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Author Notes:

Correspondence to Dr Yiming Shao; yshao08@gmail.com

WK and TT contributed equally.

Contributors: YR, WK, HX and YS designed the study.

YR, HX, SL, LL, YM, HT, TZ, GS, CH, WK, XL and PL collected the data.

CH, TT and LL conducted laboratory analysis.

XL and WK analysed the data.

KMW, VCM, YR, WK, HX, LL and YS interpreted the data.

KMW, VCM, YR, WK, TT and YS drafted the report.

All authors reviewed, revised and approved the final report.

Patient consent: Obtained.

Ethics approval: National Center for AIDS/STD Control and Prevention of the Chinese Center for Disease Control and Prevention (NCAIDS, China CDC).

Competing interests: None declared.

Subjects:

Research Funding:

This study was supported by Guangxi Center for Disease Control and Prevention, Nanning, China.

The antiretroviral drugs used in this study were provided by NFATP.

Keywords:

  • Science & Technology
  • Life Sciences & Biomedicine
  • Medicine, General & Internal
  • General & Internal Medicine
  • GENDER-DIFFERENCES
  • FOLLOW-UP
  • THERAPY
  • INFECTION
  • RISK
  • SURVEILLANCE
  • INDIVIDUALS
  • ZIDOVUDINE
  • LAMIVUDINE
  • MORTALITY
  • HIV
  • Antiretroviral treatment
  • Virological failure
  • Drug resistance
  • Gender differences
  • China

Predictors of HIV virological failure and drug resistance in Chinese patients after 48 months of antiretroviral treatment, 2008-2012: a prospective cohort study

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Journal Title:

BMJ Open

Volume:

Volume 7, Number 9

Publisher:

, Pages e016012-e016012

Type of Work:

Article | Final Publisher PDF

Abstract:

Objective To explore factors associated with HIV virological failure (VF) and HIV drug resistance (HIVDR) among HIV-positive Chinese individuals 4 years after initiating first-line lamivudine-based antiretroviral treatment (ART) in 2008 at five sentinel sites. Design First-line ART initiators who were previously treatment naïve were selected using consecutive ID numbers from the 2008 National Surveillance Database into a prospective cohort study. Questionnaires and blood samples were collected in 2011 and 2012 to assess the outcomes of interest: VF (defined as viral load ≥1000 copies/mL) and HIVDR (defined as VF with genetic drug-resistant mutations). Questionnaires and data from National Surveillance Database assessed demographics and drug adherence data. Results 536 individuals with HIV were analysed; the 4-year risk of VF was 63 (11.8%) and HIVDR was 27 (5.0%). Female participants initiating stavudine (D4T)-based regimens were more susceptible to both VF (adjusted OR (aOR)=2.5, 95% CI 1 to 6.1, p=0.04) and HIVDR (aOR=3.6, 95% CI 1 to 12.6, p=0.05) versus zidovudine-based regimens. Male participants missing doses in past month were more susceptible to both VF (aOR=2.8, 95% CI 1.1 to 7, p=0.03) and HIVDR (aOR=9.7, 95% CI 2.1 to 44.1, p < 0.01). Participants of non-Han nationality were of increased risk for HIVDR (aOR from 4.8 to 12.2, p < 0.05) and non-Han men were at increased risk for VF (aOR=2.9, 95% CI 1.1 to 7.3, p=0.02). All 27 participants detected with HIVDR had non-nucleoside reverse-transcriptase inhibitor mutations, 21 (77.8%) also had nucleoside reverse-transcriptase inhibitor mutations, and no protease inhibitor mutations were detected. Conclusions Our findings suggest successful treatment outcomes at 4 years for roughly 90% of patients. We suggest conducting further study on whether and when to change ART regimen for women initiated with D4T-based regimen, and reinforcing adherence counselling for men. Increased VF and HIVDR risk among non-Han minorities warrants further exploration, and ethnic minorities may be an important group to tailor adherence-focused interventions.

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This is an Open Access work distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License (http://creativecommons.org/licenses/by-nc/4.0/).

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