Analysis of full-length hepatitis B virus genome from chronic hepatitis B-patients with higher alanine aminotransferase elevation

被引:0
|
作者
Takahashi, Hiroshi [1 ]
Kanda, Tatsuo [1 ]
Matsumoto, Naoki [1 ]
Shibata, Toshikatsu [1 ]
Nirei, Kazushige [1 ]
Tamura, Akinori [1 ]
Matsuoka, Shunichi [1 ]
Kuroda, Kazumichi [1 ]
Moriyama, Mitsuhiko [1 ]
机构
[1] Nihon Univ, Sch Med, Dept Med, Div Gastroenterol & Hepatol,Itabashi Ku, 30-1 Oyaguchi Kamicho, Tokyo 1738610, Japan
关键词
acute exacerbation; ALT; full-length HBV sequence; HBV; HCC; reactivation; virologic breakthrough; C CHRONIC HEPATITIS; CORE PROMOTER; RESISTANT MUTATIONS; LAMIVUDINE-RESISTANCE; FULMINANT-HEPATITIS; GENOTYPE; MANAGEMENT; SEQUENCE; MUTANTS; EMERGENCE;
D O I
10.2217/fvl-2020-0104
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Background & aim: Higher elevation of alanine aminotransferase (ALT) occasionally leads to severe outcomes in hepatitis B virus (HBV)-infected patients. Our aim is to investigate the HBV sequence mutations associated with higher ALT elevation. Materials & methods: We analyzed full-length HBV sequences from patients with or without higher ALT elevation. Results: Nucleotide mutations in precore and core regions, which are associated with severe hepatitis B, were found in two HBV-infected patients with higher ALT elevation. Amino acid mutations within the pre-S1, pre-S2 and S regions were also found in a patient with HBV virologic breakthrough during the use of nucleoside analogs. Conclusion: It may be useful for HBV-infected patients with higher ALT elevation to analyze full-length HBV genome.
引用
收藏
页码:429 / 439
页数:11
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