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旧金山湾区拉丁裔女性的遗传血统与乳腺癌风险因素

Genetic ancestry and risk factors for breast cancer among Latinas in the San Francisco Bay Area.

作者信息

Ziv Elad, John Esther M, Choudhry Shweta, Kho Jennifer, Lorizio Wendy, Perez-Stable Eliseo J, Burchard Esteban Gonzalez

机构信息

Division of General Internal Medicine, University of California San Francisco, Box 1732, San Francisco, CA 94143, USA.

出版信息

Cancer Epidemiol Biomarkers Prev. 2006 Oct;15(10):1878-85. doi: 10.1158/1055-9965.EPI-06-0092.

Abstract

BACKGROUND

Genetic association studies using case-control designs are susceptible to false-positive and false-negative results if there are differences in genetic ancestry between cases and controls. We measured genetic ancestry among Latinas in a population-based case-control study of breast cancer and tested the association between ancestry and known breast cancer risk factors. We reasoned that if genetic ancestry is associated with known breast cancer risk factors, then the results of genetic association studies would be confounded.

METHODS

We used 44 ancestry informative markers to estimate individuals' genetic ancestry in 563 Latina participants. To test whether ancestry is a predictor of hormone therapy use, parity, and body mass index (BMI), we used multivariate logistic regression models to estimate odds ratios (OR) and 95% confidence intervals (95% CI) associated with a 25% increase in Indigenous American ancestry, adjusting for age, education, and the participant's and grandparents' place of birth.

RESULTS

Hormone therapy use was significantly less common among women with higher Indigenous American ancestry (OR, 0.78; 95% CI, 0.63-0.96). Higher Indigenous American ancestry was also significantly associated with overweight (BMI, 25-29.9 versus <25) and obesity (BMI, > or =30 versus <25), but only among foreign-born Latina women (OR, 3.44; 95% CI, 1.97-5.99 and OR, 1.95; 95% CI, 1.24-3.06, respectively).

CONCLUSION

Some breast cancer risk factors are associated with genetic ancestry among Latinas in the San Francisco Bay Area. Therefore, case-control genetic association studies for breast cancer should directly measure genetic ancestry to avoid potential confounding.

摘要

背景

如果病例组和对照组之间存在遗传血统差异,那么采用病例对照设计的基因关联研究容易出现假阳性和假阴性结果。在一项基于人群的乳腺癌病例对照研究中,我们测量了拉丁裔女性的遗传血统,并测试了血统与已知乳腺癌风险因素之间的关联。我们推断,如果遗传血统与已知的乳腺癌风险因素相关,那么基因关联研究的结果将会受到混淆。

方法

我们使用44个血统信息标记来估计563名拉丁裔参与者的个体遗传血统。为了测试血统是否是激素治疗使用情况、生育次数和体重指数(BMI)的预测因素,我们使用多变量逻辑回归模型来估计与美洲原住民血统增加25%相关的优势比(OR)和95%置信区间(95%CI),并对年龄、教育程度以及参与者及其祖父母的出生地进行了调整。

结果

在美洲原住民血统较高的女性中,激素治疗的使用明显较少见(OR,0.78;95%CI,0.63 - 0.96)。较高的美洲原住民血统也与超重(BMI为25 - 29.9与<25相比)和肥胖(BMI≥30与<25相比)显著相关,但仅在外国出生的拉丁裔女性中如此(OR分别为3.44;95%CI,1.97 - 5.99和OR,1.95;95%CI,1.24 - 3.06)。

结论

在旧金山湾区的拉丁裔中,一些乳腺癌风险因素与遗传血统相关。因此,乳腺癌的病例对照基因关联研究应直接测量遗传血统以避免潜在的混淆。

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