Reducing glucocorticoid dosage improves serum osteocalcin in patients with rheumatoid arthritis-results from the TOMORROW study

被引:11
作者
Tada, M. [1 ]
Inui, K. [2 ]
Sugioka, Y. [3 ]
Mamoto, K. [1 ]
Okano, T. [1 ]
Koike, T. [3 ,4 ]
Nakamura, H. [1 ]
机构
[1] Osaka City Univ, Dept Orthopaed Surg, Sch Med, Abeno Ku, 1-4-3 Asahimachi, Osaka 5458585, Japan
[2] Osaka City Univ, Dept Rheumatosurg, Sch Med, Abeno Ku, 1-4-3 Asahimachi, Osaka 5458585, Japan
[3] Osaka City Univ, Ctr Senile Degenerat Disorders, Sch Med, Abeno Ku, 1-4-3 Asahimachi, Osaka 5458585, Japan
[4] Shirahama Fdn Hlth & Welf, Search Inst Bone & Arthrit Dis, Nishimurogun Shirahamacho 1447, Wakayama 6492211, Japan
关键词
Bone metabolic marker; Cohort study; Glucocorticoid; Rheumatoid arthritis; BONE-MINERAL DENSITY; INDUCED OSTEOPOROSIS; DISEASE-ACTIVITY; RISK; HEALTH; OSTEOBLASTS; METABOLISM; PREVENTION; OSTEOCYTES; APOPTOSIS;
D O I
10.1007/s00198-015-3291-y
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
A Summary Decreasing the daily dose of glucocorticoids improved bone metabolic marker levels in patients with rheumatoid arthritis. However, changes in disease activity did not influence bone metabolism. Bone metabolism might thus remain uncontrolled even if disease activity is under good control. Decreasing glucocorticoid dosage appears important for improving bone metabolism. Introduction Patients with rheumatoid arthritis (RA) develop osteoporosis more frequently than healthy individuals. Bone resorption is increased and bone formation is inhibited in patients with RA, and glucocorticoid negatively affects bone metabolism. We aimed to investigate factors influencing bone metabolic markers in patients with RA. Methods We started the 10-year prospective cohort Total Management of Risk Factors in Rheumatoid Arthritis Patients to Lower Morbidity and Mortality (TOMORROW) study in 2010. We compared changes in urinary cross-linked N-telopeptide of type I collagen (uNTx) and serum osteocalcin (OC), as markers of bone resorption and formation, respectively, in 202 RA patients and age- and sex-matched volunteers between 2010 and 2011. We also investigated factors influencing Delta uNTx and Delta OC in the RA group using multivariate analysis. Results Values of Delta uNTx were significantly lower in patients with RA than in healthy controls (-0.51 vs. 7.41 nmol bone collagen equivalents (BCE)/mmol creatinine (Cr); p = 0.0013), whereas Delta OC values were significantly higher in RA patients (0.94 vs. 0.37 ng/ml; p = 0.0065). Changes in prednisolone dosage correlated negatively with Delta OC (beta = -0.229, p = 0.001), whereas changes in disease activity score, bisphosphonate therapy, and period of biologics therapy did not correlate significantly with Delta OC. No significant correlation was seen between Delta uNTx and change in prednisolone dosage. Conclusions Decreased glucocorticoid dosage improved bone metabolic markers in RA, but disease activity, bisphosphonate therapy, and period of biologics therapy did not influence levels of bone metabolic markers. Decreasing glucocorticoid dosage appears important for improving bone metabolic marker profiles in patients with RA.
引用
收藏
页码:729 / 735
页数:7
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