ISSN:
1432-0827
Keywords:
Key words: Stable isotopes — Bone-metabolism — Children.
Source:
Springer Online Journal Archives 1860-2000
Topics:
Biology
,
Medicine
,
Physics
Notes:
Abstract. Children with osteogenesis imperfecta (OI) type III and type IV were studied using a 42Ca stable isotope technique. Serum dilution kinetics of 42Ca were studied pre- and post-growth hormone (GH) treatment in 9 OI III (age range 5–9 years) and 8 OI IV patients (age range 5–12 years). Each subject was studied twice: at baseline and following GH therapy (range 1–1.5 years). Isotopic enrichments of 42Ca were followed over 7 days using thermal ionization mass spectrometry. A binding site model, which describes reversible and irreversible binding of calcium (Ca) ions to postulated short- and long-term binding sites in bone, was used to analyze the kinetic data. In type III patients, GH treatment (1) increased the fraction of short-term binding sites, θ (0.777 ± 0.112 versus 0.877 ± 0.05, respectively; P= 0.034); (2) increased the apparent half-life of a Ca ion attached to the long-term binding site by 76% (P= 0.009); (3) although not statistically significant (P= 0.098), a trend toward an increased growth rate was observed with increasing change in θ (Δθ); (4) patients experienced a 75% increase in growth rate during the first 6 months of treatment. In type IV patients, GH treatment increased the apparent half-life of a Ca ion attached to the long-term binding site by 83% (P= 0.048), however, no trend toward an increased growth rate was observed with increasing Δθ in these patients. These significant changes in Ca binding to bone may influence growth in type III patients.
Type of Medium:
Electronic Resource
URL:
http://dx.doi.org/10.1007/s00223001110
