Nyberg S, Eriksson B, Oxenstierna G, Halldin C, Farde L
Karolinska Institutet, Department of Clinical Neuroscience, Karolinska Hospital, Stockholm, Sweden.
Am J Psychiatry. 1999 Jun;156(6):869-75. doi: 10.1176/ajp.156.6.869.
Multicenter trials with the novel antipsychotic risperidone have suggested a standard dose of 6 mg/day. However, a dose producing the highest response rate in fixed-dose studies is likely to exceed the minimal effective dose in most patients. The aim of this positron emission tomography (PET) study was to suggest a minimal effective dose of risperidone based on measurements of dopamine D2 and serotonin 5-HT2A receptor occupancy.
Eight first-episode or drug-free schizophrenic patients were treated with risperidone, 6 mg/day, for 4 weeks and then 3 mg/day for 2 weeks. PET was performed after 4 and 6 weeks, with [11C]raclopride to measure D2 receptor occupancy and [11C]N-methylspiperone to measure 5-HT2A receptor occupancy.
Seven patients completed the study and responded to treatment with risperidone. No patient had extrapyramidal side effects at the time of inclusion in the study. At the 6-mg/day dose, mean D2 receptor occupancy was 82% (range = 79%-85%), 5-HT2A receptor occupancy was 95% (range = 86%-109%), and six patients had developed extrapyramidal side effects. After dose reduction to 3 mg/day, D2 receptor occupancy was 72% (range = 53%-78%), and 5-HT2A receptor occupancy was 83% (range = 65%-112%). Three patients had extrapyramidal side effects at this time.
Treatment with risperidone, 6 mg/day, is likely to induce unnecessarily high D2 receptor occupancy, with a consequent risk of extrapyramidal side effects. High 5-HT2A receptor occupancy did not prevent extrapyramidal side effects completely. The authors previously suggested an optimal interval for D2 receptor occupancy of 70%-80%. To achieve this, resperidone, 4 mg/day, should be a suitable initial dose for antipsychotic effect with a minimal risk of extrapyramidal side effects in most patients.
新型抗精神病药物利培酮的多中心试验表明标准剂量为6毫克/天。然而,在固定剂量研究中产生最高反应率的剂量在大多数患者中可能超过最小有效剂量。这项正电子发射断层扫描(PET)研究的目的是根据多巴胺D2和5-羟色胺5-HT2A受体占有率的测量结果,提出利培酮的最小有效剂量。
8例首发或未用过药的精神分裂症患者接受利培酮治疗,开始剂量为6毫克/天,持续4周,然后减为3毫克/天,持续2周。在第4周和第6周后进行PET检查,用[11C]雷氯必利测量D2受体占有率,用[11C]N-甲基螺哌隆测量5-HT2A受体占有率。
7例患者完成研究并对利培酮治疗有反应。纳入研究时无患者有锥体外系副作用。在6毫克/天剂量时,平均D2受体占有率为82%(范围=79%-85%),5-HT2A受体占有率为95%(范围=86%-109%),6例患者出现锥体外系副作用。剂量减至3毫克/天后,D2受体占有率为72%(范围=53%-78%),5-HT2A受体占有率为83%(范围=65%-112%)。此时3例患者有锥体外系副作用。
6毫克/天的利培酮治疗可能会导致不必要的高D2受体占有率,从而有发生锥体外系副作用的风险。高5-HT2A受体占有率并不能完全预防锥体外系副作用。作者之前提出D2受体占有率的最佳区间为70%-80%。为达到这一目标,4毫克/天的利培酮应是大多数患者抗精神病作用的合适初始剂量,且锥体外系副作用风险最小。