Li Shuai, Nguyen Tuong L, Nguyen-Dumont Tu, Dowty James G, Dite Gillian S, Ye Zhoufeng, Trinh Ho N, Evans Christopher F, Tan Maxine, Sung Joohon, Jenkins Mark A, Giles Graham G, Hopper John L, Southey Melissa C
Centre for Epidemiology and Biostatistics, Melbourne School of Population and Global Health, The University of Melbourne, Parkville, VIC 3051, Australia.
Centre for Cancer Genetic Epidemiology, Department of Public Health and Primary Care, University of Cambridge, Cambridge CB1 8RN, UK.
Cancers (Basel). 2022 Jun 2;14(11):2767. doi: 10.3390/cancers14112767.
Cumulus, Altocumulus, and Cirrocumulus are measures of mammographic density defined at increasing pixel brightness thresholds, which, when converted to mammogram risk scores (MRSs), predict breast cancer risk. Twin and family studies suggest substantial variance in the MRSs could be explained by genetic factors. For 2559 women aged 30 to 80 years (mean 54 years), we measured the MRSs from digitized film mammograms and estimated the associations of the MRSs with a 313-SNP breast cancer polygenic risk score (PRS) and 202 individual SNPs associated with breast cancer risk. The PRS was weakly positively correlated (correlation coefficients ranged 0.05−0.08; all p < 0.04) with all the MRSs except the Cumulus-white MRS based on the “white but not bright area” (correlation coefficient = 0.04; p = 0.06). After adjusting for its association with the Altocumulus MRS, the PRS was not associated with the Cumulus MRS. There were MRS associations (Bonferroni-adjusted p < 0.04) with one SNP in the ATXN1 gene and nominally with some ESR1 SNPs. Less than 1% of the variance of the MRSs is explained by the genetic markers currently known to be associated with breast cancer risk. Discovering the genetic determinants of the bright, not white, regions of the mammogram could reveal substantial new genetic causes of breast cancer.
积云状、高积云状和卷积云状是在不断增加的像素亮度阈值下定义的乳腺钼靶密度测量指标,将其转换为乳腺钼靶风险评分(MRS)后可预测乳腺癌风险。双胞胎和家族研究表明,MRS的显著差异可能由遗传因素解释。对于2559名年龄在30至80岁(平均54岁)的女性,我们从数字化乳腺钼靶片中测量了MRS,并估计了MRS与313个单核苷酸多态性(SNP)的乳腺癌多基因风险评分(PRS)以及与乳腺癌风险相关的202个个体SNP之间的关联。PRS与除基于“白色但不明亮区域”的积云状白色MRS之外的所有MRS呈弱正相关(相关系数范围为0.05 - 0.08;所有p < 0.04)(相关系数 = 0.04;p = 0.06)。在调整其与高积云状MRS的关联后,PRS与积云状MRS无关联。MRS与ATXN1基因中的一个SNP存在关联(经Bonferroni校正p < 0.04),与一些ESR1 SNP名义上存在关联。目前已知与乳腺癌风险相关的遗传标记仅解释了不到1%的MRS变异。发现乳腺钼靶片中明亮而非白色区域的遗传决定因素可能会揭示大量新的乳腺癌遗传病因。