Dabrowska Anna Maria, Tarach Jerzy Stanislaw, Wojtysiak-Duma Beata, Duma Dariusz
Department of Endocrinology, Medical University of Lublin, Poland.
Department of Biochemical Diagnostics, Medical University of Lublin, Poland.
Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub. 2015 Sep;159(3):352-9. doi: 10.5507/bp.2015.018. Epub 2015 Apr 24.
Fetuin-A, also called Alpha 2-Heremans Schmid Glycoprotein, is a multifunctional plasma agent what has been proven in animal and human studies. It plays a role as a physiological inhibitor of insulin receptor tyrosine kinase associated with insulin resistance and a negative acute phase reactant. It also regulates bone remodeling and calcium metabolism being an important inhibitor of calcium salt precipitation and vascular calcifications.
PubMed database was searched for articles from 2002 up to December 2014 to identify the role of fetuin-A in the pathogenesis of selected internal diseases.
Due to secretion of fetuin-A mainly by the liver, it may be a marker of liver function and predictor of mortality in patients with cirrhosis and hepatocellular cancer. The associations between high fetuin-A and metabolic syndrome as well as its hepatic manifestation- nonalcoholic fatty liver disease and atherogenic lipid profile have been well proven. However, fetuin-A relation with BMI is not so clear. Contrary to few reports, many authors suggest that fetuin-A may be an independent risk factor for type 2 diabetes and marker of diabetic complications. Close associations of high and low fetuin-A concentrations with cardiovascular diseases and mortality risk have been reported which is explained by differences in analyzed populations, stages of atherosclerosis and calcifications, coexistence of type 2 diabetes or kidney dysfunction and different main pathways of fetuin-A actions in various diseases.
Fetuin-A has a diagnostic potential as a biomarker for liver dysfunction, cardiovascular diseases and disorders associated with metabolic syndrome.
胎球蛋白-A,也称为α2-赫曼斯-施密德糖蛋白,是一种多功能血浆因子,已在动物和人体研究中得到证实。它作为胰岛素受体酪氨酸激酶的生理抑制剂与胰岛素抵抗相关,也是一种负急性期反应物。它还调节骨重塑和钙代谢,是钙盐沉淀和血管钙化的重要抑制剂。
检索PubMed数据库中2002年至2014年12月的文章,以确定胎球蛋白-A在选定内科疾病发病机制中的作用。
由于胎球蛋白-A主要由肝脏分泌,它可能是肝硬化和肝细胞癌患者肝功能的标志物及死亡率的预测指标。高胎球蛋白-A与代谢综合征及其肝脏表现——非酒精性脂肪性肝病和致动脉粥样硬化血脂异常之间的关联已得到充分证实。然而,胎球蛋白-A与体重指数的关系并不那么明确。与少数报道相反,许多作者认为胎球蛋白-A可能是2型糖尿病的独立危险因素和糖尿病并发症的标志物。高和低胎球蛋白-A浓度与心血管疾病和死亡风险密切相关,这可以通过分析人群的差异、动脉粥样硬化和钙化的阶段、2型糖尿病或肾功能不全的共存以及胎球蛋白-A在各种疾病中的不同主要作用途径来解释。
胎球蛋白-A作为肝功能障碍、心血管疾病和与代谢综合征相关疾病的生物标志物具有诊断潜力。