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Hepatitis B virus (HBV) gene mutations related to entecavir-resistance in patients with chronic HBV infections / 中华临床感染病杂志
Chinese Journal of Clinical Infectious Diseases ; (6): 139-142, 2015.
Article in Chinese | WPRIM | ID: wpr-466437
ABSTRACT
Objective To investigate hepatitis B virus (HBV) gene mutations related to entecavir (ETV)-resistance in patients with chronic HBV infections.Methods Serum samples were collected from 44 patients with chronic HBV infections and resistant to ETV treatment who were admitted in Ningbo No.2 Hospital during February 2010 and May 2014.The HBV polymerase regions were amplified by real-time fluorescent quantitative polymerase chain reaction (PCR) method,and the PCR products were analyzed with direct sequencing.SPSS 16.0 was used to assess the frequency of HBV polymerase gene mutations,and its relation to the viral genotype and clinical features.Results The most common HBV polymerase gene mutation was rtS202G/I (52.28%,23/44),followed by rtT184A/G/I/S (36.36%,16/44) and rtM250V/L (11.36%,5/44).Nine mutation patterns were detected,in which rtL180 + rtM204V + rtS202G/I (38.64%,17/44) and rtL180 +rtM204V + rtT184A/G/I/S (27.27%,12/44) were the most frequent ones.The difference in gene mutations between genotype B and C was of statistical significance (x2=12.294,P <0.01).Patients carrying rtT184A/G/I/S mutations were associated with worse liver function (x2 =14.499,P < 0.01),and those carrying rtM250V/L mutations were associated with lower HBeAg positive rate (x2 =10.057,P < 0.01).Conclusions rtL180M + rtM204V + rtS202G/I is the most common HBV polymerase gene mutation related to ETV resistance in patients with chronic HBV infections.Different gene mutations may be associated with HBV genotypes,severity of liver damages,and HBeAg positive rate.

Full text: Available Index: WPRIM (Western Pacific) Language: Chinese Journal: Chinese Journal of Clinical Infectious Diseases Year: 2015 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Language: Chinese Journal: Chinese Journal of Clinical Infectious Diseases Year: 2015 Type: Article