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Kinetics of hepatitis B surface antigen in pregnant women with and without tenofovir disoproxil fumarate.
Chang, Huai-Lung; Wen, Wan-Hsin; Lee, Chien-Nan; Chiu, Yu-En; Liu, Chun-Jen; Chang, Mei-Hwei; Lin, Lung-Huang; Chen, Huey-Ling.
Afiliación
  • Chang HL; School of Medicine, National Taiwan University College of Medicine, Taipei, Taiwan.
  • Wen WH; Department of Pediatrics, Cardinal Tien Hospital, New Taipei City, Taiwan.
  • Lee CN; School of Medicine, College of Medicine, Fu-Jen Catholic University, New Taipei City, Taiwan.
  • Chiu YE; Department of Obstetrics and Gynecology, National Taiwan University College of Medicine and Hospital, Taipei, Taiwan.
  • Liu CJ; Department of Pediatrics, National Taiwan University College of Medicine and Hospital, Taipei, Taiwan.
  • Chang MH; Department of Internal Medicine, National Taiwan University College of Medicine and Hospital, Taipei, Taiwan.
  • Lin LH; Hepatitis Research Center, National Taiwan University Hospital, Taipei, Taiwan.
  • Chen HL; Graduate Institute of Clinical Medicine, National Taiwan University College of Medicine, Taipei, Taiwan.
J Viral Hepat ; 29(2): 107-114, 2022 02.
Article en En | MEDLINE | ID: mdl-34724288
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.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Complicaciones Infecciosas del Embarazo / Hepatitis B Crónica / Hepatitis B Tipo de estudio: Prognostic_studies Límite: Female / Humans / Infant / Pregnancy Idioma: En Revista: J Viral Hepat Asunto de la revista: GASTROENTEROLOGIA Año: 2022 Tipo del documento: Article País de afiliación: Taiwán

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Complicaciones Infecciosas del Embarazo / Hepatitis B Crónica / Hepatitis B Tipo de estudio: Prognostic_studies Límite: Female / Humans / Infant / Pregnancy Idioma: En Revista: J Viral Hepat Asunto de la revista: GASTROENTEROLOGIA Año: 2022 Tipo del documento: Article País de afiliación: Taiwán