| Literature DB >> 24659896 |
Norie Yamada1, Ryuta Shigefuku1, Ryuichi Sugiyama1, Minoru Kobayashi1, Hiroki Ikeda1, Hideaki Takahashi1, Chiaki Okuse1, Michihiro Suzuki1, Fumio Itoh1, Hiroshi Yotsuyanagi1, Kiyomi Yasuda1, Kyoji Moriya1, Kazuhiko Koike1, Takaji Wakita1, Takanobu Kato1.
Abstract
A 47-year-old man presented with general fatigue and dark urine. The laboratory data showed increased levels of hepatic transaminases. The patient was positive for hepatitis B virus (HBV) markers and negative for anti-human immunodeficiency virus. The HBV-DNA titer was set to 7.7 log copies/mL. The patient was diagnosed with acute hepatitis B. The HBV infection route was obscure. The serum levels of hepatic transaminases decreased to normal ranges without any treatment, but the HBV-DNA status was maintained for at least 26 mo, indicating the presence of persistent infection. We isolated HBV from the acute-phase serum and determined the genome sequence. A phylogenetic analysis revealed that the isolated HBV was genotype H. In this patient, the elevated peak level of HBV-DNA and the risk alleles at human genome single nucleotide polymorphisms s3077 and rs9277535 in the human leukocyte antigen-DP locus were considered to be risk factors for chronic infection. This case suggests that there is a risk of persistent infection by HBV genotype H following acute hepatitis; further cases of HBV genotype H infection must be identified and characterized. Thus, the complete determination of the HBV genotype may be essential during routine clinical care of acute hepatitis B outpatients.Entities:
Keywords: Acute hepatitis; Chronic hepatitis; Genotyping; Hepatitis B virus; Single nucleotide polymorphisms
Mesh:
Year: 2014 PMID: 24659896 PMCID: PMC3961985 DOI: 10.3748/wjg.v20.i11.3044
Source DB: PubMed Journal: World J Gastroenterol ISSN: 1007-9327 Impact factor: 5.742