首页> 外国专利> METHOD FOR ESTIMATING RISK OF EXPRESSION OF ADVERSE DRUG REACTION CAUSED BY ADMINISTRATION OF COMPOUND, WHICH IS EITHER METABOLIZED PER SE BY UGT1A1 ENZYME OR WHOSE METABOLIC INTERMEDIATE IS METABOLIZED BY ENZYME

METHOD FOR ESTIMATING RISK OF EXPRESSION OF ADVERSE DRUG REACTION CAUSED BY ADMINISTRATION OF COMPOUND, WHICH IS EITHER METABOLIZED PER SE BY UGT1A1 ENZYME OR WHOSE METABOLIC INTERMEDIATE IS METABOLIZED BY ENZYME

机译:评估化合物管理引起的不良药物反应表达风险的方法,UGT1A1酶本身已将其代谢,或者代谢产物的中间体被酶代谢了

摘要

PPROBLEM TO BE SOLVED: To provide a method for estimating the risk of expression of an adverse drug reaction caused by the administration of irinotecan and a method for reducing adverse reaction caused by administration of irinotecan. PSOLUTION: A polymorphism on the basis of a difference in the repeating numbers of TA repetitive sequences in the promoter region of T1A1 gene and two types of polymorphisms (bases at the 211- and 686-positions) on the basis of single nucleotide polymorphisms in the exon 1 are analyzed. Further, the administration doses of irinotecan is designed for individual patients depending on the risk of the expression of the adverse drug reaction, thereby reducing the adverse drug reaction caused by the administration of irinotecan. PCOPYRIGHT: (C)2009,JPO&INPIT
机译:<要解决的问题:提供一种估计由施用伊立替康引起的药物不良反应表达风险的方法和减少由施用伊立替康引起的不良反应的方法。

解决方案:一种多态性是基于T1A1基因启动子区域中TA重复序列的重复数的差异,以及两种基于单核苷酸的多态性(211和686位碱基)分析外显子1中的多态性。此外,依立替康的给药剂量是根据药物不良反应表达的风险为个别患者设计的,从而减少了因依立替康的给药而引起的药物不良反应。

版权:(C)2009,日本特许厅&INPIT

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