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PMID: 20844293 Published · ppublish English Journal Article Meta-Analysis Multicenter Study Research Support, Non-U.S. Gov't Review

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

Gut ·Vol. 59 ·No. 12 ·2010-12-00 ·Pages 1670-9

Din FV, Theodoratou E, Farrington SM, Tenesa A, Barnetson RA, Cetnarskyj R, Stark L, Porteous ME, Campbell H, Dunlop MG

Abstract

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. 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. 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). 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.

MeSH Terms
Adolescent Adult Aged Anti-Inflammatory Agents, Non-Steroidal/administration & dosage,therapeutic use Anticarcinogenic Agents/administration & dosage,therapeutic use Aspirin/administration & dosage,therapeutic use Colorectal Neoplasms/epidemiology,prevention & control Confounding Factors, Epidemiologic Diet/statistics & numerical data Dose-Response Relationship, Drug Drug Administration Schedule Epidemiologic Methods Female Humans Life Style Male Middle Aged Poverty/statistics & numerical data Scotland/epidemiology Smoking/epidemiology Young Adult
Chemicals
Anti-Inflammatory Agents, Non-Steroidal Anticarcinogenic Agents Aspirin
Authors & Affiliations
10 authors, click to expand affiliations / ORCID
Din Farhat V N
Colon Cancer Genetics Group and Academic Coloproctology, Institute of Genetics and Molecular Medicine, University of Edinburgh and MRC Human Genetics Unit, Western General Hospital, Edinburgh EH4 2XU, UK.
Theodoratou Evropi
Farrington Susan M
Tenesa Albert
Barnetson Rebecca A
Cetnarskyj Roseanne
Stark Lesley
Porteous Mary E
Campbell Harry
Dunlop Malcolm G
Article Info
Journal
Gut
Abbr.
Gut
ISSN
1468-3288
Published
2010-12-00
Epub
2010-00-15
Pages
1670-9
Language
English
Region
England
NLM ID
2985108R
Subset
IM
Grants
Cancer Research UK · C348/A3758 · United Kingdom
Medical Research Council · MC_U127527198 · United Kingdom
Cancer Research UK · C26031/A11378 · United Kingdom
Cancer Research UK · 11378 · United Kingdom
Cancer Research UK · C31250/A10107 · United Kingdom
Cancer Research UK · C348/A8896 · United Kingdom
Medical Research Council · G0000657-53203 · United Kingdom
Chief Scientist Office · CZB/4/449 · United Kingdom
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