Acetylcholinesterase inhibitors and the risk of osteoporotic fractures: nested case-control study

被引:20
作者
Tamimi, I. [1 ]
Nicolau, B. [2 ]
Eimar, H. [3 ]
Madathil, S. Arekunnath [2 ]
Kezouh, A. [4 ]
Karp, I. [5 ]
Tamimi, F. [6 ]
机构
[1] Hosp Reg Univ Malaga, Ave Carlos Haya SN, Malaga 29010, Spain
[2] McGill Univ, Div Oral Hlth & Soc Res, Fac Dent, 2001 McGill Coll Ave, Montreal, PQ H3A 1G1, Canada
[3] Univ Alberta, Fac Med & Dent, 2J2-00WC Mackenzie Hlth Sci Ctr 8440 112 St NW, Edmonton, AB T6G 2R7, Canada
[4] Lady Davis Inst, Ctr Clin Epidemiol, Dept Epidemiol & Biostat, 3755 Cote Ste Catherine Rd, Montreal, PQ H3T 1E2, Canada
[5] Western Univ, Dept Epidemiol & Biostat, Kresge Bldg K214, London, ON N6A 5C1, Canada
[6] McGill Univ, Fac Dent, 3640 Univ St, Montreal, PQ H3A 2B2, Canada
关键词
Acetylcholinesterase inhibitors; Alzheimer's disease; Mortality; Osteoporotic fracture; Reintervention; Second fracture; ALZHEIMERS-DISEASE PATIENTS; SYMPATHETIC-NERVOUS-SYSTEM; BONE MASS; HIP FRACTURE; VASCULAR DEMENTIA; CHOLINESTERASE-INHIBITORS; LEPTIN REGULATION; DOUBLE-BLIND; DONEPEZIL; RECEPTORS;
D O I
10.1007/s00198-017-4346-z
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The objective of this study was to analyze the effect of acetylcholinesterase inhibitors (AChEIs) on the risk of osteoporotic fractures in Alzheimer patients. A nested case-control study was conducted on 1190 cases and 4760 controls. The use of AChEIs was found to decrease the risk of osteoporotic fractures in these patients. The objective of this study is to estimate the extent to which the use of AChEIs is associated with a reduction in the risk of osteoporotic fractures. A nested case-control study was conducted using data from the UK Clinical Practice Research Datalink (CPRD) and Hospital Episode Statistics (HES) database (1998-2013). The study cohort consisted of Alzheimer's Disease (AD) patients aged >= 65 years with no previous history of osteoporotic fractures at cohort baseline. Cases were individuals who suffered an osteoporotic fracture during the study period, whereas controls were subject who did not experience any osteoporotic fractures during the same period. Controls were drawn from the population time at risk while being matched to the cases in respect to age, sex, up-to-standard follow-up in the CPRD, calendar time, and duration of AD (control-to-case ratio: 4-to-1). Information on the use of AChEIs and the relevant potential confounders was ascertained from the CPRD database for all the cases and controls. We identified 1190 cases and 4760 controls. Compared to non-users, any use of AChEIs prior to the fracture was associated with a reduction in the fracture risk [adjusted odds ratio (OR) 0.80 (confidence interval (CI) 95%, 0.70-0.91)]. The use of AChEIs corresponding to a proportion of days covered of 0.8-1.0 was associated with a lower osteoporotic fracture risk compared to non-use [adjusted OR 0.76 (CI 95%, 0.66-0.87)]. In this study using large primary care databases, the use and treatment adherence to AChEIs were associated with a decreased risk of osteoporotic fractures in elderly AD patients.
引用
收藏
页码:849 / 857
页数:9
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