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TRIAGING OF PATIENTS HAVING ASYMPTOMATIC HEMATURIA USING GENOTYPIC AND PHENOTYPIC BIOMARKERS

机译:使用基因型和表型生物标志物对无症状性血尿的患者进行分类

摘要

New methods for treating patents for urothelial cancer (UC) include combining selected phenotypic variables with levels of genotypic expression into a metric, the “G+P INDEX.” The G+P INDEX combines age, sex, smoking history, presence of hematuria, and frequency of hematuria with genotypic expression of the genetic markers, MDK, CDC2, HOXA13, IGFBP5, and optionally IL8Rb, then determining of the G+P INDEX value obtained for a patient is within one of three groups, either: (1) at High Risk of UC, (2) at Risk of UC, or (3) at Low Risk of UC. For groups 1 and 2, further clinical and laboratory work up or treatment is indicated, and patients in group 3 are monitored periodically to determine the need for further clinical workup. Using the G+P INDEX can save substantial time, effort, and funds by avoiding unnecessary medical diagnostic procedures for patients having or are at risk for developing UC.
机译:治疗尿路上皮癌(UC)专利的新方法包括将选定的表型变量和基因型表达水平组合到度量标准“ G​​ + P INDEX”中。 G + P INDEX将年龄,性别,吸烟史,血尿和血尿的频率与遗传标记MDK,CDC2,HOXA13,IGFBP5和可选的IL8Rb的基因型表达结合起来,然后确定G + P INDEX值为患者获得的结果属于三组之一:(1)UC高危,(2)UC高危,或(3)UC低危。对于第1组和第2组,需要进行进一步的临床和实验室检查或治疗,并定期监测第3组的患者,以确定是否需要进行进一步的临床检查。使用G + P INDEX可以避免患有UC或有患UC风险的患者不必要的医学诊断程序,从而节省大量时间,精力和资金。

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