Center for Psychopharmacology, Diakonhjemmet Hospital, Oslo, Norway.
Division of Mental Health and Addiction, NORMENT and K.G. Jebsen Centre for Psychosis Research, University of Oslo and Oslo University Hospital, Oslo, Norway.
CNS Drugs. 2017 Nov;31(11):991-997. doi: 10.1007/s40263-017-0469-1.
Clozapine is restricted to use in patients with treatment-refractory schizophrenia due to the risk of a serious drop in absolute neutrophil granulocyte count (ANC). The formation of reactive, unstable metabolites (adducts) has been suggested as a mechanism of clozapine-induced granulocyte decline. These adducts are not detectable in vivo, but stable clozapine metabolites could potentially be indirect pharmacokinetic measures of adduct formation.
The present retrospective observational study investigated the correlation between concentrations of N-desmethylclozapine, the major stable clozapine metabolite, and ANC in a real-life population of clozapine-treated patients.
Patients were included from a therapeutic drug monitoring service at the Center for Psychopharmacology, Diakonhjemmet Hospital, Oslo, Norway, between March 2005 and December 2015. Information about clozapine and N-desmethylclozapine steady-state trough concentrations, as well as accompanying measurements of ANC, were collected from the laboratory database. Correlations of serum concentrations of N-desmethylclozapine and clozapine (and their respective ratios) with ANC were investigated by linear mixed-model analysis.
Overall, 129 patients with 855 measurements of clozapine/N-desmethylclozapine concentrations and ANC (range 0.9-19 × 10 cells/L, median 4.6) were included. Concentrations of N-desmethylclozapine, but not clozapine, correlated significantly and positively with ANC (estimated model slope 0.0011 × 10 cells/L/nM; p = 0.002), and the N-desmethylclozapine/clozapine ratio also positively correlated with ANC (p = 0.040).
N-Desmethylclozapine level and ANC significantly correlated in this real-life population of schizophrenia patients. The positive correlation, which was also present for the metabolic ratio, might reflect reduced clozapine availability for the formation of reactive metabolites potentially affecting granulocyte level. However, as our findings were based on ANC mainly within the reference range, this hypothesis should be studied further in clozapine-treated patients with neutropenia or agranulocytosis.
氯氮平由于存在严重的中性粒细胞绝对计数(ANC)下降风险,仅被限制用于治疗抵抗性精神分裂症患者。形成反应性、不稳定的代谢物(加合物)已被认为是氯氮平诱导粒细胞下降的一种机制。这些加合物在体内无法检测到,但稳定的氯氮平代谢物可能是加合物形成的间接药代动力学指标。
本回顾性观察研究调查了在接受氯氮平治疗的真实患者人群中,主要的稳定氯氮平代谢物 N-去甲基氯氮平和 ANC 浓度之间的相关性。
患者来自于挪威奥斯陆 Diakonhjemmet 医院精神药理学治疗药物监测服务中心,于 2005 年 3 月至 2015 年 12 月间入组。从实验室数据库中收集了氯氮平和 N-去甲基氯氮平稳态谷浓度以及 ANC 的相关信息。通过线性混合模型分析研究了 N-去甲基氯氮平血清浓度与 ANC 的相关性。
总体而言,共纳入 129 名患者,共 855 次氯氮平/N-去甲基氯氮平浓度和 ANC(范围 0.9-19×10 个细胞/L,中位数 4.6)测量值。N-去甲基氯氮平浓度而非氯氮平浓度与 ANC 显著正相关(估计模型斜率为 0.0011×10 个细胞/L/nM;p=0.002),N-去甲基氯氮平/氯氮平比值也与 ANC 正相关(p=0.040)。
在这一真实的精神分裂症患者人群中,N-去甲基氯氮平水平与 ANC 显著相关。这种正相关关系也存在于代谢比值中,这可能反映了形成反应性代谢物的氯氮平可用性降低,从而可能影响粒细胞水平。然而,由于我们的发现主要基于 ANC 在参考范围内,因此应在中性粒细胞减少症或粒细胞缺乏症的氯氮平治疗患者中进一步研究这一假说。