Comparison of test performance profile for blood tests of liver fibrosis in chronic hepatitis C

被引:100
作者
Halfon, Philippe
Bacq, Yannick
De Muret, Anne
Penaranda, Guillaume
Bourliere, Marc
Ouzan, Denis
Tran, Albert
Botta, Danielle
Renou, Christophe
Brechot, Marie-Claude
Degott, Claude
Paradis, Valerie
机构
[1] Lab Alphabio, F-13006 Marseille, France
[2] CHRU, Hop Trousseau, Serv Hepatogastroenterol, Tours, France
[3] CHRU, Hop Trousseau, Serv Anatomopathol, Tours, France
[4] CDL Pharma, Etudes Epidemiol, Dept Biostat, Marseille, France
[5] Hop St Joseph, Serv Hepatogastroenterol, Marseille, France
[6] Inst Arnault Tzanck, Serv Hepatogastroenterol, St Laurent Du Var, France
[7] Hop Archet, Serv Hepatogastroenterol, Nice, France
[8] Hop La Conception, Serv Hepatogastroenterol, Marseille, France
[9] Hop Gen, Serv Hepatogastroenterol, Hyeres, France
[10] CHRU Tours, Hop Trousseau, Biochim Lab, Tours, France
[11] CHU Beaujon, Serv Anat Pathol, Clichy, France
关键词
liver fibrosis; blood test; Metavir staging; liver biopsy; C chronic hepatitis; blood marker;
D O I
10.1016/j.jhep.2006.09.020
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background/Aims: We evaluated the test performance profile (TPP) of blood tests of liver fibrosis. Methods: Three hundred and fifty-six patients with C chronic hepatitis were included in two centers. Metavir staging of liver specimens by two independent pathologists and the following tests were evaluated: Fibrotest (FT), APRI, FibroMeter (FM), and Hepascore (HS). Results: Metavir stages were: F0: 4%, F1: 55%, F2: 26%, F3: 11%, and F4: 4%. The AUROCs were not significantly different, respectively, FT, FM, APRI, HS: >= F2: 0.79, 0.78, 0.76, 0.76; >= F3: 0.81, 0.85, 0.81, 0.81; and F4: 0.86, 0.94, 0.92, 0.89. The TPP relies on the paired comparison of blood-test misclassification based on liver specimen, e.g. FT vs FM, respectively: F0+1: 18 vs 28% (p = 0.0003), >= F2: 43 vs 31% (p = 0.004). There was no center effect. Conclusions: In those populations, the four blood tests had a similar performance for significant fibrosis (F >= 2), lying in the lower range of published results which is attributable to a low >= F2 prevalence, and for >= F3 and F4. However, FM and FT had performance profiles significantly different as a function of fibrosis stages or diagnostic target (fibrosis cut-off). This has to be considered during the interpretation process. Moreover, the performance should be reported with different diagnostic targets. (c) 2006 European Association for the Study of the Liver. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:395 / 402
页数:8
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