Literature DB >> 25318660

Incidence of natural resistance mutations in naïve chronic hepatitis B patients: a systematic review and meta-analysis.

Qi Zhang1, Yun Liao, Bei Cai, Yi Li, Lixin Li, Junlong Zhang, Yunfei An, Lanlan Wang.   

Abstract

BACKGROUND AND AIM: Studies focused on the naturally occurring resistance mutation rate in treatment-naïve chronic hepatitis B (CHB) patients have set off a furious dispute. We conduct this meta-analysis to appraise the pooled incidence of spontaneous hepatitis B virus resistance mutations worldwide and its distribution.
METHODS: We searched PubMed, EMBASE, Chinese Biomedical Literature Database, and China National Knowledge Infrastructure until December 31, 2013. Cross-sectional or case-control studies reporting incidence of natural resistance mutations in untreated CHB patients were included. Pooled incidence was performed in fixed- or random-effects models, and heterogeneity among studies was assessed.
RESULTS: A total of 106 studies were included involving 12,212 naive CHB patients. The summarized incidence of natural mutations worldwide was 5.73% (95% confidence interval [CI]: 4.85-6.61%), primary mutation rate 5.39% (95%CI: 4.54-6.24%), and secondary mutation rate 2.94% (95%CI: 1.59-4.29%). The pooled incidence reached up to 8.00% (95%CI: 6.63-9.38%) in China, higher than that in other countries (1.88% [95%CI: 1.06-2.69%]). Mutation rtM204V/I had the highest incidence of 4.89% (95%CI: 4.13-5.65%), and other primary mutations seldom spontaneously occurred. In subgroup analysis, genotype C hepatitis B virus infection, male, and hepatitis B antigen (HBeAg) negative patients had a slightly higher natural mutation rate.
CONCLUSION: The resistance mutations occurred frequently in untreated CHB patients, especially in China. The lamivudine resistance had the highest natural prevalence rate, while other nucleos(t)ide analogues showed rarely spontaneous resistance. Detecting the spontaneous resistance mutations will benefit the clinical management of CHB patients.
© 2014 Journal of Gastroenterology and Hepatology Foundation and Wiley Publishing Asia Pty Ltd.

Entities:  

Keywords:  antiviral drug resistance; hepatitis B virus; incidence; mutation; reverse transcriptase

Mesh:

Substances:

Year:  2015        PMID: 25318660     DOI: 10.1111/jgh.12831

Source DB:  PubMed          Journal:  J Gastroenterol Hepatol        ISSN: 0815-9319            Impact factor:   4.029


  17 in total

1.  Hepatitis B virus reverse transcriptase polymorphisms between treated and treatment-naïve chronically infected patients.

Authors:  Masoumeh Rezanezhadi; Alireza Mohebbi; Fatemeh Sana Askari; Seyyede Delafruz Hosseini; Alijan Tabarraei
Journal:  Virusdisease       Date:  2019-01-10

2.  Prevalence of hepatitis B antiviral drug resistance variants in North American patients with chronic hepatitis B not receiving antiviral treatment.

Authors:  A S Lok; L Ganova-Raeva; Y Cloonan; L Punkova; H-H S Lin; W M Lee; M G Ghany
Journal:  J Viral Hepat       Date:  2017-07-03       Impact factor: 3.728

3.  Prevalence of Potential Resistance Related Variants Among Chinese Chronic Hepatitis B Patients Not Receiving Nucleos(T)ide Analogues.

Authors:  Fuchu Qian; Weihua Zou; Fang Jin; Dongli Li; Yujuan Shen
Journal:  Infect Drug Resist       Date:  2020-07-17       Impact factor: 4.003

4.  HBV Drug Resistance Substitutions Existed before the Clinical Approval of Nucleos(t)ide Analogues: A Bioinformatic Analysis by GenBank Data Mining.

Authors:  Xizhan Xu; Kuanhui Xiang; Mingze Su; Yao Li; Wei Ji; Yutang Li; Hui Zhuang; Tong Li
Journal:  Viruses       Date:  2017-07-27       Impact factor: 5.048

5.  Genotyping of HBV and tracking of resistance mutations in treatment-naïve patients with chronic hepatitis B.

Authors:  Sidelcina Rugieri Pacheco; Maria Isabel Magalhães Andrade Dos Santos; Andreas Stocker; Maria Alice Sant'Anna Zarife; Maria Isabel Schinoni; Raymundo Paraná; Mitermayer Galvão Dos Reis; Luciano Kalabric Silva
Journal:  Infect Drug Resist       Date:  2017-07-05       Impact factor: 4.003

6.  Naturally occurring mutations in the reverse transcriptase region of hepatitis B virus polymerase from treatment-naïve Korean patients infected with genotype C2.

Authors:  Ji-Eun Kim; So-Young Lee; Hong Kim; Ki-Jeong Kim; Won-Hyeok Choe; Bum-Joon Kim
Journal:  World J Gastroenterol       Date:  2017-06-21       Impact factor: 5.742

7.  Naturally occurring genotypic drug-resistant mutations of HBV in Huzhou, China: a single-center study.

Authors:  Fuchu Qian; Weihua Zou; Jiqu Qin; Dongli Li
Journal:  Infect Drug Resist       Date:  2017-12-14       Impact factor: 4.003

8.  Performance Evaluation of the Beckman Coulter DxN VERIS Hepatitis B Virus (HBV) Assay in Comparison With the Abbott RealTime HBV Assay.

Authors:  Joonhong Park; Hanwool Cho; Seung Jun Choi; Gun Dong Lee; Sang Hyun Sin; Ji Hyeong Ryu; Hye Sun Park; Hyeyoung Lee; Yonggoo Kim; Eun Jee Oh
Journal:  Ann Lab Med       Date:  2019-01       Impact factor: 3.464

9.  Epidemiology study of HBV genotypes and antiviral drug resistance in multi-ethnic regions from Western China.

Authors:  Qi Zhang; Yun Liao; Jie Chen; Bei Cai; Zhenzhen Su; Binwu Ying; Xiaojun Lu; Chuanmin Tao; Lanlan Wang
Journal:  Sci Rep       Date:  2015-11-27       Impact factor: 4.379

Review 10.  Naturally occurring hepatitis B virus reverse transcriptase mutations related to potential antiviral drug resistance and liver disease progression.

Authors:  Yu-Min Choi; So-Young Lee; Bum-Joon Kim
Journal:  World J Gastroenterol       Date:  2018-04-28       Impact factor: 5.742

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