Risk factors for CD4 lymphopenia in patients treated with a tenofovir/didanosine high dose-containing highly active antiretroviral therapy regimen

AIDS. 2005 Jul 1;19(10):1107-8. doi: 10.1097/01.aids.0000174460.24171.0b.

Abstract

In this study, the dynamics of CD4 cell depletion during tenofovir/didanosine co-administration were analysed. Ninety-five HIV-positive patients were followed for 562 days, and 37 lost at least 50 CD4 cells, with a median delay of 274 days. Cox analysis showed that the CD4 cell decrease was associated with a duration of treatment by didanosine of more than 853 days and a didanosine dose of more than 5.50 mg/kg.

MeSH terms

  • Adenine / adverse effects
  • Adenine / analogs & derivatives*
  • Adult
  • Anti-HIV Agents / adverse effects*
  • Antiretroviral Therapy, Highly Active / adverse effects
  • CD4 Lymphocyte Count
  • CD4-Positive T-Lymphocytes*
  • Didanosine / adverse effects*
  • Female
  • HIV Infections / drug therapy*
  • Humans
  • Lymphopenia / chemically induced*
  • Male
  • Organophosphonates / adverse effects*
  • Risk Factors
  • Tenofovir

Substances

  • Anti-HIV Agents
  • Organophosphonates
  • Tenofovir
  • Adenine
  • Didanosine