Effect of aspirin and NSAIDs on risk and survival from colorectal cancer

被引:230
|
作者
Din, Farhat V. N. [1 ,2 ,3 ]
Theodoratou, Evropi
Farrington, Susan M. [1 ,2 ,3 ]
Tenesa, Albert [1 ,2 ,3 ]
Barnetson, Rebecca A. [1 ,2 ,3 ]
Cetnarskyj, Roseanne [5 ]
Stark, Lesley [1 ,2 ,3 ]
Porteous, Mary E. [4 ]
Campbell, Harry
Dunlop, Malcolm G. [1 ,2 ,3 ]
机构
[1] Univ Edinburgh, Colon Canc Genet Grp, Edinburgh EH4 2XU, Midlothian, Scotland
[2] Univ Edinburgh, Inst Genet & Mol Med, Edinburgh EH4 2XU, Midlothian, Scotland
[3] Western Gen Hosp, MRC Human Genet Unit, Edinburgh EH4 2XU, Midlothian, Scotland
[4] Western Gen Hosp, SE Scotland Clin Genet Serv, Edinburgh EH4 2XU, Midlothian, Scotland
[5] Edinburgh Napier Univ, Fac Life Sci, Edinburgh, Midlothian, Scotland
基金
英国医学研究理事会;
关键词
NONSTEROIDAL ANTIINFLAMMATORY DRUGS; LOW-DOSE ASPIRIN; SERVICES-TASK-FORCE; PRIMARY PREVENTION; RANDOMIZED-TRIAL; WOMENS HEALTH; REDUCED RISK; ADENOMAS; CHEMOPREVENTION; EXPRESSION;
D O I
10.1136/gut.2009.203000
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background Previous studies have shown that aspirin and other non-steroidal anti-inflammatory drugs (NSAIDs) lower colorectal cancer (CRC) risk. However, the lowest effective NSAID dose, treatment duration, and effects on survival are not defined. In a large population-based case-control study, we have explored the relationship between NSAID dose and duration, CRC risk and overall CRC-specific survival. Methods The relationship between NSAID use and CRC risk was examined in 2279 cases and 2907 controls. Subjects completed food-frequency and lifestyle questionnaires. NSAID categories were low-dose aspirin (75 mg), non-aspirin NSAIDs (NA-NSAIDs) and any NSAID. Users were defined as taking >4 tablets/week for >1 month. ORs were calculated by logistic regression models and adjusted for potential confounding factors. Effect of NSAID use on all-cause and CRC-specific mortality was estimated using Logrank tests and Cox's hazard models. Results In all, 354 cases (15.5%) were taking low-dose aspirin compared to 526 controls (18.1%). Low-dose aspirin use was associated with decreased CRC risk (OR 0.78 95% CI 0.65 to 0.92, p=0.004), evident after 1 year and increasing with duration of use (p(trend)=0.004). NA-NSAID and any NSAID use were also inversely associated with CRC. There was no demonstrable effect of NSAIDS on all-cause (HR 1.11, p=0.22, 0.94-1.33) or CRC-specific survival (HR 1.01, p=0.93, 0.83-1.23). Conclusion This is the first study to demonstrate a protective effect against CRC associated with the lowest dose of aspirin (75 mg per day) after only 5 years use in the general population. NSAID use prior to CRC diagnosis does not influence survival from the disease.
引用
收藏
页码:1670 / U114
页数:10
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