Effects of a single large dose of vitamin A, given during the postpartum period to HIV-positive women and their infants, on child HIV infection, HIV-free survival, and mortality

  • Jean H. Humphrey
  • , Peter J. Iliff
  • , Edmore T. Marinda
  • , Kuda Mutasa
  • , Lawrence H. Moulton
  • , Henry Chidawanyika
  • , Brian J. Ward
  • , Kusum J. Nathoo
  • , Lucie C. Malaba
  • , Lynn S. Zijenah
  • , Partson Zvandasara
  • , Robert Ntozini
  • , Faith Mzengeza
  • , Agnes I. Mahomva
  • , Andrea J. Ruff
  • , Michael T. Mbizvo
  • , Clare O. Zunguza

Research output: Contribution to journalArticlepeer-review

165 Citations (Scopus)

Abstract

Background. Low maternal serum retinol level is a risk factor for mother-to-child transmission (MTCT) of human immunodeficiency virus (HIV). Multiple-large-dose vitamin A supplementation of HIV-positive children reduces mortality. The World Health Organization recommends single-large-dose vitamin A supplementation for postpartum women in areas of prevalent vitamin A deficiency; neonatal dosing is under consideration. We investigated the effect that single-large-dose maternal/neonatal vitamin A supplementation has on MTCT, HIV-free survival, and mortality in HIV-exposed infants. Methods. A total of 14,110 mother-infant pairs were enrolled ≤96 h after delivery, and both mother and infant, mother only, infant only, or neither received vitamin A supplementation in a randomized, placebo-controlled trial with a 2 × 2 factorial design. All but 4 mothers initiated breast-feeding. A total of 4495 infants born to HIV-positive women were included in the present analysis. Results. Neither maternal nor neonatal vitamin A supplementation significantly affected postnatal MTCT or overall mortality between baseline and 24 months. However, the timing of infant HIV infection modified the effect that supplementation had on mortality. Vitamin A supplementation had no effect in infants who were polymerase chain reaction (PCR) negative for HIV at baseline. In infants who were PCR negative at baseline and PCR positive at 6 weeks, neonatal supplementation reduced mortality by 28% (P = .01), but maternal supplementation had no effect. In infants who were PCR negative at 6 weeks, all 3 vitamin A regimens were associated with ∼2-fold higher mortality (P ≤ .05). Conclusions. Targeted vitamin A supplementation of HIV-positive children prolongs their survival. However, postpartum maternal and neonatal vitamin A supplementation may hasten progression to death in breast-fed children who are PCR negative at 6 weeks. These findings raise concern about universal maternal or neonatal vitamin A supplementation in HIV-endemic areas.

Original languageEnglish
Pages (from-to)860-871
Number of pages12
JournalJournal of Infectious Diseases
Volume193
Issue number6
DOIs
Publication statusPublished - 15 Mar 2006

ASJC Scopus subject areas

  • Immunology and Allergy
  • Infectious Diseases

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