Low-dose aspirin or other nonsteroidal anti-inflammatory drug use and prostate cancer risk: a nationwide study

被引:23
作者
Skriver, Charlotte [1 ]
Dehlendorff, Christian [1 ]
Borre, Michael [2 ]
Brasso, Klaus [3 ]
Sorensen, Henrik Toft [4 ]
Hallas, Jesper [5 ]
Larsen, Signe Benzon [1 ]
Tjonneland, Anne [1 ]
Friis, Soren [1 ,4 ,6 ]
机构
[1] Danish Canc Soc, Res Ctr, Strandboulevarden 49, DK-2100 Copenhagen O, Denmark
[2] Aarhus Univ Hosp, Dept Urol, Palle Juul Jensens Blvd 99, DK-8200 Aarhus N, Denmark
[3] Rigshosp, Copenhagen Prostate Canc Ctr, Dept Urol, Blegdamsvej 9, DK-2100 Copenhagen O, Denmark
[4] Aarhus Univ Hosp, Dept Clin Epidemiol, Olof Palmes Alle 43-45, DK-8200 Aarhus N, Denmark
[5] Univ Southern Denmark, Dept Publ Hlth, Clin Pharmacol & Pharm, JB Winslows Vej 19, DK-5000 Odense C, Denmark
[6] Univ Copenhagen, Dept Publ Hlth, Oster Farimagsgade 5, DK-1014 Copenhagen K, Denmark
关键词
Aspirin; Nonsteroidal anti-inflammatory drugs; Prostate neoplasms; Risk; Epidemiology; Casecontrol study; COLORECTAL-CANCER; POPULATION; PREVENTION; METAANALYSIS; REGISTERS; COHORT;
D O I
10.1007/s10552-016-0785-7
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose Increasing evidence suggests that aspirin use may protect against prostate cancer. In a nationwide case-control study, using Danish high-quality registry data, we evaluated the association between the use of low-dose aspirin or other nonsteroidal anti-inflammatory drugs (NSAIDs) and the risk of prostate cancer. Methods We identified 35,600 patients (cases) with histologically verified prostate cancer during 2000-2012. Cases were matched to 177,992 population controls on age and residence by risk-set sampling. Aspirin and nonaspirin NSAID exposure was defined by type, estimated dose, duration, and consistency of use. We used conditional logistic regression to estimate odds ratios (ORs), with 95 % confidence intervals (CIs), for prostate cancer associated with low-dose aspirin (75-150 mg) or nonaspirin NSAID use, adjusted for potential confounders. Results Use of low-dose aspirin was associated with an OR for prostate cancer of 0.94 (95 % CI 0.91-0.97). Slightly lower ORs were seen with increasing cumulative amount, duration, and consistency of low-dose aspirin use (continuous use, >= 5 years: OR 0.89; 95 % CI 0.82-0.97; >= 10 years: OR 0.86; 95 % CI 0.70-1.06). Nonaspirin NSAID use was associated with a slightly increased OR for prostate cancer (1.13; 95 % CI 1.10-1.15); however, this association was confined to localized disease and did not vary materially with amount, duration, or consistency of nonaspirin NSAID use. Conclusions Our study indicates that long-term, consistent low-dose aspirin use may provide modest protection against prostate cancer. The slightly increased risk of only localized prostate cancer with nonaspirin NSAID use suggests a noncausal explanation of the observed association.
引用
收藏
页码:1067 / 1079
页数:13
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