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Published on: January 7, 2018
Whole-body and hepatic insulin resistance in obese children
Lorena del Rocío Ibarra-Reynoso1, Liudmila Pisarchyk1, Elva Leticia Pérez-Luque1
1Department of Medical Sciences, University of Guanajuato, Campus León, 20 de Enero 929, León Guanajuato, México.
Insights
In obese children, BMI best predicts whole-body insulin resistance, while waist-to-height ratio predicts hepatic insulin resistance. These findings highlight central obesity
Area of Science:
- Pediatric Endocrinology
- Metabolic Syndrome Research
- Obesity Studies
Background:
- Insulin resistance can manifest as whole-body or hepatic.
- Understanding factors contributing to both is crucial for pediatric metabolic health.
Purpose of the Study:
- To investigate factors associated with whole-body and hepatic insulin resistance in obese children.
- To identify key anthropometric and metabolic predictors.
Main Methods:
- Cross-sectional study of 182 obese children.
- Assessed insulin resistance using HOMA-IR (whole-body) and IGFBP-1 levels (hepatic).
- Compared BMI, waist-to-height ratio, visceral adiposity, and measured hormone and metabolite levels.
Main Results:
- 73.1% of obese children exhibited both whole-body and hepatic insulin resistance.
- HOMA-IR correlated positively with BMI, triglycerides, and leptin; IGFBP-1 correlated negatively with waist-to-height ratio and HOMA-IR.
- No association found between HOMA-IR/IGFBP-1 and fatty liver.
Conclusions:
- BMI is the optimal predictor for whole-body insulin resistance in children.
- Waist-to-height ratio is the best predictor for hepatic insulin resistance, underscoring central obesity's role.
- The inverse relationship between IGFBP-1 and HOMA-IR suggests interconnected physiological pathways.
Background:
Insulin resistance may be assessed as whole body or hepatic.
Objective:
To study factors associated with both types of insulin resistance.
Methods:
Cross-sectional study of 182 obese children. Somatometric measurements were registered, and the following three adiposity indexes were compared: BMI, waist-to-height ratio and visceral adiposity. Whole-body insulin resistance was evaluated using HOMA-IR, with 2.5 as the cut-off point. Hepatic insulin resistance was considered for IGFBP-1 level quartiles 1 to 3 (<6.67 ng/ml). We determined metabolite and hormone levels and performed a liver ultrasound.
Results:
The majority, 73.1%, of obese children had whole-body insulin resistance and hepatic insulin resistance, while 7% did not have either type. HOMA-IR was negatively associated with IGFBP-1 and positively associated with BMI, triglycerides, leptin and mother's BMI. Girls had increased HOMA-IR. IGFBP-1 was negatively associated with waist-to-height ratio, age, leptin, HOMA-IR and IGF-I. We did not find HOMA-IR or IGFBP-1 associated with fatty liver.
Conclusion:
In school-aged children, BMI is the best metric to predict whole-body insulin resistance, and waist-to-height ratio is the best predictor of hepatic insulin resistance, indicating that central obesity is important for hepatic insulin resistance. The reciprocal negative association of IGFBP-1 and HOMA-IR may represent a strong interaction of the physiological processes of both whole-body and hepatic insulin resistance.
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