首页> 外文期刊>International clinical psychopharmacology >Human leukocyte antigen typing, response to neuroleptics, and clozapine-induced agranulocytosis in jewish Israeli schizophrenic patients.
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Human leukocyte antigen typing, response to neuroleptics, and clozapine-induced agranulocytosis in jewish Israeli schizophrenic patients.

机译:以色列犹太人精神分裂症患者的人类白细胞抗原分型,对精神抑制药的反应以及氯氮平诱导的粒细胞缺乏症。

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The atypical antipsychotic agent clozapine is known to be effective in schizophrenic patients refractory to other medications; however, it induces agranulocytosis in approximately 1-2%. In Jews, this complication is associated with the haplotype HLA B38,DR4,DQ3. The aim of the present study was to determine which human leukocyte antigen (HLA) antigens are involved in clozapine-induced agranulocytosis. We performed HLA typing in 88 Jewish Israeli schizophrenic patients and in 127 ethnically matched healthy individuals. Thirty-eight patients responsive to standard antipsychotic medications were treated with haloperidol, and 50 refractory patients received clozapine. A trend was noted for elevated rates of HLA B38 among control individuals and clozapine-treated patients of Ashkenazi origin compared to individuals of non-Ashkenazi origin, but the findings failed to reach statistical significance. No association was found between HLA class I antigens and the response to haloperidol or clozapine. Neutropenia developed in two clozapine-treated patients and agranulocytosis in one. Two of these three patients were of Ashkenazi origin, and both demonstrated the HLA B38 phenotype. Although the findings did not reach a statistical significance because of the small number of patients, they may support an association between clozapine-induced neutropenia/agranulocytosis and Ashkenazi origin and the HLA B38 phenotype. The rate of agranulocytosis in our sample (2%) is similar to the usual cumulative risk of agranulocytosis but in contrast to its high frequency among Jewish American patients. One possible explanation for this difference is the high rate of Ashkenazi patients in the American sample and the preponderance of non-Ashkenazi patients in our population.
机译:已知非典型抗精神病药氯氮平对其他药物难以治疗的精神分裂症患者有效。然而,它诱导粒细胞缺乏症的比例约为1-2%。在犹太人中,这种并发症与单倍型HLA B38,DR4,DQ3有关。本研究的目的是确定氯氮平诱导的粒细胞缺乏症涉及哪些人类白细胞抗原(HLA)抗原。我们对88名以色列犹太人精神分裂症患者和127名种族匹配的健康个体进行了HLA分型。 38例对标准抗精神病药物有反应的患者接受了氟哌啶醇治疗,50例难治性患者接受了氯氮平治疗。与非Ashkenazi来源的个体相比,在对照个人和接受氯氮平治疗的Ashkenazi来源的患者中,HLA B38的发生率呈上升趋势,但该发现未能达到统计学意义。在HLA I类抗原与氟哌啶醇或氯氮平的反应之间未发现关联。两名接受氯氮平治疗的患者出现中性粒细胞减少症,一名患有粒细胞缺乏症。这三位患者中有两位来自阿什肯纳兹(Ashkenazi),均显示出HLA B38表型。尽管由于患者人数少,这些发现没有统计学意义,但它们可能支持氯氮平诱导的中性粒细胞减少/无粒细胞增多症和阿什肯纳兹起源与HLA B38表型之间的关联。在我们的样本中,粒细胞缺乏症的发生率(2%)与通常的粒细胞缺乏症的累积风险相似,但与此相反,在美国犹太人患者中粒细胞缺乏症的发生率很高。这种差异的一种可能解释是,美国样本中的Ashkenazi患者比例很高,而在我们的人口中非Ashenazi患者占优势。

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