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Suppression of bone turnover by B-cell depletion in patients with rheumatoid arthritis

Summary The role of B cells in inflammatory bone formation and resorption is controversial. We investigated this in patients with rheumatoid arthritis (RA) treated with rituximab, a B-cell depleting antibody. We found a significant suppression in bone turnover, possibly a direct effect or as a conse...

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Published in:Osteoporosis international 2011-12, Vol.22 (12), p.3067-3072
Main Authors: Wheater, G., Hogan, V. E., Teng, Y. K. O., Tekstra, J., Lafeber, F. P., Huizinga, T. W. J., Bijlsma, J. W. J., Francis, R. M., Tuck, S. P., Datta, H. K., van Laar, J. M.
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Language:English
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Summary:Summary The role of B cells in inflammatory bone formation and resorption is controversial. We investigated this in patients with rheumatoid arthritis (RA) treated with rituximab, a B-cell depleting antibody. We found a significant suppression in bone turnover, possibly a direct effect or as a consequence of a reduction in inflammation and disease activity. Introduction RA is the most prevalent inflammatory joint disease, in which B cells play an important role. However, the role of B cells in bone turnover is controversial and RA subjects treated with rituximab, a B-cell depleting monoclonal antibody, provide an ideal model for determining the role of B cells in inflammatory bone resorption. Methods Serum from 46 RA patients, collected pre- and post-rituximab therapy, was analysed for biomarkers of bone turnover (procollagen type I amino-terminal propeptide [P1NP], osteocalcin, β-isomerised carboxy-terminal telopeptide of type 1 collagen [βCTX] and osteoprotegerin [OPG]). Results A significant decrease in bone resorption was observed 6 months after rituximab (median change βCTX −50 ng/L, 95%CI −136, −8 p  
ISSN:0937-941X
1433-2965
DOI:10.1007/s00198-011-1607-0