4.3 Article

Metabolic control and growth during exclusive growth hormone treatment in X-linked hypophosphatemic rickets

Journal

HORMONE RESEARCH
Volume 69, Issue 4, Pages 212-220

Publisher

KARGER
DOI: 10.1159/000113021

Keywords

hypophosphatemia; rickets; growth hormone; metabolic control; IGF-I

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Background: GH may improve phosphate balance and height in X- linked hypophosphatemic rickets ( XLH). This study evaluated the impact of exclusive rhGH therapy on phosphate homeostasis and growth. Methods: Ten children ( median age 12.2 years) with XLH were included in a 12-month trial with GH. Conventional treatment was discontinued 1 month prior GH ( 0.033 mg/ kg/ day); 1 alpha- hydroxyvitamin D was added at 6 months and oral phosphate at 12 months, when GH was discontinued. Patients were followed 1-3 monthly until 18 months for clinical, biochemical and radiographic parameters. Results: Serum phosphate Z-score increased significantly from baseline at 6 months ( p = 0.005) and 9 months ( p = 0.009) but returned to baseline by 12 months. Serum 1,25-dihydroxyvitamin D also increased significantly. Parathyroid function normalized. The median height Z-score was - 2.2 ( - 2.7 to + 0.4) at GH onset and - 1.7 ( - 2.3 to + 0.3) at 12 months. One patient showed a significant increase in radiographic rickets activity and 3 patients aggravation of lower limb deformity; the others showed no changes or improvement in these parameters. Conclusions: GH treatment improved serum phosphate and 1,25-dihydroxyvitamin D, normalized parathyroid function and improved longitudinal growth in XLH. It may however aggravate pre- existing skeletal deformities. Copyright (c) 2008 S. Karger AG, Basel.

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