| Literature DB >> 17235688 |
Kosei Arimura1, Naomichi Arima, Kakushi Matsushita, Masaki Akimoto, Chi Young Park, Kimiharu Uozumi, Chuwa Tei.
Abstract
Behçet's disease (BD) is a systemic inflammatory disorder of unknown etiology, and rarely complicated with myelodysplastic syndrome (MDS). In the present study, we investigated the morphological myelodysplasia and apoptotic rate of bone marrow cells in 15 patients with BD in comparison with MDS patients. Morphological myelodysplasia of bone marrow cells was detected in 53.3% of BD, but none showed chromosomal abnormalities. The apoptotic rate in BD patients (26.1 +/- 8.4%) was significantly higher in normal controls (11.3 +/- 2.4%; p < 0.005) and significantly lower in patients with MDS (50.8 +/- 14.0%; p < 0.0001). These findings suggest that myelodysplasia in patients with BD is more frequent than expected, and possibly due to excess induction of apoptosis of bone marrow cells in BD. However, the rate of apoptotic bone marrow cells is lower than MDS, which may explain the slight peripheral cytopenia in BD, distinct from that in MDS.Entities:
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Year: 2007 PMID: 17235688 DOI: 10.1007/s10875-006-9064-9
Source DB: PubMed Journal: J Clin Immunol ISSN: 0271-9142 Impact factor: 8.317