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[Insulin sensitivity in children aged 6 to 16 years: association with nutritional status and pubertal development]
Raquel Burrows A1, Laura Leiva B, Medardo Burgueño A
1Instituto de Nutrición y Tecnología de los Alimentos, Universidad de Chile, José Pedro Alessandri 5540, Macul, Chile. rburrows@uec.inta.uchile.cl
Insights
Childhood obesity is common in Chile. Insulin sensitivity (IS) decreases with puberty, with fasting insulin levels increasing by 50%, impacting hyperinsulinism and insulin resistance diagnosis.
Area of Science:
- Pediatric Endocrinology
- Metabolic Health
- Obesity Research
Context:
- High prevalence of obesity and hyperinsulinism in Chilean prepuberal children.
- Need for accurate assessment of insulin sensitivity (IS) in pediatric populations.
- Evaluating metabolic health markers in relation to body composition and pubertal development.
Purpose:
- To assess insulin sensitivity (IS) using fasting insulin, HOMA, and QUICKI in Chilean children.
- To examine the correlation between IS markers and anthropometric measurements (BMI, %TBF, WC).
- To investigate the influence of pubertal maturation on insulin sensitivity.
Summary:
- Insulin sensitivity (IS) showed strong associations with total body fat percentage (%TBF) and waist circumference (WC).
- Fasting insulin (Ins), HOMA, and QUICKI correlated significantly with BMI, %TBF, and WC.
- Insulin levels and HOMA increased, while QUICKI decreased with age and puberty, indicating reduced IS.
Impact:
- Confirms the link between IS, BMI, %TBF, WC, and pubertal development.
- Highlights a significant decrease in IS and an approximate 50% increase in fasting insulin during puberty.
- Emphasizes the importance of considering pubertal changes for diagnosing hyperinsulinism and insulin resistance in children.
Background:
There is a high prevalence of obesity and hyperinsulinism among Chilean prepuberal children.
Aim:
To evaluate insulin sensitivity (IS) using fasting insulin, the Homeostasis Model Assessment (HOMA) and quantitative insulin-sensitivity check index (QUICKI) in Chilean children.
Material And Methods:
Body mass index (BMI), total body fat percentage (%TBF) using the sum of 4 skin folds, abdominal obesity determined through waist circumference (WC), pubertal maturation using five Tanner stages, fasting glucose (Glu) and insulin (Ins), were measured in 354 children aged 6 to 15 years (173 males). IS was evaluated using HOMA and QUICKI.
Results:
IS was strongly associated with %TBF and WC. Ins, HOMA and QUICKI were significantly correlated with BMI (r =0.412; 0.405 y -0.442, respectively), %TBF (r =0.370; 0.367 y -0.394, respectively), and WC (r =0.452; 0.446 y -0.481, respectively). Ins and HOMA increased and QUICKI decreased significantly (p <0.0001) with age. Children in a similar Tanner stage did not have differences in Ins, HOMA and QUICKI. No differences in Ins, HOMA and QUICKI were observed between children in Tanner stages 1 and 2. However, children in Tanner stages 1 and 2, had significantly lower Ins and HOMA and higher QUICKI than those in Tanner 3 to 5 stages. The highest Ins quartile for Tanner stages 1 and 2 was 10.0 micro UI/dl; for Tanner stages 3 to five, the figure was 15.6 microUI/dl.
Conclusions:
These results confirm the relationship of IS with BMI, %TBF, WC and pubertal maturation. IS decreases significantly and fasting Ins levels increase approximately 50% with puberty. This fact must be considered for the diagnosis of hyperinsulinism and insulin resistance in children.
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