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A case report of voriconazole therapy failure in a homozygous ultrarapid CYP2C19*17/*17 patient comedicated with carbamazepine

机译:纯康唑治疗失败的杂康唑治疗杂志CYP2C19 * 17 / * 17患者与尸毒血管瘤(Carbamazepine)的案例报告

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摘要

Recently this journal published an article in which the authors examined by literature search the clinical implication of the ultrarapid CYP2C19* 17 variant allele. The authors concluded that the CYP2C19* 17 increased enzyme activity is unlikely to be clinically significant for voricona-zole. However, a comment to this article replied that in the case of voriconazole the variant allele CYP2C19* 17 certainly is clinically relevant and that data have shown that in subjects carrying a single CYP2C79*17allele,exposure may be reduced by up to 50 percent compared with normal metabo-lizers.The authors of the comment also mention that they are not aware of published studies of homozygous CVP2C79*17/*17 patients; and they assume that these subjects would display further reduced voriconazole exposure. In this case report we present a case of voriconazole therapy failure in a homozygous CYP2C19*17/*17 patient comedicated with carbamazepine.
机译:最近,该期刊发布了一篇文章,其中文学检测的作者搜索超鲜CYP2C19 * 17变异等位基因的临床意义。 作者得出结论,CYP2C19 * 17增加的酶活性对于vioricona-Zole不太可能是临床上显着的。 然而,对本文的评论回答说,在voriconazole的情况下,变异等位基因CYP2C19 * 17当然是临床相关的并且数据表明,在携带单个CYP2C79 * 17的受试者中,相比,暴露可能降低至多50% 正常的梅纳博利斯。评论的作者还提到他们不知道出版的纯合CVP2C79 * 17 / * 17名患者的研究; 他们认为这些受试者将显示进一步减少的伏立康唑暴露。 在本例中,我们提出了一种纯合CYP2C19 * 17 / * 17患者在纯合的CYP2C19 * 17患者中进行的voriconazole治疗失败的情况。

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