Precore and core promoter mutations of hepatitis B virus and hepatitis B e antigen-negative chronic hepatitis B in Korea. 2003

Byung Chul Yoo, and Joong-Won Park, and Hyung Joon Kim, and Dong Ho Lee, and Young Ju Cha, and Sill Moo Park
Division of Gastroenterology, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, South Korea. bcyoo@smc.samsung.co.kr

OBJECTIVE The aims of this study were to determine the frequency of precore/core promoter mutations and hepatitis B e antigen (HBeAg)-negative chronic hepatitis B (e-CHB) in Korea. METHODS Patients with chronic hepatitis B virus (HBV) infection were tested for HBeAg, anti-HBe, liver profile and HBV-DNA by a branched DNA (bDNA) assay. Serum HBV-DNA was amplified by a polymerase chain reaction and the precore/core promoter sequence was determined. RESULTS Among the 413 consecutive HBeAg-negative patients, 19.6% were bDNA-positive. Evidence of liver disease was found in 90.1% of bDNA-positive and 41.7% of bDNA-negative patients. Overall, 17.7% of HBeAg-negative patients had e-CHB. Precore mutation (A1896) was detected in 93.7% of HBeAg-negative bDNA-positive and 93.9% of HBeAg-negative bDNA-negative patients. In 59 HBeAg-positive patients, 78% had wild-type and 22% had a mixture of wild-type and A1896 mutant. Core promoter TA mutation was detected in 89.9% of HBeAg-negative bDNA-positive patients, 89.8% of HBeAg-negative bDNA-negative patients, and 74.6% of HBeAg-positive patients. No correlation was found between the presence of precore/core promoter mutations and HBV-DNA levels or disease severity. CONCLUSIONS In Korean patients infected with HBV genotype C, precore mutation occurred almost invariably along with HBeAg seroconversion and core promoter TA mutation was frequent irrespective of viral replication levels or disease severity.

UI MeSH Term Description Entries
D008297 Male Males
D008875 Middle Aged An adult aged 45 - 64 years. Middle Age
D009154 Mutation Any detectable and heritable change in the genetic material that causes a change in the GENOTYPE and which is transmitted to daughter cells and to succeeding generations. Mutations
D011401 Promoter Regions, Genetic DNA sequences which are recognized (directly or indirectly) and bound by a DNA-dependent RNA polymerase during the initiation of transcription. Highly conserved sequences within the promoter include the Pribnow box in bacteria and the TATA BOX in eukaryotes. rRNA Promoter,Early Promoters, Genetic,Late Promoters, Genetic,Middle Promoters, Genetic,Promoter Regions,Promoter, Genetic,Promotor Regions,Promotor, Genetic,Pseudopromoter, Genetic,Early Promoter, Genetic,Genetic Late Promoter,Genetic Middle Promoters,Genetic Promoter,Genetic Promoter Region,Genetic Promoter Regions,Genetic Promoters,Genetic Promotor,Genetic Promotors,Genetic Pseudopromoter,Genetic Pseudopromoters,Late Promoter, Genetic,Middle Promoter, Genetic,Promoter Region,Promoter Region, Genetic,Promoter, Genetic Early,Promoter, rRNA,Promoters, Genetic,Promoters, Genetic Middle,Promoters, rRNA,Promotor Region,Promotors, Genetic,Pseudopromoters, Genetic,Region, Genetic Promoter,Region, Promoter,Region, Promotor,Regions, Genetic Promoter,Regions, Promoter,Regions, Promotor,rRNA Promoters
D003062 Codon A set of three nucleotides in a protein coding sequence that specifies individual amino acids or a termination signal (CODON, TERMINATOR). Most codons are universal, but some organisms do not produce the transfer RNAs (RNA, TRANSFER) complementary to all codons. These codons are referred to as unassigned codons (CODONS, NONSENSE). Codon, Sense,Sense Codon,Codons,Codons, Sense,Sense Codons
D004279 DNA, Viral Deoxyribonucleic acid that makes up the genetic material of viruses. Viral DNA
D005260 Female Females
D006513 Hepatitis B e Antigens A closely related group of antigens found in the plasma only during the infective phase of hepatitis B or in virulent chronic hepatitis B, probably indicating active virus replication; there are three subtypes which may exist in a complex with immunoglobulins G. HBeAg,Hepatitis B e Antigen,Hepatitis Be Antigen,e Antigen,e Antigens,HBe Ag-1,HBe Ag-2,Hepatitis Be Antigens,Antigen, Hepatitis Be,Antigen, e,Antigens, Hepatitis Be,Antigens, e,Be Antigen, Hepatitis,Be Antigens, Hepatitis
D006515 Hepatitis B virus The type species of the genus ORTHOHEPADNAVIRUS which causes human HEPATITIS B and is also apparently a causal agent in human HEPATOCELLULAR CARCINOMA. The Dane particle is an intact hepatitis virion, named after its discoverer. Non-infectious spherical and tubular particles are also seen in the serum. Dane Particle,Hepatitis Virus, Homologous Serum,B virus, Hepatitis,Hepatitis B viruses,Particle, Dane,viruses, Hepatitis B
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man

Related Publications

Byung Chul Yoo, and Joong-Won Park, and Hyung Joon Kim, and Dong Ho Lee, and Young Ju Cha, and Sill Moo Park
May 2006, Journal of viral hepatitis,
Byung Chul Yoo, and Joong-Won Park, and Hyung Joon Kim, and Dong Ho Lee, and Young Ju Cha, and Sill Moo Park
April 2009, Journal of medical virology,
Byung Chul Yoo, and Joong-Won Park, and Hyung Joon Kim, and Dong Ho Lee, and Young Ju Cha, and Sill Moo Park
February 2013, Alimentary pharmacology & therapeutics,
Byung Chul Yoo, and Joong-Won Park, and Hyung Joon Kim, and Dong Ho Lee, and Young Ju Cha, and Sill Moo Park
October 2004, Journal of medical virology,
Byung Chul Yoo, and Joong-Won Park, and Hyung Joon Kim, and Dong Ho Lee, and Young Ju Cha, and Sill Moo Park
November 2002, The Journal of infectious diseases,
Byung Chul Yoo, and Joong-Won Park, and Hyung Joon Kim, and Dong Ho Lee, and Young Ju Cha, and Sill Moo Park
April 2011, Virologie (Montrouge, France),
Byung Chul Yoo, and Joong-Won Park, and Hyung Joon Kim, and Dong Ho Lee, and Young Ju Cha, and Sill Moo Park
March 2007, The Journal of infection,
Byung Chul Yoo, and Joong-Won Park, and Hyung Joon Kim, and Dong Ho Lee, and Young Ju Cha, and Sill Moo Park
March 2013, Hepatology (Baltimore, Md.),
Byung Chul Yoo, and Joong-Won Park, and Hyung Joon Kim, and Dong Ho Lee, and Young Ju Cha, and Sill Moo Park
September 2002, Journal of hepatology,
Byung Chul Yoo, and Joong-Won Park, and Hyung Joon Kim, and Dong Ho Lee, and Young Ju Cha, and Sill Moo Park
January 1993, Gastroenterology,
Copied contents to your clipboard!