Key result
Children with insulin-dependent diabetes mellitus had lower serum IGF-I and IGFBP-3 levels during puberty compared to healthy controls.
Why the study?
Are serum IGF-I and IGFBP-3 levels altered in children with insulin-dependent diabetes mellitus compared to healthy controls?
Case-Control (n=50)
Are serum IGF-I and IGFBP-3 levels altered in children with insulin-dependent diabetes mellitus compared to healthy controls?
Children with insulin-dependent diabetes mellitus have disturbed regulation of IGF-I and IGFBP-3 concentrations, particularly during adolescence, with lower levels compared to healthy controls.
Answers are grounded in this paper and cite their sources.
May prompt growth monitoring in pubertal IDDM; leaves open whether IGF axis modulation improves outcomes.
Pubertal development has recently been evaluated from the standpoint of changes in insulin-like growth factor (IGF)-I and IGF-binding protein-3 (IGFBP-3) levels in healthy children. We studied puberty related changes in serum IGF-I and IGFBP-3 levels in 24 patients (11 prepubertal) with insulin dependent diabetes mellitus (IDDM) and 26 healthy subjects (14 prepubertal). Serum IGF-I and IGFBP-3 levels were assayed using immunoradiometric assays and radioimmunoassays, respectively. Serum IGF-I and IGFBP-3 levels in diabetics did not increase during puberty, as opposed to those in healthy children. Serum IGF-I and IGFBP-3 levels of diabetic patients were found to be lower than those of control subjects during puberty (p < 0.0001 and p < 0.05, respectively). Proteolysis is believed to be a general mechanism to increase IGF bioavailability in the presence of IGFBPs. Increased IGFBP-3 protease activity has been shown in sera of children with IDDM as well as a decrease in this activity in response to insulin therapy. Our data displaying low IGFBP-3 levels in diabetic children may be due to increased proteolysis, which also causes a shift in IGF-I to its lower molecular weight forms. Higher rate of clearance of the latter may be the reason for the low IGF-I levels we observed in children with IDDM. The moderate correlation between insulin dose and IGFBP-3 levels (r = 0.5, p < 0.01) may suggest insulin to be a contributing factor in the regulation of IGFBP-3 levels. We conclude that regulation of IGF-I and IGFBP-3 concentrations is disturbed in children with IDDM, in particular during adolescence.
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Cınaz et al. (1996) conducted a case-control in Insulin-Dependent Diabetes Mellitus (n=50). Insulin-dependent diabetes mellitus vs. Healthy controls was evaluated on Serum IGF-I and IGFBP-3 levels during puberty (p=<0.0001). Children with insulin-dependent diabetes mellitus had lower serum IGF-I and IGFBP-3 levels during puberty compared to healthy controls.
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