Oral Bisphosphonate Use and All-Cause Mortality in Patients With Moderate-Severe (Grade 3B-5D) Chronic Kidney Disease: A Population-Based Cohort Study

被引:7
作者
Alarkawi, Dunia [1 ]
Ali, M. Sanni [2 ,3 ]
Bliuc, Dana [1 ]
Pallares, Natalia [4 ]
Tebe, Cristian [4 ]
Elhussein, Leena [2 ,3 ]
Caskey, Fergus J. [5 ,6 ]
Arden, Nigel K. [2 ,3 ]
Ben-Shlomo, Yoav [5 ]
Abrahamsen, Bo [2 ,3 ,7 ,8 ]
Diez-Perez, Adolfo [9 ]
Pascual, Julio [10 ]
Perez-Saez, Maria Jose [10 ]
Center, Jacqueline R. [1 ,11 ]
Judge, Andrew [2 ,3 ,12 ,13 ]
Cooper, Cyrus [2 ,3 ,13 ]
Javaid, Muhammad K. [2 ,3 ,13 ]
Prieto-Alhambra, Daniel [2 ,3 ,14 ]
机构
[1] Univ New South Wales, Garvan Inst Med Res, Sch Med, Bone Biol Div, Sydney, NSW, Australia
[2] Univ Oxford, Ctr Stat Med, Oxford, England
[3] Univ Oxford, Nuffield Dept Orthopaed Rheumatol & Musculoskelet, Oxford, England
[4] Bellvitge Biomed Res Inst IDIBELL, Biostat Unit, Barcelona, Spain
[5] Univ Bristol, Populat Hlth Sci, Bristol, Avon, England
[6] UK Renal Registry, Bristol, Avon, England
[7] Univ Southern Denmark, Odense Patient Data Explorat Network, Odense, Denmark
[8] Holbaek Cent Hosp, Dept Med, Holbaek, Denmark
[9] Univ Barcelona UAB, Hosp del Mar, Inst Med Invest, Ctr Invest Biomed Red Fragilidad & Envejecimiento, Barcelona, Spain
[10] Hosp del Mar, Dept Nephrol, Barcelona, Spain
[11] St Vincents Hosp, Sch Clin, Sydney, NSW, Australia
[12] Univ Bristol, Biomed Res Ctr Translat Hlth Sci, Natl Inst Hlth Res, Bristol, Avon, England
[13] Univ Southampton, MRC, Lifecourse Epidemiol Unit, Southampton, Hants, England
[14] Univ Autonoma Barcelona, Ctr Invest Biomed Red Fragilidad & Envejecimiento, Idiap Jordi Gol Primary Care Res Inst, GREMPAL,Res Grp, Barcelona, Spain
基金
英国医学研究理事会;
关键词
BISPHOSPHONATES; CHRONIC KIDNEY DISEASE; EPIDEMIOLOGY; MORTALITY; OSTEOPOROSIS; HIP FRACTURE; SUBSEQUENT FRACTURE; RENAL-FUNCTION; ZOLEDRONIC ACID; INCREASED RISK; BONE-DISEASE; DENOSUMAB; SAFETY; WOMEN; MEN;
D O I
10.1002/jbmr.3961
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Oral bisphosphonates (oBPs) have been associated with reduced fractures and mortality. However, their risks and benefits are unclear in patients with moderate-severe CKD. This study examined the association between oBPs and all-cause mortality in G3B-5D CKD. This is a population-based cohort study including all subjects with an estimated glomerular filtration rate (eGFR) <45/mL/min/1.73 m(2) (G3B: eGFR <45/mL/min/1.73 m(2) G4: eGFR 15-29/mL/min/1.73 m(2) G5: eGFR <15/mL/min/1.73 m(2) G5D: hemodialysis) aged 40+ years from the UK Clinical Practice Research Datalink (CPRD) and the Catalan Information System for Research in Primary Care (SIDIAP). Previous and current users of other anti-osteoporosis drugs were excluded. oBP use was modeled as a time-varying exposure to avoid immortal time bias. Treatment episodes in oBP users were created by concatenating prescriptions until patients switched or stopped therapy or were censored or died. A washout period of 180 days was added to (date of last prescription +180 days). Propensity scores (PSs) were calculated using prespecified predictors of mortality including age, gender, baseline eGFR, socioeconomic status, comorbidities, previous fracture, co-medications, and number of hospital admissions in the previous year. Cox models were used for PS adjustment before and after PS trimming (the first and last quintiles). In the CPRD, of 19,351 oBP users and 210,954 non-oBP users, 5234 (27%) and 85,105 (40%) deaths were recorded over 45,690 and 915,867 person-years of follow-up, respectively. oBP users had 8% lower mortality risk compared to non-oBP users (hazard ratio [HR] 0.92; 95% CI, 0.89 to 0.95). Following PS trimming, this became nonsignificant (HR 0.98; 95% CI, 0.94 to 1.04). In the SIDIAP, of 4146 oBP users and 86,127 non-oBP users, 1330 (32%) and 36,513 (42%) died, respectively. oBPs were not associated with mortality in PS adjustment and trimming (HR 1.04; 95% CI, 0.99 to 1.1 and HR 0.95; 95% CI, 0.89 to 1.01). In this observational, patient-based cohort study, oBPs were not associated with increased mortality among patients with moderate-severe CKD. However, further studies are needed on other effects of oBPs in CKD patients. (c) 2020 American Society for Bone and Mineral Research (c) 2020 American Society for Bone and Mineral Research.
引用
收藏
页码:894 / 900
页数:7
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