Vaspin is related to gender, puberty and deteriorating insulin sensitivity in children
1Department of Women and Child Health, University Hospital for Children & Adolescents, University of Leipzig, Leipzig, Germany.
Insights
Visceral adipose tissue-derived serine protease inhibitor (vaspin) levels differ by sex and age in children. Lower vaspin is linked to insulin resistance and cardiovascular issues, decreasing after glucose provocation in insulin-resistant adolescents.
Area of Science:
- Pediatric Endocrinology
- Metabolic Research
- Adipokine Signaling
Background:
- Visceral adipose tissue-derived serine protease inhibitor (vaspin) is a novel adipocytokine implicated in adult obesity and insulin sensitivity.
- Understanding vaspin's role in pediatric metabolic health is crucial for early intervention.
Purpose of the Study:
- To quantify serum vaspin concentrations in lean and obese children.
- To investigate the relationship between vaspin, physical development, obesity, and metabolic/cardiovascular phenotypes.
- To assess the acute vaspin response to glucose provocation and tissue expression patterns.
Main Methods:
- Serum vaspin levels were measured in 65 lean and 67 obese children.
- Acute vaspin response to oral glucose tolerance test was assessed in 20 obese adolescents.
- Vaspin mRNA expression was evaluated in human tissues.
Main Results:
- Vaspin levels were higher in girls, increasing with age and puberty, unlike in boys.
- Obese girls had lower vaspin than lean controls, but no BMI correlation.
- Lower vaspin correlated with better insulin sensitivity, higher systolic blood pressure, and impaired endothelial function.
- In insulin-resistant adolescents, vaspin levels decreased ~25% post-glucose provocation.
- Vaspin mRNA was expressed in adipose tissue, liver, pancreas, and skin.
Conclusions:
- Gender differences in vaspin emerge during female pubertal progression.
- Vaspin elevation is associated with worsening insulin resistance in children, independent of obesity.
- Acute vaspin down-regulation post-glucose challenge occurs in insulin-resistant adolescents.
- Liver and pancreas expression may contribute to circulating vaspin levels.
Background:
Visceral adipose tissue-derived serine protease inhibitor (vaspin) has been suggested as a novel adipocytokine related to obesity and insulin sensitivity in adults.
Design:
We quantified vaspin serum concentrations in 65 lean and 67 obese children and aimed to evaluate the relationship of vaspin with physical development, obesity, and metabolic and cardiovascular phenotypes in children. We further assessed the acute vaspin response to glucose provocation in 20 obese adolescents and evaluated tissue expression patterns of vaspin in humans.
Results:
Vaspin levels were significantly higher in girls than in boys. In girls, vaspin increased with age and pubertal stage, whereas there was no change with development in boys. Obese girls had lower vaspin serum levels than those of lean controls, but there was no significant correlation with body mass index (BMI). Independent of sex, age and BMI, lower vaspin was associated with better insulin sensitivity, with higher systolic blood pressure and impaired endothelial function. In response to glucose provocation during an oral glucose tolerance test, vaspin serum levels declined by approximately 25% in adolescents with hyperinsulinemia, whereas there was no significant decline in normoinsulinemic patients. In support of our clinical data, we not only confirmed vaspin mRNA expression in adipose tissue but also found consistent expression of vaspin in the liver and indications for expression in the pancreas and the skin.
Conclusion:
We showed that gender differences in circulating vaspin levels develop during pubertal progression in girls. Although vaspin's association with obesity remains controversial, vaspin was increased with worsening insulin resistance already in children and was acutely down-regulated following glucose provocation in insulin-resistant adolescents independent of obesity. Besides adipose tissue, vaspin expression in the liver and the pancreas may potentially contribute to circulating vaspin levels and their regulation.
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