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Boosted Lopinavir- Versus Boosted Atazanavir-Containing Regimens and Immunologic, Virologic, and Clinical Outcomes: A Prospective Study of HIV-Infected Individuals in High-Income Countries

Authors :
Isabel Hurtado
Santiago Pérez-Hoyos
Consuelo Viladés
Adilia Warris
Federico Pulido
Eva Calabuig
Oscar Murillo Rubio
Dimitrios Paraskevis
Julia Del amo
Pablo Barreiro
INMA JARRIN
Arantza Sanvisens
Enrique Bernal Morell
Roberto Muga
Mariona Xercavins
Jean-Francois Bergmann
Aba Mahamat
Ignacio Pérez Valero
DAVID DALMAU
Clifford Leen
Dominique Costagliola
Jim Young
Vicente Soriano
Montserrat Vargas Laguna
Marcela Guevara
Soraya Boucherit
Jesus Castilla
Jean-Marie Michot
José A. Oteo
Maria Jose Amengual
Vicente Boix
Jonathan Sterne
Valerie Delpech
Jane Anderson
Alexandra Montoliu
Esperanza Merino de Lucas
Sophie Matheron
Michael Kozal
Caroline Sabin
André Cabié
Susana Monge
Luis Fernando Lopez.Cortes
Sylvie ABEL
Cedric Arvieux
Félix Gutiérrez
Bart Rijnders
Eulalia Valle-Garay
Juan Berenguer
Carmen Cabellos
Amy Justice
Felipe García
Joaquín Portilla
Mariana Gerschenson
Amsterdam institute for Infection and Immunity
Amsterdam Public Health
Global Health
Graduate School
Other departments
Infectious diseases
Paediatric Infectious Diseases / Rheumatology / Immunology
General Internal Medicine
Center of Experimental and Molecular Medicine
Dermatology
Medical Microbiology and Infection Prevention
Centre Hospitalier Universitaire de Nîmes (CHU Nîmes)
Medische Microbiologie
RS: CAPHRI School for Public Health and Primary Care
RS: CAPHRI - R4 - Health Inequities and Societal Participation
Interne Geneeskunde
Source :
Clinical infectious diseases, 60(8), 1262-1268. Oxford University Press, Clinical Infectious Diseases, Clinical Infectious Diseases, Oxford University Press (OUP), 2015, 60 (8), pp.1262-1268. ⟨10.1093/cid/ciu1167⟩, Clinical Infectious Diseases, 60(8), 1262-1268. Oxford University Press, Clinical Infectious Diseases, 60, 1262-8, Clinical Infectious Diseases, 60(8), 1262-8. Oxford University Press, Clinical Infectious Diseases, 60, 8, pp. 1262-8
Publication Year :
2015

Abstract

Current clinical guidelines consider regimens consisting of either ritonavir-boosted atazanavir or ritonavir-boosted lopinavir and a nucleoside reverse transcriptase inhibitor (NRTI) backbone among their recommended and alternative first-line antiretroviral regimens. However, these guidelines are based on limited evidence from randomized clinical trials and clinical experience.We compared these regimens with respect to clinical, immunologic, and virologic outcomes using data from prospective studies of human immunodeficiency virus (HIV)-infected individuals in Europe and the United States in the HIV-CAUSAL Collaboration, 2004-2013. Antiretroviral therapy-naive and AIDS-free individuals were followed from the time they started a lopinavir or an atazanavir regimen. We estimated the 'intention-to-treat' effect for atazanavir vs lopinavir regimens on each of the outcomes.A total of 6668 individuals started a lopinavir regimen (213 deaths, 457 AIDS-defining illnesses or deaths), and 4301 individuals started an atazanavir regimen (83 deaths, 157 AIDS-defining illnesses or deaths). The adjusted intention-to-treat hazard ratios for atazanavir vs lopinavir regimens were 0.70 (95% confidence interval [CI], .53-.91) for death, 0.67 (95% CI, .55-.82) for AIDS-defining illness or death, and 0.91 (95% CI, .84-.99) for virologic failure at 12 months. The mean 12-month increase in CD4 count was 8.15 (95% CI, -.13 to 16.43) cells/?L higher in the atazanavir group. Estimates differed by NRTI backbone.Our estimates are consistent with a lower mortality, a lower incidence of AIDS-defining illness, a greater 12-month increase in CD4 cell count, and a smaller risk of virologic failure at 12 months for atazanavir compared with lopinavir regimens.? The Author 2015. Published by Oxford University Press on behalf of the Infectious Diseases Society of America. All rights reserved. For Permissions, please e-mail: journals.permissions@oup.com.

Details

Language :
English
ISSN :
10584838 and 15376591
Database :
OpenAIRE
Journal :
Clinical infectious diseases, 60(8), 1262-1268. Oxford University Press, Clinical Infectious Diseases, Clinical Infectious Diseases, Oxford University Press (OUP), 2015, 60 (8), pp.1262-1268. ⟨10.1093/cid/ciu1167⟩, Clinical Infectious Diseases, 60(8), 1262-1268. Oxford University Press, Clinical Infectious Diseases, 60, 1262-8, Clinical Infectious Diseases, 60(8), 1262-8. Oxford University Press, Clinical Infectious Diseases, 60, 8, pp. 1262-8
Accession number :
edsair.doi.dedup.....d0a14e9dc8dd797739eba92f150c49b5