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Method for predicting the risk of developing side effects due to administration of compounds whose own or intermediate metabolites are metabolized by the UGT1A1 enzyme

机译:预测由于施用其自身或中间代谢物被UGT1A1酶代谢的化合物而产生副作用的风险的方法

摘要

A method of estimating a risk of the expression of an adverse drug reaction caused by the administration of irinotecan; and a method of reducing the adverse drug reaction caused by the administration of irinotecan. A polymorphism on the basis of a difference in the repeating numbers of TA repetitive sequences in the promoter region of UGT1 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. Based on the analytical data, the risk of the expression of an adverse drug reaction caused by the administration of irinotecan is estimated. 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 cased by the administration of irinotecan. IMAGE
机译:一种估计由伊立替康给药引起的药物不良反应表达风险的方法;以及减少由伊立替康给药引起的药物不良反应的方法。基于UGT1基因启动子区域中TA重复序列重复数的差异的多态性和基于外显子1中单核苷酸多态性的两种类型的多态性(基于211和686位碱基)被分析。基于分析数据,估计了由伊立替康给药引起的药物不良反应表达的风险。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。 <图像>

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