Skip to main navigation Skip to search Skip to main content

HIV-1 drug resistance mutations emerging on darunavir therapy in PI-naive and -experienced patients in the UK

  • UK HIV Drug Resistance Database (UKHDRD)
  • , UK Collaborative HIV Cohort (UK CHIC) Study Steering Committees
  • University College London
  • Medical Research Council
  • UK Health Security Agency
  • King's College Hospital NHS Foundation Trust
  • Imperial College Healthcare NHS Trust
  • University of Edinburgh
  • Chelsea and Westminster Hospital NHS Foundation Trust
  • University of KwaZulu-Natal
  • NHS Greater Glasgow and Clyde
  • West of Scotland Specialist Virology Laboratory
  • South Tees Hospitals NHS Foundation Trust
  • University Hospitals Sussex NHS Foundation Trust
  • Barts Health NHS Trust
  • HIV i-BASE
  • Guy's and St Thomas' NHS Foundation Trust
  • Imperial College London
  • University of Liverpool
  • Leeds Teaching Hospitals NHS Trust
  • London School of Hygiene and Tropical Medicine
  • PHE-Virus Reference Department
  • King's College Hospital
  • University Hospitals Birmingham NHS Foundation Trust
  • Royal Infirmary of Edinburgh
  • Manchester Royal Infirmary
  • Cambridge University Hospitals NHS Foundation Trust
  • Specialist Virology Centre
  • Ashford and St Peter's Hospitals NHS Foundation Trust

Research output: Contribution to journalArticlepeer-review

22 Citations (Scopus)

Abstract

Background: Darunavir is considered to have a high genetic barrier to resistance. Most darunavir-associated drug resistance mutations (DRMs) have been identified through correlation of baseline genotype with virological response in clinical trials. However, there is little information on DRMs that are directly selected by darunavir in clinical settings. Objectives: We examined darunavir DRMs emerging in clinical practice in the UK. Patients and methods: Baseline and post-exposure protease genotypes were compared for individuals in the UK Collaborative HIV Cohort Study who had received darunavir; analyses were stratified for PI history. A selection analysis was used to compare the evolution of subtype B proteases in darunavir recipients and matched PInaive controls. Results: Of 6918 people who had received darunavir, 386 had resistance tests pre- and post-exposure. Overall, 2.8% (11/386) of these participants developed emergent darunavir DRMs. The prevalence of baseline DRMs was 1.0% (2/198) among PI-naive participants and 13.8% (26/188) among PI-experienced participants. Emergent DRMs developed in 2.0% of the PI-naive group (4 mutations) and 3.7% of the PI-experienced group (12 mutations). Codon 77 was positively selected in the PI-naive darunavir cases, but not in the control group. Conclusions: Our findings suggest that although emergent darunavir resistance is rare, it may be more common among PI-experienced patients than those who are PI-naive. Further investigation is required to explore whether codon 77 is a novel site involved in darunavir susceptibility.

Original languageEnglish
Pages (from-to)3487-3494
Number of pages8
JournalJournal of Antimicrobial Chemotherapy
Volume71
Issue number12
DOIs
Publication statusPublished - Dec 2016
Externally publishedYes

Bibliographical note

Publisher Copyright:
© The Author 2016.

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Cite this