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Published on: September 11, 2015
Serum Milk Fat Globule Epidermal Growth Factor 8 Concentrations in Children with Obesity
Chao Liu1, Linhao Wang2, Shuang Guo1
1Department of Pediatrics, The Second Affiliated Hospital of Xi'an Jiaotong University, Xi'an, China.
Insights
Elevated Milk fat globule epidermal growth factor 8 (MFGE8) levels are linked to pediatric obesity. This suggests MFGE8 may contribute to childhood obesity and its metabolic complications.
Area of Science:
- Endocrinology
- Metabolic Syndrome
- Pediatric Health
Background:
- Milk fat globule epidermal growth factor 8 (MFGE8) is an integrin ligand influencing metabolic processes.
- MFGE8's role in pediatric obesity is not well understood.
- Obesity pathogenesis is linked to MFGE8, necessitating pediatric investigation.
Purpose of the Study:
- To investigate the association between serum MFGE8 concentrations and obesity-related parameters in children.
- To explore MFGE8's relationship with anthropometric, metabolic, and inflammatory markers in pediatric obesity.
Main Methods:
- 104 children (64 obese, 40 controls) participated.
- Serum MFGE8 levels were measured using ELISA.
- Evaluated BMI, blood pressure, lipids, glucose, insulin, and inflammatory markers.
Main Results:
- Obese children had significantly higher MFGE8 levels than controls.
- MFGE8 correlated positively with BMI, blood pressure, and insulin resistance (HOMA-IR).
- MFGE8 also correlated with inflammatory markers like TNF-α, adiponectin, and leptin.
Conclusions:
- Elevated MFGE8 is associated with pediatric obesity and related metabolic issues.
- MFGE8 may play a role in the development of childhood obesity.
- Further research is warranted to understand MFGE8's precise contribution to metabolic complications.
Introduction:
Milk fat globule epidermal growth factor 8 (MFGE8) represents a recently characterized secreted integrin ligand involved in modulating systemic metabolic processes through impacts on nutrient absorption, gastrointestinal motility, and lipid homeostasis. Current literature supports its relevance in obesity pathogenesis. However, the exploration of MFGE8's function specifically within pediatric obesity contexts remains insufficient. This investigation aimed to delineate relationships between circulating MFGE8 concentrations and diverse obesity-associated parameters in children.
Methods:
Our study included 104 participants (32 females, 72 males), consisting of 64 children diagnosed with obesity and 40 normal-weight controls. We measured serum MFGE8 levels employing enzyme-linked immunosorbent assay methodology. Multiple clinical and biochemical measures were evaluated, encompassing body mass index (BMI), waist and hip circumferences, blood pressure, hepatic enzyme patterns, cholesterol parameters, and fasting insulin (FINS).
Results:
Obese participants exhibited substantially increased serum MFGE8 concentrations relative to non-obese controls (p < 0.05). MFGE8 levels correlated positively with numerous anthropometric measures: systolic blood pressure, heart rate (BPM), bone age, height, weight, BMI, waist circumference, hip circumference, waist-to-hip ratio, and waist-to-height ratio. Additionally, MFGE8 demonstrated significant positive relationships with multiple metabolic and inflammatory indicators: alanine aminotransferase, triglyceride, FINS, homeostatic model assessment of insulin resistance (HOMA-IR), basal metabolic rate, body fat percentage, uric acid, glutamyl transpeptidase, tumor necrosis factor-α, adiponectin, and leptin. Inverse correlations were identified with albumin and direct bilirubin. Multivariable linear regression modeling identified BMI, HOMA-IR, and male gender as independent positive predictors of MFGE8 concentrations.
Conclusion:
Our results demonstrate that elevated MFGE8 levels are linked to pediatric obesity, implying its potential contribution to the development of this condition and associated metabolic complications.
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