Amsterdam Institute for Addiction Research, Department of Psychiatry, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands; Department of Nuclear Medicine, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands; Collaborative Antwerp Psychiatric Research Institute (CAPRI), University of Antwerp, Antwerp, Belgium.
Eur Neuropsychopharmacol. 2013 Dec;23(12):1714-23. doi: 10.1016/j.euroneuro.2013.05.002. Epub 2013 May 31.
Methylphenidate (MPH) occupies brain striatal dopamine transporters (DATs) and is an effective treatment for attention deficit hyperactivity disorder (ADHD). However, patients with ADHD and comorbid cocaine dependence do not benefit significantly from treatment with MPH. To better understand the neurobiology of this phenomenon, we examined DAT availability and the effects of MPH treatment on DAT occupancy in ADHD patients with and without cocaine dependence. ADHD patients without a comorbid substance use disorder (N=16) and ADHD patients with comorbid cocaine dependence (N=8) were imaged at baseline and after two weeks MPH treatment using single photon emission computed tomography (SPECT) with the DAT tracer [(123)I]FP-CIT. Changes in ADHD symptoms were measured with the ADHD symptom rating scale (ASRS). At baseline, we observed lower striatal DAT availability in ADHD patients with cocaine dependence. Following fixed MPH treatment, MPH occupied significantly less striatal DATs in cocaine-dependent than in non-cocaine dependent ADHD patients. There were no significant correlations between baseline DAT availability or DAT occupancy by MPH and ADHD symptom improvement. However, we did find significant correlations between DAT occupancy by MPH and decreases in impulsivity scores and years of cocaine use. These preliminary findings suggest that low DAT occupancy is not the reason why ADHD patients with cocaine dependence do not benefit from MPH treatment. It also suggests that higher dosages of MPH in these patients are probably not the solution and that medications directed at other pharmacological targets should be considered in these comorbid ADHD patients. This trial is registered at the Dutch Trial Register, www.trialregister.nl, under Trial ID number NTR3127.
哌醋甲酯(MPH)占据大脑纹状体多巴胺转运体(DATs),是治疗注意力缺陷多动障碍(ADHD)的有效方法。然而,患有 ADHD 且合并可卡因依赖的患者并没有从 MPH 治疗中获得显著的益处。为了更好地理解这种现象的神经生物学机制,我们研究了 ADHD 患者中是否存在可卡因依赖,以及 DAT 可用性以及 MPH 治疗对 DAT 占有率的影响。无共病物质使用障碍的 ADHD 患者(N=16)和伴有可卡因依赖的 ADHD 患者(N=8)在基线和 MPH 治疗两周后使用单光子发射计算机断层扫描(SPECT)用 DAT 示踪剂[(123)I]FP-CIT 进行成像。使用 ADHD 症状评定量表(ASRS)测量 ADHD 症状的变化。在基线时,我们观察到可卡因依赖的 ADHD 患者纹状体 DAT 可用性较低。在固定 MPH 治疗后,可卡因依赖的 ADHD 患者中,MPH 占据的纹状体 DAT 明显较少。基线 DAT 可用性或 MPH 占据的 DAT 与 ADHD 症状改善之间无显著相关性。然而,我们确实发现 MPH 占据的 DAT 与冲动性评分和可卡因使用年限之间存在显著相关性。这些初步发现表明,DAT 占有率低不是可卡因依赖的 ADHD 患者不能从 MPH 治疗中获益的原因。这也表明,这些患者可能需要更高剂量的 MPH,但这并不是解决问题的方法,应该考虑针对这些共病 ADHD 患者的其他药理学靶点的药物。本试验在荷兰试验注册处(www.trialregister.nl)注册,注册号为 NTR3127。