Cardiovascular Safety and Fracture Prevention Effectiveness of Denosumab Versus Oral Bisphosphonates in Patients Receiving Dialysis: A Target Trial Emulation

被引:0
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作者
Masuda, Soichiro [1 ,2 ]
Fukasawa, Toshiki [2 ,3 ,4 ]
Matsuda, Shuichi [5 ]
Kawakami, Koji [3 ]
机构
[1] Kyoto Univ, Kyoto City Hosp, Dept Orthoped Surg, Kyoto, Japan
[2] Kyoto Univ, Grad Sch Med & Publ Hlth, Dept Pharmacoepidemiol, Kyoto, Japan
[3] Kyoto Univ, Grad Sch Med & Publ Hlth, Dept Pharmacoepidemiol, Yoshida Konoecho,Sakyoku, Kyoto 6068501, Japan
[4] Kyoto Univ, Grad Sch Med & Publ Hlth, Dept Digital Hlth & Epidemiol, Kyoto, Japan
[5] Kyoto Univ, Grad Sch Med, Dept Orthoped Surg, Kyoto, Japan
关键词
INTRAVENOUS BISPHOSPHONATES; OSTEOPOROSIS; DISEASE; RISK;
D O I
10.7326/ANNALS-24-03237
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Dialysis patients have high rates of fracture morbidity, but evidence on optimal management strategies for osteoporosis is scarce. Objective: To determine the risk for cardiovascular events and fracture prevention effects with denosumab compared with oral bisphosphonates in dialysis-dependent patients. Design: An observational study that attempts to emulate a target trial. Setting: A Japanese administrative claims database (April 2014 to October 2022). Patients: Adults aged 50 years or older who have initiated denosumab or oral bisphosphonates for osteoporosis in dialysis-dependent patients. Measurements: The safety outcome was major adverse cardiac events (MACE). The effectiveness outcome was a composite of all fractures. Follow-up was 3 years. Results: A total of 1032 patients were identified (658 denosumab users and 374 oral bisphosphonate users). Overall average age was 74.5 years, and 62.9% were women. The weighted 3-year risk difference for MACE was 8.2% (95% CI, -0.2% to 16.7%), with a weighted 3-year risk ratio of 1.36 (CI, 0.99 to 1.87). The weighted 3-year risk difference for composite fractures was -5.3% (CI, -11.3% to -0.6%), and the weighted 3-year risk ratio was 0.55 (CI, 0.28 to 0.93). Limitations: Lack of clinical data on kidney or osteoporosis disease severity and cardiovascular or other metabolic risk with residual confounding. Safety outcomes did not include kidney end points. Conclusion: It was estimated that, compared with oral bisphosphonates, denosumab lowered the risk for fractures by 45% and increased the risk for MACE by 36%. The estimates, however, are imprecise and need to be confirmed in future studies.
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页数:11
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