Department of Psychiatry, Post Graduate Institute of Medical Education and Research, Chandigarh, India.
Department of Internal Medicine, Post Graduate Institute of Medical Education and Research, Chandigarh, India.
Clin Psychopharmacol Neurosci. 2016 May 31;14(2):212-7. doi: 10.9758/cpn.2016.14.2.212.
Agranulocytosis as a side effect of clozapine has been reported to be associated with initial phases of treatment, i.e., first six months. Agranulocytosis with clozapine during the initial phases of treatment has been linked to genetic vulnerability in the form of variations in the human leukocyte-antigen haplotypes. However, there is limited literature on late onset agranulocytosis with clozapine and this has very rarely been linked to human leukocyte-antigen haplotypes vulnerability. In this report we review the existing data on late onset agranulocytosis with clozapine and describe the case of a young man, who developed agranulocytosis with clozapine after 35 months of treatment and was found to have genetic vulnerability in form of being positive for HLA DR4. This case highlights underlying autoimmune immune mechanism in clozapine-induced agranulocytosis and the need for frequent blood count monitoring on clozapine even after the initial 6 months of starting treatment especially in patients with genetic vulnerability to develop this condition.
粒细胞缺乏症作为氯氮平的副作用,据报道与治疗的初始阶段有关,即前六个月。在治疗的初始阶段,氯氮平引起的粒细胞缺乏症与人类白细胞抗原单倍型的遗传易感性有关。然而,关于氯氮平引起的迟发性粒细胞缺乏症的文献有限,而且这种情况很少与人类白细胞抗原单倍型易感性有关。在本报告中,我们回顾了氯氮平引起的迟发性粒细胞缺乏症的现有数据,并描述了一名年轻男性的病例,他在接受氯氮平治疗 35 个月后出现粒细胞缺乏症,并且被发现具有 HLA-DR4 阳性的遗传易感性。该病例强调了氯氮平诱导的粒细胞缺乏症中潜在的自身免疫机制,以及即使在开始治疗后的最初 6 个月后,也需要频繁监测氯氮平的血细胞计数,特别是在易发生这种情况的患者中。