Literature DB >> 21889468

Relative performances of FibroTest, Fibroscan, and biopsy for the assessment of the stage of liver fibrosis in patients with chronic hepatitis C: a step toward the truth in the absence of a gold standard.

Thierry Poynard1, Victor de Ledinghen, Jean Pierre Zarski, Carol Stanciu, Mona Munteanu, Julien Vergniol, Julie France, Anca Trifan, Gilles Le Naour, Jean Christophe Vaillant, Vlad Ratziu, Frederic Charlotte.   

Abstract

BACKGROUND & AIMS: Liver fibrosis stage is traditionally assessed with biopsy, an imperfect gold standard. Two widely used techniques, FibroTest®, and liver stiffness measurement (LSM) using Fibroscan® have been validated using biopsy, and therefore the true performances of these estimates are still unknown in the absence of a perfect reference. The aim was to assess the relative accuracy of FibroTest, LSM, and biopsy using methods without gold standard in patients with chronic hepatitis C (CHC) and controls.
METHODS: A total of 1289 patients with CHC and 604 healthy volunteers, with assessment of fibrosis stage by the three techniques, and alanine aminotransferase (ALT) taken as a control test, were analyzed by latent class method with random effects. In the volunteers, the false positive risk of biopsy was obtained from a large surgical sample of four normal livers.
RESULTS: The latent class model with random effects permitted to conciliate the observed data and estimates of test performances. For advanced fibrosis, the specificity/sensitivity was for FibroTest 0.93/0.70, LSM 0.96/0.45, ALT 0.79/0.78 and biopsy 0.67/0.63, and for cirrhosis FibroTest 0.87/0.41, LSM 0.93/0.39, ALT 0.78/0.08 and biopsy 0.95/0.51. The analysis of the discordances between pairs suggested that the variability of the model was mainly related to the discordances between biopsy and LSM (residuals>10; p<0.0001).
CONCLUSIONS: A method without the use of a gold standard confirmed the accuracy of FibroTest and Fibroscan for the diagnosis of advanced fibrosis and cirrhosis in patients with chronic hepatitis C. The variability of the model was mostly due to the discordances between Fibroscan and biopsy.
Copyright © 2011 European Association for the Study of the Liver. Published by Elsevier B.V. All rights reserved.

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Year:  2011        PMID: 21889468     DOI: 10.1016/j.jhep.2011.08.007

Source DB:  PubMed          Journal:  J Hepatol        ISSN: 0168-8278            Impact factor:   25.083


  28 in total

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7.  Point shear wave elastography method for assessing liver stiffness.

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8.  Multiplex protein analysis to determine fibrosis stage and progression in patients with chronic hepatitis C.

Authors:  Keyur Patel; Katja S Remlinger; Terence G Walker; Peter Leitner; Joseph E Lucas; Stephen D Gardner; John G McHutchison; Will Irving; Indra Neil Guha
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9.  Dietary fructose intake and severity of liver disease in hepatitis C virus-infected patients.

Authors:  Gia L Tyson; Peter A Richardson; Donna L White; Jill Kuzniarek; David J Ramsey; Shahriar Tavakoli-Tabasi; Hashem B El-Serag
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