Léon Bérard Cancer Center, UNICANCER, Lyon, France.
Cancer Research Centre of Lyon, French Institute of Health and Medical Research (INSERM) 1052, French National Centre for Scientific Research (CNRS) 5286, Lyon, France.
Am J Clin Nutr. 2019 Mar 1;109(3):597-605. doi: 10.1093/ajcn/nqy313.
Soy-based dietary supplements have been promoted as natural alternatives to menopausal hormone therapy, but their potential effect on breast cancer development is controversial.
We examined the relation between the consumption of soy supplements and the risk of breast cancer, overall and by tumor hormone receptor status, among women aged >50 y.
In total, 76,442 women from the Etude Epidemiologique aupres de Femmes de la Mutuelle Generale de l'Education Nationale (E3N) cohort, born between 1925 and 1950, were followed from 2000 to 2011 (11.2 y on average, starting at a mean age of 59.5 y; 3608 incident breast cancers), with soy supplement use assessed every 2-3 y. HRs of breast cancer were estimated with the use of multivariable Cox models.
Compared with never using soy supplements, the HRs associated with current use of soy supplements were 0.92 (95% CI: 0.76, 1.11) for all, 0.78 (95% CI: 0.60, 0.99) for estrogen receptor (ER)-positive, and 2.01 (95% CI: 1.41, 2.86) for ER-negative breast cancers. There was no association between past use of soy supplements and breast cancer. HRs for current use were 1.36 (95% CI: 0.95, 1.93) and 0.82 (95% CI: 0.65, 1.02) among women with and without a family history of breast cancer, respectively (P-interaction = 0.03) and 1.06 (95% CI: 0.87, 1.30) ≥5 y after menopause compared with 0.50 (95% CI: 0.31, 0.81) in premenopause or ≤5 y postmenopause (P-interaction = 0.04).
In this cohort of women aged >50 y, we report opposing associations of soy supplements with ER-positive and ER-negative breast cancer risk. Our results also caution against the use of these supplements in women with a family history of breast cancer. Whether the risk profile of soy supplements could be more favorable among premenopausal or recently postmenopausal women deserves further investigation.
大豆膳食补充剂已被宣传为更年期激素替代疗法的天然替代品,但它们对乳腺癌发展的潜在影响仍存在争议。
我们研究了大豆补充剂的摄入与 50 岁以上女性乳腺癌风险之间的关系,整体及按肿瘤激素受体状态进行分层。
共有 76442 名女性参与了女性教育全国互助会队列(E3N)研究,她们出生于 1925 年至 1950 年之间,随访时间从 2000 年至 2011 年(平均 11.2 年,起始年龄平均为 59.5 岁;共发生 3608 例乳腺癌),每隔 2-3 年评估一次大豆补充剂的使用情况。使用多变量 Cox 模型估计乳腺癌的 HR。
与从不使用大豆补充剂相比,当前使用大豆补充剂与所有乳腺癌(HR:0.92,95%CI:0.76,1.11)、雌激素受体(ER)阳性乳腺癌(HR:0.78,95%CI:0.60,0.99)和 ER 阴性乳腺癌(HR:2.01,95%CI:1.41,2.86)的风险相关。过去使用大豆补充剂与乳腺癌之间无关联。有乳腺癌家族史的女性当前使用大豆补充剂的 HR 为 1.36(95%CI:0.95,1.93),无家族史的女性为 0.82(95%CI:0.65,1.02)(P 交互=0.03);绝经后≥5 年与绝经前或≤5 年(HR:1.06,95%CI:0.87,1.30)相比,绝经后 5 年内(HR:0.50,95%CI:0.31,0.81)(P 交互=0.04)。
在这项 50 岁以上女性队列研究中,我们报告了大豆补充剂与 ER 阳性和 ER 阴性乳腺癌风险之间相反的关联。我们的结果还提示有乳腺癌家族史的女性不应使用这些补充剂。大豆补充剂的风险特征是否在绝经前或近期绝经后女性中更为有利,值得进一步研究。