Mortality risk reduction differs according to bisphosphonate class: a 15-year observational study
Dana Bliuc, For the CaMOS Research Group , Thach Tran
Tineke van Geel, Jonathan D Adachi, Claudie Berger, Joop P. van den Bergh, John A Eisman, Joop van den Bergh, Piet Geusens, David Goltzman, David A Hanley, Christopher S Kovacs, Lisa Langsetmo, Jerilynn C Prior, Tuan V Nguyen, CaMOS Research Group , Jacqueline R Center, Robert G Josse, S Kaiser
In this prospective cohort of 6120 participants aged 50+, nitrogen-bisphosphonates but not non-nitrogen bisphosphonates were associated with a significant 34% mortality risk reduction compared to non-treated propensity score matched controls. These findings open new avenues for research into mechanistic pathways.
Introduction
Emerging evidence suggests that bisphosphonates (BP), first-line treatment of osteoporosis, are associated with reduced risks for all-cause mortality. This study aimed to determine the association between different BP types and mortality risk in participants with or without a fracture.
Methods
A prospective cohort study of users of different BPs matched to non-users by propensity score (age, gender, co-morbidities, fragility fracture status) and time to starting the BP medication from the population-based Canadian Multicentre Osteoporosis Study from nine Canadian centres followed from 1995 to 2013. Mortality risk for bisphosphonate users vs matched non-users was assessed using pairwise multivariable Cox proportional hazards models.
Results
There were 2048 women and 308 men on BP and 1970 women and 1794 men who did not receive medication for osteoporosis. The relationship between BP and mortality risk was explored in three separate 1:1 propensity score-matched cohorts of BP users and no treatment (etidronate, n = 599, alendronate, n = 498, and risedronate n = 213). Nitrogen BP (n-BP) (alendronate and risedronate) was associated with lower mortality risks [pairwise HR, 0.66 (95% CI, 0.48-0.91)] while the less potent non-n-BP, etidronate, was not [pairwise HR: 0.89 (95% CI, 0.66-1.20)]. A direct comparison between n-BP and etidronate (n = 340 pairs) also suggested a better survival for n-BP [paired HR, 0.47 (95%CI, (95% CI, 031-0.70)] for n-BP vs. etidronate].
Conclusion
Compared to no treatment, nitrogen but not non-nitrogen bisphosphonates appear to be associated with better survival.
bisphosphonate class mortality risk reduction prospective cohort, nitrogen bisphosphonate vs non-nitrogen bisphosphonate survival, alendronate risedronate etidronate mortality comparison, Prior JC bisphosphonate osteoporosis mortality, propensity score matched bisphosphonate treatment outcomes, Canadian Multicentre Osteoporosis Study bisphosphonate survival, osteoporosis treatment all-cause mortality reduction, bisphosphonate type fracture mortality risk older adults, nitrogen bisphosphonate mechanistic pathways survival benefit, postmenopausal women bisphosphonate therapy long-term outcomes, Cox proportional hazards bisphosphonate mortality 15 year follow-up
PMID 30607457 30607457 DOI 10.1007/s00198-018-4806-0 10.1007/s00198-018-4806-0
Cite this article
Bliuc, D., Tran, T., van Geel, T., Adachi, J. D., Berger, C., van den Bergh, J., Eisman, J. A., Geusens, P., Goltzman, D., Hanley, D. A., Josse, R. G., Kaiser, S., Kovacs, C. S., Langsetmo, L., Prior, J. C., Nguyen, T. V., Center, J. R., & CaMOS Research Group (2019). Mortality risk reduction differs according to bisphosphonate class: a 15-year observational study. Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA, 30(4), 817-828. https://doi.org/10.1007/s00198-018-4806-0
Bliuc D, Tran T, van Geel T, Adachi JD, Berger C, van den Bergh J, et al. Mortality risk reduction differs according to bisphosphonate class: a 15-year observational study. Osteoporos Int. 2019;30(4):817-828. doi:10.1007/s00198-018-4806-0
Bliuc, D., et al. "Mortality risk reduction differs according to bisphosphonate class: a 15-year observational study." Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA, vol. 30, no. 4, 2019, pp. 817-828.
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