University of Kentucky Mental Health Research Center at Eastern State Hospital, Lexington, KY, USA; Biomedical Research Centre in Mental Health Net (CIBERSAM), Santiago Apóstol Hospital, University of the Basque Country, Vitoria, Spain.
Eur Neuropsychopharmacol. 2022 May;58:80-85. doi: 10.1016/j.euroneuro.2022.03.001. Epub 2022 Mar 18.
Recently, Salagre and Vieta commented on the complexity of implementing precision medicine in psychiatry. For 25 years, this author has focused on a circumscribed type of precision medicine: personalized dosing using pharmacokinetic mechanisms to stratified patients. This short communication focuses on personalized dosing of three oral antipsychotics (clozapine, risperidone and paliperidone) and presents their maintenance dosing in a table which provides dose-correction factors generated by pharmacokinetic studies. Inhibitors need dose-correction factors < 1 and inducers need correction factors >1. Clozapine maintenance dosing is based on the dose needed to reach 350 ng/ml (the minimum plasma therapeutic concentration in treatment-resistant schizophrenia). Clozapine maintenance dosing is influenced by 3 levels of complexity: 1) ancestry groups (Asians/Native Americans; Europeans and Blacks), 2) sex-smoking subgroups (lowest dose in female non-smokers and highest in male smokers) and 3) presence/absence of poor metabolizer status (due to genetic and non-genetic causes including co-prescription of inhibitors, obesity or inflammation). Risperidone and paliperidone maintenance dosing are based on the dose needed to reach plasma concentrations of 20-60 ng/ml. Risperidone PMs need approximately half the dose, which can be explained by genetics (CYP2D6 PMs) or co-prescription of CYP2D6 inhibitors. Fluoxetine co-prescription may require one fourth the risperidone maintenance dose. Carbamazepine co-prescription may require twice the risperidone maintenance dose. Although not well studied, two groups may need higher doses of oral paliperidone: Koreans may need 1.5 times higher doses while those taking carbamazepine may need 3 times higher paliperidone maintenance doses. Precision dosing in psychiatry requires using blood levels of individuals.
最近,Salagre 和 Vieta 评论了在精神病学中实施精准医学的复杂性。作者 25 年来一直专注于一种特定类型的精准医学:使用药代动力学机制对患者进行分层的个体化给药。本简讯重点介绍三种口服抗精神病药物(氯氮平、利培酮和帕利哌酮)的个体化给药,并提供了一个表格,其中列出了药代动力学研究产生的剂量校正因子。抑制剂需要校正因子 < 1,诱导剂需要校正因子 >1。氯氮平的维持剂量基于达到 350ng/ml(治疗抵抗性精神分裂症的最低血浆治疗浓度)所需的剂量。氯氮平的维持剂量受 3 个复杂程度的影响:1)种族群体(亚洲人/美洲原住民;欧洲人和黑人),2)性别-吸烟亚组(女性非吸烟者最低剂量,男性吸烟者最高剂量),3)是否存在代谢不良者状态(由于遗传和非遗传原因,包括同时处方抑制剂、肥胖或炎症)。利培酮和帕利哌酮的维持剂量基于达到 20-60ng/ml 血浆浓度所需的剂量。利培酮 PM 大约需要一半的剂量,这可以用遗传学(CYP2D6 PM)或同时处方 CYP2D6 抑制剂来解释。氟西汀同时处方可能需要利培酮维持剂量的四分之一。卡马西平同时处方可能需要利培酮维持剂量的两倍。虽然研究不多,但有两个群体可能需要更高剂量的口服帕利哌酮:韩国人可能需要 1.5 倍的剂量,而同时服用卡马西平的人可能需要 3 倍的帕利哌酮维持剂量。精神病学中的精准给药需要使用个体的血药浓度。