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Denosumab and Mortality in a Real-World Setting: A Comparative Study.
Alarkawi, Dunia; Tran, Thach; Chen, Weiwen; March, Lyn M; Blyth, Fiona M; Blank, Robert D; Bliuc, Dana; Center, Jacqueline R.
Afiliación
  • Alarkawi D; Skeletal Diseases Program, Garvan Institute of Medical Research, University of New South Wales, Sydney, Australia.
  • Tran T; Skeletal Diseases Program, Garvan Institute of Medical Research, University of New South Wales, Sydney, Australia.
  • Chen W; Skeletal Diseases Program, Garvan Institute of Medical Research, University of New South Wales, Sydney, Australia.
  • March LM; Clinical School, Faculty of Medicine, St Vincent's Hospital, University of New South Wales, Sydney, Australia.
  • Blyth FM; Institute of Bone and Joint Research, Kolling Institute, Sydney, Australia.
  • Blank RD; Clinical School, Royal North Shore Hospital, St Leonards, Australia.
  • Bliuc D; Clinical School, Concord Repatriation General Hospital, Sydney, Australia.
  • Center JR; Skeletal Diseases Program, Garvan Institute of Medical Research, University of New South Wales, Sydney, Australia.
J Bone Miner Res ; 38(12): 1757-1770, 2023 12.
Article en En | MEDLINE | ID: mdl-37915252
Denosumab (Dmab) is increasingly prescribed worldwide. Unlike bisphosphonates (BPs), its effect on mortality has yet to be well explored. This study examined the association between Dmab and all-cause mortality compared with no treatment in subjects with a fracture and BPs in subjects without a fracture. The study population was from the Sax Institute's 45 and Up Study (n = 267,357), a prospective population-based cohort with questionnaire data linked to hospital admissions (Admitted Patients Data Collection [APDC] data were linked by the Centre for Health Record Linkage), medication records (Pharmaceutical Benefits Scheme [PBS] provided by Services Australia), and stored securely (secure data access was provided through the Sax Institute's Secure Unified Research Environment [SURE]). The new-user cohort design with propensity-score (PS) matching was implemented. In the fracture cohort, Dmab and oral BP users were matched 1:2 to no treatment (Dmab: 617 women, 154 men; oral BPs: 615 women, 266 men). In the no-fracture cohort, Dmab users were matched 1:1 with oral BPs and zoledronic acid (Zol) users (Dmab:oral BPs: 479 men, 1534 women; Dmab:Zol: 280 men, 625 women). Mortality risk was measured using sex-specific pairwise multivariable Cox models. In the fracture cohort, compared with no treatment, Dmab was associated with 48% lower mortality in women (hazard ratio [HR] = 0.52, 95% confidence interval [CI] 0.36-0.72) but not in men. Oral BPs were associated with 44% lower mortality in both sexes (women HR = 0.56, 95% CI 0.42-0.77; men HR = 0.56, 95% CI 0.40-0.78). In the no-fracture cohort, compared with BPs, Dmab was associated with 1.5- to 2.5-fold higher mortality than oral BPs (women HR = 1.49, 95% CI 1.13-1.98; men HR = 2.74; 95% CI 1.82-4.11) but similar mortality to Zol. Dmab in women and oral BPs were associated with lower post-fracture mortality than no treatment. However, Dmab users had generally higher mortality than oral BP users in those without fractures. © 2023 American Society for Bone and Mineral Research (ASBMR).
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Fracturas Óseas / Conservadores de la Densidad Ósea Límite: Female / Humans / Male Idioma: En Revista: J Bone Miner Res Asunto de la revista: METABOLISMO / ORTOPEDIA Año: 2023 Tipo del documento: Article País de afiliación: Australia

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Fracturas Óseas / Conservadores de la Densidad Ósea Límite: Female / Humans / Male Idioma: En Revista: J Bone Miner Res Asunto de la revista: METABOLISMO / ORTOPEDIA Año: 2023 Tipo del documento: Article País de afiliación: Australia