NSAIDs and colorectal cancer risk: do administrative data support a chemopreventive effect?

NSAIDs and colorectal cancer risk: do administrative data support a chemopreventive effect?
复制标题

非甾体抗炎药和结直肠癌风险:管理数据是否支持化学预防作用?

DOI:
10.1007/s11606-007-0256-7
复制
发表时间:
2007
影响因子:
5.7
通讯作者:
Lauderdale,DianeS
Lauderdale,DianeS
中科院分区:
医学2区
文献类型:
--
作者:
Lamont,ElizabethB;Dias,LaurenE;Lauderdale,DianeS

文献摘要

相似文献

BackgroundRandomized trials show non-steroidal anti-inflammatory drugs (NSAIDs) reduce precancerous polyps. Observational studies of the NSAID aspirin (ASA) suggest that it reduces invasive colorectal cancer (CRC) incidence, but because ASA use may also be a marker for healthy behaviors, these studies may be subject to selection bias. We sought to estimate the effectiveness of NSAIDs in CRC prevention in the population of elderly Medicare beneficiaries, minimizing this selection bias.MethodsWith National Ambulatory Medical Care Survey data, we find that patients with a diagnosis of osteoarthritis (OA) are 4.4 times more likely to concurrently have NSAID use documented than patients without such a diagnosis. We use this figure to estimate the expected NSAID-mediated reduction in CRC risk associated with a diagnosis of OA. Using Survival Epidemiology and End-Results (SEER)-Medicare data, we compare cases of elderly Medicare beneficiaries diagnosed with CRC in 1995 to persons without CRC to determine if their odds of antecedent OA differ.ResultsWe estimate the expected NSAID-mediated reduction in CRC associated with an OA diagnosis to be between 6 and 16% (i.e., RR, 0.84–0.94). In the SEER-Medicare data, we find that individuals with a diagnosis of OA in Medicare claims in the previous 3 years had 15% lower odds of being diagnosed with CRC than individuals whose claims did not reflect antecedent OA (OR 0.85, 95%CI 0.80–0.91).ConclusionsThis case-control study finds that elderly Medicare beneficiaries with histories of OA have 15% lower odds of developing CRC. These results are consistent with a preventive role for NSAIDs in CRC among the elderly.