Mortality risk reduction differs according to bisphosphonate class: a 15-year observational study

被引:31
作者
Bliuc, D. [1 ]
Tran, T. [1 ]
van Geel, T. [2 ]
Adachi, J. D. [3 ]
Berger, C. [4 ]
van den Bergh, J. [5 ,6 ]
Eisman, J. A. [1 ,7 ]
Geusens, P. [2 ,8 ]
Goltzman, D. [9 ]
Hanley, D. A. [10 ]
Josse, R. G. [11 ]
Kaiser, S. [12 ]
Kovacs, C. S. [13 ]
Langsetmo, L. [14 ]
Prior, J. C. [15 ]
Nguyen, T., V [1 ,16 ,17 ]
Center, J. R. [1 ,16 ]
机构
[1] Garvan Inst Med Res, Osteoporosis & Bone Biol, Sydney, NSW, Australia
[2] Maastricht Univ, Med Ctr, Res Sch CAPHRI, Care & Publ Hlth Res Inst, Maastricht, Netherlands
[3] McMaster Univ, Dept Med, Hamilton, ON, Canada
[4] McGill Univ, CaMos Natl Coordinating Ctr, Montreal, PQ, Canada
[5] Maastricht Univ, Med Ctr, Res Sch Nutrim, Dept Internal Med,Subdiv Rheumatol, Maastricht, Netherlands
[6] VieCuri Med Ctr Noord Limburg, Dept Internal Med, Venlo, Netherlands
[7] Univ Notre Dame Australia, Sch Med Sydney, Sydney, NSW, Australia
[8] Univ Hasselt, Biomed Res Inst, Hasselt, Belgium
[9] McGill Univ, Dept Med, Montreal, PQ, Canada
[10] Univ Calgary, Dept Med, Calgary, AB, Canada
[11] Univ Toronto, Dept Med, Toronto, ON, Canada
[12] Dalhousie Univ, Dept Med, Halifax, NS, Canada
[13] Mem Univ, Fac Med, St John, NF, Canada
[14] Univ Minnesota, Sch Publ Hlth, Minneapolis, MN USA
[15] Univ British Columbia, Dept Med & Endocrinol, Vancouver, BC, Canada
[16] UNSW, Fac Med, Clin Sch, St Vincents Hosp, Sydney, NSW, Australia
[17] Univ Technol Sydney, Sch Biomed Engn, Sydney, NSW, Australia
基金
英国医学研究理事会; 加拿大健康研究院;
关键词
Bisphosphonate; Fracture; Mortality risk; Osteoporosis; Prospective study; DELTA T-CELLS; SUBSEQUENT FRACTURE; BONE LOSS; OSTEOPOROTIC FRACTURE; ZOLEDRONIC ACID; HIP FRACTURE; WOMEN; MEN; PAMIDRONATE; EFFICACY;
D O I
10.1007/s00198-018-4806-0
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
A Summary 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.
引用
收藏
页码:817 / 828
页数:12
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