Powell Mark J, Von Behren Julie, Neuhausen Susan, Reynolds Peggy, Benz Christopher C
Zero Breast Cancer, San Rafael, CA, USA.
Buck Institute for Research on Aging, Novato, CA, USA.
Cancer Causes Control. 2017 Oct;28(10):1027-1032. doi: 10.1007/s10552-017-0942-7. Epub 2017 Aug 18.
Hypertension in pregnancy has been associated with decreased future risk of breast cancer in many but not all studies. In the Marin Women's Study, pregnancy-induced hypertension was shown to interact with the T allele of a functional IGF1R gene variant, rs2016347, to result in lower breast density, as well as decreased breast cancer risk. Our objective was to explore these findings in a larger sample of women from the California Teachers Study (CTS).
The CTS cohort consists of over 130,000 female educators. DNA was available from a nested case-control study, which included 2,030 non-Hispanic white women who developed breast cancer and 1,552 controls. The current study included all participants from the case-control group with a self-reported history of preeclampsia (80 cases/57 controls).
Comparing TT to GG genotypes revealed adjusted odds ratios of 0.38 (CI 0.13, 1.14) for all invasive breast cancers, 0.26 (CI 0.07, 0.89) for hormone receptor-positive (HR+) breast cancers, 0.15 (CI 0.04, 0.56) for those with age at first birth (AFB) < 30, and 0.10 (CI 0.02, 0.49) for those with AFB < 30 and HR+ breast cancers. Trend analysis yielded p values of 0.09, 0.03, 0.005, and 0.004 respectively, suggesting a biological effect for each T allele.
Study findings indicate that the T allele of IGF1R variant rs2016347 is associated with a significant reduction in breast cancer risk in women with a history of preeclampsia, most marked for HR+ breast cancer and in women with AFB < 30.
许多但并非所有研究都表明,孕期高血压与未来患乳腺癌风险降低有关。在马林妇女研究中,妊娠高血压被证明与功能性IGF1R基因变体rs2016347的T等位基因相互作用,导致乳房密度降低以及乳腺癌风险降低。我们的目的是在加利福尼亚教师研究(CTS)中更大的女性样本中探索这些发现。
CTS队列由超过130,000名女性教育工作者组成。DNA来自一项巢式病例对照研究,其中包括2,030名患乳腺癌的非西班牙裔白人女性和1,552名对照。本研究纳入了病例对照组中所有有子痫前期自我报告病史的参与者(80例病例/57例对照)。
比较TT与GG基因型,所有浸润性乳腺癌的校正比值比为0.38(95%置信区间0.13, 1.14),激素受体阳性(HR+)乳腺癌为|0.26(95%置信区间0.07, 0.89),首次生育年龄(AFB)<30岁的女性为0.15(95%置信区间0.04, 0,56),AFB<30岁且患HR+乳腺癌的女性为0.10(95%置信区间0.02, 0.49)。趋势分析分别得出p值为0.09、0.03、0.005和0.004,表明每个T等位基因都有生物学效应。
研究结果表明,IGF1R变体rs2016347的T等位基因与有子痫前期病史的女性患乳腺癌风险显著降低有关,在HR+乳腺癌和AFB<30岁的女性中最为明显。