Chronic arthritis directly induces quantitative and qualitative bone disturbances leading to compromised biomechanical properties

Clin Exp Rheumatol. 2009 May-Jun;27(3):475-82.

Abstract

Objectives: Rheumatoid arthritis (RA) is associated with an increased risk of fragility fractures. In RA patients, the direct effect of inflammation on bone is difficult to study because their skeleton is also affected by medication with corticosteroids and other drugs as well as aging and menopause, which contribute to bone fragility. This study used an animal model of chronic arthritis to evaluate the direct impact of chronic inflammation on biomechanical properties and structure of bone.

Methods: In the SKG mouse chronic arthritis model three point bending tests were performed on femoral bones and compression tests on vertebral bodies. Collagen structure was analysed using second-harmonic generation (SHG) imaging with a two-photon microscope, ultramorphology by scanning electron microscopy (SEM) coupled with energy dispersive x-ray spectroscopy (EDS) and bone density using water pycnometer.

Results: Arthritic bones had poor biomechanical quality compared to control bones. SHG, SEM and pycnometry disclosed variable signs of impaired collagen organization, poor trabecular architecture and low bone density.

Conclusion: Present data demonstrate for the first time that chronic inflammation per se, without confounding influence of drugs and aging, leads to impairment of bone biomechanics in terms of stiffness, ductility and ultimate strength (fracture).

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Arthritis / metabolism
  • Arthritis / pathology*
  • Arthritis / physiopathology*
  • Biomechanical Phenomena
  • Bone Density / physiology
  • Chronic Disease
  • Collagen / metabolism
  • Collagen / ultrastructure
  • Disease Models, Animal
  • Female
  • Femur / metabolism
  • Femur / pathology*
  • Femur / physiopathology*
  • Lumbar Vertebrae / metabolism
  • Lumbar Vertebrae / pathology*
  • Lumbar Vertebrae / physiopathology*
  • Mice
  • Mice, Inbred BALB C
  • Mice, Mutant Strains
  • Microscopy, Electron, Scanning
  • Spectrometry, X-Ray Emission

Substances

  • Collagen