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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.
Kidney International
|May 1, 1991
Summary
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.