Pharmacogenomic screening for agranulocytosis and efficacy with clozapine

M. Shad
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Abstract

Aim: To review genetic biomarkers of agranulocytosis and efficacy with clozapine as a screening tool for the safe and effective use of clozapine. Methods: A PubMed search was performed using PRISMA guidelines for English articles. Separate searches were conducted using “clozapine” AND “agranulocytosis,” and “clozapine” AND (“response” OR efficacy “outcome”) AND “schizophrenia”. Eligible studies reported positive findings with genetic polymorphism(s) associated with clozapine-induced agranulocytosis (CIA) and clozapine’s efficacy. Case reports/series, abstracts, systematic reviews, and meta-analyses were excluded. Negative and genome-wide studies were not formally reviewed but included in the discussion. Results: Twelve out of 572 CIA studies and 32 out of 126 efficacy studies met the eligibility criteria for this review. Most reviewed studies were conducted in small samples of Jewish, Caucasian, and Asian populations using a candidate gene approach. Conclusion: Future research needs to address the limitations of the findings from the reviewed studies to enable a combined genetic screening for CIA and clozapine response to optimize the safe and effective use of clozapine without unnecessarily exposing potential clozapine nonresponders to CIA or neutropenia.
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氯氮平对粒细胞缺乏症的药物基因组学筛查及其疗效
目的:回顾氯氮平对粒细胞缺乏症的遗传生物标志物和疗效,作为氯氮平安全有效使用的筛选工具。方法:使用PRISMA指南对英文文章进行PubMed检索。分别使用“氯氮平”和“粒细胞缺乏症”、“氯氮平”和(“反应”或“疗效”)和“精神分裂症”进行搜索。符合条件的研究报告了与氯氮平诱导的粒细胞缺乏症(CIA)和氯氮平疗效相关的基因多态性阳性结果。排除病例报告/系列、摘要、系统评价和荟萃分析。阴性和全基因组研究没有正式审查,但包括在讨论中。结果:572项CIA研究中有12项和126项疗效研究中有32项符合本综述的资格标准。大多数研究都是在犹太人、高加索人和亚洲人的小样本中使用候选基因方法进行的。结论:未来的研究需要解决所回顾研究结果的局限性,以便对CIA和氯氮平反应进行联合遗传筛查,以优化氯氮平的安全有效使用,而不会不必要地使潜在的氯氮平无应答者暴露于CIA或中性粒细胞减少症。
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