[Resistance to anti-retroviral therapy in Chilean patients with HIV-1 from 2002 to 2005]

Rev Med Chil. 2007 Oct;135(10):1237-44. Epub 2007 Dec 20.
[Article in Spanish]

Abstract

Background: Resistance limits the effectiveness of anti-retroviral therapy. In Chile, there is free access to highly active anti-retroviral therapy since 2001, but there is no information about the frequency of mutations associated to drug resistance.

Aim: To determine the most common mutations associated to anti-retroviral drug resistance in Chile.

Materials and methods: Retrospective study of 710 genotype analysis coming from 568 patients aged 22 to 70 years (85% males) with virological failure. The analysis was performed using a commercially available sequencing kit (Trugene HIV-1 genotypic assay from Bayer S.A).

Results: Mean CD4(+) cell count and viral load were 154 cells/microl and 228784 RNA copies/ml, respectively. The frequency of resistance to nucleoside RT inhibitors (NRTI), non nucleoside RT inhibitors (NNRTI) and protease inhibitors (PI) was 71 %, 62% and 22%, respectively. The most common mutations found were T215Y (46%), L10F (44%), Ml84V (3896), K103N (35%) and M41L (32%). Fifty five percent of mutations corresponded to the TAM (thymidine analogue mutations) group. Multiresistance was 47% to NNRTI, 7% to NRTI, 4% to PI and 0.7% to all groups. During the four years of the study, there was a significant increase in NNRTI resistance.

Conclusions: These data provides important information about the epidemiology of drug resistance mutations and should help to design new HAART strategies.

Publication types

  • English Abstract

MeSH terms

  • Adult
  • Aged
  • Anti-HIV Agents / therapeutic use*
  • Antiretroviral Therapy, Highly Active*
  • CD4 Lymphocyte Count
  • Chile
  • Drug Resistance, Multiple, Viral / genetics*
  • Female
  • Genotype
  • HIV Infections / drug therapy
  • HIV Infections / virology*
  • HIV-1 / drug effects
  • HIV-1 / enzymology
  • HIV-1 / genetics*
  • Humans
  • Male
  • Middle Aged
  • Mutation / genetics*
  • Protease Inhibitors / therapeutic use
  • RNA, Viral / analysis
  • Retrospective Studies
  • Reverse Transcriptase Inhibitors / therapeutic use
  • Viral Load

Substances

  • Anti-HIV Agents
  • Protease Inhibitors
  • RNA, Viral
  • Reverse Transcriptase Inhibitors