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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.
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页码:429 / 439
页数:11
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