National Institute of Environmental Health Sciences, POB 12233, Research Triangle, NC, USA.
Int J Epidemiol. 2021 Mar 3;50(1):97-104. doi: 10.1093/ije/dyaa201.
Familial clustering of age at onset would have implications for both personalized screening and aetiology, but has not been studied for breast cancer.
We prospectively studied a cohort of 23 145 sisters to explore whether their breast cancer risk changed near the age at diagnosis of a previously affected older sister. Using an age-time-dependent variable in a Cox regression model, we estimated hazard ratios for breast cancer when participants were near their sister's diagnosis age, relative to similarly aged women whose sister was diagnosed at a very different age. To rule out a correlation driven by young-onset familial cancer, we separately investigated women who had enrolled at age 50 or older.
Of the 23 145 women, 1412 developed breast cancer during follow-up (median 9.5 years). The estimated hazard ratio was 1.80 (95% confidence interval: 1.18, 2.74) at their sister's age at diagnosis, suggesting a substantial increase in risk compared with women of the same age but whose sister was diagnosed at a very different age. Restriction to women who enrolled at or after age 50 produced similar results.
This familial clustering suggests that there may be important genetic and/or early environmental risk factors that influence the timing of breast cancer, even when onset is late in life. Personalized screening might need to account for the age at which a sister was earlier diagnosed with breast cancer.
发病年龄的家族聚集性对个性化筛查和病因都有影响,但尚未对乳腺癌进行研究。
我们前瞻性地研究了一个由 23145 对姐妹组成的队列,以探讨她们的乳腺癌风险是否会在以前受影响的姐姐发病年龄附近发生变化。在 Cox 回归模型中使用年龄-时间相关变量,我们估计了参与者在接近姐姐诊断年龄时发生乳腺癌的风险比,与姐姐诊断年龄相差很大的同龄女性相比。为了排除由早发性家族性癌症引起的相关性,我们分别调查了在 50 岁或以上入组的女性。
在 23145 名女性中,1412 人在随访期间患上乳腺癌(中位随访时间为 9.5 年)。与年龄相同但姐姐诊断年龄相差很大的女性相比,其姐姐诊断时的估计风险比为 1.80(95%置信区间:1.18,2.74),表明风险显著增加。限制在 50 岁或以上入组的女性中也得到了类似的结果。
这种家族聚集性表明,即使发病年龄较晚,也可能存在影响乳腺癌发生时间的重要遗传和/或早期环境风险因素。个性化筛查可能需要考虑姐姐更早诊断为乳腺癌的年龄。