Carolan, Eirin and Hogan, Andrew E. and Corrigan, Michelle and Gaotswe, Gadintshware and O'Connell, Jean and Foley, Niamh and O'Neill, Luke A. and Cody, Declan and O'Shea, Donal
(2014)
The Impact of Childhood Obesity on Inflammation,
Innate Immune Cell Frequency, and Metabolic
MicroRNA Expression.
Journal of Clinical Endocrinology and Metabolism, 99 (3).
pp. 474-478.
ISSN 0021-972X
Abstract
Background: Obesity is characterized by chronic inflammation, immune dysregulation, and alteration of gene expression, associated with type 2 diabetes mellitus and cardiovascular disease. The
degree to which these changes occur in childhood obesity is not fully defined.
Aims and Methods: The aim was to investigate the effect of childhood obesity on immune cell
frequency, macrophage activation, cytokine production, and specific regulators of metabolic gene
expression. Profiling was performed on peripheral blood from 29 obese and 20 nonobese children
using real-time PCR, ELISA, and flow cytometry.
Results: Fasting glucose was similar in both groups, but there was a higher degree of insulin resistance
in obese subjects (homeostasis model of assessment for insulin resistance, 4.8 vs 0.84; P .001). Soluble
CD163, a marker of macrophage polarization to a proinflammatory profile, was elevated in the obese
compared to nonobese children (135 vs 105 ng/mL; P .03). Invariant natural killer T cells were reduced
in the obese children (CD3 T cells, 0.31 vs 0.53%; P .001). Cytokine profiling revealed significantly
elevated TNF- (6.7 vs 5.1 pg/mL; P .01) and leptin (1186 vs 432 pg/mL; P .001) and reduced
adiponectin (884 vs 1321 pg/mL; P .001) in obese compared to nonobese children. Stimulation of
peripheral blood mononuclear cells from obese children resulted in higher levels of IL-1 (2100 vs 1500
pg/mL; P .018). There was a 4-fold increase in expression of microRNA33a (P .001) and a 3-fold
increase in microRNA33b (P .017) in obese children.
Conclusion: Childhood obesity is associated with changes in immune cell frequency, inflammatory
environment, and regulation of metabolic gene expression. These changes have been causally
linked to the onset of metabolic disease in adulthood and suggest the future trajectory of obese
children to the development of type 2 diabetes mellitus and premature cardiovascular disease
Item Type: |
Article
|
Keywords: |
SYSTEMIC INFLAMMATION; INSULIN-RESISTANCE; ADIPOSE; TISSUE; SOLUBLE; CD163; DISORDERS; |
Academic Unit: |
Faculty of Science and Engineering > Biology |
Item ID: |
12422 |
Identification Number: |
https://doi.org/10.1210/jc.2013-3529 |
Depositing User: |
Andrew Hogan
|
Date Deposited: |
17 Feb 2020 15:14 |
Journal or Publication Title: |
Journal of Clinical Endocrinology and Metabolism |
Publisher: |
Oxford University Press |
Refereed: |
Yes |
URI: |
|
Use Licence: |
This item is available under a Creative Commons Attribution Non Commercial Share Alike Licence (CC BY-NC-SA). Details of this licence are available
here |
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