Integrase strand transfer inhibitors (INSTIs) resistance mutations in HIV-1 infected Turkish patients
No Thumbnail Available
Date
2016
Journal Title
Journal ISSN
Volume Title
Publisher
Taylor & Francis
Abstract
Objectives: Integrase strand transfer inhibitor (INSTI) is a new class of antiretroviral (ARV) drugs designed to block the action of the integrase viral enzyme, which is responsible for insertation of the HIV-1 genome into the host DNA. The aim of this study was to evaluate for the first time INSTI resistance mutations in Turkish patients. Methods: This study was conducted in Turkey, between April 2013 and April 2015 using 169 HIV-1-infected patients (78 ARV naive patients and 91 ARV-experienced patients). Laboratory and clinical characteristics of ARV naive and ARV-experienced patients were as follows: gender (M/F): 71/7 and 80/11, median age: 38 and 38.4; median CD4+ T-cell: 236 and 216 cells/mm3, median HIV-1 RNA: 4.95+ E5 and 1.08E+ 6 copies/ml. Population-based seqeunces of the reverse transcriptase, protease, and integrase domains of the HIV-1 pol gene were used to detect HIV-1 drug resistance mutations. Result: INSTI resistance mutations were not found in recently diagnosed HIV-1-infected patients. However, ARV-experienced patients had major resistance mutations associated with raltegravir and elvitegravir; the following results were generated: F121Y, Y143R, Q148R and E157Q (6/91 - 6.6%). Conclusions: The prevalence of INSTI resistant mutations in ART-experienced patients suggested that resistance testing must be incorporated as an integral part of HIV management with INSTI therapies.
Description
Keywords
Infectious diseases, Pharmacology & pharmacy, Hiv-1 integrase, Integrase inhibitors, Raltegravir, Elvitegravir, Dolutegravir, Drug, Resistance, Dna sequencing, Antiretroviral-naive patients, Natural polymorphisms, HIV-1, Individuals, Therapy, Update, Turkey
Citation
Sayan, M. vd. (2016). "Integrase strand transfer inhibitors (INSTIs) resistance mutations in HIV-1 infected Turkish patients". HIV Clinical Trials, 17(3), 109-113.