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Metabolic, Mitochondrial, and Inflammatory Effects of Efavirenz, Emtricitabine, and Tenofovir Disoproxil Fumarate in Asymptomatic Antiretroviral-Naïve People with HIV. | LitMetric

AI Article Synopsis

  • The study evaluated the effects of the efavirenz, emtricitabine, and tenofovir disoproxil fumarate (EFV/FTC/TDF) treatment on metabolic, mitochondrial, and inflammatory parameters in people with HIV compared to untreated individuals.
  • Results showed that while treatment significantly improved viral outcomes, it also led to increased levels of glucose, cholesterol, and triglycerides, indicating metabolic changes.
  • Despite these metabolic alterations, mitochondrial function was mostly preserved, with some recovery in mitochondrial DNA, and a reduction in inflammatory markers was observed following treatment, suggesting some overall benefit.

Article Abstract

This study aimed to comprehensively assess the metabolic, mitochondrial, and inflammatory effects of first-line efavirenz, emtricitabine, and tenofovir disoproxil fumarate (EFV/FTC/TDF) single-tablet regimen (STR) relative to untreated asymptomatic HIV infection. To this end, we analyzed 29 people with HIV (PWH) treated for at least one year with this regimen vs. 33 antiretroviral-naïve PWH. Excellent therapeutic activity was accompanied by significant alterations in metabolic parameters. The treatment group showed increased plasmatic levels of glucose, total cholesterol and its fractions (LDL and HDL), triglycerides, and hepatic enzymes (GGT, ALP); conversely, bilirubin levels (total and indirect fraction) decreased in the treated cohort. Mitochondrial performance was preserved overall and treatment administration even promoted the recovery of mitochondrial DNA (mtDNA) content depleted by the virus, although this was not accompanied by the recovery in some of their encoded proteins (since cytochrome c oxidase II was significantly decreased). Inflammatory profile (TNFα, IL-6), ameliorated after treatment in accordance with viral reduction and the recovery of TNFα levels correlated to mtDNA cell restoration. Thus, although this regimen causes subclinical metabolic alterations, its antiviral and anti-inflammatory properties may be associated with partial improvement in mitochondrial function.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11313075PMC
http://dx.doi.org/10.3390/ijms25158418DOI Listing

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