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Effect of growth hormone treatment on calcium kinetics in patients with osteogenesis Imperfecta Type III and IV
Using a dual stable isotope technique, the effect of growth hormone (GH) on whole body calcium (Ca) metabolism was studied in children (ages 5–14 years) with type III (n = 9) and IV (n = 8) osteogenesis imperfecta. Each subject was studied twice: at baseline and following a GH (0.1–0.2 U/kg per day)...
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Published in: | Bone (New York, N.Y.) N.Y.), 1999-10, Vol.25 (4), p.501-505 |
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Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Using a dual stable isotope technique, the effect of growth hormone (GH) on whole body calcium (Ca) metabolism was studied in children (ages 5–14 years) with type III (n = 9) and IV (n = 8) osteogenesis imperfecta. Each subject was studied twice: at baseline and following a GH (0.1–0.2 U/kg per day) treatment period of 1–1.5 years. Subjects were given
42Ca intravenously and
44Ca orally. The sera and urine
42Ca and
44Ca isotopic enrichments were followed over 7 days using thermal ionization mass spectrometry. The S
aam program was used to fit a three-compartment model to the tracer data. No significant differences were observed between: (1) children with type III and IV disease; or (2) baseline studies of boys and girls within each disease type. However, GH treatment significantly increased: (1) the exchangeable calcium pool (EP) in type III patients (2086 vs. 4422 mg/day,
p = 0.02); and (2) the parameter associated with bone calcium accretion in type IV patients (Vo
+: 973 vs. 1560 mg/day,
p = 0.03) with boys responding with a significantly greater increase than girls
(p = 0.008). Although not statistically significant, a trend toward an increase in Vo
+ in type III patients and in EP in type IV was observed following treatment. Our observations imply that more Ca was available for bone mineralization following GH treatment in these subjects. |
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ISSN: | 8756-3282 1873-2763 |
DOI: | 10.1016/S8756-3282(99)00186-6 |