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Enhanced insulin sensitivity in prepubertal children with constitutional delay of growth and development
Dyanne A Wilson1, Paul L Hofman, Harriet L Miles
1Liggins Institute and National Research Centre for Growth and Development, University of Auckland, Private Bag 92019, Auckland, New Zealand.
Insights
Children with constitutional delay of growth and development (CDGD) show significantly enhanced insulin sensitivity. This finding supports the link between insulin sensitivity and the timing of puberty onset.
Area of Science:
- Pediatric Endocrinology
- Metabolic Regulation
- Growth and Development
Background:
- Constitutional delay of growth and development (CDGD) is a common condition in children.
- The relationship between insulin sensitivity and pubertal timing in CDGD is not fully understood.
Purpose of the Study:
- To investigate insulin sensitivity in prepubertal children with presumed CDGD.
- To test the hypothesis that enhanced insulin sensitivity is associated with later pubertal onset in these children.
Main Methods:
- A frequently sampled intravenous glucose tolerance test was performed.
- Evaluated insulin sensitivity, glucose regulation, and growth markers in 21 children with CDGD and 23 controls.
Main Results:
- Children with CDGD exhibited 40% greater insulin sensitivity compared to controls.
- The CDGD group had reduced acute insulin response and lower insulin-like growth factor binding protein 3 levels.
- Lower serum insulin-like growth factor-II levels were observed in the CDGD group.
Conclusions:
- Prepubertal children with CDGD possess enhanced insulin sensitivity.
- This supports the hypothesis linking insulin sensitivity to pubertal timing.
- Enhanced insulin sensitivity may confer long-term benefits, including reduced risk of metabolic syndrome and malignancy.
Objective:
To test the hypothesis that prepubertal children with presumed constitutional delay of growth and development (CDGD) have enhanced insulin sensitivity and, therefore, insulin sensitivity is associated with later onset of puberty.
Study Design:
Twenty-one prepubertal children with presumed CDGD and 23 prepubertal control children, underwent a frequently sampled intravenous glucose tolerance test to evaluate insulin sensitivity and other markers of insulin, glucose, and growth regulation.
Results:
Children in the CDGD group were shorter and leaner than control subjects. Children with presumed CDGD were 40% more insulin sensitive (17.0 x 10(-4) min(-1)/[mU/L] versus 12.1 x 10(-4) min(-1)/[mU/L]; P = .0006) and had reduced acute insulin response, thus maintaining euglycemia (216 mU/L versus 330 mU/L; P = .02) compared with control subjects. In addition, the CDGD group had lower serum insulin-like growth factor binding protein 3 levels (3333 ng/mL versus 3775 ng/mL; P = .0004) and a trend toward lower serum insulin-like growth factor-II levels (794 ng/mL versus 911 ng/mL; P = .06).
Conclusion:
Prepubertal children with presumed CDGD have enhanced insulin sensitivity, supporting the hypothesis that insulin sensitivity is associated with timing of puberty. It may signify long-term biological advantages with lower risk of metabolic syndrome and malignancy.
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