The virological and immunological outcomes in patients carrying multiclass-resistant HIV-1, their predictors, and their impact on disease progression were investigated. Antiretroviral-experienced patients carrying at least one primary resistance mutation (IAS-USA 2006) to two to three classes of antiretroviral drugs were analyzed for achieving an HIV-1 RNA <50 copies/ml, a CD4 count increase of >200 cells/μl from baseline, and progression to an AIDS-defining event or death. Survival analysis was performed using the Kaplan-Meier estimates and predictors of different outcomes were analyzed using Cox's regression models. A total of 236 patients were identified. Of these 73% reached HIV-1 RNA <50 copies/ml. Higher genotypic sensitivity score of the salvage regimen, lower viral load, and more recent calendar year at genotyping were independently associated with virological response. Immunological response (58%) was predicted by a more recent calendar year, the achievement of an undetectable viral load, and higher CD4 counts at genotyping. Thirty-three patients showed clinical progression: achieving HIV-1 RNA <50 copies/ml predicted AIDS-free survival, independently from other significant cofactors. In individuals with multiclass-resistant HrV-1, virological suppression and immunological recovery are becoming more easily accessible with more recent therapies. The achievement of virological suppression is a strong predictor of reduced clinical progression. © Mary Ann Liebert, Inc.

Virological suppression reduces clinical progression in patients with multiclass-resistant HIV type 1 / Laura, Bracciale; Simona Di, Giambenedetto; Manuela, Colafigli; LA TORRE, Giuseppe; Mattia, Prosperi; Rosaria, Santangelo; Simona, Marchetti; Roberto, Cauda; Giovanni, Fadda; Andrea De, Luca. - In: AIDS RESEARCH AND HUMAN RETROVIRUSES. - ISSN 0889-2229. - 25:3(2009), pp. 261-267. [10.1089/aid.2008.0136]

Virological suppression reduces clinical progression in patients with multiclass-resistant HIV type 1

LA TORRE, Giuseppe;
2009

Abstract

The virological and immunological outcomes in patients carrying multiclass-resistant HIV-1, their predictors, and their impact on disease progression were investigated. Antiretroviral-experienced patients carrying at least one primary resistance mutation (IAS-USA 2006) to two to three classes of antiretroviral drugs were analyzed for achieving an HIV-1 RNA <50 copies/ml, a CD4 count increase of >200 cells/μl from baseline, and progression to an AIDS-defining event or death. Survival analysis was performed using the Kaplan-Meier estimates and predictors of different outcomes were analyzed using Cox's regression models. A total of 236 patients were identified. Of these 73% reached HIV-1 RNA <50 copies/ml. Higher genotypic sensitivity score of the salvage regimen, lower viral load, and more recent calendar year at genotyping were independently associated with virological response. Immunological response (58%) was predicted by a more recent calendar year, the achievement of an undetectable viral load, and higher CD4 counts at genotyping. Thirty-three patients showed clinical progression: achieving HIV-1 RNA <50 copies/ml predicted AIDS-free survival, independently from other significant cofactors. In individuals with multiclass-resistant HrV-1, virological suppression and immunological recovery are becoming more easily accessible with more recent therapies. The achievement of virological suppression is a strong predictor of reduced clinical progression. © Mary Ann Liebert, Inc.
2009
01 Pubblicazione su rivista::01a Articolo in rivista
Virological suppression reduces clinical progression in patients with multiclass-resistant HIV type 1 / Laura, Bracciale; Simona Di, Giambenedetto; Manuela, Colafigli; LA TORRE, Giuseppe; Mattia, Prosperi; Rosaria, Santangelo; Simona, Marchetti; Roberto, Cauda; Giovanni, Fadda; Andrea De, Luca. - In: AIDS RESEARCH AND HUMAN RETROVIRUSES. - ISSN 0889-2229. - 25:3(2009), pp. 261-267. [10.1089/aid.2008.0136]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/128762
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