Morali Gilles, Maor Yaacov, Klar Rachel, Braun Marius, Ben Ari Ziv, Bujanover Yoram, Zuckerman Eli, Boger Sarah, Halfon Philippe
Department of Gastroenterology, Shaare Zedek Medical Center, Jerusalem, Israel.
Isr Med Assoc J. 2007 Aug;9(8):588-91.
The Fibrotest-Actitest is a six-parameter scoring system that allows quantification of liver fibrosis and inflammation. This test has been validated by several studies in hepatitis B and C viruses and alcoholic liver disease, with a high correlation between the liver biopsy and the results of the FT-AT (AUROC between 0.78 and 0.95). The FT-AT was introduced in Israel (Rambam Laboratory) in March 2005.
To assess the results of HCV patients who underwent the test during the period March 2005 to February 2006.
Serum was taken and brought to the central laboratory performing the tests within 4 hours. Six parameters were evaluated using commercial kits approved by the designer of the test (Biopredictive): total bilirubin, gamma-glutamyltransferase, alpha-2 macroglobulin, haptoglobin, alanine aminotransferase, and apolipoprotein-A1. The results were sent to the website of Biopredictive (France), which provided the FT-AT score online using a patented formula.
Of the 325 patients tested, only 4 were not interpretable because of hemolysis. Patients' age ranged from 7 to 72 years (median 42); 54% were female. Liver biopsy was performed in 81 patients and was compared with the results of the Fibrotest. Findings were as follows: 27% of the patients were F0, 19% F1, 20% F2, 17% F3 and 17% F4; 18% were A0, 32% A1, 28% A2 and 22% A3. The AUROC curve comparing the Fibrotest with liver biopsy with a cutoff point at F2 and A2 for significant fibrosis and inflammation was 0.85 and 0.79 respectively.
Fibrotest is a simple and effective method to assess liver fibrosis and inflammation and can be considered an alternative to liver biopsy in most patients with HCV.
Fibrotest-Actitest是一种六参数评分系统,可对肝纤维化和炎症进行量化。该检测已在多项针对乙型和丙型肝炎病毒以及酒精性肝病的研究中得到验证,肝活检结果与Fibrotest-Actitest(FT-AT)结果之间具有高度相关性(受试者工作特征曲线下面积在0.78至0.95之间)。FT-AT于2005年3月在以色列(兰巴姆实验室)引入。
评估2005年3月至2006年2月期间接受该检测的丙型肝炎病毒(HCV)患者的检测结果。
采集血清并在4小时内送至进行检测的中央实验室。使用该检测方法设计者(Biopredictive)批准的商用试剂盒评估六个参数:总胆红素、γ-谷氨酰转移酶、α-2巨球蛋白、触珠蛋白、丙氨酸氨基转移酶和载脂蛋白A1。结果被发送至Biopredictive(法国)的网站,该网站使用专利公式在线提供FT-AT评分。
在325名接受检测的患者中,仅有4名因溶血无法进行解读。患者年龄在7至72岁之间(中位数为42岁);54%为女性。81名患者进行了肝活检,并将结果与Fibrotest的结果进行比较。结果如下:27%的患者为F0,19%为F1,20%为F2,17%为F3,17%为F4;18%为A0,32%为A1,28%为A2,22%为A3。将Fibrotest与肝活检进行比较的受试者工作特征曲线,以F2和A2作为显著纤维化和炎症的截断点,其曲线下面积分别为0.85和0.79。
Fibrotest是评估肝纤维化和炎症的一种简单有效的方法,在大多数HCV患者中可被视为肝活检的替代方法。