Maternal Malaria and Perinatal HIV Transmission, Western Kenya

  • John G. Ayisi
  • , Anna Van Eijk
  • , Robert D. Newman
  • , Feiko Ter Kuile
  • , Ya Ping Shi
  • , Chunfu Yang
  • , Margarette S. Kolczak
  • , Juliana A. Otieno
  • , Ambrose O. Misore
  • , Piet A. Kager
  • , Renu B. Lal
  • , Richard W. Steketee
  • , Bernard L. Nahlen

Research output: Contribution to journalArticlepeer-review

92 Citations (Scopus)

Abstract

To determine whether maternal placental malaria is associated with an increased risk for perinatal mother-to-child HIV transmission (MTCT), we studied HIV-positive women in western Kenya. We enrolled 512 mother-infant pairs; 128 (25.0%) women had placental malaria, and 102 (19.9%) infants acquired HIV perinatally. Log10 HIV viral load and episiotomy or perineal tear were associated with increased perinatal HIV transmission, whereas low-density placental malaria (<10,000 parasites/μL) was associated with reduced risk (adjusted relative risk [ARR] 0.4). Among women dually infected with malaria and HIV, high-density placental malaria (≥10, 000 parasites/μL) was associated with increased risk for perinatal MTCT (ARR 2.0), compared to low-density malaria. The interaction between placental malaria and MTCT appears to be variable and complex: placental malaria that is controlled at low density may cause an increase in broad-based immune responses that protect against MTCT; uncontrolled, high-density malaria may simultaneously disrupt placental architecture and generate substantial antigen stimulus to HIV replication and increase risk for MTCT.
Original languageEnglish
Pages (from-to)643-652
Number of pages10
JournalEmerging Infectious Diseases
Volume10
Issue number4
DOIs
Publication statusPublished - 1 Apr 2004
Externally publishedYes

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