Your browser doesn't support javascript.

Secretaria de Estado da Saúde - BVS

Rede de Informação e Conhecimento

Home > Pesquisa > ()
XML
Imprimir Exportar

Formato de exportação:

Exportar

Email
Adicionar mais destinatários
| |

Resistance to antiretroviral therapy (ART) in patients with HIV/AIDS after therapeutic failure / Resistencia a la terapia antirretroviral (TAR) en pacientes VIH/SIDA en fracaso terapéutico

Agudelo-Rojas, Lina María; Coral-Orbes, María Victoria; Galindo-Orrego, Ximena; Mueses-Marín, Héctor Fabio; Galindo-Quintero, Jaime.
Acta méd. colomb ; 44(4): 3-10, Oct.-Dec. 2019. tab, graf
Artigo Inglês | LILACS, COLNAL | ID: biblio-1124055
Abstract

Introduction:

HIV replication and the suboptimal use of antiretrovirals are directly related to the appearance of resistant mutations. The objective of this study was to describe the resistance mutations (RMs) present in HIV infected patients who experienced antiretroviral treatment failure between 2002 and 2015 in Cali, Colombia.

Method:

403 genotypes of adult patients with HIV/AIDS who received ART and experienced virological failure were analyzed. With informed consent, resistance genotype testing was performed using TRUGENE HIV-1; the RMs were defined according to the International AIDS Society-2015 list. The sample was subdivided by periods (2002-2006 vs 2007-2015) and early versus late genotyping. Mutations with ≥15 points to some ARV were considered, according to the Stanford HIV database.

Results:

comparing the periods, there were more RMs for non-nucleoside reverse transcriptase inhibitors (NNRTIs) in 2007-2015 than in 2002-2006 (85% vs. 60%, respectively, p<0.0001), but protease inhibitors were less affected in 2007-2015 than in 2002-2006 (11% vs. 29%, respectively, p < 0.001). The M184V and K103 N mutations were the most frequent RMs in reverse transcriptase (RT) for NRTIs and NNRTIs, respectively. A total of 67.5% were early genotypes. There was a higher prevalence of certain RMs in late genotypes compared to early ones, mainly for RMs to PIs (D30N, L90M) and NRTIs (M41L, D67N, K70R, L210W); but a lower prevalence of RMs to NNRTIs (Y181C).

Conclusion:

the late resistance genotypes were associated with higher levels of resistance mutations, mainly to the NNRTI and NRTI families, limiting their use as a rescue therapy alternative. (Acta Med Colomb 2019; 44. DOIhttps//doi.org/10.36104/amc.2019.1546).
Biblioteca responsável: CO70
Selo DaSilva