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Stimulation of Collagen Synthesis and Linear Growth by Growth Hormone in Glucocorticoid-Treated Children
[摘要] Impaired linear growth and skeletal maturation associated with chronic glucocorticoid therapy may result from (1) inhibited insulin-like growth factor 1 (IGF-1) activity; (2) impaired type 1 collagen synthesis; or (3) suppressed growth hormone (GH) secretory response to growth hormone-releasing hormone. Each mechanism could potentially be improved by exogenous GH treatment. Seven slowly growing glucocorticoid-treated children received recombinant DNA human GH (0.3 mg/kg/per week) for 6 to 21 (mean 13.1 ± 4.9) months. Height, weight, IGF-1 activity, glycosylated hemoglobin level, and C-terminal type 1 procollagen level were measured every 3 months and growth velocity was calculated. Skeletal maturation and 2-hour postprandial serum glucose and insulin levels were assessed every 6 months. All patients showed increased growth velocity during treatment with GH. Mean growth velocity increased from 3.43 ± 0.65 cm/y to 6.72 ± 0.84 cm/y with GH therapy ( P < .005). Growth velocity standard deviation scores corrected for bone age ( P < .005), IGF-1 levels ( P < .05), and C-terminal type 1 procollagen levels ( P < .005) also increased with GH therapy. C-terminal type 1 procollagen levels correlated well with growth velocity ( r = .652) while IGF-1 levels did not ( r = .17). Glycosylated hemoglobin levels remained unchanged, but 2-hour postprandial glucose levels rose during GH treatment. Slowly growing glucocorticoid-treated children receiving GH therapy increased growth velocity for 6 to 21 months. Initially diminished C-terminal type 1 procollagen levels rose with GH therapy, a change which corresponded with growth acceleration. This observation, combined with normal or elevated baseline IGF-1 levels, supports both inhibition of IGF-1 effects and collagen synthesis as growth-retarding effects of glucocorticoid therapy. Mild alterations in carbohydrate metabolism are detected in some glucocorticoid-treated children receiving GH.
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[效力级别]  [学科分类] 儿科学
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