Author/Authors :
Wang, Jing Department of Rheumatology - First Affiliated Hospital - School of Medicine - Xi’an Jiaotong University, china , Liu, Jinfeng Department of Infectious Diseases - First Affiliated Hospital - School of Medicine - Xi’an Jiaotong University, China , Yu, Qiang Department of Pediatric Surgery - Second Affiliated Hospital - School of Medicine, Xi’an Jiaotong University, China , Jin, Li Department of Infectious Diseases - First Affiliated Hospital - School of Medicine - Xi’an Jiaotong University, China , Yao, Naijuan Department of Infectious Diseases - First Affiliated Hospital - School of Medicine - Xi’an Jiaotong University, China , Yang, Yuan Department of Infectious Diseases - First Affiliated Hospital - School of Medicine - Xi’an Jiaotong University, China , Yan, Taotao Department of Infectious Diseases - First Affiliated Hospital - School of Medicine - Xi’an Jiaotong University, China , Hu, Chunhua Department of Infectious Diseases - First Affiliated Hospital - School of Medicine - Xi’an Jiaotong University, China , He, Yingli Department of Infectious Diseases - First Affiliated Hospital - School of Medicine - Xi’an Jiaotong University, China , Zhao, Yingren Department of Infectious Diseases - First Affiliated Hospital - School of Medicine - Xi’an Jiaotong University, China , Chen, Tianyan Department of Infectious Diseases - First Affiliated Hospital - School of Medicine - Xi’an Jiaotong University, China , Zheng, Jie Department of Infectious Diseases - First Affiliated Hospital - School of Medicine - Xi’an Jiaotong University, China
Abstract :
Background
HBV-resistant mutants in treatment-naïve patients may lead to antiviral treatment failure. It is not clear if HBV mutants are present in pregnant women and about the influence of the preexisting mutants on the short-term antiviral therapy during pregnancy.
Method
We enrolled 73 pregnant women with high HBV DNA load and telbivudine (TBV) treatment during pregnancy in this retrospective study. The UDPS was used to detect the HBV mutations before and after the TBV treatment.
Results
Before TBV treatment, the complexity of HBV quasispecies of all subjects was 0.40 ± 0.09; 41.1% (30/73) and 53.4% (39/73) subjects had rtM204I/V and rtN236 T/A detected, respectively; and 9.6% (7/73) patients had more than 20% frequency mutation of rtM204I/V, which was also similar with high frequency of rtN236 T/A mutation (41.1% vs. 53.4%, P=0.136; frequencies >20%: 9.6% vs. 5.5%, P=0.347). After TBV treatment, 71.2% (52/73) subjects had HBV DNA load ≥ 103 IU/mL at delivery. Among them, 75.0% of patients with rtM204I positive had HBV DNA load ≥103 IU/mL at delivery, which was comparable with the subjects without rtM204I (75.0% vs. 70.8%, P=0.710). No changes were found in the frequencies and the complexity of HBV quasispecies of rtM204I mutation after the TVB treatment.
Conclusion
The prevalence of preexisting drug-resistant mutations among pregnant women was high using UPDS. However, the preexisting HBV mutation had limited influence on the efficacy of short-term TBV treatment, and TBV treatment during late pregnancy seemed not to increase the risk of emerging HBV-resistant mutants.
Keywords :
High Prevalence , HBV Polymerase Mutations , Pregnant Women , Antiviral Therapy Efficacy