Body fat evolution as predictor of retinal microvasculature in children

C J C Van Aart1, N Michels1, I Sioen1,2

  • 1Department of Public Health, Faculty of Medicine and Health Sciences, Ghent University, Ghent, Belgium.

Insights

Changes in children's body fat over time are linked to retinal microvasculature changes, particularly in boys. This suggests early cardiovascular aging markers may be influenced by childhood adiposity.

Area of Science:

  • Pediatric cardiovascular health
  • Ophthalmology
  • Developmental biology

Background:

  • Overweight in children is a growing concern linked to cardiovascular disease.
  • Microvascular changes are potential early indicators of cardiovascular aging.
  • Understanding the link between body fat and vascular health in children is crucial.

Purpose of the Study:

  • To investigate the association between changes in children's body fat over time and retinal microvasculature.
  • To explore if body fat accumulation in childhood predicts cardiovascular aging markers.
  • To examine sex-specific differences in these associations.

Main Methods:

  • Longitudinal study of 171 healthy Flemish children over 7 years.
  • Measurements included body mass index (zBMI), waist circumference (zWC), and fat mass index (zFMI).
  • Retinal microvasculature (CRAE, CRVE) assessed using digital retinal photographs and IVAN software.

Main Results:

  • Higher fat mass index (zFMI) in boys was cross-sectionally associated with higher central retinal venular equivalent (CRVE).
  • Boys with high zFMI also showed a lower central retinal arteriolar to venular equivalent ratio.
  • Longitudinal analysis revealed changes in zFMI over time were positively associated with CRVE in boys.

Conclusions:

  • Changes in body fat during childhood are associated with retinal microvascular alterations, specifically the CRVE.
  • These findings highlight potential early cardiovascular aging effects in children related to adiposity.
  • The association was particularly evident in boys, suggesting sex-specific effects.
Abstract

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