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Enhanced Myeloid Leukocytes in Obese Children and Adolescents at Risk for Metabolic Impairment.

Citation
Gállego-Suárez, C., et al. “Enhanced Myeloid Leukocytes In Obese Children And Adolescents At Risk For Metabolic Impairment.”. Frontiers In Endocrinology, p. 327.
Center University of Michigan
Author Cecilia Gállego-Suárez, Ayse Bulan, Emily Hirschfeld, Phillip Wachowiak, Simin Abrishami, Cameron Griffin, Julie Sturza, Abigail Tzau, Taryn Hayes, Susan J Woolford, Carey N Lumeng, Joyce M Lee, Kanakadurga Singer
Keywords CRP, inflammation, Insulin resistance, monocytes, Pediatric obesity
Abstract

We aimed to examine if myeloid leukocyte profiles are associated with metabolic impairment in children and adolescents with obesity, and if sex, age, or race influence this relationship. 282 children ages 8-17 were evaluated. Predictor measures were absolute neutrophil counts (ANC), absolute monocyte count, monocyte subtypes and C reactive protein (CRP). Outcome variables were waist circumference, fasting glucose and insulin, HOMA-IR, HbA1c (%) and lipid profiles. Pearson correlation coefficients were used to determine associations between predictor and outcome variables. Wilcoxon two-sample tests were used to evaluate differences by sex. CRP ( < 0.0001), ANC ( < 0.0018), and classical monocytes ( = 0.05) were significantly higher in children with obesity. CRP, ANC and classical monocytes showed positive correlations with waist circumference, insulin, HOMA-IR and triglycerides. CRP was positively associated with ANC overall ( = 0.05). ANC demonstrated positive correlation with monocytes ( < 0.001). The associations between predictor and outcome variables were influenced by sex, race, and age. CRP and myeloid leukocyte populations, specifically classical monocytes and neutrophils associate with both body composition and metabolic parameters in children with obesity suggesting that these cells may play a critical role in metabolic impairment. Race, gender and age interactions between monocytes and metabolic parameters were significant.

Year of Publication
2020
Journal
Frontiers in endocrinology
Volume
11
Number of Pages
327
Date Published
05/2020
ISSN Number
1664-2392
DOI
10.3389/fendo.2020.00327
Alternate Journal
Front Endocrinol (Lausanne)
PMID
32528415
PMCID
PMC7266967
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