, MET suppressed free testosterone to a greater extent than BUP:[12.26 nmol/l vs 16.32 nmol/l). BUP group approached normal testosterone level. Gambling urge, smoking urge and alcohol urge are highly inter-related ( p < 0.05). Gambling urge correlated significantly (P < 0.05) with SCL-90(Symptom-Check-list) score of obsessive-compulsiveness in mixed male/female PG cohort (n=50). The findings of our study implicate that testosterone dysregulation underlies the link of OUD and GD , and explain the efficacy of naltrexone, opiate receptor antagonist, in blocking gambling craving through resetting opiate-testosterone signaling modulating behavioral and cognitive impulsivity ,decision- making and reward-punishment sensitivity in GD.