Wu Xueyao, Jiang Shu, Ge Aaron, Turman Constance, Colditz Graham, Tamimi Rulla M, Kraft Peter
Division of Cancer Epidemiology and Genetics, National Cancer Institute, Rockville, Maryland, USA.
Washington University School of Medicine in St. Louis, St. Louis, Missouri, USA.
medRxiv. 2025 Feb 20:2025.02.18.25322419. doi: 10.1101/2025.02.18.25322419.
The mammogram risk score (MRS), an AI-driven texture feature derived from digital mammograms, strongly predicts breast cancer risk independently of breast density, though underlying mechanisms remain unclear. This study investigated relationships between established breast cancer risk factors, covering anthropometrics, reproductive factors, family history, and mammographic density metrics, and MRS.
Using data from the Nurses' Health Study II (292 cases, 561 controls), we validated MRS's association with breast cancer using logistic regression and evaluated its relationships with risk factors through: linear regressions of MRS on observed risk factors and polygenic scores associated with risk factors, and Mendelian randomization (MR) analysis via two-stage least squares regression. We conducted two-sample MR of MRS using summary statistics from genome-wide association studies of risk factors.
MRS was significantly associated with breast cancer risk before adjustment for BI-RADS density (OR=1.92 per SD increase in MRS; 95%CI:1.57-2.33; AUC=0.69) and after (OR=1.85; 95%CI:1.49-2.30). Early life body size and adult body mass index (BMI) were inversely associated with MRS, while history of benign breast disease and BI-RADS density showed positive associations; after adjusting for BI-RADS density, associations between MRS and the other three risk factors attenuated. Higher polygenic score for dense area was associated with increased MRS (β=0.16 SD increase in MRS per SD increase in polygenic score; 95%CI: 0.06-0.25), as was percent density (β=0.14; 95%CI:0.05-0.23). Two-sample MR identified associations between genetically predicted dense area (β=0.83 SD increase in MRS per SD increase in dense area; 95%CI:0.39-1.27) and percent density (β=1.14; 95%CI:0.55-1.74) with MRS. After adjusting for BI-RADS density and BMI, higher waist-to-hip ratio was significantly associated with increased MRS in polygenic score and two-sample MR analyses. No significant associations were observed with other risk factors.
We validated MRS's association with breast cancer risk in cases diagnosed 0.5-10.1 years (median 2.6) after mammogram acquisition. Our findings reveal robust associations between breast density measures and MRS and suggest a potential impact of central obesity on MRS. Future larger-scale studies are crucial to validate these results and explore their potential to enhance our understanding of breast cancer etiology and refine risk prediction models.
乳房X线摄影风险评分(MRS)是一种从数字乳房X线摄影中提取的人工智能驱动的纹理特征,它能独立于乳房密度强烈预测乳腺癌风险,但其潜在机制尚不清楚。本研究调查了既定的乳腺癌风险因素(包括人体测量学、生殖因素、家族史和乳房X线摄影密度指标)与MRS之间的关系。
利用护士健康研究II的数据(292例病例,561例对照),我们通过逻辑回归验证了MRS与乳腺癌的关联,并通过以下方式评估其与风险因素的关系:对观察到的风险因素和与风险因素相关的多基因评分进行MRS的线性回归,以及通过两阶段最小二乘回归进行孟德尔随机化(MR)分析。我们使用风险因素全基因组关联研究的汇总统计数据对MRS进行两样本MR分析。
在调整BI-RADS密度之前(MRS每增加1个标准差,OR = 1.92;95%CI:1.57 - 2.33;AUC = 0.69)和之后(OR = 1.85;95%CI:1.49 - 2.30),MRS与乳腺癌风险均显著相关。早年体型和成年体重指数(BMI)与MRS呈负相关,而良性乳腺疾病史和BI-RADS密度呈正相关;在调整BI-RADS密度后,MRS与其他三个风险因素之间的关联减弱。致密区域的多基因评分越高,MRS越高(多基因评分每增加1个标准差,MRS增加0.16个标准差;95%CI:0.06 - 0.25),密度百分比也是如此(β = 0.14;95%CI:0.05 - 0.23)。两样本MR分析确定了基因预测的致密区域(致密区域每增加1个标准差,MRS增加0.83个标准差;95%CI:0.39 - 1.27)和密度百分比(β = 1.14;95%CI:0.55 - 1.74)与MRS之间的关联。在调整BI-RADS密度和BMI后,在多基因评分和两样本MR分析中,较高的腰臀比与MRS升高显著相关。未观察到与其他风险因素有显著关联。
我们在乳房X线摄影采集后0.5 - 10.1年(中位数2.6年)诊断的病例中验证了MRS与乳腺癌风险的关联。我们的研究结果揭示了乳房密度测量与MRS之间的紧密关联,并表明中心性肥胖对MRS有潜在影响。未来更大规模的研究对于验证这些结果以及探索其增强我们对乳腺癌病因的理解和完善风险预测模型的潜力至关重要。