Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
4
pubmed:dateCreated
2007-11-5
pubmed:abstractText
After hepatitis B e antigen (HBeAg) seroconversion, hepatitis B may become inactive or progress to HBeAg-negative hepatitis with persistent or intermittent alanine aminotransferase (ALT) elevation. The aim of this study was to prospectively identify factors predictive of the clinical course in HBeAg-negative chronic hepatitis B (CHB). Patients were stratified by ALT and HBeAg status and followed every 3 months for up to 5 years. Kaplan-Meier and Cox regression analysis using the change from normal ALT to elevated ALT as endpoints were performed to determine factors associated with ALT elevation/normalization. Seventy-four HBeAg-negative and 32 HBeAg-positive patients were prospectively evaluated. For HBeAg-negative patients, hepatitis B virus (HBV) DNA was predictive of future ALT. Only 1 patient with normal ALT and an HBV DNA value lower than 10,000 copies/mL developed an elevated ALT within the subsequent year, whereas 67% with an HBV DNA value greater than 100,000 copies/mL had a rise in ALT above normal within 1 year. Patients with a previous history of ALT elevation and longer follow-up at all levels of HBV DNA were more likely to experience ALT elevations. For HBeAg-negative patients with elevated ALT and all HBeAg-positive patients, HBV DNA did not predict future ALT. Other viral and host factors were not predictive of future ALT. CONCLUSION: HBeAg-negative CHB has a fluctuating course. HBV DNA values lower than 10,000 copies/mL predict persistently normal ALT for at least 1 year. Patients with HBV DNA values between 10,000 and 100,000 copies/mL can safely be followed at 6 monthly intervals, whereas HBV DNA values greater than 100,000 copies/mL are highly predictive of future ALT elevation and should prompt regular follow-up.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Oct
pubmed:issn
0270-9139
pubmed:author
pubmed:issnType
Print
pubmed:volume
46
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
1057-70
pubmed:dateRevised
2010-11-18
pubmed:meshHeading
pubmed-meshheading:17654702-Adult, pubmed-meshheading:17654702-Aged, pubmed-meshheading:17654702-Alanine Transaminase, pubmed-meshheading:17654702-Biopsy, pubmed-meshheading:17654702-Cohort Studies, pubmed-meshheading:17654702-DNA, Viral, pubmed-meshheading:17654702-Disease Progression, pubmed-meshheading:17654702-Female, pubmed-meshheading:17654702-Follow-Up Studies, pubmed-meshheading:17654702-Hepatitis B, Chronic, pubmed-meshheading:17654702-Hepatitis B e Antigens, pubmed-meshheading:17654702-Hepatitis B virus, pubmed-meshheading:17654702-Humans, pubmed-meshheading:17654702-Kaplan-Meier Estimate, pubmed-meshheading:17654702-Liver, pubmed-meshheading:17654702-Male, pubmed-meshheading:17654702-Middle Aged, pubmed-meshheading:17654702-Mutation, pubmed-meshheading:17654702-Predictive Value of Tests, pubmed-meshheading:17654702-Prognosis, pubmed-meshheading:17654702-Proportional Hazards Models, pubmed-meshheading:17654702-Prospective Studies
pubmed:year
2007
pubmed:articleTitle
Hepatitis B virus DNA prediction rules for hepatitis B e antigen-negative chronic hepatitis B.
pubmed:affiliation
Department of Medicine, University of Toronto, Toronto, Canada. feldj@niddk.nih.gov
pubmed:publicationType
Journal Article, Comparative Study, Research Support, Non-U.S. Gov't, Evaluation Studies, Research Support, N.I.H., Intramural