Use of proton pump inhibitors and risk of hip/femur fracture: a population-based case-control study

被引:78
|
作者
Pouwels, S. [1 ]
Lalmohamed, A. [1 ]
Souverein, P. [1 ]
Cooper, C. [2 ,5 ]
Veldt, B. J. [3 ]
Leufkens, H. G. [1 ]
de Boer, A. [1 ]
van Staa, T. [1 ,2 ,4 ]
de Vries, F. [1 ,2 ,4 ]
机构
[1] Univ Utrecht, Utrecht Inst Pharmaceut Sci, Div Pharmacoepidemiol & Pharmacotherapy, NL-3508 TB Utrecht, Netherlands
[2] Univ Southampton, Southampton Gen Hosp, MRC Epidemiol Resource Ctr, Southampton, Hants, England
[3] Erasmus MC Univ Med Ctr, Dept Gastroenterol & Hepatol, Rotterdam, Netherlands
[4] Med & Healthcare Prod Regulatory Agcy, London, England
[5] Univ Oxford, Inst Musculoskeletal Sci, Oxford, England
基金
英国医学研究理事会;
关键词
Fracture risk; Histamine H-2-receptor antagonist; Proton pump inhibitor; TERM OMEPRAZOLE TREATMENT; CALCIUM-ABSORPTION; BONE-RESORPTION; CELIAC-DISEASE; K+-ATPASE; EPIDEMIOLOGY; OSTEOPOROSIS; MEDICATIONS; CARBONATE; DRUGS;
D O I
10.1007/s00198-010-1337-8
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Previous studies evaluated the association between proton pump inhibitor (PPI) use and subsequent fracture risk, but they showed ambiguous results. Therefore, the objective was to evaluate this association in a different study population. Our findings show that there is probably no causal relationship between PPI use and hip fracture risk. Previous studies evaluated the association between PPI use and subsequent fracture risk, but they showed ambiguous results. To further test these conflicting results, the objective of this study was to evaluate the association between the use of PPIs and the risk of hip/femur fracture in a different study population. A case-control study was conducted using data from the Dutch PHARMO record linkage system. The study population included 6,763 cases aged 18 years and older with a first hip/femur fracture during enrolment and 26,341 age-, gender- and region-matched controls. Current users of PPIs had an increased risk of hip/femur fracture yielding an adjusted odds ratio (AOR) of 1.20 (95% CI 1.04-1.40). Fracture risk attenuated with increasing durations of use, resulting in AORs of 1.26 (95% CI 0.94-1.68) in the first 3 months, 1.31 (95% CI 0.97-1.75) between 3 and 12 months, 1.18 (95% CI 0.92-1.52) between 13 and 36 months and 1.09 (95% CI 0.81-1.47) for use longer than 36 months. Our findings show that there is probably no causal relationship between PPI use and hip fracture risk. The observed association may be the result of unmeasured distortions: although current use of PPIs was associated with a 1.2-fold increased risk of hip/femur fracture, the positive association was attenuated with longer durations of continuous use. Our findings do not support that discontinuation of PPIs decreases risk of hip fracture in elderly patients.
引用
收藏
页码:903 / 910
页数:8
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