Journal
PEDIATRIC RESEARCH
Volume 70, Issue 2, Pages 208-212Publisher
NATURE PUBLISHING GROUP
DOI: 10.1203/PDR.0b013e3182226a0c
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Small for GA (SGA) children are at risk for developing the metabolic syndrome. Those who do not catch up, and remain short (SSGA), may benefit from GH therapy. 11 beta Hydroxysteroid dehydrogenase type 1 (11 beta-HSD-1) is expressed in visceral fat and is implicated in metabolic morbidity. We hypothesized that SSGA children will have increased basal and glucocorticoid (GC)stimulated 11 beta-HSD-1 activity. Twenty SSGA children, aged 7.1 +/- 1 y (mean +/- SD), were studied before and while on GH therapy and compared with 12 normal age-matched controls. 11 beta-HSD-1 activity was evaluated by gas chromatography mass spectrometry (GCMS) of urinary steroid product/substrate ratios. GC-stimulated 11 beta-HSD-1 activity was assessed after overnight dexamethazone (DEX), by oral cortisone conversion to cortisol. In SSGA children, 11 beta-HSD-1 activity was lower (p < 0.05) and GC-stimulated activity enhanced. SSGA children had maximal cortisol generation of 883 108 compared with 690 +/- 63 nmol/L in controls (p < 0.04). GH treatment suppressed 11 beta-HSD-1 activity. GC-stimulated enzyme activity correlated negatively with GA (r = -0.53, p < 0.01) and birth weight (r = -0.55, p < 0.01). SSGA is associated with enhanced GC-stimulated 11 beta-HSD-1 activity. This may be programmed in utero, as it is not a function of body composition or secondary metabolic derangement. GH therapy normalizes GC-stimulated 11 beta-HSD-1 activity. (Pediatr Res 70: 208-212, 2011)
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