Cortical-Bone Fragility--Insights from sFRP4 Deficiency in Pyle's Disease

N Engl J Med. 2016 Jun 30;374(26):2553-2562. doi: 10.1056/NEJMoa1509342.

Abstract

Background: Cortical-bone fragility is a common feature in osteoporosis that is linked to nonvertebral fractures. Regulation of cortical-bone homeostasis has proved elusive. The study of genetic disorders of the skeleton can yield insights that fuel experimental therapeutic approaches to the treatment of rare disorders and common skeletal ailments.

Methods: We evaluated four patients with Pyle's disease, a genetic disorder that is characterized by cortical-bone thinning, limb deformity, and fractures; two patients were examined by means of exome sequencing, and two were examined by means of Sanger sequencing. After a candidate gene was identified, we generated a knockout mouse model that manifested the phenotype and studied the mechanisms responsible for altered bone architecture.

Results: In all affected patients, we found biallelic truncating mutations in SFRP4, the gene encoding secreted frizzled-related protein 4, a soluble Wnt inhibitor. Mice deficient in Sfrp4, like persons with Pyle's disease, have increased amounts of trabecular bone and unusually thin cortical bone, as a result of differential regulation of Wnt and bone morphogenetic protein (BMP) signaling in these two bone compartments. Treatment of Sfrp4-deficient mice with a soluble Bmp2 receptor (RAP-661) or with antibodies to sclerostin corrected the cortical-bone defect.

Conclusions: Our study showed that Pyle's disease was caused by a deficiency of sFRP4, that cortical-bone and trabecular-bone homeostasis were governed by different mechanisms, and that sFRP4-mediated cross-regulation between Wnt and BMP signaling was critical for achieving proper cortical-bone thickness and stability. (Funded by the Swiss National Foundation and the National Institutes of Health.).

Publication types

  • Case Reports
  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Animals
  • Biomarkers / blood
  • Bone Density / genetics*
  • Bone Morphogenetic Proteins / metabolism
  • Bone Remodeling / genetics*
  • Bone Remodeling / physiology
  • Bone and Bones / pathology
  • Bone and Bones / physiology
  • Child, Preschool
  • Disease Models, Animal
  • Female
  • Gene Deletion
  • Homeostasis
  • Humans
  • Male
  • Mice
  • Mice, Knockout
  • Middle Aged
  • Osteochondrodysplasias / genetics*
  • Osteochondrodysplasias / physiopathology
  • Proto-Oncogene Proteins / deficiency*
  • Proto-Oncogene Proteins / genetics*
  • Sequence Analysis, DNA
  • Signal Transduction
  • Wnt Proteins / metabolism

Substances

  • Biomarkers
  • Bone Morphogenetic Proteins
  • Proto-Oncogene Proteins
  • SFRP4 protein, human
  • Sfrp4 protein, mouse
  • Wnt Proteins

Supplementary concepts

  • Pyle disease