Kinon Bruce J, Ahl Jonna, Stauffer Virginia L, Hill Angela L, Buckley Peter F
Lilly Research Laboratories, Eli Lilly and Company, Lilly Corporate Center, Drop Code 4133, Indianapolis, IN 46285, USA.
CNS Drugs. 2004;18(9):597-616. doi: 10.2165/00023210-200418090-00005.
Based on information from clinical trials, both the efficacy and adverse effects of conventional antipsychotics in the treatment of schizophrenia are dose related. The overlapping nature of these dose-response profiles limits the use of these agents. Atypical antipsychotics provide greater relief across the comorbid symptom domains of schizophrenia, but dose-response studies and clinical experience have revealed that some of these drugs also have dose limitations. This article reviews the dose-response relationships of the atypical antipsychotics as presented predominantly in pivotal, randomised studies (double-blind and otherwise). Limited data indicate that clozapine shows dose-related efficacy up to 600 mg/day in patients with treatment-resistant schizophrenia. However, higher dosages of clozapine may be associated with the risk of seizures. Risperidone demonstrates dose-related adverse events that compromise efficacy. The dose-response relationships for ziprasidone, quetiapine and aripiprazole are less well established. The efficacy of olanzapine appears to be dose related within the recommended dosage range of 10-20 mg/day, but clinical trials that have explored higher dosages suggest improved efficacy. Furthermore, the higher doses are not associated with a significantly increased incidence of adverse events. Further studies are clearly needed to fully characterise the dose-response relationships of atypical antipsychotics.
基于临床试验信息,传统抗精神病药物治疗精神分裂症的疗效和不良反应均与剂量相关。这些剂量反应曲线的重叠特性限制了这些药物的使用。非典型抗精神病药物能在精神分裂症的共病症状领域提供更大程度的缓解,但剂量反应研究和临床经验表明,其中一些药物也存在剂量限制。本文主要回顾在关键的随机研究(双盲及其他)中呈现的非典型抗精神病药物的剂量反应关系。有限的数据表明,对于难治性精神分裂症患者,氯氮平在每日600毫克的剂量范围内显示出与剂量相关的疗效。然而,更高剂量的氯氮平可能与癫痫发作风险相关。利培酮表现出与剂量相关的不良事件,这会影响疗效。齐拉西酮、喹硫平和阿立哌唑的剂量反应关系尚不明确。在10 - 20毫克/天的推荐剂量范围内,奥氮平的疗效似乎与剂量相关,但探索更高剂量的临床试验表明疗效有所改善。此外,更高剂量与不良事件发生率的显著增加无关。显然需要进一步研究以全面描述非典型抗精神病药物的剂量反应关系。