Wood Marie E, Sprague Brian L, Oustimov Andrew, Synnstvedt Marie B, Cuke Melissa, Conant Emily F, Kontos Despina
Department of Medicine, University of Vermont School of Medicine, Burlington, VT, USA.
Department of Surgery, University of Vermont School of Medicine, Burlington, VT, USA.
Breast Cancer Res Treat. 2017 Apr;162(3):419-425. doi: 10.1007/s10549-017-4127-6. Epub 2017 Feb 4.
Observational and biologic studies suggest that aspirin is a promising prevention therapy for breast cancer. However, clinical trials to date have not corroborated this evidence, potentially due to study design. We evaluated the effect of aspirin on mammographic density (MD), an established modifiable risk factor for breast cancer.
Electronic medical records from the University of Pennsylvania were evaluated for women who underwent screening mammography, saw their primary care provider, and had a confirmed list of medications during 2012-2013. Logistic regression was performed to test for associations between clinically recorded MD and aspirin use, after adjusting for age, body mass index (BMI), and ethnicity.
We identified 26,000 eligible women. Mean age was 57.3, mean BMI was 28.9 kg/m, 41% were African American, and 19.7% reported current aspirin use. Aspirin users were significantly older and had higher BMI. There was an independent, inverse association between aspirin use and MD (P < 0.001). Women with extremely dense breasts were less likely to be aspirin users than women with scattered fibroglandular density (OR 0.73; 95% CI 0.57-0.93). This association was stronger for younger women (P = 0.0002) and for African Americans (P = 0.011). The likelihood of having dense breasts decreased with aspirin dose (P = 0.007), suggesting a dose response.
We demonstrate an independent association between aspirin use and lower MD in a large, diverse screening cohort. This association was stronger for younger and African American women: two groups at greater risk for ER- breast cancer. These results contribute to the importance of investigating aspirin for breast cancer prevention.
观察性研究和生物学研究表明,阿司匹林是一种很有前景的乳腺癌预防疗法。然而,迄今为止的临床试验尚未证实这一证据,这可能是由于研究设计的原因。我们评估了阿司匹林对乳腺钼靶密度(MD)的影响,乳腺钼靶密度是一种已确定的可改变的乳腺癌风险因素。
对宾夕法尼亚大学2012年至2013年期间接受乳腺钼靶筛查、看初级保健医生并拥有确认用药清单的女性的电子病历进行评估。在调整年龄、体重指数(BMI)和种族后,进行逻辑回归以检验临床记录的MD与阿司匹林使用之间的关联。
我们确定了26000名符合条件的女性。平均年龄为57.3岁,平均BMI为28.9kg/m,41%为非裔美国人,19.7%报告目前正在使用阿司匹林。使用阿司匹林的人年龄明显更大,BMI更高。阿司匹林使用与MD之间存在独立的负相关(P<0.001)。与具有散在纤维腺密度的女性相比,乳腺极度致密的女性使用阿司匹林的可能性较小(OR 0.73;95%CI 0.57-0.93)。这种关联在年轻女性(P=0.0002)和非裔美国人中更强(P=0.011)。乳腺致密的可能性随着阿司匹林剂量的增加而降低(P=0.007),表明存在剂量反应。
我们在一个大型、多样化的筛查队列中证明了阿司匹林使用与较低的MD之间存在独立关联。这种关联在年轻女性和非裔美国女性中更强,这两组女性患雌激素受体阴性乳腺癌的风险更高。这些结果有助于说明研究阿司匹林预防乳腺癌的重要性。