The effect of statin use on the incidence of prostate cancer: A population-based nested case-control study

被引:12
|
作者
Dawe, David E. [1 ,2 ]
Ye, Xibiao [3 ]
Czaykowski, Piotr [1 ,2 ,3 ]
Jassal, Davinder [1 ,2 ]
Singh, Harminder [1 ,2 ,3 ]
Skarsgard, David [5 ]
Aprikian, Armen [6 ]
Mahmud, Salaheddin M. [3 ,4 ]
机构
[1] CancerCare Manitoba, Dept Hematol & Med Oncol, Winnipeg, MB, Canada
[2] Univ Manitoba, Dept Internal Med, Fac Hlth Sci, Winnipeg, MB, Canada
[3] Univ Manitoba, Dept Community Hlth Sci, Fac Hlth Sci, Winnipeg, MB, Canada
[4] CancerCare Manitoba, Dept Epidemiol & Canc Registry, Winnipeg, MB, Canada
[5] Univ Calgary, Dept Oncol, Calgary, AB, Canada
[6] McGill Univ, Dept Oncol, Montreal, PQ, Canada
基金
加拿大健康研究院;
关键词
statins; prostate cancer; epidemiology; chemoprevention; pharmacoepidemiology; ANTIINFLAMMATORY DRUG-USE; RISK; SASKATCHEWAN; FINASTERIDE; PREVENTION; CANADA; TESTS;
D O I
10.1002/ijc.31295
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Preclinical studies suggest statins may help prevent prostate cancer (PC), but epidemiologic results are mixed. Many epidemiological studies have relatively short prediagnosis drug exposure data, which may miss some statin use. We completed a nested case-control study investigating the impact of statin use on PC diagnosis and clinically significant PC using data from men aged >= 40 years in the Canadian province of Saskatchewan between 1990 and 2010. Drug exposure histories were derived from a population-based prescription drug database. We used conditional logistic regression to model use of statins as a class and stratified analyses for groups defined by lipophilicity. Clinically significant PC was defined as Gleason score 8-10 OR stage C or D or III or IV at diagnosis. 12,745 cases of PC were risk-set matched on age and geographic location to 50,979 controls. Greater than 90% of subjects had prediagnosis drug exposure histories >15 years. 2,064 (16.2%) cases and 7,956 (15.6%) controls were dispensed one or more statin prescriptions. In multivariable models, ever prescription of statins was not associated with PC diagnosis (OR 0.97; 95% CI 0.90-1.05). Neither lipophilic statins (OR 0.96, 95% CI 0.88-1.04) nor hydrophilic statins (OR 1.06, 95% CI 0.95-1.20) impacted PC diagnosis. There was no effect of the dose or duration of statin use. Diagnosis of clinically significant PC decreased with statin use (OR 0.84, 95% CI 0.73-0.97). Statin use is not associated with overall PC risk, regardless of duration or dose of statin exposure. Statin use is associated with a decreased risk of clinically significant PC.
引用
收藏
页码:190 / 198
页数:9
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