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Incidence of natural resistance mutations in naive chronic hepatitis B patients: A systematic review and meta-analysis

期刊

JOURNAL OF GASTROENTEROLOGY AND HEPATOLOGY
卷 30, 期 2, 页码 252-261

出版社

WILEY
DOI: 10.1111/jgh.12831

关键词

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

资金

  1. National Natural Science Foundation of China [81072443, 81100536, 81273256]

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Background and AimStudies focused on the naturally occurring resistance mutation rate in treatment-naive 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. MethodsWe 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. ResultsA total of 106 studies were included involving 12212 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. ConclusionThe 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.

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