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乳腺钼靶密度家族聚集性的遗传模型。

Genetic models for the familial aggregation of mammographic breast density.

作者信息

Kataoka Masako, Antoniou Antonis, Warren Ruth, Leyland Jean, Brown Judith, Audley Tina, Easton Doug

机构信息

Department of Radiology, University of Cambridge, Cambridge, UK.

出版信息

Cancer Epidemiol Biomarkers Prev. 2009 Apr;18(4):1277-84. doi: 10.1158/1055-9965.EPI-08-0568. Epub 2009 Mar 31.

DOI:10.1158/1055-9965.EPI-08-0568
PMID:19336563
Abstract

BACKGROUND

Mammographic breast density (MBD) has a strong genetic component. Investigating the genetic models for mammographic density may provide further insights into the genetic factors affecting breast cancer risk.

PURPOSE

To evaluate the familial aggregation of MBD and investigate the genetic models of susceptibility.

METHODS

We used data on 746 women from 305 families participating in the Sisters in Breast Screening study. Retrieved mammograms were digitized, and percent mammographic density was determined using the Cumulus software. Linear regression analysis was done to identify the factors that are associated with mammographic density and a multivariate regression model was constructed. Familial correlations between relative pairs were calculated using the residuals from these models. Genetic models of susceptibility were investigated using segregation analysis.

RESULTS

After adjusting for covariates, the intraclass correlation coefficient among the residuals was 0.26 (95% confidence interval, 0.16-0.36) in sister-sister pairs and 0.67 (0.27-1.00) among the monozygotic twin pairs. The most parsimonious model was a Mendelian single major gene model in which an allele with population frequency 0.39 (95% confidence interval, 0.33-0.46) influenced mammographic density in an additive fashion. This model explained 66% of the residual variance.

CONCLUSION

These results confirm that MBD has a strong heritable basis, and suggest that major genes may explain some of the familial aggregation. These results may have implications for the search of genes that control mammographic density.

摘要

背景

乳腺钼靶密度(MBD)具有很强的遗传成分。研究乳腺钼靶密度的遗传模式可能会为影响乳腺癌风险的遗传因素提供进一步的见解。

目的

评估MBD的家族聚集性并研究易感性的遗传模式。

方法

我们使用了参与乳腺筛查姐妹研究的305个家庭中746名女性的数据。检索到的乳房X光照片被数字化,并使用Cumulus软件确定乳腺钼靶密度百分比。进行线性回归分析以确定与乳腺钼靶密度相关的因素,并构建多元回归模型。使用这些模型的残差计算相对对之间的家族相关性。使用分离分析研究易感性的遗传模式。

结果

在调整协变量后,姐妹对中残差的组内相关系数为0.26(95%置信区间,0.16 - 0.36),同卵双胞胎对中为0.67(0.27 - 1.00)。最简约的模型是孟德尔单主基因模型,其中群体频率为0.39(95%置信区间,0.33 - 0.46)的一个等位基因以加性方式影响乳腺钼靶密度。该模型解释了66%的残差方差。

结论

这些结果证实MBD有很强的遗传基础,并表明主基因可能解释部分家族聚集性。这些结果可能对寻找控制乳腺钼靶密度的基因有启示意义。

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