Porta Mauro, Sassi Marco, Cavallazzi Mario, Fornari Maurizio, Brambilla Arianna, Servello Domenico
Tourette Clinic and Functional Neurosurgery, IRCCS Galaezzi Hospital, Milan, Italy.
Clin Drug Investig. 2008;28(7):443-59. doi: 10.2165/00044011-200828070-00006.
Gilles de la Tourette's syndrome (Tourette's syndrome; TS) is an inherited tic disorder commonly associated with other neurobehavioural conditions such as attention-deficit hyperactivity disorder (ADHD) and obsessive-compulsive disorder (OCD). While the clinical presentation of TS and other features of this disorder have been well characterized, the genetic and neurobiological basis of the disease remains incompletely elucidated. The suggestion of a central role of dopamine in the aetiology of TS has been made on the basis of experimental studies, evidence from neuroimaging studies and the therapeutic response patients with TS have to agents that antagonize or interfere with putative dopaminergic pathways. Tetrabenazine is such an agent; it depletes presynaptic dopamine and serotonin stores and blocks postsynaptic dopamine receptors. In clinical studies, tetrabenazine has been found to be effective in a wide range of hyperkinetic movement disorders, including small numbers (<50) of patients with TS in some studies. Results of a retrospective chart review enrolling only patients with TS (n = 77; mean age approximately 15 years) showed that 2 years' treatment with tetrabenazine resulted in an improvement in functioning and TS-related symptoms in over 80% of patients, findings that suggest that treatment with tetrabenazine may have long-term benefits. The authors' experience with 120 heavily co-medicated patients with TS confirms these findings. Long-term (mean 19 months) tetrabenazine treatment resulted in a Clinical Global Impressions of Change scale rating of 'improved' in 76% of patients. Such findings are promising and suggest that tetrabenazine may be suitable as add-on therapy in patients for whom additional suppression of tics is required.
吉勒·德·拉·图雷特综合征(图雷特综合征;TS)是一种遗传性抽动障碍,通常与其他神经行为疾病有关,如注意力缺陷多动障碍(ADHD)和强迫症(OCD)。虽然TS的临床表现和该疾病的其他特征已得到很好的描述,但该疾病的遗传和神经生物学基础仍未完全阐明。基于实验研究、神经影像学研究的证据以及TS患者对拮抗或干扰假定多巴胺能途径的药物的治疗反应,有人提出多巴胺在TS病因中起核心作用。丁苯那嗪就是这样一种药物;它消耗突触前多巴胺和5-羟色胺储备,并阻断突触后多巴胺受体。在临床研究中,已发现丁苯那嗪对多种运动亢进性疾病有效,在一些研究中包括少数(<50例)TS患者。一项仅纳入TS患者(n = 77;平均年龄约15岁)的回顾性病历审查结果显示,丁苯那嗪治疗2年使超过80%的患者功能和TS相关症状得到改善,这些结果表明丁苯那嗪治疗可能具有长期益处。作者对120例联合使用多种药物的重度TS患者所做的研究证实了这些发现。丁苯那嗪长期(平均19个月)治疗使76%的患者临床总体印象变化量表评分为“改善”。这些发现很有前景,表明丁苯那嗪可能适合作为需要进一步抑制抽动的患者的附加疗法。