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首页> 外文期刊>Neuropsychopharmacology >Plasma Clozapine and Desmethylclozapine Levels in Clozapine-Induced Agranulocytosis
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Plasma Clozapine and Desmethylclozapine Levels in Clozapine-Induced Agranulocytosis

机译:氯氮平诱导的粒细胞缺乏症中的血浆氯氮平和去甲基氯氮平水平

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摘要

Clozapine may produce agranulocytosis in 1–2% of patients treated with it for 4 weeks or longer. Three mechanisms have been suggested: a direct toxic effect of metabolite of clozapine, an immunologic mechanism or a combination of both. N-desmethylclozapine, the major metabolite of clozapine, has been reported to be more toxic than clozapine itself (Gerson et al., 1994). In this study, plasma levels of clozapine and desmethylclozapine were measured in five patients who developed agranulocytosis. The levels of both parent compound and metabolite were within the range found in other patients and below the toxic range. If a toxic mechanism is involved in clozapine-induced agranulocytosis, an additional vulnerability factor must be important.
机译:氯氮平治疗4周或更长时间的患者中,1-2%的患者可能会产生粒细胞缺乏症。已经提出了三种机制:氯氮平代谢产物的直接毒性作用,免疫机制或两者的组合。 N-去甲基氯氮平是氯氮平的主要代谢产物,据报道比氯氮平本身毒性更大(Gerson等,1994)。在这项研究中,测定了五名发生粒细胞缺乏症的患者的氯氮平和去甲基氯氮平的血浆水平。母体化合物和代谢产物的水平都在其他患者中发现的范围内,并且低于毒性范围。如果氯氮平诱导的粒细胞缺乏症涉及一种毒性机制,那么额外的脆弱性因素就必须很重要。

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