Abstract

Introduction: Treatment for All recommendations have allowed access to antiretroviral (ARV) treatment for an increasing number of patients. This minimizes the transmission of infection but can potentiate the risk of transmitted (TDR) and acquired drug resistance (ADR). Objective: To study the trends of TDR and ADR in patients followed up in Portuguese hospitals between 2001 and 2017. Methods: In total, 11,911 patients of the Portuguese REGA database were included. TDR was defined as the presence of one or more surveillance drug resistance mutation according to the WHO surveillance list. Genotypic resistance to ARV was evaluated with Stanford HIVdb v7.0. Patterns of TDR, ADR and the prevalence of mutations over time were analyzed using logistic regression. Results and Discussion: The prevalence of TDR increased from 7.9% in 2003 to 13.1% in 2017 (p < 0.001). This was due to a significant increase in both resistance to nucleotide reverse transcriptase inhibitors (NRTIs) and non-nucleotide reverse transcriptase inhibitors (NNRTIs), from 5.6% to 6.7% (p = 0.002) and 2.9% to 8.9% (p < 0.001), respectively. TDR was associated with infection with subtype B, and with lower viral load levels (p < 0.05). The prevalence of ADR declined from 86.6% in 2001 to 51.0% in 2017 (p < 0.001), caused by decreasing drug resistance to all antiretroviral (ARV) classes (p < 0.001). Conclusions: While ADR has been decreasing since 2001, TDR has been increasing, reaching a value of 13.1% by the end of 2017. It is urgently necessary to develop public health programs to monitor the levels and patterns of TDR in newly diagnosed patients.

Highlights

  • Treatment for All recommendations have allowed access to antiretroviral (ARV) treatment for an increasing number of patients

  • In Portugal, the first line regimen recommends the use of an integrase strand inhibitor (INSTI), such as dolutegravir (DTG), raltegravir (RAL) or evitelgravir (EVG/c), together with a combination of nucleoside reverse transcriptase inhibitors (NRTI), such as tenofovir/entricitabine (TDF/FTC) or abacavir/lamivudine (ABC/3TC)

  • We aim to describe the temporal trends of transmitted drug resistance (TDR) and acquired drug resistance (ADR) between 2001 and 2017, as well as the most prevalent drug resistance mutations, and to identify predictors of TDR among HIV-1 infected patients treated in Portuguese hospitals

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Summary

Introduction

Treatment for All recommendations have allowed access to antiretroviral (ARV) treatment for an increasing number of patients This minimizes the transmission of infection but can potentiate the risk of transmitted (TDR) and acquired drug resistance (ADR). International guidelines consistently recommend that newly diagnosed individuals should be tested for ARV drug resistance, to detect potential transmitted drug resistance (TDR) and guide the selection of ART regimens [6,7]. This procedure minimizes the risk of experiencing virologic failure after starting ART due to the selection of resistant strains. Another option is to use a non-nucleoside reverse transcriptase inhibitor (NNRTI), such as rilpivirine (RPV), together with a combination of NRTI (TDF/FTC or ABC/3TC)

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