Department of Psychiatry and Psychotherapy, Klinikum Offenbach GmbH, Mainz, Germany.
Int Clin Psychopharmacol. 2010 Mar;25(2):101-6. doi: 10.1097/YIC.0b013e32833643fd.
Eight schizophrenic inpatients without manifest comorbidity were longitudinally studied. The aim was to find whether clozapine, the prototype of atypical antipsychotic drugs, altered their serum concentrations of high sensitive C-reactive protein (hsCRP), an inflammatory marker of high clinical importance. Following first-time therapy with clozapine, predominantly as the sole antipsychotic for 8 weeks, hsCRP profiles increased subclinically by 600%. This rise, and the Spearman correlation between hsCRP values and corresponding leukocyte counts, was statistically significant. A one-time cross-section investigation of 25 long-term clozapine patients and 25 patient controls did not show an elevation of hsCRP under clozapine after 1 year and more. It is assumed that the clozapine-evoked increase of hsCRP is part of a transient acute-phase response. The underlying inflammatory process needs clarification.
对 8 名无明显合并症的精神分裂症住院患者进行了纵向研究。目的是确定作为典型抗精神病药物原型的氯氮平是否会改变其血清高敏 C 反应蛋白 (hsCRP)浓度,hsCRP 是一种具有重要临床意义的炎症标志物。在首次接受氯氮平治疗(主要是作为单一抗精神病药物)8 周后,hsCRP 水平亚临床上升了 600%。这种升高以及 hsCRP 值与相应白细胞计数之间的斯皮尔曼相关性均具有统计学意义。对 25 名长期氯氮平患者和 25 名患者对照进行的一次性横断面调查显示,在 1 年及更长时间后,氯氮平并未引起 hsCRP 的升高。据推测,氯氮平引起的 hsCRP 升高是短暂急性期反应的一部分。需要阐明潜在的炎症过程。