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首页> 外文期刊>European journal of immunogenetics: official journal of the British Society for Histocompatibility and Immunogenetics >HLA-B38 and clozapine-induced agranulocytosis in Israeli Jewish schizophrenic patients.
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HLA-B38 and clozapine-induced agranulocytosis in Israeli Jewish schizophrenic patients.

机译:以色列犹太人精神分裂症患者的HLA-B38和氯氮平诱导的粒细胞缺乏症。

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摘要

To further substantiate reports of an association between the major histocompatibility complex subtypes and clozapine-induced agranulocytosis, HLA typing was performed in 61 Jewish Israeli schizophrenic patients, in 11 of whom agranulocytosis developed following clozapine treatment and in 50 (controls) of whom it did not. Of the 11 agranulocytosis patients, seven (63%) were of Ashkenazi origin and four (37%) of Sephardi origin. There was no difference in ethnic origin between the arganulocytosis and non-agranulocytosis groups (chi 2 = 2.4, d.f. = 1, P = 0.11), although the agranulocytosis patients had a higher frequency of the HLA B38 antigen (8/11 or 72% vs. 6/50 or 12%; chi 2 = 18.7, d.f. = 1, P < 0.001). These results suggest that major histocompatibility complex gene products could be involved in clozapine-mediated haematological complications.
机译:为了进一步证实主要组织相容性复杂亚型与氯氮平诱导的粒细胞缺乏症之间存在关联的报道,对61名以色列以色列精神分裂症患者进行了HLA分型,其中11名在氯氮平治疗后出现粒细胞缺乏症,而其中的50名(对照组)则没有。在11名粒细胞缺乏症患者中,有7名(63%)来自阿什肯纳兹族,四名(37%)来自Sephardi。尽管粒细胞缺乏症患者的HLA B38抗原发生率较高(8/11或72%),但粒细胞缺乏症和非粒细胞缺乏症组的族裔差异没有统计学意义(chi 2 = 2.4,df = 1,P = 0.11)。 vs.6 / 50或12%; chi 2 = 18.7,df = 1,P <0.001)。这些结果表明,主要的组织相容性复合基因产物可能与氯氮平介导的血液学并发症有关。

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