Clozapine/norclozapine plasma concentrations and their ratio in treatment resistant, early psychosis patients.

Q3 Medicine
Psychiatrike = Psychiatriki Pub Date : 2025-04-07 Epub Date: 2025-03-24 DOI:10.22365/jpsych.2025.001
Andreas Karampas, Dimitra Florou, Giorgos Markozannes, Alexandros Asimakopoulos, Giorgos Georgiou, Marios Plakoutsis, Thomas Hyphantis, Vasiliki Boumba, Petros Petrikis
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Abstract

Treatment-resistant schizophrenia affects approximately 30% of schizophrenia patients, and clozapine is the antipsychotic of choice for their treatment. Despite its effectiveness, clozapine is considerably under-prescribed for the aforementioned patients' group, probably due to its severe side effects. Measurement of plasma concentrations of clozapine and its active metabolite, norclozapine, in plasma could help clinicians to monitor compliance to treatment and reduce the possibility of severe side effects. Such measurements are currently not included in routine clinical practice, although clozapine plasma concentrations seem to be influenced by many different factors and do not usually reflect the prescribed dose. The aim of the present study was to measure clozapine and norclozapine plasma concentrations and their ratio in a group of early psychosis, treatment-resistant, schizophrenia patients and to investigate possible associations among the prescribed clozapine daily dose and socio- demographic variables. Thirty-eight patients were included in the study, and 342 blood samples were collected. Clozapine and norclozapine plasma concentration measurements were performed by UHPLC-MS/MS. Mixed-effects linear regression models were performed to associate blood clozapine and norclozapine levels and their ratio to clozapine dose. The median clozapine dose, clozapine, norclozapine plasma concentrations, and their ratio at first and last measurement were as follows: 400mg/day (IQR = 350mg/day to 500mg/day) and 425mg/day (IQR = 350mg/day to 600mg/day), 335 ng/ml (IQR = 191 ng/ml to 427 ng/ml) and 389 ng/ml (IQR = 276 ng/ml to 523 ng/ml), 129 ng/ml (IQR = 62 ng/ml to 218 ng/ml) and 135 ng/ml (IQR = 82 ng/ml to 209 ng/ml), 2.5 (IQR = 1.6 to 4.8) and 2.9 (IQR = 1.7 to 4.4). An increase of clozapine dose by 50mg/day was associated with higher blood clozapine and norclozapine levels but with lower clozapine/norclozapine ratio. Clozapine dose was positively associated with blood clozapine and norclozapine levels and negatively with the clozapine/norclozapine ratio.

抗药早期精神病患者氯氮平/去甲氮平血药浓度及其比值。
难治性精神分裂症影响了大约30%的精神分裂症患者,氯氮平是他们治疗的首选抗精神病药物。尽管氯氮平很有效,但对于上述患者来说,它的处方还是相当少的,可能是由于其严重的副作用。测定血浆中氯氮平及其活性代谢物去氯氮平的浓度可以帮助临床医生监测治疗的依从性,减少严重副作用的可能性。虽然氯氮平的血浆浓度似乎受到许多不同因素的影响,通常不能反映处方剂量,但这种测量目前尚未纳入常规临床实践。本研究的目的是测量氯氮平和去甲氯氮平在一组早期精神病、治疗抵抗、精神分裂症患者中的血药浓度及其比值,并调查氯氮平处方日剂量与社会人口统计学变量之间的可能关联。38名患者参与了这项研究,收集了342份血液样本。采用UHPLC-MS/MS法测定氯氮平和去氯氮平的血药浓度。采用混合效应线性回归模型分析血液氯氮平和去氯氮平水平及其与氯氮平剂量的比值。中等剂量氯氮平、氯氮平norclozapine血浆浓度,和他们比在第一个和最后一个测量如下:400毫克/天(IQR = 350毫克/天至500毫克/天)和425毫克/天(IQR = 350毫克/天至600毫克/天),335 ng / ml (IQR = 191 ng / ml 427 ng / ml)和389 ng / ml (IQR = 276 ng / ml 523 ng / ml), 129 ng / ml (IQR = 62 ng / ml 218 ng / ml)和135 ng / ml (IQR = 82 ng / ml 209 ng / ml), 2.5 (IQR = 1.6 - 4.8)和2.9 (IQR = 1.7 - 4.4)。氯氮平剂量增加50mg/天与血氯氮平和去氯氮平水平升高有关,但与氯氮平/去氯氮平比值降低有关。氯氮平剂量与血氯氮平和去氯氮平水平呈正相关,与氯氮平/去氯氮平比值呈负相关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Psychiatrike = Psychiatriki
Psychiatrike = Psychiatriki Medicine-Medicine (all)
CiteScore
2.60
自引率
0.00%
发文量
37
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