HBV mutation literature information.


  Hepatitis B virus genotype B with G1896A and A1762T/G1764A mutations is associated with hepatitis B related acute-on-chronic liver failure.
 PMID: 21739444       2011       Journal of medical virology
Abstract: In genotype B patients, the A1762T/G1764A, A1846T, and G1896A mutations were significantly more prevalent in patients with acute-on-chronic liver failure than CHB (50.7% vs.


  T1846 and A/G1913 are associated with acute on chronic liver failure in patients infected with hepatitis B virus genotypes B and C.
 PMID: 21503912       2011       Journal of medical virology
Abstract: The results of longitudinal study showed that C53T, A1846T, and G1896A were the most common mutations in association with ACLF.


  Association between the various mutations in viral core promoter region to different stages of hepatitis B, ranging of asymptomatic carrier state to hepatocellular carcinoma.
 PMID: 20959817       2011       The American journal of gastroenterology
Abstract: A1846T and T1674C/G are novel factors independently associated with cirrhosis and HCC, respectively.
Abstract: Multivariate regression analyses showed that age, male, abnormal alanine aminotransferase (ALT), T1768A, A1762T/G1764A, and A1846T were independently associated with cirrhosis compared with ASCs and the patients with CHB.


  A case-control study on sequence variations in the enhancer II/core promoter/precore and X genes of hepatitis B virus in patients with hepatocellular carcinoma.
 PMID: 21063480       2010       Hepatology international
Abstract: No significant difference between groups was found with respect to G1613A, C1653T, C1766T/T1768A, A1846T/C, T1858C, and G1896A mutations.


  Prevalent HBV point mutations and mutation combinations at BCP/preC region and their association with liver disease progression.
 PMID: 20846420       2010       BMC infectious diseases
Result: Univariate binary logistic regression analysis showed significant correlation of several substitutions with the HBeAg negativity, including G1776A (OR = 8.1, 95% CI: 1.7-39; P = 0.009), A1846T (OR = 3.8, 95% CI: 1.2-11.8; P = 0.02), G1896A (OR = 3.5, 95% CI: 1.4-8.6; P = 0.007), and the number of individual point mutations >= 3 (OR = 2.8, 95% CI: 1.1-6.8; P = 0.027).


  Molecular and clinical characteristics of hepatitis B virus in Korea.
 PMID: 20513074       2010       Journal of medical virology
Abstract: A number of amino acid/nucleotide substitutions were associated with HCC, namely sR24K (HBsAg), SI126T (HBsAg), and pcA1846T (precore gene) mutations (P = 0.029, 0.001, and 0.008, respectively).


  A study on sequence variations in pre-S/surface, X and enhancer II/core promoter/precore regions of occult hepatitis B virus in non-B, non-C hepatocellular carcinoma patients in Taiwan.
 PMID: 19431214       2009       International journal of cancer
Abstract: Compared with the HBsAg-positive HCC controls, occult HBV-infected HCC patients had higher frequencies of M1I and Q2K in pre-S2 gene, G185R and S210N in surface gene, A36T and A44L in X gene, and G1721A in enhancer II gene, and had lower rates of pre-S deletions and A1762T/G1764A,  PMID: 12667359       2002       Zhonghua liu xing bing xue za zhi
Abstract: Among samples with stopped mutation, 4 samples had mutation at nt1846 (A-->T), 2 samples at nt1862 (G-->T).



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