Kinetics of hepatitis B surface antigen in pregnant women with and without tenofovir disoproxil fumarate
Journal
Journal of Viral Hepatitis
Journal Volume
29
Journal Issue
2
Pages
107
Date Issued
2022
Author(s)
Chang, Huai-Lung
Wen, Wan-Hsin
Chiu, Yu-En
Chang, Mei-Hwei
Lin, Lung-Huang
Abstract
Tenofovir disoproxil fumarate (TDF) is the preferred treatment to prevent mother-to-infant transmission in highly viremic HBV-infected women. Data on hepatitis B surface antigen (HBsAg) levels in pregnant women are lacking. We aimed to investigate prepartum and postpartum HBsAg kinetics and its correlation with HBV DNA in pregnant women. HBV-infected mothers with HBV DNA ≥7.5 log10 IU/ml were tested for HBsAg and HBV DNA from baseline to 6 months postpartum. Of the 186 pregnant women with comparable baseline HBsAg and HBV DNA, 101 received TDF from the third trimester until 1 month postpartum. At delivery, TDF group had mildly lower HBsAg (4.32 ± 0.47 vs. 4.54 ± 0.35 log10 IU/ml, p = .0004) and markedly lower HBV DNA (4.26 ± 0.97 vs. 8.11 ± 0.70 log10 IU/ml, p < .0001) than the control group. In the TDF group, mean reduction of HBsAg and HBV DNA from baseline to delivery were 0.22 ± 0.38 and 3.96 ± 0.93 log10 IU/ml. HBsAg reduction had a positive correlation (r = .309; p = .0017) with HBV DNA reduction, and was predictive of HBV DNA reduction ≥3 log10 IU/ml (area under the receiver operating characteristic curve, 0.67; 95% confidence interval, 0.50-0.82). At 6 months postpartum, TDF and control group had comparable HBsAg and HBV DNA. In conclusion, HBsAg decreased slightly at delivery in pregnant women receiving TDF. For monitoring the effect of antiviral therapy during pregnancy, HBV DNA is a better marker than HBsAg. Our data provided valuable information regarding monitoring HBV-infected pregnant women using antiviral therapy.
Subjects
antiviral agents; hepatitis B virus; infectious disease transmission; maternal-foetal relations; pregnancy
SDGs
Other Subjects
antivirus agent; hepatitis B surface antigen; tenofovir; virus DNA; chronic hepatitis B; female; genetics; hepatitis B; Hepatitis B virus; human; infant; kinetics; pregnancy; pregnancy complication; pregnant woman; prevention and control; vertical transmi
Publisher
WILEY
Type
journal article