McGovern Medical School, University of Texas Health Science Center at Houston, Houston, TX, USA.
UT-Houston Center for Clinical Research and Evidence-Based Medicine, Houston, TX, USA.
Addiction. 2017 Oct;112(10):1861-1868. doi: 10.1111/add.13868. Epub 2017 Jul 3.
Pioglitazone (PIO), a potent agonist of PPAR-gamma, is a promising candidate treatment for cocaine use disorder (CUD). We tested the effects of PIO on targeted mechanisms relevant to CUD: cocaine craving and brain white matter (WM) integrity. Feasibility, medication compliance and tolerability were evaluated.
Two-arm double-blind randomized controlled proof-of-concept pilot trial of PIO or placebo (PLC).
Single-site out-patient treatment research clinic in Houston, TX, USA.
Thirty treatment-seeking adults, 18 to 60 years old, with CUD. Eighteen participants (8 = PIO; 10 = PLC) completed diffusion tensor imaging (DTI) of WM integrity at pre-/post-treatment.
Study medication was dispensed at thrice weekly visits along with once-weekly cognitive behavioral therapy for 12 weeks.
Measures of target engagement mechanisms of interest included cocaine craving assessed by the Brief Substance Craving Scale (BSCS), the Obsessive Compulsive Drug Use Scale (OCDUS), a visual analog scale (VAS) and change in WM integrity. Feasibility measures included number completing treatment, medication compliance (riboflavin detection) and tolerability (side effects, serious adverse events).
Target engagement change in mechanisms of interest, defined as a ≥ 0.75 Bayesian posterior probability of an interaction existing favoring PIO over PLC, was demonstrated on measures of craving (BSCS, VAS) and WM integrity indexed by fractional anisotropy (FA) values. Outcomes indicated greater decrease in craving and greater increase in FA values in the PIO group. Feasibility was demonstrated by high completion rates among those starting treatment (21/26 = 80%) and medication compliance (≥ 80%). There were no reported serious adverse events for PIO.
Compared with placebo, patients receiving pioglitazone show a higher likelihood of reduced cocaine craving and improved brain white matter integrity as a function of time in treatment. Pioglitazone shows good feasibility as a treatment for cocaine use disorder.
吡格列酮(PIO)是一种强效过氧化物酶体增殖物激活受体-γ(PPAR-γ)激动剂,是治疗可卡因使用障碍(CUD)的有希望的候选药物。我们测试了 PIO 对与 CUD 相关的靶向机制的影响:可卡因渴望和脑白质(WM)完整性。评估了可行性、药物依从性和耐受性。
PIO 或安慰剂(PLC)的双盲随机对照概念验证性试验。
美国德克萨斯州休斯顿的单站点门诊治疗研究诊所。
30 名寻求治疗的成年人,年龄在 18 至 60 岁之间,患有 CUD。18 名参与者(8 名=PIO;10 名=PLC)完成了 WM 完整性的弥散张量成像(DTI)在治疗前/后。
研究药物在每周三次就诊时分配,并在 12 周内每周一次进行认知行为疗法。
感兴趣的目标参与机制的测量包括可卡因渴望,通过简短物质渴望量表(BSCS)、强迫性药物使用量表(OCDUS)、视觉模拟量表(VAS)和 WM 完整性变化来评估。可行性措施包括完成治疗的人数、药物依从性(核黄素检测)和耐受性(副作用、严重不良事件)。
目标参与机制的变化,定义为 PIO 与 PLC 相比存在交互作用的贝叶斯后验概率≥0.75,在渴望(BSCS,VAS)和 WM 完整性的指标上得到了证明,以各向异性分数(FA)值表示。结果表明,PIO 组的渴望降低和 FA 值增加更大。高治疗开始率(21/26=80%)和药物依从性(≥80%)证明了可行性。PIO 没有报告严重不良事件。
与安慰剂相比,接受吡格列酮治疗的患者在治疗期间表现出降低可卡因渴望和改善脑白质完整性的可能性更高。吡格列酮作为可卡因使用障碍的治疗方法具有良好的可行性。