Migliardi Gaetana, D'Arrigo Concetta, Santoro Vincenza, Bruno Antonio, Cortese Lara, Campolo Domenica, Cacciola Massimo, Spina Edoardo
Section of Pharmacology, Department of Clinical and Experimental Medicine and Pharmacology, University of Messina, Messina, Italy.
Clin Neuropharmacol. 2007 Mar-Apr;30(2):107-13. doi: 10.1097/01.wnf.0000240955.49315.65.
To investigate the effect of topiramate on the steady-state plasma concentrations of the second-generation antipsychotics--clozapine, olanzapine, risperidone, and quetiapine--in patients with schizophrenia or bipolar disorder.
Thirty-eight outpatients on long-term treatment with clozapine (250-500 mg/d, n = 10), olanzapine (10-20 mg/d, n = 12), risperidone (3-6 mg/d, n = 9), or quetiapine (200-600 mg/d, n = 7) received adjunctive topiramate, gradually titrated up to a final dosage of 200 mg/d for 6 weeks. Pharmacokinetic assessments were made at baseline and at the end of treatment weeks 4 and 8 at topiramate dosages of 100 and 200 mg/d, respectively.
Plasma concentrations of clozapine and its metabolite (norclozapine), olanzapine, risperidone and its metabolite (9-hydroxy-risperidone), and quetiapine were not significantly modified during concomitant administration of topiramate. Adjunctive topiramate therapy was well tolerated in all groups.
These findings indicate that topiramate, at the dosages recommended for use as a mood stabilizer, does not affect the plasma levels of the new antipsychotics-clozapine, olanzapine, risperidone, and quetiapine.
研究托吡酯对精神分裂症或双相情感障碍患者第二代抗精神病药物(氯氮平、奥氮平、利培酮和喹硫平)稳态血药浓度的影响。
38例长期服用氯氮平(250 - 500mg/d,n = 10)、奥氮平(10 - 20mg/d,n = 12)、利培酮(3 - 6mg/d,n = 9)或喹硫平(200 - 600mg/d,n = 7)的门诊患者接受托吡酯辅助治疗,逐渐滴定至最终剂量200mg/d,持续6周。分别在基线以及托吡酯剂量为100mg/d和200mg/d时治疗第4周和第周结束时进行药代动力学评估。
在同时服用托吡酯期间,氯氮平及其代谢物(去甲氯氮平)、奥氮平、利培酮及其代谢物(9 - 羟基利培酮)和喹硫平的血药浓度未发生显著改变。所有组对托吡酯辅助治疗耐受性良好。
这些研究结果表明,以推荐用作心境稳定剂的剂量使用托吡酯,不会影响新型抗精神病药物(氯氮平、奥氮平、利培酮和喹硫平)的血药水平。