AI Article Synopsis

  • The study examines drug resistance patterns in HIV-1 patients in Portugal, focusing on both transmitted drug resistance (TDR) and acquired drug resistance (ADR) among a sample of 1,050 cases.
  • Findings reveal that about 20% of the patients had drug resistance mutations, with TDR at 12.6% and ADR at 41.1%, particularly noting several specific mutations prevalent in both ART-naive and experienced patients.
  • The research also identifies risk factors associated with higher rates of drug resistance, including age over 50, origin from Portuguese-speaking African countries, specific HIV-1 subtypes, and low CD4 counts, while men and patients with high viral loads showed lower chances of resistance mutations.

Article Abstract

Background: The global scale-up of antiretroviral treatment (ART) offers significant health benefits by suppressing HIV-1 replication and increasing CD4 cell counts. However, incomplete viral suppression poses a potential threat for the emergence of drug resistance mutations (DRMs), limiting ART options, and increasing HIV transmission.

Objective: We investigated the patterns of transmitted drug resistance (TDR) and acquired drug resistance (ADR) among HIV-1 patients in Portugal.

Methods: Data were obtained from 1050 HIV-1 patient samples submitted for HIV drug resistance (HIVDR) testing from January 2022 to June 2023. Evaluation of DRM affecting viral susceptibility to nucleoside/tide reverse transcriptase inhibitors (NRTIs), non-nucleoside reverse transcriptase inhibitors (NNRTIs), protease inhibitors (PIs), and integrase strand transfer inhibitors (INSTIs) was performed using an NGS technology, the Vela Diagnostics Sentosa SQ HIV-1 Genotyping Assay.

Results: About 71% of patients were ART naïve and 29% were experienced. Overall, 20% presented with any DRM. The prevalence of TDR and ADR was 12.6% and 41.1%, respectively. M184V, T215S, and M41L mutations for NRTI, K103N for NNRTI, and M46I/L for PIs were frequent in naïve and treated patients. E138K and R263K mutations against INSTIs were more frequent in naïve than treated patients. TDR and ADR to INSTIs were 0.3% and 7%, respectively. Patients aged 50 or over (OR: 1.81, = 0.015), originating from Portuguese-speaking African countries (PALOPs) (OR: 1.55, = 0.050), HIV-1 subtype G (OR: 1.78, = 0.010), and with CD4 < 200 cells/mm (OR: 1.70, = 0.043) were more likely to present with DRMs, while the males (OR: 0.63, = 0.003) with a viral load between 4.1 to 5.0 Log (OR: 0.55, = 0.003) or greater than 5.0 Log (OR: 0.52, < 0.001), had lower chances of presenting with DRMs.

Conclusions: We present the first evidence on TDR and ADR to INSTI regimens in followed up patients presenting for healthcare in Portugal. We observed low levels of TDR to INSTIs among ART-naïve and moderate levels in ART-exposed patients. Regimens containing PIs could be an alternative second line in patients with intermediate or high-level drug resistance, especially against second-generation INSTIs (dolutegravir, bictegravir, and cabotegravir).

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11054263PMC
http://dx.doi.org/10.3390/v16040622DOI Listing

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