4.4 Article

Effect of vitamin D3 treatment on bone density in neurofibromatosis 1 patients: A retrospective clinical study

期刊

JOINT BONE SPINE
卷 80, 期 3, 页码 315-319

出版社

ELSEVIER FRANCE-EDITIONS SCIENTIFIQUES MEDICALES ELSEVIER
DOI: 10.1016/j.jbspin.2012.07.010

关键词

Neurofibromatosis 1; Cholecalciferol; Bone mineral density; Dual energy X-ray absorptiometry (DXA); 25-hydroxy vitamin D-3 deficiency

资金

  1. Orion Pharma
  2. Wealth-Cup
  3. Stiftung Hilfe aus Dank
  4. German Lay Organisation Bundesverb and Neurofibromatose

向作者/读者索取更多资源

Objectives: We have previously demonstrated reduced bone density and an increased incidence of 25-hydroxy vitamin D3 (25-OH D-3) deficiency in adults with neurofibromatosis 1 (NF1) compared to healthy controls. Vitamin D-3 is a cheap, safe, and effective supplement in the general population, but its value in NF1 patients has not been demonstrated. This study investigates the therapeutic potential of oral vitamin D-3 on bone mineral density (BMD) in NF1 patients with vitamin D-3 deficiency. Methods: We measured serum 25-OH D-3, parathyroid hormone, calcium, and bone alkaline phosphatase concentrations, urinary deoxypyridinoline concentrations, and BMD in 35 adults with NF1. Nineteen patients received vitamin D-3 supplementation for 2 years, six patients received supplementation for 1 year and 10 patients received no supplementation. Supplementation was administered in a dose that maintained the serum 25-OH D-3 level above 30 mu g/l. BMD was measured again at 1 and 2 years, and biochemical assessments of bone metabolism were measured at least every half year during therapy. Results: Treated subjects had significantly reduced loss of BMD, as measured by T score at the hip (p = 0.011) and lumbar spine (p = 0.022). The effect on hip BMD was apparent at 1 year in comparison to baseline (p = 0.02) and was greater at 2 years in comparison to measurements at 1 year (p = 0.02). Conclusions: Vitamin D-3 supplementation improves BMD in adult NF1 patients. Further studies are needed to elucidate the mechanisms responsible for reduced BMD in NF1 patients. (C) 2012 Societe francaise de rhumatologie. Published by Elsevier Masson SAS. All rights reserved.

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