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Journal of the International AIDS Society logoLink to Journal of the International AIDS Society
. 2014 Nov 2;17(4Suppl 3):19667. doi: 10.7448/IAS.17.4.19667

Difference in factors associated with low-level viraemia and virological failure: results from the Austrian HIV Cohort Study

Gisela Leierer 1, Armin Rieger 2, Andrea Steuer 3, Mario Sarcletti 1, Maria Geit 4, Bernhard Haas 5, Ninon Taylor 6, Manfred Kanatschnig 7, Michaela Rappold 1, Bruno Ledergerber 8, Robert Zangerle 1
PMCID: PMC4225379  PMID: 25397417

Abstract

Introduction

For some patients, it remains a challenge to achieve complete virological suppression which is the goal of antiretroviral therapy (ART). Identifying factors associated with low-level viraemia (LLV) and virological failure (VF) under ART might help to optimize management of these patients.

Materials and Methods

We investigated patients from the Austrian HIV Cohort Study receiving unmodified ART for >6 months with two nucleoside reverse-transcriptase inhibitors (NRTIs) with either a non-nucleoside reverse-transcriptase inhibitor (NNRTI) or a boosted protease inhibitor (PI) or an integrase inhibitor (INSTI) between 1 July 2012 and 1 July 2013 with at least one viral load (VL) measurement below the limit of detection (BLD) or below level of quantification (BLQ) in their treatment history. VF was defined as HIV-RNA levels ≥200 copies/mL and all other quantifiable measurements were classified as LLV. Factors associated with LLV and VF compared to BLD and BLQ were identified by using logistic regression models.

Results

Of the 2,276 patients analyzed, 1,972 (86.6%) were BLD or BLQ, 222 (9.8%) showed LLV and 82 (3.6%) had VF. A higher risk for LLV and VF was found in patients with ART interruptions and in patients with boosted PI therapy. The risk for LLV and VF was lower in patients from a centre which uses Abbott RealTime HIV-1 assay compared to the other centres measuring VL by the Roche Cobas AmpliPrep/Cobas TaqMan 2.0. A higher risk for LLV but not for VF was found in patients with a higher VL before ART and shorter ART duration. A higher risk for VF but not for LLV was found in patients of younger age, originating from a high prevalence country, with a lower CD4 count and in male injecting drug users.

Conclusions

This study of well-defined patients on stable ART over a period of more than six months gives insights into the different factors associated with LLV and VF. In patients with VF, factors associated with adherence play a prominent role, whereas in patients with LLV, the biology of viral replication comes additionally into effect. Despite its observational design, it has implications for patient management and forms the basis for future outcome studies.


Table 1.

Multivariable logistic regression results: Association between different factors and low-level viraemia and virological failure compared to viral load below the limit of detection or below level of quantification

LLV<200 VF≥200
Outcome OR (95% CI) OR (95% CI)
Age at VL measurement
  < 30 years 1.01 (0.58–1.76) 2.95 (1.07–8.18)
 30–50 years 0.98 (0.70–1.36) 2.80 (1.28–6.10)
  > 50 years 1.00 (Reference) 1.00 (Reference)
HIV transmission category
 Male injecting drug user 1.07 (0.66–1.73) 2.04 (1.00–4.18)
 Female injecting drug user 0.42 (0.16–1.08) 1.44 (0.48–4.28)
 Male heterosexual 0.85 (0.58–1.25) 0.69 (0.31–1.54)
 Female heterosexual 0.62 (0.41–0.94) 1.11 (0.55–2.24)
 Other 1.36 (0.72–2.58) 1.27 (0.35–4.61)
 Men who have sex with men 1.00 (Reference) 1.00 (Reference)
Nationality
 High prevalence countries 2.14 (1.04–4.41)
 Low prevalence countries 1.00 (Reference)
CD4 count at VL measurement
 Missing 2.12 (1.07–4.19) 0.65 (0.08–5.08)
  < 200 cells/µL 1.70 (0.86–3.36) 9.17 (4.18–20.13)
 200–349 cells/µL 0.98 (0.62–1.57) 2.81 (1.48–5.32)
 350–499 cells/µL 0.94 (0.62–1.41) 2.53 (1.38–4.65)
  ≥ 500 cells/µL 1.00 (Reference) 1.00 (Reference)
Ever ART interruptions
  ≥ 1 1.80 (1.33–2.43) 2.49 (1.53–4.05)
 None 1.00 (Reference) 1.00 (Reference)
Assay used
 Abbott RealTime (single centre) 0.34 (0.21–0.53) 0.11 (0.03–0.35)
 Roche TaqMan 2.0 (6 centres) 1.00 (Reference) 1.00 (Reference)
ART regimen
 2 NRTI + PI/r 1.53 (1.14–2.05) 2.35 (1.43–3.86)
 2 NRTI + NNRTI/INSTI 1.00 (Reference) 1.00 (Reference)
VL before ART
 Missing 2.12 (1.03–4.37) 1.14 (0.42–3.07)
  > 99.999 copies/mL 3.66 (1.92–7.00) 1.32 (0.59–2.98)
 9.999–99.999 copies/mL 2.17 (1.11–4.22) 1.99 (0.90–4.41)
  ≤ 9.999 copies/mL 1.00 (Reference) 1.00 (Reference)
ART duration
  < 9 months 2.50 (1.33–4.72) 0.72 (0.16–3.24)
 9–18 months 0.99 (0.57–1.71) 1.24 (0.55–2.79)
  > 18 months 1.00 (Reference) 1.00 (Reference)

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