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Beta 2-microglobulin deposition in bone in chronic renal failure

S Onishi1, D L Andress, N A Maloney

  • 1Division of Nephrology, Veterans Administration Medical Center, Seattle, Washington.

Insights

Beta 2 microglobulin (beta 2 m) amyloid deposition is common in the bones of patients on long-term hemodialysis, particularly after 10 years. This bone deposition is linked to an increased risk of femoral neck fractures.

Area of Science:

  • Nephrology
  • Orthopedic Surgery
  • Pathology

Background:

  • Beta 2 microglobulin (beta 2 m) amyloidosis is increasingly reported in soft tissues of dialysis patients.
  • Bone involvement of beta 2 m amyloid deposition is less understood.
  • Long-term hemodialysis is a risk factor for amyloid accumulation.

Purpose of the Study:

  • To determine the prevalence of beta 2 m deposition in bone biopsies from hemodialysis patients.
  • To assess the relationship between beta 2 m deposits and bone histomorphometry.
  • To investigate the association between bone beta 2 m deposition and fracture risk.

Main Methods:

  • Analysis of bone biopsy specimens from 224 patients undergoing long-term hemodialysis.
  • Immunohistochemical staining for beta 2 m deposition.
  • Histomorphometric analysis of bone structure.
  • Comparison of fracture incidence in patients with and without beta 2 m deposition.

Main Results:

  • Beta 2 m deposits were found in 8% of patients, increasing to 19% in those on dialysis for over 10 years.
  • Deposition was observed in various bone sites, notably the iliac crest periosteum.
  • Patients with iliac crest beta 2 m deposition had a significantly higher rate of femoral neck fractures (62% vs 4%).
  • Osteitis fibrosa appeared more common in patients with beta 2 m deposits.

Conclusions:

  • Beta 2 m deposition in bone is a frequent finding in uremic patients with over 10 years of hemodialysis.
  • Periosteal beta 2 m deposition in the iliac crest may predict susceptibility to femoral fractures.
  • Further research is warranted to understand the mechanism linking beta 2 m deposition to bone fragility and fractures.

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