ADVANTAGES OF BIOCHEMICAL METHODS OF DIAGNOSING FIBROSIS IN NON-ALCOHOLIC FATTY LIVER DISEASE IN ADOLESCENTS WITH OBESITY

O. Buznytska
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Abstract

Non-alcoholic fatty liver disease occurs in most obese people, the main pathway of which is the process of fibrogenesis. This disorder is currently classified into two types: hepatic steatosis and nonalcoholic steatohepatitis. Hepatic steatosis is a reversible condition in which large vacuoles of triglyceride fat accumulate in the liver cells, causing nonspecific inflammation. Most people with this condition experience few, if any, symptoms, and it does not usually lead to scarring or serious liver damage. The majority of patients with nonalcoholic fatty liver disease have this type. Nonalcoholic steatohepatitis is the more severe, progressive form that involves not only fat accumulation (steatosis) in the liver but also inflammation. Steatohepatitis can lead to fibrosis and eventually to cirrhosis, which is severe scarring that can lead to liver failure. The real frequency of the prevalence of the disease is difficult to establish, due to the insufficient use of non-invasive screening diagnostic methods, through which it is possible to detect the initial forms of the disease. The aim: to study the diagnostic significance of the serum biomarkers of liver fibrogenesis in adolescents with obesity. Methods. On the base of the Department of Endocrinology, SI “Institute of children and adolescence health care of NAMS” (Kharkov) 226 patients with obesity aged 8–18 years were examined. Investigation of liver fibrosis consisted of measurement in blood the levels of fibronectin, collagen type IV, N-terminal propeptides and C-terminal telopeptides of type I collagen by IFA method. Results. The study of liver fibrogenesis revealed a significant increase in levels of type IV collagen and fibronectin in children with obesity (p<0.05). As diagnostic criteria for two physiologically diverse processes – fibrogenesis and fibrolysis, the levels of N-terminal propeptides and C-terminal telopeptides of type I collagen, respectively, were determined. The serum level of N-terminal propeptides of type I collagen significantly exceeds the normal values in all children with obesity, in contrast to the children of the control group (p<0.05). Conclusion. It has been established that a biochemical method for determining the level of type IV collagen, fibronectin, N-terminal propeptides and C-terminal telopeptides of type I collagen has a high sensitivity for the diagnosis of liver fibrogenesis.
生化方法诊断青少年肥胖非酒精性脂肪肝纤维化的优势
非酒精性脂肪性肝病发生于大多数肥胖者,其主要途径是纤维化过程。这种疾病目前分为两种类型:肝性脂肪变性和非酒精性脂肪性肝炎。肝脂肪变性是一种可逆性疾病,甘油三酯脂肪大液泡积聚在肝细胞中,引起非特异性炎症。大多数患有这种疾病的人几乎没有症状,而且通常不会导致疤痕或严重的肝损伤。大多数非酒精性脂肪性肝病患者属于这种类型。非酒精性脂肪性肝炎是更为严重的进行性形式,不仅涉及肝脏脂肪积累(脂肪变性),还涉及炎症。脂肪性肝炎可导致纤维化,最终导致肝硬化,这是一种严重的疤痕,可导致肝功能衰竭。由于没有充分使用非侵入性筛查诊断方法,因此很难确定该疾病流行的真实频率,通过这种方法可以检测出该疾病的初始形式。目的:探讨血清纤维化标志物对青少年肥胖症的诊断意义。方法。在哈尔科夫国立科学院儿童青少年保健研究所内分泌科的基础上,对226例8-18岁的肥胖患者进行了检查。肝纤维化的研究包括用IFA法测定血液中纤维连接蛋白、IV型胶原、I型胶原n端前肽和c端端肽的水平。结果。肝纤维化研究显示肥胖儿童IV型胶原蛋白和纤维连接蛋白水平显著升高(p<0.05)。作为两种不同生理过程的诊断标准——纤维发生和纤维溶解,分别测定了I型胶原n端前肽和c端端肽的水平。肥胖患儿血清I型胶原n端前肽水平均明显高于正常值,与对照组比较差异有统计学意义(p<0.05)。结论。已经证实,用生化方法检测IV型胶原蛋白、纤维连接蛋白、I型胶原蛋白n端前肽和c端端肽水平对肝纤维化的诊断具有较高的敏感性。
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