Longitudinal changes in mitochondrial-associated measures and insulin resistance in youth with perinatally-acquired HIV in the U.S

Mitochondrion. 2024 Sep:78:101936. doi: 10.1016/j.mito.2024.101936. Epub 2024 Jul 14.

Abstract

HIV infection and its treatment are associated with mitochondrial dysfunction and metabolic derangement. However, longitudinal changes in oxidative phosphorylation activities [Complex I (C1) and Complex IV (C4)], or venous lactate/pyruvate ratios (LPR), and their relationships with insulin resistance (IR), remain unclear in youth living with perinatally-acquired HIV (YPHIV). We measured venous LPR, C1, and C4 activities in blood cells and homeostatic model assessment for IR (HOMA-IR) over two years. Limited longitudinal differences in mitochondrial-related measures and IR were observed in YPHIV vs youth perinatally HIV-exposed but uninfected. There were no systematic differences in C1, C4, or HOMA-IR between the groups.

Keywords: Insulin resistance; Lactate; Mitochondria; Oxidative phosphorylation; Perinatal HIV; Youth.

MeSH terms

  • Adolescent
  • Child
  • Electron Transport Complex I / metabolism
  • Electron Transport Complex IV / genetics
  • Electron Transport Complex IV / metabolism
  • Female
  • HIV Infections*
  • Humans
  • Infectious Disease Transmission, Vertical
  • Insulin Resistance*
  • Lactic Acid / blood
  • Lactic Acid / metabolism
  • Longitudinal Studies
  • Male
  • Mitochondria / metabolism
  • Oxidative Phosphorylation
  • Pyruvic Acid / blood
  • Pyruvic Acid / metabolism
  • United States / epidemiology
  • Young Adult

Substances

  • Lactic Acid
  • Pyruvic Acid
  • Electron Transport Complex IV
  • Electron Transport Complex I