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家族史、乳腺密度与乳腺癌风险。

Family history, mammographic density, and risk of breast cancer.

机构信息

Campbell Family Institute for Breast Cancer Research, Ontario Cancer Institute, Toronto, Ontario, Canada.

出版信息

Cancer Epidemiol Biomarkers Prev. 2010 Feb;19(2):456-63. doi: 10.1158/1055-9965.EPI-09-0881.

DOI:10.1158/1055-9965.EPI-09-0881
PMID:20142244
Abstract

PURPOSE

Mammographic density is a strong and highly heritable risk factor for breast cancer. The purpose of this study was to examine the extent to which mammographic density explains the association of family history of breast cancer with risk of the disease.

SUBJECTS AND METHODS

We carried out three nested case-control studies in screening programs that included in total 2,322 subjects (1,164 cases and 1,158 controls). We estimated the independent and combined associations of family history and percent mammographic density at baseline with subsequent breast cancer risk.

RESULTS

After adjustment for age and other risk factors, compared with women with no affected first-degree relatives, percent mammographic density was 3.1% greater for women with one affected first-degree relative, and 7.0% greater for women with two or more affected relatives (P = 0.001 for linear trend across family history categories). The odds ratios for breast cancer risk were 1.37 [95% confidence interval (95% CI), 1.10-1.72] for having one affected relative, and 2.45 (95% CI, 1.30-4.62) for having two or more affected relatives (P for trend = 0.0002). Adjustment for percent mammographic density reduced these odds ratios by 16% and 14%, respectively. Percent mammographic density explained 14% (95% CI, 4-39%) of the association of family history (at least one affected first-degree relative) with breast cancer risk.

CONCLUSIONS

Percent mammographic density has features of an intermediate marker for breast cancer, and some of the genes that explain variation in percent mammographic density might be associated with familial risk of breast cancer.

摘要

目的

乳腺密度是乳腺癌的一个强烈且高度可遗传的危险因素。本研究旨在探讨乳腺密度在多大程度上解释了家族乳腺癌史与疾病风险之间的关联。

对象和方法

我们在包括 2322 名受试者(1164 例病例和 1158 例对照)的筛查项目中进行了三项嵌套病例对照研究。我们估计了家族史和基线时乳腺密度百分比与随后乳腺癌风险的独立和联合关联。

结果

在调整年龄和其他危险因素后,与无一级亲属受影响的女性相比,有一级亲属受影响的女性乳腺密度增加 3.1%,有两个或更多受影响亲属的女性乳腺密度增加 7.0%(家族史类别中线性趋势的 P=0.001)。乳腺癌风险的比值比(OR)分别为有一个受影响亲属的 1.37(95%置信区间(95%CI),1.10-1.72),有两个或更多受影响亲属的 2.45(95%CI,1.30-4.62)(趋势 P=0.0002)。调整乳腺密度百分比后,这些比值比分别降低了 16%和 14%。乳腺密度百分比解释了家族史(至少有一个一级亲属受影响)与乳腺癌风险之间关联的 14%(95%CI,4-39%)。

结论

乳腺密度百分比具有乳腺癌中间标志物的特征,解释乳腺密度百分比变化的一些基因可能与乳腺癌的家族风险相关。

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