| Literature DB >> 15168185 |
Kenshiro Inatomi1, Tomoko Matsumoto, Tadashi Tomonaga, Masao Eto, Hiroyuki Shindo, Tomayoshi Hayashi, Hiroaki Konishi.
Abstract
Dialysis-related spondyloarthropathy (DRS) is a severe complication of long-term hemodialysis that ultimately leads to functional disability of the upper and lower extremities. Although the cause of this disease is still unknown, it is thought that amyloid deposits are involved. beta2-Microglobulin (beta2M) is a major component of amyloid fibrils, some of which are modified with the advanced glycation end-product (AGE). To clarify the pathophysiology of DRS we histologically examined the ligamentum flavum of the cervical spine in 15 patients with DRS. The mean duration of hemodialysis was 20 years (12-27 years). In addition to the congo red stain for amyloid, beta2M and AGE were detected by immunohistochemical methods. Macrophages were stained with CD68 antibody. Amyloid deposits were found in tissues, although the extent of the stained area differed among the patients. Part of the amyloid deposit area was positively immunostained for beta2M and AGE. In 10 cases macrophages positive for CD68 infiltrated around the amyloid deposits. Comparing these histological findings with the dialysis duration, more positive staining areas for beta2M and AGE were found in the tissue from patients with long-term dialysis. These findings suggest that both beta2M and AGE play roles in the pathogenesis of DRS. The Japanese Orthopaedic AssociationEntities:
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Year: 2004 PMID: 15168185 DOI: 10.1007/s00776-004-0767-6
Source DB: PubMed Journal: J Orthop Sci ISSN: 0949-2658 Impact factor: 1.601