慢性丙型肝炎患者血清骨桥蛋白和细胞角蛋白-18的研究

G. El-Saeed, Gamal Y Aboraia, R. Noreldin, Ayman Alghoraieb
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引用次数: 3

摘要

慢性丙型肝炎是一个全球性的卫生问题;大多数患者都有发生纤维化和肝硬化的风险。肝活检的组织学检查是目前检测早期肝损伤的金标准,但迫切需要更好的非侵入性方法。本研究的目的是评估血清骨桥蛋白(OPN)水平、血清细胞角蛋白18m30 (ck - 18m30)新表位水平与丙型肝炎病毒(HCV)诱导患者肝纤维化组织学严重程度的关系。对象和方法:本研究纳入89例受试者,其中慢性丙型肝炎病毒感染70例,根据METAVIR纤维化分期分为2组:I组(2期及以下为轻度肝纤维化)50例,II组(3期及以上为广泛肝纤维化)20例,年龄和性别匹配的健康者19例作为对照组。所有受试者均接受了以下检查:通过病史记录、完整的临床检查,采用酶联免疫吸附试验(ELISA)测定血清骨桥蛋白和细胞角蛋白18m30新表位的浓度。结果显示,OPN和CK-18 M30在患者与对照组之间存在高度显著差异(P<0.001)。轻度纤维化组与广泛纤维化组比较,OPN有显著性差异(P<0.001), CK-18 M30有显著性差异(P=0.02)。血清OPN浓度与肝纤维化严重程度呈高度显著相关(r=0.75, P<0.001),血清CK-18 M30浓度与肝纤维化严重程度呈显著相关(r=0.33, P=0.005)。ROC曲线上,3.1 ng/ml的血清OPN可区分轻度和广泛纤维化,敏感性为95%;293 ng/ml的血清CK-18 M30可区分轻度和广泛纤维化,敏感性为70%。最后,根据所获得的研究结果,血清OPN水平比CK-18 M30更好地识别肝纤维化程度,可作为评估HCV患者纤维化分期的生物标志物,有助于减少肝活检次数。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Serum Osteopontin and Cytokeratin-18 in Chronic Hepatitis C Patients
Chronic hepatitis C is a global health problem; most patients are at risk for developing fibrosis and cirrhosis. Histological examination of liver biopsies is currently the gold standard for the detection of early liver damage, but there is a strong need for better noninvasive methods. The aim of this study was to evaluate the association between serum osteopontin (OPN) level, serum cytokeratin 18 M30 (CK-18 M30) neoepitope level and the histological severity of hepatic fibrosis in hepatitis C virus (HCV) induced patients. Subjects and methods: This study included 89 subjects, 70 with chronic hepatitis C virus infection, they were classified into 2 groups according to METAVIR fibrosis stage as follows: group I (stage 2 or less was considered as mild liver fibrosis) included 50 patient, group II (stage 3 or more was considered as extensive fibrosis) included 20 patients and 19 healthy matched age and gender as a control group. All subjects were submitted to the following: Through history taking, complete clinical examination, and serum concentrations of osteopontin and cytokeratin 18 M30 neoepitope were measured by enzyme linked immunosorbent assay (ELISA). The results revealed that there were high significant differences of OPN and CK-18 M30 between patients and control (P<0.001). There was a high significant difference of OPN (P<0.001) and a significant difference of CK-18 M30 (P=0.02) when compared between mild fibrosis and extensive fibrosis groups. There was a high significant correlation of serum OPN concentrations with severity of liver fibrosis degree (r=0.75, P<0.001), while the serum CK-18 M30 concentrations showed a significant correlation (r=0.33, P=0.005). In ROC curve serum OPN at the cut-off point of 3.1 ng/ml could discriminate mild from extensive fibrosis with sensitivity of 95%, serum CK-18 M30 at the cut-off point of 293 ng/ml could discriminate mild from extensive fibrosis with sensitivity of 70%. Finally from obtained study, results showed that serum OPN levels was better than CK-18 M30 in identification the degree of hepatic fibrosis and could be used as a biomarker to assess the stage of fibrosis in HCV patients which would help to reduce the number of liver biopsies.
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