Longitudinal changes in body fat and metabolic complications in young people with perinatally acquired HIV

HIV Med. 2024 Feb;25(2):233-244. doi: 10.1111/hiv.13566. Epub 2023 Oct 16.

Abstract

Background: The role of body fat on metabolic complications remains poorly understood in young people living with perinatally acquired HIV (YPHIV).

Objective: Our objective was to assess the association of changes in adiposity over 2 years with metabolic outcomes in YPHIV.

Methods: The PHACS Adolescent Master Protocol (AMP) study enrolled YPHIV from 2007 to 2009 across 15 US sites, including Puerto Rico. We included YPHIV aged 7-19 years with body composition data assessed by whole-body dual-energy X-ray absorptiometry (DXA) at baseline and 2 years later. Metabolic outcomes included homeostatic model assessment of insulin resistance (HOMA-IR) and non-high-density lipoprotein cholesterol (non-HDL-C). We fitted linear regression models to assess the association of increase in body fat over 2 years with metabolic outcomes at years 2 and 3.

Results: In all, 232 participants had a second DXA and either HOMA-IR or non-HDL-C measured at year 2. Participant characteristics at the first DXA were: age 12 years (9-14) [median (Q1-Q3)], 69% Black, and median CD4 count 714 cells/μL; 70% with HIV RNA <400 copies/mL. In adjusted analyses for every 1% increase in body fat from baseline to year 2, HOMA-IR was higher by 1.03-fold at year 3 (95% CI: 1.00, 1.05). We observed that for every 1% increase in body fat from baseline to year 2, non-HDL-C was 0.72 mg/dL higher at year 2 (95% CI: -0.04-1.49) and 0.81 mg/dL higher at year 3 (95% CI: -0.05-1.66).

Conclusions: Increases in adiposity over time may lead to downstream decreased insulin sensitivity and dyslipidaemia in YPHIV.

Keywords: HIV; adiposity; adolescents; metabolic outcomes; perinatally acquired.

MeSH terms

  • Absorptiometry, Photon
  • Adipose Tissue / diagnostic imaging
  • Adiposity
  • Adolescent
  • Cholesterol
  • HIV Infections* / complications
  • Humans
  • Insulin Resistance*
  • Obesity / complications

Substances

  • Cholesterol