首页> 外国专利> METHODS AND KITS FOR DETERMINING WHETHER A PATIENT WITH CIRRHOSIS IS AT RISK OF HAVING CLINICALLY SIGNIFICANT PORTAL HYPERTENSION

METHODS AND KITS FOR DETERMINING WHETHER A PATIENT WITH CIRRHOSIS IS AT RISK OF HAVING CLINICALLY SIGNIFICANT PORTAL HYPERTENSION

机译:确定患有肝硬化患者是否有临床上显着的门脉高压症的风险的方法和试剂盒

摘要

The present invention relates to a method for determining whether a patient with cirrhosis is at risk of having clinically significant portal hypertension comprising the steps consisting of i) quantifying the levels of leuko-endothelial (CD31+/41−), pan-leukocyte (CD11a+), lymphocyte (CD4+), erythrocyte (CD235a+) and hepatocyte-derived (cytokeratin-18+) microparticles in a blood sample obtained from the patient and ii) comparing said levels with predetermined reference values wherein a difference between the levels quantified at step i) and the predetermined reference values is indicative whether the patient is at risk of having clinically significant portal hypertension.
机译:本发明涉及一种确定肝硬化患者是否有临床上显着的门静脉高压症的风险的方法,该方法包括以下步骤:i)定量白细胞内皮细胞(CD31 + / 41-),泛白细胞(CD11a +)的水平,从患者获得的血液样本中的淋巴细胞,淋巴细胞(CD4 +),红细胞(CD235a +)和肝细胞衍生的(细胞角蛋白18+)微粒,以及ii)将所述水平与预定参考值进行比较,其中在步骤i)中量化的水平之间的差异预定参考值指示患者是否有临床上显着的门脉高压症的风险。

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