Rostami Sahar, Parsian Hadi
Student Research Committee, Babol University of Medical Sciences, Babol, IR Iran ; Department of Biochemistry, Faculty of Medical Sciences, Tarbiat Modares University, Tehran, IR Iran.
Cellular and Molecular Biology Research Center, Babol University of Medical Sciences, Babol, IR Iran ; Department of Biochemistry and Biophysics, Babol University of Medical Sciences, Babol, IR Iran.
Hepat Mon. 2013 Dec 14;13(12):e13787. doi: 10.5812/hepatmon.13787.
Hyaluronic acid (HA) is a high molecular weight polysaccharide that is distributed in all bodily tissues and fluids. The liver is the most important organ involved in the synthesis and degradation of HA. Research has shown that liver cell injury can affect serum HA levels. In this review, authors aimed to describe the biochemical and physiological roles of this glycosaminoglycan and its changes in various liver diseases.
Liver fibrosis and in more severe form, cirrhosis are results of an imbalance between fibrogenesis and fibrinolysis. Liver biopsy is the gold standard to assess liver necro inflammatory injuries. This method is invasive and has some major side effects; therefore it is an unfavorable method for both physicians and patients. Now, a wide variety of noninvasive methods have been introduced based on evaluating serum level of different markers. They are safe, readily available, and more favorable. Serum HA levels are used by some researchers to assess stages of liver fibrosis.
There are several scientific studies indicating HA as a biomarker for high score fibrosis and cirrhosis in various liver diseases alone or in algorithm models. It seems from various algorithm models that the use of HA as a major constituent has more diagnostic reliability and accuracy than the use of HA alone.
Use of HA in an algorithm model, is an extra and valuable tool for assessing liver necro inflammatory injuries- in parallel with liver biopsy- but more comprehensive studies are needed to approve the use of HA as an appropriate clinical tool.
透明质酸(HA)是一种高分子量多糖,分布于所有身体组织和体液中。肝脏是参与HA合成与降解的最重要器官。研究表明,肝细胞损伤会影响血清HA水平。在本综述中,作者旨在描述这种糖胺聚糖的生化和生理作用及其在各种肝脏疾病中的变化。
肝纤维化以及更严重的肝硬化是纤维生成和纤维蛋白溶解失衡的结果。肝活检是评估肝脏坏死性炎症损伤的金标准。这种方法具有侵入性且有一些主要副作用;因此,对医生和患者来说都是一种不理想的方法。现在,基于评估不同标志物的血清水平,已经引入了多种非侵入性方法。它们安全、易于获得且更受欢迎。一些研究人员使用血清HA水平来评估肝纤维化阶段。
有几项科学研究表明,HA单独或在算法模型中可作为各种肝脏疾病中高评分纤维化和肝硬化的生物标志物。从各种算法模型来看,将HA作为主要成分使用比单独使用HA具有更高的诊断可靠性和准确性。
在算法模型中使用HA,是一种与肝活检并行的、用于评估肝脏坏死性炎症损伤的额外且有价值的工具,但需要更全面的研究来批准将HA用作合适的临床工具。