@article{91b3078dccf94cedae5b1c8075d1ba69,
title = "Determination of hepatitis B phenotype using biochemical and serological markers",
abstract = "The aim of this study was to assess the validity of categorization of chronic hepatitis B viral infection into stages or phases based upon measures of disease activity and viral load, assuming these phenotypes will be useful for prognostication and determining the need for antiviral therapy. We assessed the phenotype of hepatitis B of 1,390 adult participants enrolled in the Hepatitis B Research Network Cohort Study, using a computer algorithm. Only 4% were immune tolerant, while 35% had chronic hepatitis B (18% e antigen positive and 17% e antigen negative) while 23% were inactive carriers. Strikingly, 38% of participants did not fit clearly into any one of these groups and were considered indeterminant. The largest subset of indeterminants had elevated serum aminotransferases with low levels of HBV DNA (less than 10,000 iu/mL). Subsequent determination of hepatitis B phenotype on the next available laboratory tests showed that 64% remained indeterminant. These findings call into question the validity of conventional staging of hepatitis B, in large part because of the substantial proportion of patients who do not fit readily into one of the usual stages or phases. Further studies are needed of the indeterminant category of chronic hepatitis B viral infection, including assessments of whether patients in this group are perhaps in transition to another phase or if they are a distinct phenotype with a need to assess liver disease severity and need for antiviral therapy. (ClinicalTrials.gov identifier NCT01263587).",
keywords = "algorithm, hepatitis B, phases, phenotype, stages",
author = "{the Hepatitis B Research Network (HBRN)} and {Di Bisceglie}, {A. M.} and M. Lombardero and J. Teckman and L. Roberts and Janssen, {H. L.A.} and Belle, {S. H.} and Hoofnagle, {J. H.} and Lau, {Daryl T.Y.} and Chung, {Raymond T.} and Smith, {Coleman I.} and Mauricio Melman and Wong, {David K.} and Joshua Juan and Jordan Feld and Colina Yim and Jenny Heathcote and Lee, {William M.} and Robert Perrillo and Son Do and Han, {Steven Huy B.} and Tran, {Tram T.} and Terrault, {Norah A.} and Mandana Khalili and Cooper, {Stewart L.} and Lok, {Anna Suk Fong} and Fontana, {Robert J.} and Fried, {Michael W.} and Keyur Patel and Donna Evon and Carithers, {Robert C.} and Margaret Shuhart and Kowdley, {Kris V.} and Wang, {Chia C.} and Sterling, {Richard K.} and Ghany, {Marc G.} and {Jake Liang}, T. and Edward Doo and Chang, {Kyong Mi} and Park, {Jang June} and Abdus Wahed and Yona Cloonan and David Kleiner",
note = "Funding Information: Funding The HBRN was funded by a U01 grant from the National Institute of Diabetes and Digestive and Kidney Diseases to the following investigators Lewis R. Roberts, MB, ChB, PhD (DK082843), Anna Suk-Fong Lok, MD (DK082863), Steven H. Belle, PhD, MScHyg (DK082864), Kyong-Mi Chang, MD (DK082866), Michael W. Fried, MD (DK082867), Adrian M. Di Bisceglie, MD (DK082871), William M. Lee, MD (U01 DK082872), Harry L. A. Janssen, MD, PhD (DK082874), Daryl T-Y Lau, MD, MPH (DK082919), Richard K. Sterling, MD, MSc (DK082923), Steven-Huy B. Han, MD (DK082927), Robert C. Carithers, MD (DK082943), Norah A. Terrault, MD, MPH (U01 DK082944), an interagency agreement with NIDDK: Lilia M. Ganova-Raeva, PhD (A-DK-3002-001) and support from the intramural programme, NIDDK, NIH: Marc G. Ghany, MD. Additional funding to support this study was provided to Kyong-Mi Chang, MD, the Immunology Center, (NIH/NIDDK Center of Molecular Studies in Digestive and Liver Diseases P30DK50306, NIH Public Health Service Research Grant M01-RR00040), Richard K. Sterling, MD, MSc (UL1TR000058, NCATS (National Center for Advancing Translational Sciences, NIH), Norah A. Terrault, MD, MPH (CTSA Grant Number UL1TR000004), Michael W. Fried, MD (CTSA Grant Number UL1TR001111) and Anna Suk-Fong Lok (CTSA Grant Number UL1RR024986.) Additional support was provided by Gilead Sciences, Inc. and Roche Molecular Systems via a CRADA through the NIDDK. Publisher Copyright: {\textcopyright} 2016 John Wiley & Sons Ltd",
year = "2017",
month = apr,
day = "1",
doi = "10.1111/jvh.12643",
language = "English (US)",
volume = "24",
pages = "320--329",
journal = "Journal of viral hepatitis",
issn = "1352-0504",
publisher = "Wiley-Blackwell",
number = "4",
}