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Volume 133, Issue 5, Pages 1452-1457 (November 2007)


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Clearance of Hepatitis B e Antigen in Patients With Chronic Hepatitis B and Genotypes A, B, C, D, and F

Stephen E. LivingstonCorresponding Author Informationemail address, Josephine P. Simonetti, Lisa R. Bulkow, Chriss E. Homan, Mary M. Snowball, Henry H. Cagle, Susan E. Negus, Brian J. McMahon

Received 18 May 2007; accepted 26 July 2007. published online 07 August 2007.

Refers to article:
Hepatitis B: Explosion of New Knowledge
Emmet B. Keeffe
Gastroenterology
November 2007 (Vol. 133, Issue 5, Pages 1718-1721)
Full Text | Full-Text PDF (104 KB)

Background & Aims: Persistence of hepatitis B e antigen (HBeAg) in chronic hepatitis B has been associated with increased risk for development of cirrhosis and hepatocellular carcinoma. Five hepatitis B virus genotypes were identified in Alaska Native persons; we analyzed clearance of HBeAg by age and genotype. Methods: In this prospective cohort study, 1158 Alaska Native persons throughout Alaska were tested serially for HBeAg for a median of 20.5 years and were genotyped. Initial and final HBeAg-positive specimens, time to clearance, age at clearance, and subsequent HBeAg results were analyzed for persons initially HBeAg-positive. Subsequent HBeAg results were analyzed for persons initially negative. Results: Genotypes A, B, C, D, and F were identified. Genotype C persons initially HBeAg-positive were more likely than those with other genotypes to be positive on initial and final specimens (P < .001 for each) and time to HBeAg clearance was longer (P < .001). Age at which 50% of persons cleared HBeAg was <20 years for those infected with genotypes A, B, D, and F and 47.8 years in genotype C (P < .001). After losing HBeAg, those with genotypes C and F were more likely to revert to the HBeAg-positive state (P < .001). Conclusions: Genotype may have a strong effect on mode of transmission and outcome. Genotype C may have been responsible for most perinatal transmission, given that seroconversion from HBeAg occurs decades later than in other genotypes.

 Liver Disease & Hepatitis Program, Alaska Native Tribal Health Consortium, Anchorage, Alaska

 Arctic Investigations Program, National Center for Infectious Diseases, Centers for Disease Control and Prevention, Anchorage, Alaska

Corresponding Author InformationAddress requests for reprints to: Stephen E. Livingston, MD, Alaska Native Tribal Health Consortium, Liver Disease & Hepatitis Program, 4315 Diplomacy Drive, ANC-HEP, Anchorage, Alaska 99508. fax: (907) 729-1570.

 Supported by Native American Research Centers for Health (NARCH) grant 1 U26 94 00005-01 from the US Indian Health Services.

PII: S0016-5085(07)01456-4

doi:10.1053/j.gastro.2007.08.010


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