Hepatitis B virus genotypes, precore and core promoter variants among predominantly Asian patients with chronic HBV infection in a Canadian center
dc.contributor.author | Fung, Scott K. | en_US |
dc.contributor.author | Wong, Florence S. H. | en_US |
dc.contributor.author | Wong, David K. H. | en_US |
dc.contributor.author | Hussain, Munira T. | en_US |
dc.contributor.author | Lok, Anna Suk-Fong | en_US |
dc.date.accessioned | 2010-06-01T18:34:24Z | |
dc.date.available | 2010-06-01T18:34:24Z | |
dc.date.issued | 2006-09 | en_US |
dc.identifier.citation | Fung, Scott K . ; Wong, Florence S . H . ; Wong, David K . H . ; Hussain, Munira T . ; Lok, Anna S . F . (2006). "Hepatitis B virus genotypes, precore and core promoter variants among predominantly Asian patients with chronic HBV infection in a Canadian center." Liver International 26(7): 796-804. <http://hdl.handle.net/2027.42/71778> | en_US |
dc.identifier.issn | 1478-3223 | en_US |
dc.identifier.issn | 1478-3231 | en_US |
dc.identifier.uri | https://hdl.handle.net/2027.42/71778 | |
dc.identifier.uri | http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=16911461&dopt=citation | en_US |
dc.description.abstract | The epidemiology of hepatitis B virus (HBV) infection in North America may be changing as a result of immigration from endemic countries. The purpose of this study was to determine the prevalence of HBV genotypes, precore (PC) and core promoter (CP) variants, and the proportion of patients meeting treatment criteria for HBV. Methods : A cross-sectional study of consecutive HBV patients attending a Canadian tertiary liver center was conducted. HBV DNA was quantified by polymerase chain reaction assay. HBV genotypes and variants were determined using a line probe assay. Results : Two hundred and seventy-two patients were enrolled; 200 were not receiving treatment at enrollment, of whom 116 were men and 84 women with a mean age 42±14 years. Among this group, 177 (88%) patients were Asian and 19 (10%) were Caucasian and 69 (35%) patients were hepatitis B e antigen (HBeAg) positive. Genotypes B and C were found in 42% and 50% untreated patients, respectively; while CP and PC were detected in 52% and 43% patients, respectively. Approximately 20% patients not receiving treatment (29% HBeAg positive, 14% HBeAg negative) met AASLD guidelines for antiviral therapy. If lower cutoff values for alanine aminotransferase and HBV DNA levels were used, 49% patients would qualify for treatment. Conclusions : The vast majority of patients at a Canadian tertiary referral center were Asian. Virological and clinical characteristics of these patients reflect their country of origin. Our findings highlight the need to monitor the changing patterns of HBV infection in countries with large immigrant populations. | en_US |
dc.format.extent | 166403 bytes | |
dc.format.extent | 3109 bytes | |
dc.format.mimetype | application/pdf | |
dc.format.mimetype | text/plain | |
dc.publisher | Blackwell Publishing Ltd | en_US |
dc.rights | © 2006 Blackwell Munksgaard | en_US |
dc.subject.other | Antiviral Therapy | en_US |
dc.subject.other | Core Promoter Variant | en_US |
dc.subject.other | HBV DNA | en_US |
dc.subject.other | HBV Genotypes | en_US |
dc.subject.other | Hepatitis B Virus | en_US |
dc.subject.other | Precore Variant | en_US |
dc.title | Hepatitis B virus genotypes, precore and core promoter variants among predominantly Asian patients with chronic HBV infection in a Canadian center | en_US |
dc.type | Article | en_US |
dc.subject.hlbsecondlevel | Internal Medicine and Specialties | en_US |
dc.subject.hlbtoplevel | Health Sciences | en_US |
dc.description.peerreviewed | Peer Reviewed | en_US |
dc.contributor.affiliationum | Division of Gastroenterology, University of Michigan, Ann Arbor, MI, USA | en_US |
dc.contributor.affiliationother | Department of Medicine, University of Toronto, Toronto, ON, Canada , | en_US |
dc.identifier.pmid | 16911461 | en_US |
dc.description.bitstreamurl | http://deepblue.lib.umich.edu/bitstream/2027.42/71778/1/j.1478-3231.2006.01297.x.pdf | |
dc.identifier.doi | 10.1111/j.1478-3231.2006.01297.x | en_US |
dc.identifier.source | Liver International | en_US |
dc.identifier.citedreference | McMahon B, Alberts S R, Wainwright R B, Bulkow L, Lanier A P. Hepatitis B-related sequelae: prospective study in 1400 hepatitis B surface antigen-positive Alaskan native carriers. Arch Internal Med 1990; 150: 1051 – 4. | en_US |
dc.identifier.citedreference | McMahon B, Holck P, Bulkow L, Snowball M M. Serologic and clinical outcomes of 1536 Alaska natives chronically infected with hepatitis B virus. Ann Internal Med 2001; 135: 759 – 68. | en_US |
dc.identifier.citedreference | Minuk G, Uhanova J. Viral hepatitis in the Canadian Inuit and First Nations populations. Can J Gastroenterol 2003; 17: 707 – 12. | en_US |
dc.identifier.citedreference | Miller J, Finelli L, Bell B P. Incidence of acute hepatitis B – United States, 1990–2002. J Am Med Assoc 2004; 291: 416 – 47. | en_US |
dc.identifier.citedreference | Lindh M, Andersson A, Gusdal A. Genotypes, nt 1858 variants, and geographic origin of hepatitis B virus – large scale analysis using a new genotyping method. J Infect Dis 1997; 175: 1285 – 93. | en_US |
dc.identifier.citedreference | Magnius L O, Norder H. Subtypes, genotypes and molecular epidemiology of the hepatitis B virus as reflected by sequence variability of the S-gene. Intervirology 1995; 38: 24 – 34. | en_US |
dc.identifier.citedreference | Sugauchi F, Orito E, Ichida T, et al. Hepatitis B virus of genotype B with or without recombination with genotype C over the precore region plus the core gene. J Virol 2002; 76: 5985 – 92. | en_US |
dc.identifier.citedreference | Sugauchi F, Kumada H, Sakugawa H, et al. Two subtypes of genotype B (Ba and Bj) of hepatitis B virus in Japan. Clin Infect Dis 2004; 38: 1222 – 8. | en_US |
dc.identifier.citedreference | Sugauchi F, Orito E, Ichida T, et al. Epidemiologic and virologic characteristics of hepatitis B virus genotype B having the recombination with genotype C. Gastroenterology 2003; 124: 925 – 32. | en_US |
dc.identifier.citedreference | Janssen H L, Senturk H, Zeuzem S, et al. Peginterferon alfa-2b and lamivudine combination therapy compared with peginterferon alfa-2b for chronic HBeAg-positive chronic hepatitis B: a randomized controlled trial in 307 patients (abstract). Hepatology 2003; 38 :( Suppl ): 246A. | en_US |
dc.identifier.citedreference | Chu C, Hussain M, Lok A. Hepatitis B virus genotype B is associated with earlier spontaneous seroconversion than hepatitis B virus genotype C. Gastroenterology 2003; 122: 1756 – 62. | en_US |
dc.identifier.citedreference | Chan H L Y, Wong M L, Hui A Y, Hung L C T, Chan F K L, Sung J J Y. Hepatitis B virus genotype C takes a more aggressive disease course than hepatitis B virus genotype B in hepatitis B e antigen-positive patients. J Clin Microbiol 2003; 41: 1277 – 9. | en_US |
dc.identifier.citedreference | Yuen M F, Fung S K, Tanaka Y, et al. Longitudinal study of hepatitis activity and viral replication before and after HBeAg seroconversion in chronic hepatitis B patients infected with genotypes B and C. J Clin Microbiol 2004; 42: 5036 – 40. | en_US |
dc.identifier.citedreference | Janssen H L, van Zonneveld M, Senturk H, et al. Pegylated interferaon alpha-2b alone or in combination with lamivudine for HBeAg-positive chronic hepatitis B: a randomised trial. Lancet 2005; 365: 123 – 9. | en_US |
dc.identifier.citedreference | Carman W F, Jacyna M R, Hadziyannis S, et al. Mutation preventing formation of hepatitis B e antigen in patients with chronic hepatitis B infection. Lancet 1989; 2: 588 – 91. | en_US |
dc.identifier.citedreference | Naoumov N V, Schneider R, Grotzinger T, et al. Precore mutant hepatitis B virus infection and liver disease. Gastroenterology 1992; 102: 538 – 43. | en_US |
dc.identifier.citedreference | Chu C M, Chiu C T, Sheen I S, Liaw Y F, Yeh C T. Precore mutant of hepatitis B virus prevails in acute and chronic infections in an area in which hepatitis B is endemic. J Clin Microbiol 1996; 34: 1815 – 8. | en_US |
dc.identifier.citedreference | Laras A, Koskinas J, Avgidis K, Hadziyannis S J. Incidence and clinical significance of hepatitis B virus precore gene translation initiation mutations in e antigen-negative patients. J Viral Hepatitis 1998; 5: 241 – 8. | en_US |
dc.identifier.citedreference | Brunetto M R, Oliveri F, Rocca G, et al. Natural course and response to interferon of chronic hepatitis B accompanied by antibody to hepatitis B e antigen. Hepatology 1989; 10: 198 – 202. | en_US |
dc.identifier.citedreference | Grandjacques C, Paradat P, Stuyver L, et al. Rapid detection of genotypes and mutations in the pre-core promoter and the pre-core region of hepatitis B virus genome: correlation with viral persistence and disease severity. J Hepatol 2000; 33: 430 – 9. | en_US |
dc.identifier.citedreference | Chu C J, Keefe E, Han S H, et al. Hepatitis B virus genotypes in the United States: results of a nationwide study. Gastroenterology 2003; 125: 444 – 51. | en_US |
dc.identifier.citedreference | Chu C J, Keeffe E, Han S H, et al. Prevalence of HBV precore/core promoter variants in the United States. Hepatology 2003; 38: 619 – 28. | en_US |
dc.identifier.citedreference | 23. Anonymous. Hepatitis B vaccination coverage among Asian and Pacific Islander children – United States, 1998. Morbid Mortal Weekly Rep 2000; 49: 616 – 9. | en_US |
dc.identifier.citedreference | Chao S, Le P V, Prapong W, Su J, So S. High prevalence of chronic hepatitis B (HBV) infection in Chinese Americans living in California (abstract). Hepatology 2004; 40 ( Suppl. 1 ): 717A. | en_US |
dc.identifier.citedreference | Lok A, McMahon B. Chronic Hepatitis B. Hepatology 2001; 34: 1225 – 41. | en_US |
dc.identifier.citedreference | Lok A S F, McMahon B J. Chronic Hepatitis B: update of recommendations. Hepatology 2004; 39: 857 – 61. | en_US |
dc.identifier.citedreference | Chan H L Y, Hussain M, Lok A S. Different hepatitis B virus genotypes are associated with different mutations in the core promoter and precore regions during hepatitis B e antigen seroconversion. Hepatology 1999; 29: 976 – 84. | en_US |
dc.identifier.citedreference | Lok A S F, Hussain M, Cursano C, et al. Evolution of hepatitis B virus polymerase gene mutations in hepatitis B e antigen-negative patients receiving lamivudine therapy. Hepatology 2000; 32: 1145 – 53. | en_US |
dc.identifier.citedreference | Lok A S F, Zoulim F, Locarnini S, et al. Monitoring drug resistance in chronic hepatitis B virus (HBV)-infected patients during lamivudine therapy: evaluation of performance of INNO-LiPA HBV DR assay. J Clin Microbiol 2002; 40: 3729 – 34. | en_US |
dc.identifier.citedreference | 30. Statistics Canada. Census 2001, http://www.statcan.ca. 2001. | en_US |
dc.identifier.citedreference | 31. EASL Jury. EASL International Consensus Conference on Hepatitis B. J Hepatol 2003; 39: S3 – 25. | en_US |
dc.identifier.citedreference | Liaw Y F, Leung N W, Guan R, et al. Asian-Pacific consensus statement on the management of chronic hepatitis B: a 2005 update. Liver Int 2005; 25: 472 – 89. | en_US |
dc.identifier.citedreference | Sherman M, Bain V, Villeneuve J P, et al. Management of viral hepatitis: a Canadian Consensus Conference 2003/2004. Can J Gastroenterol 2004; 18: 715 – 28. | en_US |
dc.identifier.citedreference | Keeffe E, Dieterich D T, Han S H B, et al. A treatment algorithm for the management of chronic hepatitis B virus infection in the United States. Clin Gastroenterol Hepatol 2004; 2: 86 – 107. | en_US |
dc.identifier.citedreference | Chan H, Leung N, Hussain M, Wong M, Lok A. Hepatitis B e antigen-negative chronic hepatitis B in Hong Kong. Hepatology 2000; 31: 763 – 8. | en_US |
dc.identifier.citedreference | Kim W R, Benson J T, Therneau T M, Torgerson H A, Yawn B P, Melton L J III. Changing epidemiology of hepatitis B in a US community. Hepatology 2004; 39: 811 – 6. | en_US |
dc.owningcollname | Interdisciplinary and Peer-Reviewed |
Files in this item
Remediation of Harmful Language
The University of Michigan Library aims to describe library materials in a way that respects the people and communities who create, use, and are represented in our collections. Report harmful or offensive language in catalog records, finding aids, or elsewhere in our collections anonymously through our metadata feedback form. More information at Remediation of Harmful Language.
Accessibility
If you are unable to use this file in its current format, please select the Contact Us link and we can modify it to make it more accessible to you.