Abstract
The liver, muscles and adipose mass of adults with long-lasting obesity are insulin resistant. This explains why, despite chronic hyperinsulinism, they produce and utilize glucose at a similar rate than normal adults. We studied (d2-glucose tracing, iv somatostatin, euglycemic clamp) 7 children (13 ± 0.5 yrs), obese (176 ± 9% ideal BW) for 5 ± 0.5 yrs, gaining 13.5 ± 1.4 kg kg/yr. Normoglycemic (82 ± 4 mg/dl) and hyperinsulinemic (22 ± 4 μU/ml) in the fasting state, they produce 2.5 times more glucose (295 ± 18 mg/min) than age-matched controls (C) and than obese adults. The similar increase of glucose utilization suggests a large glucose uptake by the adipose tissue of pPOb. Normalized to BW, the glucose uptake of pPOb (3.6 ± 0.2 mg/kg.min) equalled that of C (3.7 ± 0.2). This indicates that the main component of BW in pPOb, adipose tissue, takes up a similar relative amount of glucose than the main component of BW in C, lean body mass(as opposed to obese adults). Suppression of insulin by somatostatin reduced glucose utilization by 110 ± 19 mg/min in pPOb (C: 41 ± 14), as expected from an insulin-sensitive enlarged adipose mass. But hyperinsulinic clamp increased glucose uptake in pPOb (250 ± 20 mg/ M2.min, insulin 402 uU/ml) much less than in C (366 ± 31, insulin 366 μU/ml), as expected from insulin-resistant muscles. Glucose overproduction by the liver, overutilization by adipose tissue contrasting with muscle insulin resistance characterize recent obesity in prepubertal children.
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Bougnères, P., Artavia, E. EARLY ALTERATIONS OF GLUCOSE METABOLISM IN PREPUBERTAL OBESITY (pPOb). Pediatr Res 23, 136 (1988). https://doi.org/10.1203/00006450-198801000-00212
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DOI: https://doi.org/10.1203/00006450-198801000-00212