Tamimi Rulla M, Cox David, Kraft Peter, Colditz Graham A, Hankinson Susan E, Hunter David J
Channing Laboratory, Department of Medicine, Brigham and Women's Hospital and Harvard Medical School, 181 Longwood Avenue, Boston, MA, 02115, USA.
Breast Cancer Res. 2008;10(4):R66. doi: 10.1186/bcr2127. Epub 2008 Aug 5.
Recently, the Breast Cancer Association Consortium (BCAC) conducted a multi-stage genome-wide association study and identified 11 single nucleotide polymorphisms (SNPs) associated with breast cancer risk. Given the high degree of heritability of mammographic density and its strong association with breast cancer, it was hypothesised that breast cancer susceptibility loci may also be associated with breast density and provide insight into the biology of breast density and how it influences breast cancer risk.
We conducted an analysis in the Nurses' Health Study (n = 1121) to assess the relation between 11 breast cancer susceptibility loci and mammographic density. At the time of their mammogram, 217 women were premenopausal and 904 women were postmenopausal. We used generalised linear models adjusted for covariates to determine the mean percentage of breast density according to genotype.
Overall, no association between the 11 breast cancer susceptibility loci and mammographic density was seen. Among the premenopausal women, three SNPs (rs12443621 [TNRc9/LOC643714], rs3817198 [lymphocyte-specific protein-1] and rs4666451) were marginally associated with mammographic density (p < 0.10). All three of these SNPs showed an association that was consistent with the direction in which these alleles influence breast cancer risk. The difference in mean percentage mammographic density comparing homozygous wildtypes to homozygous variants ranged from 6.3 to 8.0%. None of the 11 breast cancer loci were associated with postmenopausal breast density.
Overall, breast cancer susceptibility loci identified through a genome-wide association study do not appear to be associated with breast cancer risk.
最近,乳腺癌协会联盟(BCAC)开展了一项多阶段全基因组关联研究,并鉴定出11个与乳腺癌风险相关的单核苷酸多态性(SNP)。鉴于乳腺X线密度的高度遗传性及其与乳腺癌的强关联,研究假设乳腺癌易感基因座可能也与乳腺密度相关,并有助于深入了解乳腺密度的生物学特性及其影响乳腺癌风险的机制。
我们在护士健康研究(n = 1121)中进行了一项分析,以评估11个乳腺癌易感基因座与乳腺X线密度之间的关系。在进行乳腺X线检查时,217名女性处于绝经前,904名女性处于绝经后。我们使用针对协变量进行调整的广义线性模型,根据基因型确定乳腺密度的平均百分比。
总体而言,未发现11个乳腺癌易感基因座与乳腺X线密度之间存在关联。在绝经前女性中,3个SNP(rs12443621 [TNRc9/LOC643714]、rs3817198 [淋巴细胞特异性蛋白-1]和rs4666451)与乳腺X线密度存在边缘关联(p < 0.10)。所有这3个SNP显示的关联与这些等位基因影响乳腺癌风险的方向一致。纯合野生型与纯合变异型相比,乳腺X线密度平均百分比的差异在6.3%至8.0%之间。11个乳腺癌基因座均与绝经后乳腺密度无关。
总体而言,通过全基因组关联研究鉴定出的乳腺癌易感基因座似乎与乳腺癌风险无关。