Magnitude of virologic blips is associated with a higher risk for virologic rebound in HIV-infected individuals: a recurrent events analysis

Grennan, J.Troy.; Loutfy, M.R.; Su, D.; Harrigan, P.Richard.; Cooper, C.; Klein, M.; Machouf, N.; Montaner, J.S.G.; Rourke, S.; Tsoukas, C.; Hogg, B.; Raboud, J.; Hosein, S.; Lemay, B.; Margolese, S.; Ssengendo, E.; Aykroyd, G.; Balfour, L.; Bayoumi, A.; Cairney, J.; Calzavara, L.; Cooper, C.; Gough, K.; Guillemi, S.; Harrigan, P..Richard.; Harris, M.; Hatzakis, G.; Hogg, R.; Kilby, D.; Klein, M.; Lalonde, R.; Lima, V.; Loutfy, M.; Machouf, N.; Mills, E.; Millson, P.; Montaner, J.; Moore, D.; Pa

Journal of Infectious Diseases 205(8): 1230-1238

2012


ISSN/ISBN: 0022-1899
PMID: 22438396
DOI: 10.1093/infdis/jis104
Accession: 054224170

Download citation:  
Text
  |  
BibTeX
  |  
RIS

Article/Abstract emailed within 0-6 h
Payments are secure & encrypted
Powered by Stripe
Powered by PayPal

Abstract
The importance of human immunodeficiency virus (HIV) blip magnitude on virologic rebound has been raised in clinical guidelines relating to viral load assays. Antiretroviral-naive individuals initiating combination antiretroviral therapy (cART) after 1 January 2000 and achieving virologic suppression were studied. Negative binomial models were used to identify blip correlates. Recurrent event models were used to determine the association between blips and rebound by incorporating multiple periods of virologic suppression per individual. 3550 participants (82% male; median age, 40 years) were included. In a multivariable negative binomial regression model, the Amplicor assay was associated with a lower blip rate than branched DNA (rate ratio, 0.69; P < .01), controlling for age, sex, region, baseline HIV-1 RNA and CD4 count, AIDS-defining illnesses, year of cART initiation, cART type, and HIV-1 RNA testing frequency. In a multivariable recurrent event model controlling for age, sex, intravenous drug use, cART start year, cART type, assay type, and HIV-1 RNA testing frequency, blips of 500-999 copies/mL were associated with virologic rebound (hazard ratio, 2.70; P = .002), whereas blips of 50-499 were not. HIV-1 RNA assay was an important determinant of blip rates and should be considered in clinical guidelines. Blips ≥500 copies/mL were associated with increased rebound risk.