Inflammation and fatness in adolescents with and without Down syndrome: UP & DOWN study

J Intellect Disabil Res. 2020 Feb;64(2):170-179. doi: 10.1111/jir.12697. Epub 2019 Dec 20.

Abstract

Background: The main objective of this study was to describe the inflammatory status of adolescents with Down syndrome (DS) and their relationship with adiposity.

Methods: Ninety-five adolescents with DS (44.2% girls) and a control group of 113 adolescents (47.8% girls), aged between 11 and 18 years old, from the UP & DOWN study were included in this substudy. Serum C-reactive protein, C3 and C4 complement factors, total proteins, interleukin-6, tumour necrosis factor-α, insulin, cortisol, leptin, adiponectin, galactin-3 and visfatin were analysed; homeostatic model assessment index was calculated. In order to evaluate adiposity, we measured the following body fat variables: weight, height, waist circumference and skinfold thicknesses. Birth weight was obtained by questionnaire. In addition, body mass index, waist-to-height ratio (WHtR) and body fat percentage (BF%) were calculated.

Results: Down syndrome group showed higher levels of body mass index, WHtR, waist circumference, BF% and lower birth weight than controls (P < 0.001). In the general linear model in the total sample, WHtR was positively associated with C3 and C4 (P < 0.001) as well as with leptin levels (P = 0.015). BF% was positively associated with total proteins (P = 0.093) and leptin levels (P < 0.001). DS was positively associated with total proteins (P < 0.001), C3 (P = 0.047) and C4 (P = 0.019). Despite the higher levels of adiposity found in DS group, no direct association was found between BF% and leptin levels, comparing with the control group.

Conclusions: These findings suggest that abdominal obesity should be controlled in adolescents because of its relationship with acute phase-inflammatory biomarkers but especially in DS adolescents who may show a peculiar metabolic status according to their relationship between adiposity and inflammatory biomarkers.

Keywords: Down syndrome; adiposity; adolescents; inflammatory biomarkers.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adiposity / immunology
  • Adiposity / physiology*
  • Adolescent
  • Biomarkers / blood
  • Child
  • Comorbidity
  • Down Syndrome* / epidemiology
  • Down Syndrome* / immunology
  • Down Syndrome* / metabolism
  • Female
  • Follow-Up Studies
  • Humans
  • Inflammation* / epidemiology
  • Inflammation* / immunology
  • Inflammation* / metabolism
  • Male
  • Pediatric Obesity* / epidemiology
  • Pediatric Obesity* / immunology
  • Pediatric Obesity* / metabolism

Substances

  • Biomarkers