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Simple fasting methods to assess insulin sensitivity in childhood
Wayne S Cutfield1, Paul L Hofman
1Liggins Institute, University of Auckland, Auckland, New Zealand. w.cutfield@auckland.ac.nz
Indirect measures like HOMA and QUICKI are increasingly used to assess insulin sensitivity in children. However, these methods show poor correlation with gold standards and lack validation in pediatric populations, necessitating further research before widespread adoption.
Area of Science:
- Pediatric Endocrinology
- Metabolic Research
- Biostatistics
Background:
- Accurate measurement of insulin sensitivity is crucial in pediatric metabolic research.
- Gold standard methods like the hyperinsulinaemic-euglycaemic clamp and minimal model are complex and invasive.
- Simpler indirect methods, including homeostatic model assessment (HOMA) and quantitative insulin sensitivity check index (QUICKI), are increasingly used in children despite limited validation.
Purpose of the Study:
- To evaluate the validity of indirect insulin sensitivity measures (HOMA, QUICKI) against gold standard techniques in pre-pubertal children.
- To assess the ability of HOMA and QUICKI to detect changes in insulin sensitivity related to obesity and growth hormone therapy.
- To determine if HOMA or QUICKI offer advantages over fasting insulin in assessing insulin sensitivity in children with normal glucose levels.
Main Methods:
- Study involved 79 pre-pubertal children.
- Compared correlations between the minimal model and RHOMA, fasting insulin, and QUICKI.
- Assessed the ability of HOMA and QUICKI to detect changes in insulin sensitivity during growth hormone therapy and with obesity.
Main Results:
- Correlation between the minimal model and RHOMA (r = -0.4) was not superior to fasting insulin (r = 0.4).
- Correlation between the minimal model and QUICKI (r = 0.2) was weak.
- HOMA and QUICKI failed to detect reduced insulin sensitivity in obese children or during growth hormone therapy, unlike the minimal model.
- Neither HOMA nor QUICKI demonstrated superiority over fasting insulin in children with normal glucose levels.
Conclusions:
- Current indirect measures of insulin sensitivity (HOMA, QUICKI) lack sufficient validation in pediatric populations.
- These methods may not accurately reflect insulin sensitivity or detect changes in children, especially in smaller or longitudinal studies.
- Further validation of derivation formulas is required before widespread use in childhood studies; precise methods are recommended for small or longitudinal studies.
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