IS CONTINUOUS INTRANASAL SALMON-CALCITONIN EFFECTIVE IN TREATING AXIAL BONE LOSS IN PATIENTS WITH ACTIVE RHEUMATOID-ARTHRITIS RECEIVING LOW-DOSE GLUCOCORTICOID THERAPY

Citation
A. Kotaniemi et al., IS CONTINUOUS INTRANASAL SALMON-CALCITONIN EFFECTIVE IN TREATING AXIAL BONE LOSS IN PATIENTS WITH ACTIVE RHEUMATOID-ARTHRITIS RECEIVING LOW-DOSE GLUCOCORTICOID THERAPY, Journal of rheumatology, 23(11), 1996, pp. 1875-1879
Citations number
22
Categorie Soggetti
Rheumatology
Journal title
ISSN journal
0315162X
Volume
23
Issue
11
Year of publication
1996
Pages
1875 - 1879
Database
ISI
SICI code
0315-162X(1996)23:11<1875:ICISEI>2.0.ZU;2-V
Abstract
Objective. To investigate the efficacy of intranasal salmon calcitonin (sCT) in treating axial bone loss in patients with rheumatoid arthrit is (RA) taking low dose glucocorticoids. Methods. In this open, multic enter study 32 women with RA were treated one year with sCT 100 IU/day and calcium (Ca) 500 mg/day, 31 women were treated with Ca alone. Bon e mineral density (BMD) was measured at the lumbar spine and proximal femur (femoral neck, Ward's triangle, trochanter) before sCT therapy a nd again after 6 and 12 months. Results. Among valid completers treate d with sCT and Ca (n = 26), the mean BMD increased at the lumbar spine (L1-L4), femoral neck, and Ward's triangle. In contrast, valid comple ters treated with Ca (n = 23) showed bone loss at the spine (L1-L4), f emoral neck, Ward's triangle, and trochanter area, The differences of the changes in BMD were statistically significant between these groups at the femoral neck, Ward's triangle, and trochanter. There were no s ignificant differences between groups in bone loss over 12 months at t he lumbar spine (L1-L4), although analysis of the upper segment (L1-L2 ) suggested some possible benefit of sCT. Conclusion. Intranasal sCT ( 100 IU/day) appears to have beneficial effects on bone loss at the pro ximal femur in patients with active RA treated with low dose glucocort icoids for 12 months; longer studies are needed to exclude transient b one remodelling effects.