首页> 外国专利> METHOD FOR IDENTIFYING A SUBSET OF POLYNUCLEOTIDES FROM AN INITIAL SET OF POLYNUCLEOTIDES CORRESPONDING TO THE HUMAN GENOME FOR THE IN VITRO DETERMINATION OF THE SEVERITY OF THE HOST RESPONSE OF A PATIENT

METHOD FOR IDENTIFYING A SUBSET OF POLYNUCLEOTIDES FROM AN INITIAL SET OF POLYNUCLEOTIDES CORRESPONDING TO THE HUMAN GENOME FOR THE IN VITRO DETERMINATION OF THE SEVERITY OF THE HOST RESPONSE OF A PATIENT

机译:从与人类基因组相对应的多核苷酸的初始集合中识别多核苷酸的子集的方法,用于体外确定患者宿主反应的严重性

摘要

The invention relates to a method for identifying a subset of polynucleotides from an initial set of polynucleotides corresponding to the human genome for the in vitro determination, in a sample, of the severity of the host response of a patient in an acute infectious and/or acute inflammatory state, wherein a measuring device is used, which has a plurality of different gene probes, which represent substantially the entire human genome, wherein the test subjects are classified into at least two of the clinically determined phenotype groups according to the infection status and/or inflammation status of the test subjects, the changes of the gene expression signals between the phenotype groups are statistically compared, and gene probes whose gene expression signals are changed between at least two phenotype groups in a statistically significant manner are selected. A master score is determined therefrom as a measure of the severity of the host response, and a number of polynucleotides considerably reduced compared to the initial set is identified by determining a score that does not exceed a specified deviation from the master score. Said score can be used to diagnose, predict the development of, or monitor an acute infectious and/or inflammatory state of a patient and/or to monitor the course of therapy and/or for focus monitoring.
机译:本发明涉及一种用于从对应于人类基因组的多核苷酸的初始集合中鉴定多核苷酸的子集的方法,用于在样品中体外确定患者在急性感染和/或宿主反应中的严重性。急性炎症状态,其中使用的测量装置具有多种不同的基因探针,这些探针基本上代表整个人类基因组,其中,根据感染状况,将测试对象分为至少两个临床确定的表型组/或测试对象的炎症状态,对表型组之间的基因表达信号的变化进行统计学比较,并选择其基因表达信号以统计学上显着的方式在至少两个表型组之间改变的基因探针。由此确定主分数作为宿主反应严重性的量度,并且通过确定不超过主分数的指定偏差的分数来鉴定与初始组相比显着减少的多核苷酸的数目。所述分数可以用于诊断,预测患者的急性感染和/或炎性状态的发展或监测患者的急性感染和/或炎性状态,和/或用于监测治疗过程和/或用于焦点监测。

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