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Regional adiposity and markers of inflammation in pre-school age children
Kerri Z Delaney1,2,3, Catherine A Vanstone4, Hope A Weiler4
1Department of Health, Kinesiology, and Applied Physiology, Concordia University, Montreal, Quebec, Canada.
Insights
Overweight preschool children exhibit higher systemic inflammation, linked to increased body fat. This suggests early adiposity may pose health risks, warranting further investigation into long-term consequences.
Area of Science:
- Pediatric Health
- Metabolic Disease Research
- Inflammation Studies
Background:
- Systemic inflammation and upper body fat are linked to metabolic disease in adults.
- The relationship between adiposity and inflammation in preschool-aged children is not well understood.
Purpose of the Study:
- To investigate the association between adiposity and systemic inflammation in preschool-aged children.
- To determine if excess body fat, particularly abdominal fat, correlates with inflammatory markers in young children.
Main Methods:
- A subset of 71 preschool children (3.7 ± 1.0 years) from Montréal, QC, were analyzed.
- Adiposity was measured using dual-energy x-ray absorptiometry.
- Blood concentrations of C-reactive protein (CRP) and tumor necrosis factor alpha (TNFα) were quantified.
Main Results:
- Overweight (OW) children had a higher android:gynoid ratio (indicating abdominal fat) and higher CRP levels compared to healthy weight (HW) children.
- Total body fat percentage correlated positively with CRP and TNFα concentrations.
- CRP levels correlated with android adiposity, and TNFα levels correlated with gynoid adiposity.
Conclusions:
- Increased adiposity in preschool-aged children is associated with elevated systemic inflammation.
- Abdominal fat distribution may play a role in this inflammatory response.
- Longitudinal studies are necessary to ascertain the long-term health implications of early-life adiposity.
Abstract:
In adults, upper body fat partially increases metabolic disease risk through increasing systemic inflammation. Our objective was to determine if this relationship exists in preschool-aged children. A subset of children (n = 71, 35 males), 3.7 ± 1.0 y, were studied from n = 515 children recruited from randomly selected daycares in Montréal, QC. According to WHO charts for 2-5 y, 49 children were healthy weight (HW) and 21 were overweight (OW). Adiposity was determined through dual-energy x-ray absorptiometry. Blood concentrations of C-reactive protein (CRP) and tumour necrosis factor alpha (TNFα) were determined via enzyme-linked immunosorbent and multiplex assays, respectively. OW children had higher (p = 0.03) android:gynoid ratio 0.50 ± 0.09 compared to HW children 0.56 ± 0.12, indicating excess fat was predominantly stored in the abdominal depot. CRP was higher (p = 0.01) in OW children 1.45 ± 2.02 mg/L compared to HW 0.74 ± 1.38 mg/L. Percent fat was correlated with CRP (r = 0.32; p < 0.01) and TNFα (r = 0.25; p = 0.04) concentrations. CRP also correlated with android adiposity (r = 0.24; p = 0.04) and TNFα correlated with gynoid adiposity (r = 0.24; p = 0.04). We observed that greater adiposity is associated with higher systemic inflammation in pre-school aged children. Future longitudinal studies are needed to understand the long term consequences of excess total and regional body fat in young children.
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