Endothelial biomarker soluble CD146 suggests that angiogenesis plays an important role in progression of fibrosis in liver disease

Efrossini Nomikou, A. Alexopoulou, L. Vasilieva, S. Dourakis
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Abstract

CD146, an element of the endothelial junction- has been evaluated in several pathological conditions with altered endothelial function but never before in patients with liver disease. As angiogenesis and inflammation were implicated in the development of liver fibrosis, we have explored this suggestion by evaluating levels of sCD146 in a group of patients with chronic liver diseases (CLD) and in cirrhotic patients. The results indicated that there is a clear connection between sCD146 levels and the progression of liver disease. They can differentiate noncirrhotic patients with CLD from cirrhotics, supporting the usefulness of CD146 in the noninvasive diagnosis of liver cirrhosis. Furthermore, our findings provided evidence of sCD146 upregulation in decompensated compared to compensated cirrhosis and sCD146 values were clearly associated with Model for End Stage Liver Disease (MELD) score. Thus, by using an easy to perform ELISA method, we demonstrated that sCD146 can accurately distinguish advanced fibrosis and prognosticate decompensation in cirrhosis.
内皮生物标志物可溶性CD146提示血管生成在肝病纤维化进展中起重要作用
CD146是内皮连接的一个元件,已经在几种内皮功能改变的病理条件下进行了评估,但从未在肝病患者中进行过评估。由于血管生成和炎症与肝纤维化的发展有关,我们通过评估一组慢性肝病(CLD)患者和肝硬化患者的sCD146水平来探讨这一观点。结果表明,sCD146水平与肝脏疾病的进展之间存在明确的联系。它们可以区分非肝硬化CLD患者和肝硬化患者,支持CD146在肝硬化无创诊断中的有效性。此外,我们的研究结果提供了sCD146在失代偿肝硬化中与代偿肝硬化相比上调的证据,并且sCD146值与终末期肝病模型(MELD)评分明显相关。因此,通过使用一种易于执行的ELISA方法,我们证明sCD146可以准确区分肝硬化的晚期纤维化和预后失代偿。
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