Caroff Stanley N, Walker Patricia, Campbell Cabrina, Lorry Alan, Petro Christopher, Lynch Kevin, Gallop Robert
Department of Veterans Affairs Medical Center, University of Pennsylvania School of Medicine, Philadelphia, USA.
J Clin Psychiatry. 2007 Mar;68(3):410-5. doi: 10.4088/jcp.v68n0309.
Recent evidence suggests that tar-dive dyskinesia may result from antipsychotic-induced damage to striatal cholinergic neurons. To test whether cholinesterase inhibitors compensate for diminished cholinergic activity, we conducted a 30-week randomized, double-blind, placebo-controlled crossover trial of galantamine in patients with tardive dyskinesia.
Patients with tardive dyskinesia were recruited between June 2001 and June 2004. After a 2-week baseline period, 35 male schizophrenia patients, on stable doses of antipsychotics, were randomly assigned to receive galantamine (8-24 mg) or placebo for two 12-week phases separated by a 4-week washout period. Patients were evaluated every 2 weeks for changes in extrapyramidal symptoms and before and after each treatment for effects on psychiatric symptoms and cognition.
Galantamine reduced mean total Abnormal Involuntary Movement Scale (AIMS) scores more than placebo, but this difference was not statistically significant (p = .08). However, patients initially randomly assigned to galantamine showed a reversal of AIMS scores after switching to placebo. Simpson-Angus Scale ratings of parkinsonism were significantly higher with galantamine than placebo (p = .0005) and correlated with age. There were no significant differences between groups in akathisia, cognition, or psychiatric symptoms. More patients dropped out while receiving galantamine, but this outcome did not significantly influence the results.
In contrast to previous reports, reductions in tardive dyskinesia associated with galantamine were not statistically significant compared with placebo in this trial. However, galantamine was associated with a modest rebound in dyskinesia scores after discontinuation and clinically minor but statistically higher ratings of parkinsonism. These findings support the need for further investigations of cholinergic mechanisms underlying tardive dyskinesia and extrapyramidal effects of cholinesterase inhibitors when used in combination with antipsychotics in susceptible patients.
ClinicalTrials.gov identifier NCT00164242.
近期证据表明,迟发性运动障碍可能是抗精神病药物导致纹状体胆碱能神经元受损所致。为了测试胆碱酯酶抑制剂是否能弥补胆碱能活性的降低,我们对迟发性运动障碍患者进行了一项为期30周的加兰他敏随机、双盲、安慰剂对照交叉试验。
2001年6月至2004年6月招募迟发性运动障碍患者。经过2周的基线期后,35名稳定服用抗精神病药物剂量的男性精神分裂症患者被随机分配接受加兰他敏(8 - 24毫克)或安慰剂,为期两个12周阶段,中间有4周的洗脱期。每2周评估患者锥体外系症状的变化,并在每次治疗前后评估对精神症状和认知的影响。
加兰他敏降低的异常不自主运动量表(AIMS)平均总分比安慰剂多,但这种差异无统计学意义(p = 0.08)。然而,最初随机分配接受加兰他敏治疗的患者在换用安慰剂后AIMS评分出现逆转。加兰他敏治疗的帕金森症患者辛普森 - 安格斯量表评分显著高于安慰剂(p = 0.0005),且与年龄相关。在静坐不能、认知或精神症状方面,两组之间无显著差异。接受加兰他敏治疗时更多患者退出,但这一结果并未对结果产生显著影响。
与之前的报告不同,在本试验中,与安慰剂相比,加兰他敏所致迟发性运动障碍的减轻无统计学意义。然而,加兰他敏与停药后运动障碍评分的适度反弹相关,且帕金森症的临床症状轻微但在统计学上评分较高。这些发现支持需要进一步研究迟发性运动障碍潜在的胆碱能机制以及胆碱酯酶抑制剂与抗精神病药物联合用于易感患者时的锥体外系效应。
ClinicalTrials.gov标识符NCT00164242。