TY - JOUR
T1 - Bone modeling indexes at onset and during the first year of follow-up in insulin-dependent diabetic children
AU - Bonfanti, R.
AU - Mora, S.
AU - Prinster, C.
AU - Bognetti, E.
AU - Meschi, F.
AU - Puzzovio, M.
AU - Proverbio, M. C.
AU - Chiumello, G.
PY - 1997/5
Y1 - 1997/5
N2 - Osteopenia has been described as a complication of insulin-dependent diabetes mellitus (IDDM). We measured bone modeling indexes during the first year of IDDM. At each time point the values obtained from diabetic children have been compared with those of control subjects. We selected 27 prepubertal children with IDDM (6.35 ± 2.16 years). We also enrolled 30 healthy prepubertal children of comparable age (5.85 ± 3.05 years). Height, height standard deviation scores, glycated haemoglobin (HbA1(C)), basal c-peptide concentrations, insulin dose, serum concentrations of procollagen type I C- terminal propeptide (PICP), and collagen type I C-terminal telopeptide (ICTP) were measured at onset of IDDM and at 3, 6 and 12 months. ICTP was in the normal range at onset of IDDM and decreased during the follow-up to reach a significant difference compared to controls after 3, 6 and 12 months of insulin treatment (P <0.04). PICP concentrations increased significantly at 3 months (P = 0.05) compared to onset. At 3 and 12 months PICP values were significantly higher than those of control children (P = 0.04). Correlations were found between PICP concentrations and HbA1(C) and c-peptide at onset of diabetes (r = -0.45 and r = 0.47, respectively). Bone formation at onset of IDDM is not impaired; the introduction of insulin therapy, together with the achievement of a good metabolic control, determines an increase of bone matrix formation coupled with a decrease of bone resorption, that determines a positive balance of bone modeling.
AB - Osteopenia has been described as a complication of insulin-dependent diabetes mellitus (IDDM). We measured bone modeling indexes during the first year of IDDM. At each time point the values obtained from diabetic children have been compared with those of control subjects. We selected 27 prepubertal children with IDDM (6.35 ± 2.16 years). We also enrolled 30 healthy prepubertal children of comparable age (5.85 ± 3.05 years). Height, height standard deviation scores, glycated haemoglobin (HbA1(C)), basal c-peptide concentrations, insulin dose, serum concentrations of procollagen type I C- terminal propeptide (PICP), and collagen type I C-terminal telopeptide (ICTP) were measured at onset of IDDM and at 3, 6 and 12 months. ICTP was in the normal range at onset of IDDM and decreased during the follow-up to reach a significant difference compared to controls after 3, 6 and 12 months of insulin treatment (P <0.04). PICP concentrations increased significantly at 3 months (P = 0.05) compared to onset. At 3 and 12 months PICP values were significantly higher than those of control children (P = 0.04). Correlations were found between PICP concentrations and HbA1(C) and c-peptide at onset of diabetes (r = -0.45 and r = 0.47, respectively). Bone formation at onset of IDDM is not impaired; the introduction of insulin therapy, together with the achievement of a good metabolic control, determines an increase of bone matrix formation coupled with a decrease of bone resorption, that determines a positive balance of bone modeling.
KW - Bone modeling
KW - Children
KW - Insulin-dependent diabetes mellitus
KW - Procollagen type I propeptide
KW - Type I C- terminal telopeptide
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U2 - 10.1007/s002239900251
DO - 10.1007/s002239900251
M3 - Article
C2 - 9115153
AN - SCOPUS:0030997097
SN - 0171-967X
VL - 60
SP - 397
EP - 400
JO - Calcified Tissue International
JF - Calcified Tissue International
IS - 5
ER -