Ozdemir V, Kalow W, Okey A B, Lam M S, Albers L J, Reist C, Fourie J, Posner P, Collins E J, Roy R
Department of Pharmacology, University of Toronto, Ontario, Canada.
J Clin Psychopharmacol. 2001 Dec;21(6):603-7. doi: 10.1097/00004714-200112000-00011.
Antipsychotic response to clozapine varies markedly among patients with schizophrenia. The disposition of clozapine is dependent, in part, on the cytochrome P-450 (CYP) 1A2 enzyme in vivo. In theory, a very high CYP1A2 activity may lead to subtherapeutic concentrations and treatment resistance to clozapine. This prospective case study evaluates the clinical significance of ultrarapid CYP1A2 activity and a recently discovered single nucleotide (C --> A) polymorphism in intron 1 of the CYP1A2 gene (CYP1A2*F) for treatment resistance to clozapine. In addition, we describe the effect of grapefruit juice or low-dose fluvoxamine (25-50 mg/d) coadministration on clozapine and active metabolite norclozapine steady-state plasma concentration and antipsychotic response.
精神分裂症患者对氯氮平的抗精神病反应差异显著。氯氮平的体内处置部分依赖于细胞色素P-450(CYP)1A2酶。理论上,CYP1A2活性过高可能导致氯氮平血药浓度低于治疗水平并产生治疗抵抗。本前瞻性病例研究评估了CYP1A2超快速活性以及最近发现的CYP1A2基因第1内含子中的单核苷酸(C→A)多态性(CYP1A2*F)对氯氮平治疗抵抗的临床意义。此外,我们描述了同时服用葡萄柚汁或低剂量氟伏沙明(25 - 50毫克/天)对氯氮平和活性代谢产物去甲氯氮平稳态血药浓度及抗精神病反应的影响。