Metabolic, Mitochondrial, and Inflammatory Effects of Efavirenz, Emtricitabine, and Tenofovir Disoproxil Fumarate in Asymptomatic Antiretroviral-Naïve People with HIV.
Humans
HIV Infections
/ drug therapy
Male
Female
Adult
Mitochondria
/ metabolism
Alkynes
Benzoxazines
/ therapeutic use
Anti-HIV Agents
/ therapeutic use
Cyclopropanes
/ therapeutic use
Tenofovir
/ therapeutic use
Middle Aged
Emtricitabine
/ therapeutic use
DNA, Mitochondrial
/ metabolism
Inflammation
HIV
antiretroviral treatment
efavirenz
emtricitabine
inflammatory effects
metabolic profile
mitochondrial DNA
mitochondrial toxicity
tenofovir
Journal
International journal of molecular sciences
ISSN: 1422-0067
Titre abrégé: Int J Mol Sci
Pays: Switzerland
ID NLM: 101092791
Informations de publication
Date de publication:
01 Aug 2024
01 Aug 2024
Historique:
received:
23
05
2024
revised:
20
07
2024
accepted:
25
07
2024
medline:
10
8
2024
pubmed:
10
8
2024
entrez:
10
8
2024
Statut:
epublish
Résumé
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.
Identifiants
pubmed: 39125986
pii: ijms25158418
doi: 10.3390/ijms25158418
pii:
doi:
Substances chimiques
efavirenz
JE6H2O27P8
Alkynes
0
Benzoxazines
0
Anti-HIV Agents
0
Cyclopropanes
0
Tenofovir
99YXE507IL
Emtricitabine
G70B4ETF4S
DNA, Mitochondrial
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Subventions
Organisme : Instituto de Salud Carlos III
ID : Grant code PI21/00935
Organisme : Centre for Biomedical Network Research on Rare Diseases
ID : 2021 SGR 01423
Organisme : Government of Catalonia
ID : CD21/00019