Alboraie Mohamed A, Afifi Mahmoud E, Elghamry Fathy G, Shalaby Helmy A, Elshennawy Gamal E, Abdelaziz Ahmed A, Shaheen Mohamed U, Abo El-Seoud Amany R
Department of Internal Medicine, Al-Azhar University, Cairo, Egypt.
Hepat Mon. 2013 Jun 16;13(6):e10810. doi: 10.5812/hepatmon.10810. eCollection 2013.
Non-invasive methods for assessment of hepatic fibrosis are increasingly needed. Recent studies showed that combined elevation of tumor markers CA 19-9 and CA 125 is predictive of severe hepatic fibrosis or cirrhosis with high specificity.
We aimed at developing a new panel of surrogate biomarkers for prediction of the stage of hepatic fibrosis by combining tumor markers with other known biomarkers of hepatic fibrosis.
A total of 92 patients with different types of chronic liver diseases (chronic hepatitis B, chronic hepatitis C and autoimmune hepatitis), were prospectively enrolled in our cohort. They were subjected to: ALT, AST, GGT, ALP, total bilirubin, INR, total cholesterol, albumin, platelet count, cancer antigen 19-9 (CA 19-9), cancer antigen 125 (CA 125), cancer antigen 15-3 (CA 15-3), haptoglobin, alpha-2-macroglobulin, apolipoprotein A1, abdominal ultrasound, liver biopsy and histological staging of hepatic fibrosis using the METAVIR system.
Combined elevation of CA 19-9 and CA 125 with a summated value > 37 U/mL is predictive of severe hepatic fibrosis or cirrhosis (stage F3-F4 METAVIR) with a probability of 77.6%. Multivariate analysis showed that the most relevant collection of biomarkers for prediction of stage of hepatic fibrosis is: CA 19-9, age, alpha-2- macroglobulin, total bilirubin, platelet count & albumin. We developed a new score, named the "Egy-Score", using a regression equation composed of this panel of biomarkers. Egy-Score could differentiate no or early fibrosis (stage F0-F2 METAVIR) from severe fibrosis or cirrhosis (stage F3-F4 METAVIR) with 83.7% accuracy.
Non-invasive assessment of hepatic fibrosis could be done using the Egy-Score. Egy-Score could differentiate no or early fibrosis (stage F0-F2 METAVIR) from severe fibrosis or cirrhosis (stage F3 - F4 METAVIR) with 83.7% accuracy.
对肝纤维化进行评估的非侵入性方法的需求日益增加。最近的研究表明,肿瘤标志物CA 19-9和CA 125的联合升高对严重肝纤维化或肝硬化具有较高特异性的预测价值。
我们旨在通过将肿瘤标志物与其他已知的肝纤维化生物标志物相结合,开发一组新的替代生物标志物,用于预测肝纤维化的阶段。
共有92例不同类型的慢性肝病(慢性乙型肝炎、慢性丙型肝炎和自身免疫性肝炎)患者前瞻性纳入我们的队列。他们接受了以下检查:谷丙转氨酶(ALT)、谷草转氨酶(AST)、γ-谷氨酰转肽酶(GGT)、碱性磷酸酶(ALP)、总胆红素、国际标准化比值(INR)、总胆固醇、白蛋白、血小板计数、癌抗原19-9(CA 19-9)、癌抗原125(CA 125)、癌抗原15-3(CA 15-3)、触珠蛋白、α-2-巨球蛋白、载脂蛋白A1、腹部超声、肝活检以及使用METAVIR系统进行肝纤维化的组织学分期。
CA 19-9和CA 125联合升高且总和值>37 U/mL可预测严重肝纤维化或肝硬化(METAVIR分期F3-F4),概率为77.6%。多变量分析表明,预测肝纤维化阶段最相关的生物标志物组合是:CA 19-9、年龄、α-2-巨球蛋白、总胆红素、血小板计数和白蛋白。我们使用由该生物标志物组合构成的回归方程开发了一种名为“Egy评分”的新评分。Egy评分能够以83.7%的准确率区分无纤维化或早期纤维化(METAVIR分期F0-F2)与严重纤维化或肝硬化(METAVIR分期F3-F4)。
可使用Egy评分对肝纤维化进行非侵入性评估。Egy评分能够以83.7%的准确率区分无纤维化或早期纤维化(METAVIR分期F0-F2)与严重纤维化或肝硬化(METAVIR分期F3-F4)。