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

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 evalua...

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Bibliographic Details
Published in:Journal of hepatology 2007-03, Vol.46 (3), p.395-402
Main Authors: Halfon, Philippe, Bacq, Yannick, De Muret, Anne, Penaranda, Guillaume, Bourliere, Marc, Ouzan, Denis, Tran, Albert, Botta, Danielle, Renou, Christophe, Bréchot, Marie-Claude, Degott, Claude, Paradis, Valérie
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Language:English
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Summary: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.
ISSN:0168-8278
1600-0641
DOI:10.1016/j.jhep.2006.09.020