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An Accurate Definition of the Status of Inactive Hepatitis B Virus Carrier by a Combination of Biomarkers (FibroTest-ActiTest) and Viral Load

BACKGROUND: The combination of transaminases (ALT), biopsy, HBeAg and viral load have classically defined the inactive status of carriers of chronic hepatitis B. The use of FibroTest (FT) and ActiTest (AT), biomarkers of fibrosis and necroinflammatory activity, has been previously validated as alter...

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Autores principales: Ngo, Yen, Benhamou, Yves, Thibault, Vincent, Ingiliz, Patrick, Munteanu, Mona, Lebray, Pascal, Thabut, Dominique, Morra, Rachel, Messous, Djamila, Charlotte, Frederic, Imbert-Bismut, Françoise, Rousselot-Bonnefont, Dominique, Moussalli, Joseph, Ratziu, Vlad, Poynard, Thierry
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2440801/
https://www.ncbi.nlm.nih.gov/pubmed/18596917
http://dx.doi.org/10.1371/journal.pone.0002573
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author Ngo, Yen
Benhamou, Yves
Thibault, Vincent
Ingiliz, Patrick
Munteanu, Mona
Lebray, Pascal
Thabut, Dominique
Morra, Rachel
Messous, Djamila
Charlotte, Frederic
Imbert-Bismut, Françoise
Rousselot-Bonnefont, Dominique
Moussalli, Joseph
Ratziu, Vlad
Poynard, Thierry
author_facet Ngo, Yen
Benhamou, Yves
Thibault, Vincent
Ingiliz, Patrick
Munteanu, Mona
Lebray, Pascal
Thabut, Dominique
Morra, Rachel
Messous, Djamila
Charlotte, Frederic
Imbert-Bismut, Françoise
Rousselot-Bonnefont, Dominique
Moussalli, Joseph
Ratziu, Vlad
Poynard, Thierry
author_sort Ngo, Yen
collection PubMed
description BACKGROUND: The combination of transaminases (ALT), biopsy, HBeAg and viral load have classically defined the inactive status of carriers of chronic hepatitis B. The use of FibroTest (FT) and ActiTest (AT), biomarkers of fibrosis and necroinflammatory activity, has been previously validated as alternatives to biopsy. We compared the 4-year prognostic value of combining FT-AT and viral load for a better definition of the inactive carrier status. METHODS AND FINDINGS: 1,300 consecutive CHB patients who had been prospectively followed since 2001 were pre-included. The main endpoint was the absence of liver-related complications, transplantation or death. We used the manufacturers' definitions of normal FT (< = 0.27), normal AT (< = 0.29) and 3 standard classes for viral load. The adjustment factors were age, sex, HBeAg, ethnic origin, alcohol consumption, HIV-Delta-HCV co-infections and treatment. RESULTS: 1,074 patients with baseline FT-AT and viral load were included: 41 years old, 47% African, 27% Asian, 26% Caucasian. At 4 years follow-up, 50 complications occurred (survival without complications 93.4%), 36 deaths occurred (survival 95.0%), including 27 related to HBV (survival 96.1%). The prognostic value of FT was higher than those of viral load or ALT when compared using area under the ROC curves [0.89 (95%CI 0.84–0.93) vs 0.64 (0.55–0.71) vs 0.53 (0.46–0.60) all P<0.001], survival curves and multivariate Cox model [regression coefficient 5.2 (3.5–6.9; P<0.001) vs 0.53 (0.15–0.92; P = 0.007) vs −0.001 (−0.003−0.000;P = 0.052)] respectively. A new definition of inactive carriers was proposed with an algorithm combining “zero” scores for FT-AT (F0 and A0) and viral load classes. This new algorithm provides a 100% negative predictive value for the prediction of liver related complications or death. Among the 275 patients with the classic definition of inactive carrier, 62 (23%) had fibrosis presumed with FT, and 3 died or had complications at 4 year. CONCLUSION: In patients with chronic hepatitis B, a combination of FibroTest-ActiTest and viral load testing accurately defined the prognosis and the inactive carrier status.
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spelling pubmed-24408012008-07-02 An Accurate Definition of the Status of Inactive Hepatitis B Virus Carrier by a Combination of Biomarkers (FibroTest-ActiTest) and Viral Load Ngo, Yen Benhamou, Yves Thibault, Vincent Ingiliz, Patrick Munteanu, Mona Lebray, Pascal Thabut, Dominique Morra, Rachel Messous, Djamila Charlotte, Frederic Imbert-Bismut, Françoise Rousselot-Bonnefont, Dominique Moussalli, Joseph Ratziu, Vlad Poynard, Thierry PLoS One Research Article BACKGROUND: The combination of transaminases (ALT), biopsy, HBeAg and viral load have classically defined the inactive status of carriers of chronic hepatitis B. The use of FibroTest (FT) and ActiTest (AT), biomarkers of fibrosis and necroinflammatory activity, has been previously validated as alternatives to biopsy. We compared the 4-year prognostic value of combining FT-AT and viral load for a better definition of the inactive carrier status. METHODS AND FINDINGS: 1,300 consecutive CHB patients who had been prospectively followed since 2001 were pre-included. The main endpoint was the absence of liver-related complications, transplantation or death. We used the manufacturers' definitions of normal FT (< = 0.27), normal AT (< = 0.29) and 3 standard classes for viral load. The adjustment factors were age, sex, HBeAg, ethnic origin, alcohol consumption, HIV-Delta-HCV co-infections and treatment. RESULTS: 1,074 patients with baseline FT-AT and viral load were included: 41 years old, 47% African, 27% Asian, 26% Caucasian. At 4 years follow-up, 50 complications occurred (survival without complications 93.4%), 36 deaths occurred (survival 95.0%), including 27 related to HBV (survival 96.1%). The prognostic value of FT was higher than those of viral load or ALT when compared using area under the ROC curves [0.89 (95%CI 0.84–0.93) vs 0.64 (0.55–0.71) vs 0.53 (0.46–0.60) all P<0.001], survival curves and multivariate Cox model [regression coefficient 5.2 (3.5–6.9; P<0.001) vs 0.53 (0.15–0.92; P = 0.007) vs −0.001 (−0.003−0.000;P = 0.052)] respectively. A new definition of inactive carriers was proposed with an algorithm combining “zero” scores for FT-AT (F0 and A0) and viral load classes. This new algorithm provides a 100% negative predictive value for the prediction of liver related complications or death. Among the 275 patients with the classic definition of inactive carrier, 62 (23%) had fibrosis presumed with FT, and 3 died or had complications at 4 year. CONCLUSION: In patients with chronic hepatitis B, a combination of FibroTest-ActiTest and viral load testing accurately defined the prognosis and the inactive carrier status. Public Library of Science 2008-07-02 /pmc/articles/PMC2440801/ /pubmed/18596917 http://dx.doi.org/10.1371/journal.pone.0002573 Text en Ngo et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Ngo, Yen
Benhamou, Yves
Thibault, Vincent
Ingiliz, Patrick
Munteanu, Mona
Lebray, Pascal
Thabut, Dominique
Morra, Rachel
Messous, Djamila
Charlotte, Frederic
Imbert-Bismut, Françoise
Rousselot-Bonnefont, Dominique
Moussalli, Joseph
Ratziu, Vlad
Poynard, Thierry
An Accurate Definition of the Status of Inactive Hepatitis B Virus Carrier by a Combination of Biomarkers (FibroTest-ActiTest) and Viral Load
title An Accurate Definition of the Status of Inactive Hepatitis B Virus Carrier by a Combination of Biomarkers (FibroTest-ActiTest) and Viral Load
title_full An Accurate Definition of the Status of Inactive Hepatitis B Virus Carrier by a Combination of Biomarkers (FibroTest-ActiTest) and Viral Load
title_fullStr An Accurate Definition of the Status of Inactive Hepatitis B Virus Carrier by a Combination of Biomarkers (FibroTest-ActiTest) and Viral Load
title_full_unstemmed An Accurate Definition of the Status of Inactive Hepatitis B Virus Carrier by a Combination of Biomarkers (FibroTest-ActiTest) and Viral Load
title_short An Accurate Definition of the Status of Inactive Hepatitis B Virus Carrier by a Combination of Biomarkers (FibroTest-ActiTest) and Viral Load
title_sort accurate definition of the status of inactive hepatitis b virus carrier by a combination of biomarkers (fibrotest-actitest) and viral load
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2440801/
https://www.ncbi.nlm.nih.gov/pubmed/18596917
http://dx.doi.org/10.1371/journal.pone.0002573
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