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

Author:

Barroso Sergio123,Guitart-Mampel Mariona123,García-García Francesc Josep123,Cantó-Santos Judith123,Valls-Roca Laura123,Andújar-Sánchez Félix123,Vilaseca-Capel Adrià123ORCID,Tobías Ester123,Arias-Dimas Angela4,Quesada-López Tania56,Artuch Rafael34ORCID,Villarroya Francesc56ORCID,Giralt Marta56ORCID,Martínez Esteban78,Lozano Ester9ORCID,Garrabou Glòria123ORCID

Affiliation:

1. Inherited Metabolic Diseases and Muscular Disorders Research Lab, Cellex-Institut d’Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Faculty of Medicine and Health Sciences, University of Barcelona (UB), 08036 Barcelona, Spain

2. Department of Internal Medicine, Hospital Clinic of Barcelona, 08036 Barcelona, Spain

3. CIBERER-Spanish Biomedical Research Centre in Rare Diseases, Carlos III Health Institute, 28029 Madrid, Spain

4. Department of Clinical Biochemistry, Institut de Recerca Sant Joan de Déu, Esplugues de Llobregat, 08950 Barcelona, Spain

5. Biochemistry and Molecular Biomedicine Department, Biomedicine Institute (IBUB), University of Barcelona (UB), 08014 Barcelona, Spain

6. CIBER Physiopathology of Obesity and Nutrition (CIBEROBN), Carlos III Health Institute, 28029 Madrid, Spain

7. Infectious Diseases Department, Hospital Clinic of Barcelona, 08036 Barcelona, Spain

8. CIBER of Infectious Diseases (CIBERINFEC), Carlos III Health Institute, 28029 Madrid, Spain

9. Department of Cell Biology, Physiology and Immunology, Faculty of Biology, University of Barcelona (UB), 08028 Barcelona, Spain

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.

Funder

Fondo de Investigaciones Sanitarias del Instituto de Salud Carlos III

El Centro de Investigación Biomédica en Red de Enfermedades Raras

Carmen de Torres grants

Generalitat de Catalunya

ISCIII-FSE+

ISCIII-NextGenerationEU

Publisher

MDPI AG

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