Genetic Ancestry and Risk of Breast Cancer among US Latinas

被引:100
作者
Fejerman, Laura [1 ,4 ]
John, Esther M. [6 ,7 ,8 ]
Huntsman, Scott [1 ,4 ]
Beckman, Kenny [9 ]
Choudhry, Shweta [2 ,3 ]
Perez-Stable, Eliseo [1 ,4 ,5 ]
Burchard, Esteban Gonzalez [2 ,3 ]
Ziv, Elad [1 ,4 ]
机构
[1] Univ Calif San Francisco, Div Gen Internal Med, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Dept Med, Lung Biol Ctr, San Francisco, CA 94143 USA
[3] Univ Calif San Francisco, Dept Biopharmaceut Sci, San Francisco, CA 94143 USA
[4] Univ Calif San Francisco, Helen Diller Family Comprehens Canc Ctr, San Francisco, CA 94143 USA
[5] Univ Calif San Francisco, Med Effectiveness Res Ctr Diverse Populat, San Francisco, CA 94143 USA
[6] No Calif Canc Ctr, Fremont, CA USA
[7] Stanford Sch Med, Stanford, CA USA
[8] Stanford Canc Ctr, Stanford, CA USA
[9] Childrens Hosp, Res Inst, Oakland, CA 94609 USA
关键词
D O I
10.1158/0008-5472.CAN-08-2039
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
U.S. Latinas have a lower incidence of breast cancer compared with non-Latina White women. This difference is partially explained by differences in the prevalence of known risk factors. Genetic factors may also contribute to this difference in incidence. Latinas are an admixed population with most of their genetic ancestry from Europeans and Indigenous Americans. We used genetic markers to estimate the ancestry of Latina breast cancer cases and controls and assessed the association with genetic ancestry, adjusting for reproductive and other risk factors. We typed a set of 106 ancestry informative markers in 440 Latina women with breast cancer and 597 Latina controls from the San Francisco Bay area and estimated genetic ancestry using a maximum likelihood method. Odds ratios (OR) and 95% confidence intervals (95% CI) for ancestry modeled as a continuous variable were estimated using logistic regression with known risk factors included as covariates. Higher European ancestry was associated with increased breast cancer risk. The OR for a 25% increase in European ancestry was 1.79 (95% CI, 1.28-2.79; P < 0.001). When known risk factors and place of birth were adjusted for, the association with European ancestry was attenuated but remained statistically significant (OR, 1.39; 95% CI, 1.06-2.11; P = 0.013). Further work is needed to determine if the association is due to genetic differences between populations or possibly due to environmental factors not measured. [Cancer Res 2008;68(23):9723-8]
引用
收藏
页码:9723 / 9728
页数:6
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