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首页> 外文期刊>Breast Cancer Research >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
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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

机译:选择性环氧化酶-2抑制剂的处方,非选择性非甾体抗炎药,以及基于人群的案例对照研究中的乳腺癌风险

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IntroductionNon-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.MethodsWe 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.ResultsOverall, 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.ConclusionsOverall, we found no compelling evidence of a reduced risk of breast cancer associated with use of sCox-2 inhibitors, aspirin, or non-selective NSAIDs.
机译:术语 - 甾体抗炎药(NSAIDs)防止了动物模型中乳腺肿瘤的生长。两种基于人群的案例对照研究表明,与选择性环氧化酶-2(SCox-2)抑制剂使用相关的乳腺癌风险降低,但有关乳腺癌发生和使用非选择性NSAID的关联的数据是冲突的..一种方法使用丹麦医疗保健数据库的基于人口的案例控制研究,以检查是否使用NSAID,包括Scox-2抑制剂,与乳腺癌的风险降低有关。我们包括1991年至2006年诊断的8,195次入射乳腺癌病例,81,950人的人口控制。培斯-2抑制剂的用户(> 2个处方)中发现没有减少的乳腺癌风险(OTS比率(或)= 1.08,95%置信区间(95%CI)= 0.99,118),阿司匹林(或= 0.98,95%CI = 0.90-1.07),或非选择性NSAIDs或= 1.04,(95%CI = 0.98,1.10))。 SCOX-2抑制剂,阿司匹林或非选择性NSAID的最近使用(> 2个处于指数日期的处方)同样与乳腺癌风险不同(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))。 NSAID使用的持续时间(<10,10至15,15,15岁以下)或强度(低/中/高)的风险估计也接近统一。无论强度,短期或长期的NSAID使用都没有明显与乳腺癌风险有显着相关.Clclusionsoverall,我们发现没有令人兴奋的证据证明与使用Scox-2抑制剂,阿司匹林或非选择性NSAID相关的乳腺癌的风险降低。

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