Biological Disease-Modifying Antirheumatic Drugs and Osteoporotic Fracture Risk in Patients with Rheumatoid Arthritis: A Danish Cohort Study

被引:10
作者
Abtahi, Shahab [1 ,2 ,3 ]
Cordtz, Rene [4 ,5 ,6 ]
Dreyer, Lene [4 ,5 ,6 ,7 ,8 ]
Driessen, Johanna H. M. [1 ,2 ,3 ,9 ]
Boonen, Annelies [10 ,11 ]
Burden, Andrea M. [1 ,12 ]
机构
[1] Maastricht Univ, Dept Clin Pharm & Toxicol, Med Ctr, Maastricht, Netherlands
[2] Maastricht Univ, Cardiovasc Res Inst Maastricht CARIM, Maastricht, Netherlands
[3] Univ Utrecht, Utrecht Inst Pharmaceut Sci, Div Pharmacoepidemiol & Clin Pharmacol, Utrecht, Netherlands
[4] Aalborg Univ, Dept Clin Med, Aalborg, Denmark
[5] Aalborg Univ, Dept Rheumatol, Aalborg, Denmark
[6] Aalborg Univ Hosp, Aalborg, Denmark
[7] Copenhagen Univ Hosp Gentofte, Ctr Rheumatol & Spine Dis, Copenhagen, Denmark
[8] DANBIO Danish Rheumatol Database, Copenhagen, Denmark
[9] Maastricht Univ, NUTRIM Sch Nutr & Translat Res Metab, Med Ctr, Maastricht, Netherlands
[10] Maastricht Univ, Div Rheumatol, Dept Internal Med, Med Ctr, Maastricht, Netherlands
[11] Maastricht Univ, Care & Publ Hlth Res Inst CAPHRI, Maastricht, Netherlands
[12] Swiss Fed Inst Technol, Inst Pharmaceut Sci, Dept Chem & Appl Biosci, Zurich, Switzerland
关键词
Biological products; Disease-modifying antirheumatic drugs; Osteoporotic fractures; Rheumatoid arthritis; BONE-MINERAL DENSITY; CLINICAL REGISTER; SERUM-LEVELS; TOCILIZUMAB; INFLIXIMAB; VALIDITY; SCORE;
D O I
10.1016/j.amjmed.2022.01.017
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
OBJECTIVES: Clinical trials have shown a beneficial effect from biological disease-modifying antirheumatic drugs (bDMARDs) on hand or axial bone loss in patients with rheumatoid arthritis; however, it is unclear if this translates to a reduced fracture risk. We investigated the effect of bDMARDs on osteoporotic fracture risk compared to no biological treatment in rheumatoid arthritis. METHODS: A cohort of patients with rheumatoid arthritis aged 18+ from DANBIO was linked to population-based health registries in Denmark (2006-2016). Adopting a prevalent new-user design, we matched bDMARD users to bDMARD-naive patients using time-conditional propensity scores. The risk of incident osteoporotic fractures (including hip, vertebrae, humerus, and forearm) was estimated among the matched patients by Cox proportional hazards models. RESULTS: Out of 24,678 patients with rheumatoid arthritis, 4265 bDMARD users were matched to the same number of bDMARD-naive patients (mean age 56.2 years, 74% female). During follow-up, 229 osteoporotic fractures occurred among bDMARD users and 205 fractures among bDMARD-naive patients (incidence rates 12.1 and 13.0 per 1000 person-years, respectively). The use of bDMARDs was not associated with a reduced risk of osteoporotic fractures among patients with rheumatoid arthritis (hazard ratio 0.97, 95% confidence interval 0.78-1.20), compared with no biological treatment. The risk estimates were similar for all osteoporotic fracture sites. CONCLUSION: We found no independent beneficial effect from using bDMARDs on reducing the risk of osteoporotic fractures in patients with rheumatoid arthritis. (c) 2022 Published by Elsevier Inc.
引用
收藏
页码:879 / +
页数:13
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