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Non-invasive biomarkers for monitoring the fibrogenic process in liver:A short survey

查看全文 作  者:Axel M [1]Gressner;Chun-Fang [2]Gao;Olav A [1]Gressner 高影响力作者 机构地区:[1]Institute of Clinical Chemistry and Pathobiochemistry, Central Laboratory, RWTH- University Hospital Aachen, Pauwelsstr. 30, 52074 Aachen, Germany;[2]Department of Laboratory Medicine, Eastern Hepatobiliary Hospital, Second Military Medical University, 225 Shanghai Road, Shanghai 200438, China高影响力机构 出  处:《World Journal of Gastroenterology》索引2009年第15卷第20期,共8页高影响力期刊 摘  要:The clinical course ofchronic liver diseases is significantly dependent on the progression rate and the extent offibrosis, i.e. the non-structured replacement of necrotic parenchyma by extracellular matrix. Fibrogenesis, i.e. the development offibrosis can be regarded as an unlimited wound healing process, which is based on matrix (connective tissue) synthesis in activated hepatic stellate cells, fibroblasts (fibrocytes), hepatocytes and biliary epithelial cells, which are converted to matrix-producing (myo-)fibroblasts by a process defined as epithelial-mesenchymal transition. Blood (noninvasive) biomarkers offibrogenesis and fibrosis can be divided into class and class analytes. Class biomarkers are those single tests, which are based on the pathophysiology offibrosis, whereas class biomarkers aremostly multiparametric algorithms, which have been statistically evaluated with regard to the detection and activity ofongoing fibrosis. Currently available markers fulfil the criteria ofideal clinical-chemical tests only partially, but increased understanding ofthe complex pathogenesis offibrosis offers additional ways for pathophysiologically well based serum (plasma) biomarkers. They include TGF-β-driven marker proteins, bone marrow-derived cells (fibrocytes), and cytokines, which govern proand anti-fibrotic activities. Proteomic and glycomic approaches ofserum are under investigation to set up specific protein or carbohydrate profiles in patients with liver fibrosis. These and other novel parameters will supplement or eventually replaceliver biopsy/histology, high resolution imaging analysis, and elastography for the detection and monitoring of patients at risk ofdeveloping liver fibrosis. 关 键 词:生物标志物 肝纤维化 侵入性 进程 监测
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