Maternal and Infant Bone Mineral Density 1 Year After Delivery in a Randomized, Controlled Trial of Maternal Tenofovir Disoproxil Fumarate to Prevent Mother-to-child Transmission of Hepatitis B Virus

Clin Infect Dis. 2019 Jun 18;69(1):144-146. doi: 10.1093/cid/ciy982.

Abstract

In a randomized, double-blind, placebo-controlled trial of tenofovir disoproxil fumarate (TDF) use from 28 weeks gestational age to 2 months postpartum to prevent mother-to-child transmission of hepatitis B virus, there was no significant effect of maternal TDF use on maternal or infant bone mineral density 1 year after delivery/birth. Clinical Trials Registration. NCT01745822.

Keywords: bone mineral density; growth; hepatitis B; pregnancy; tenofovir disoproxil fumarate.

Publication types

  • Clinical Trial, Phase III
  • Randomized Controlled Trial
  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Antiviral Agents / therapeutic use*
  • Bone Density / drug effects*
  • Double-Blind Method
  • Female
  • Gestational Age
  • Hepatitis B / drug therapy*
  • Hepatitis B virus
  • Humans
  • Infant
  • Infectious Disease Transmission, Vertical / prevention & control*
  • Male
  • Postpartum Period
  • Pregnancy
  • Pregnancy Complications, Infectious / prevention & control
  • Pregnancy Complications, Infectious / virology
  • Tenofovir / therapeutic use*
  • Viral Load / drug effects
  • Young Adult

Substances

  • Antiviral Agents
  • Tenofovir

Associated data

  • ClinicalTrials.gov/NCT01745822