High bone turnover and accumulation of osteoid in patients with neurofibromatosis 1

Osteoporos Int. 2010 Jan;21(1):119-27. doi: 10.1007/s00198-009-0933-y. Epub 2009 May 5.

Abstract

Although it is known that neurofibromatosis 1 (NF1) patients suffer from vitamin D deficiency and display decreased bone mineral density (BMD), a systematic clinical and histomorphometrical analysis is absent. Our data demonstrate that NF1 patients display high bone turnover and accumulation of osteoid and that supplementation of vitamin D has a beneficial effect on their BMD.

Introduction: Neurofibromatosis 1 results in a wide range of clinical manifestations, including decreased BMD. Although it has been reported that NF1 patients have decreased vitamin D serum levels, the manifestation of the disease at the bone tissue level has rarely been analyzed.

Methods: Thus, we performed a clinical evaluation of 14 NF1 patients in comparison to age- and sex-matched control individuals. The analysis included dual X-ray absorptiometry osteodensitometry, laboratory parameters, histomorphometric and quantitative backscattered electron imaging (qBEI) analyses of undecalcified bone biopsies.

Results: NF1 patients display significantly lower 25-(OH)-cholecalciferol serum levels and decreased BMD compared to control individuals. Histomorphometric analysis did not only reveal a reduced trabecular bone volume in biopsies from NF1 patients, but also a significantly increased osteoid volume and increased numbers of osteoblasts and osteoclasts. Moreover, qBEI analysis revealed a significant decrease of the calcium content in biopsies from NF1 patients. To address the question whether a normalization of calcium homeostasis improves BMD in NF1 patients, we treated four patients with cholecalciferol for 1 year, which resulted in a significant increase of BMD.

Conclusion: Taken together, our data provide the first complete histomorphometric analysis from NF1 patients. Moreover, they suggest that low vitamin D levels significantly contribute to the skeletal defects associated with the disease.

MeSH terms

  • Absorptiometry, Photon / methods
  • Adult
  • Aged
  • Biopsy
  • Bone Density / drug effects
  • Bone Density / physiology
  • Bone Density Conservation Agents / therapeutic use
  • Bone Remodeling / physiology*
  • Calcifediol / blood
  • Calcium / blood
  • Cholecalciferol / therapeutic use
  • Female
  • Hip Joint / physiopathology
  • Humans
  • Ilium / pathology
  • Lumbar Vertebrae / physiopathology
  • Male
  • Middle Aged
  • Neurofibromatosis 1 / blood
  • Neurofibromatosis 1 / complications*
  • Neurofibromatosis 1 / pathology
  • Neurofibromatosis 1 / physiopathology
  • Osteoporosis / drug therapy
  • Osteoporosis / etiology*
  • Osteoporosis / pathology
  • Osteoporosis / physiopathology
  • Parathyroid Hormone / blood
  • Phosphates / blood
  • Vitamin D Deficiency / blood
  • Vitamin D Deficiency / etiology
  • Young Adult

Substances

  • Bone Density Conservation Agents
  • Parathyroid Hormone
  • Phosphates
  • Cholecalciferol
  • Calcifediol
  • Calcium