Pregnenolone Reduces Provoked Craving and Cocaine Use in Men and Women with Cocaine Use Disorder: A Pilot Trial.

Elcin Sakmar, Stephanie Wemm, Nia Fogelman, Gretchen Hermes, Rajita Sinha, Verica Milivojevic
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Abstract

Aim: Chronic cocaine use is associated with decreases in neuroactive steroid levels. These adaptations may contribute to continued cocaine use and high relapse risk in individuals with cocaine use disorder (CUD). Thus, this pilot study assessed chronic treatment with 2 supraphysiologic doses of the neuroactive steroid precursor pregnenolone (PREG, 300 mg/day; 500 mg/day) to boost endogenous neuroactive steroid levels and assess its impact on provoked craving and cocaine use outcomes in an 8-week trial in men and women with CUD.

Methods: Fifty-five treatment-seeking individuals with CUD were randomly assigned to receive either placebo (PLA; n=18; 12M/6F), 300mg PREG/day (n=20; 15M/5F) or 500mg PREG/day (n=17; 12M/5F) for 8 weeks, along with outpatient weekly relapse prevention treatment. Plasma was collected at weeks 2, 5 and 7 to assess circulating pregnenolone levels. A subset of subjects participated in a 3-day experimental component of guided imagery exposure to stress, cocaine cue and neutral conditions in about week 2 of the trial to assess craving response. Cocaine use outcomes was also assessed over the 8-week treatment period. Intent-to-treat analyses were conducted using linear mixed effects models.

Results: There were no differences between treatment groups on demographic variables and baseline cocaine use. Plasma pregnenolone levels were higher in the 300mg and 500mg PREG groups compared to PLA ( p's < 0.032). Participant trial completion rates were 100% for PLA, 90% for 300mg and 94% for 500mg PREG groups. Placebo group had increased craving in response to stress ( p < .001) and cocaine cue ( p < .001) provocation, whereas the PREG groups showed no increased in provoked cocaine craving. For cocaine use outcomes during the 8-week trial, a significant main effect of treatment group ( p = .005) on the weekly amounts of cocaine use showed e significantly lower amounts used in the 300mg PREG compared to the 500mg PREG group ( p = 0.01) and to PLA ( p = .047). There was also a trend for a treatment group main effect for days of cocaine used (p<.12).

Conclusions: These pilot findings suggest that supraphysiologic neuroactive steroid PREG doses reduces cocaine craving and may also improve cocaine use outcomes in treatment seeking individuals with CUD. Findings support further assessment and development of PREG in the treatment of CUD.

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孕烯醇酮可减少男性和女性可卡因使用障碍患者的诱发性渴望和可卡因使用:一项试点试验。
目的:长期使用可卡因与神经活性类固醇水平降低有关。这些适应可能导致可卡因使用障碍(CUD)患者持续使用可卡因和高复发风险。因此,这项初步研究评估了2次超生理剂量的神经活性类固醇前体孕烯醇酮(PREG, 300 mg/天;500毫克/天)提高内源性神经活性类固醇水平,并评估其对诱发性渴望和可卡因使用结果的影响,在一项为期8周的男女CUD试验中。方法:55名寻求治疗的CUD患者被随机分配接受安慰剂(PLA;n = 18;12M/6F), 300mg PREG/天(n=20;15M/5F)或500mg PREG/天(n=17;12M/5F)治疗8周,同时每周进行门诊预防复发治疗。在第2、5和7周收集血浆,评估循环孕烯醇酮水平。一部分受试者在试验的第2周左右参加了为期3天的应激、可卡因提示和中性条件下的引导意象暴露实验,以评估渴望反应。在8周的治疗期间,还评估了可卡因使用结果。意向治疗分析使用线性混合效应模型进行。结果:治疗组在人口学变量和基线可卡因使用方面没有差异。300mg和500mg PREG组血浆孕烯醇酮水平高于PLA组(p < 0.032)。PLA组的试验完成率为100%,300mg组为90%,500mg PREG组为94%。安慰剂组在应激(p < 0.001)和可卡因提示(p < 0.001)刺激下的渴望增加,而PREG组在刺激下的渴望没有增加。对于8周试验期间的可卡因使用结果,治疗组对每周可卡因使用量的显著主效应(p = 0.005)表明,与500mg PREG组(p = 0.01)和PLA组(p = 0.047)相比,300mg PREG组的使用量显着降低(p = 0.01)。结论:这些初步研究结果表明,超生理神经活性类固醇PREG剂量可减少对可卡因的渴望,也可能改善寻求治疗的CUD患者的可卡因使用结果。研究结果支持进一步评估和发展PREG治疗CUD。
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