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基于人群的病例对照研究中,选择性环氧化酶-2 抑制剂、非选择性非甾体抗炎药处方与乳腺癌风险。

Prescriptions for selective cyclooxygenase-2 inhibitors, non-selective non-steroidal anti-inflammatory drugs, and risk of breast cancer in a population-based case-control study.

机构信息

Department of Clinical Epidemiology, Aarhus University Hospital, Olof Palmes Alle 43-45, Aarhus N, Denmark.

出版信息

Breast Cancer Res. 2010;12(2):R15. doi: 10.1186/bcr2482. Epub 2010 Mar 1.

Abstract

INTRODUCTION

Non-steroidal anti-inflammatory drugs (NSAIDs) prevent the growth of mammary tumours in animal models. Two population-based case-control studies suggest a reduced risk of breast cancer associated with selective cyclooxygenase-2 (sCox-2) inhibitor use, but data regarding the association between breast cancer occurrence and use of non-selective NSAIDs are conflicting.

METHODS

We conducted a population-based case-control study using Danish healthcare databases to examine if use of NSAIDs, including sCox-2 inhibitors, was associated with a reduced risk of breast cancer. We included 8,195 incident breast cancer cases diagnosed in 1991 through 2006 and 81,950 population controls.

RESULTS

Overall, we found no reduced breast cancer risk in ever users (>2 prescriptions) of sCox-2 inhibitors (odds ratio (OR) = 1.08, 95% confidence interval (95% CI) = 0.99, 1.18), aspirin (OR = 0.98, 95% CI = 0.90-1.07), or non-selective NSAIDs OR = 1.04, (95% CI = 0.98, 1.10)). Recent use (>2 prescriptions within two years of index date) of sCox-2 inhibitors, aspirin, or non-selective NSAIDs was likewise not associated with breast cancer risk (Ors = 1.06 (95% CI = 0.96, 1.18), 0.96 (95% CI = 0.87, 1.06) and 0.99 (95% CI = 0.85, 1.16), respectively). Risk estimates by duration (<10, 10 to 15, 15+ years) or intensity (low/medium/high) of NSAID use were also close to unity. Regardless of intensity, shorter or long-term NSAID use was not significantly associated with breast cancer risk.

CONCLUSIONS

Overall, we found no compelling evidence of a reduced risk of breast cancer associated with use of sCox-2 inhibitors, aspirin, or non-selective NSAIDs.

摘要

简介

非甾体抗炎药 (NSAIDs) 可阻止动物模型中的乳腺肿瘤生长。两项基于人群的病例对照研究表明,选择性环氧化酶-2 (sCox-2) 抑制剂的使用与乳腺癌风险降低相关,但关于乳腺癌发生与非选择性 NSAIDs 使用之间关联的数据存在冲突。

方法

我们使用丹麦医疗保健数据库进行了一项基于人群的病例对照研究,以检查 NSAIDs(包括 sCox-2 抑制剂)的使用是否与乳腺癌风险降低相关。我们纳入了 1991 年至 2006 年间诊断出的 8195 例乳腺癌新发病例和 81950 名人群对照。

结果

总体而言,我们发现 sCox-2 抑制剂(比值比 (OR) = 1.08,95%置信区间 (95% CI) = 0.99,1.18)、阿司匹林(OR = 0.98,95% CI = 0.90-1.07)或非选择性 NSAIDs(OR = 1.04,95% CI = 0.98,1.10)的长期使用者(>2 次处方)的乳腺癌风险并未降低。最近使用(索引日期前两年内 >2 次处方)sCox-2 抑制剂、阿司匹林或非选择性 NSAIDs 与乳腺癌风险也无关联(ORs = 1.06(95% CI = 0.96,1.18),0.96(95% CI = 0.87,1.06)和 0.99(95% CI = 0.85,1.16))。根据 NSAID 使用时间(<10 年、10-15 年、15+ 年)或强度(低/中/高)划分的风险估计值也接近 1。无论强度如何,短期或长期 NSAID 使用与乳腺癌风险均无显著关联。

结论

总体而言,我们没有发现 sCox-2 抑制剂、阿司匹林或非选择性 NSAIDs 使用与乳腺癌风险降低相关的有力证据。

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