氯氮平:n -去甲基氯氮平(CLZ: NDMC)比值的可靠性

Shirlee Daniela Solomon, V. Powell, M. Sanches, C. Borlido, L. Burton, Dr Vincenzo De Luca, Dr Tarek Rajji, Dr Gary Remington
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引用次数: 2

摘要

氯氮平是唯一被批准用于治疗难治性精神分裂症(TRS)的药物。明确的剂量指南很难划定,治疗药物监测(TDM)已成为指导临床使用的常用方法。在这种情况下,人们的注意力也集中在氯氮平(CLZ)与其代谢物n -去甲基氯氮平(NDMC)之间的比例上。CLZ:NDMC比率与认知有关,认知是精神分裂症的一个重要临床领域,各种临床人口统计学因素被认为会影响它。迄今为止,CLZ:NDMC比率的可靠性尚未建立,本研究旨在(i)计算CLZ:NDMC比率的类内相关系数(ICC)以评估可靠性,以及(ii)调查选定的临床人口学因素的影响。样本包括100名被诊断为精神分裂症或分裂情感性障碍的患者,他们接受氯氮平治疗,稳定在当前剂量,并能够提供至少2个TDM样本。CLZ:NDMC比值的计算ICC为0.65,而性别和共同服用情绪稳定剂,特别是双丙戊酸钠,被发现对该比值有显著影响。综上所述,CLZ:NDMC比值是中等可靠的,可能受到临床变量的影响,值得进一步研究。目前研究的主要局限性包括无法收集相关变量的数据,如吸烟和种族,以及分类排除已知的氯氮平代谢抑制剂/诱导剂。同时,这些限制强调了在临床实践中利用这些措施的挑战。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Reliability of the clozapine: N-desmethylclozapine (CLZ: NDMC) ratio
Clozapine represents the only agent approved for treatment resistant schizophrenia (TRS). Clear dosing guidelines have been difficult to delineate, and therapeutic drug monitoring (TDM) has become a common method to guide clinical use. In this context, attention has also focused on the ratio between clozapine (CLZ) and its metabolite, N-desmethylclozapine (NDMC). The CLZ:NDMC ratio has been implicated in cognition, an important clinical domain in schizophrenia, and various clinico-demographic factors are thought to impact it. To date, the reliability of the CLZ:NDMC ratio has not been established, and the present study aimed to (i) calculate the intraclass correlation coefficient (ICC) for the CLZ:NDMC ratio to assess reliability, and (ii) investigate the effect of selected clinico-demographic factors. The sample consisted of 100 patients diagnosed with schizophrenia or schizoaffective disorder being treated with clozapine, stabilized on their current dose, and able to provide at least 2 TDM samples. The calculated ICC for the CLZ:NDMC ratio was 0.65, while sex and co-administration of a mood stabilizer, specifically divalproex sodium, were found to significantly impact the ratio. In conclusion, the CLZ:NDMC ratio is moderately reliable, and can be influenced by clinical variables that warrant further investigation. Key limitations of the present investigation include inability to collect data on relevant variables such as smoking and ethnicity, as well as categorical exclusion of known inhibitors/inducers of clozapine metabolism. At the same time, these limitations underscore the challenges in utilizing such measures in clinical practice.
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