Cohn Barbara A, Cirillo Piera M, Hopper Bill R, Siiteri Pentti K
Child Health and Development Studies, Public Health Institute, Berkeley, California 94709.
J Clin Endocrinol Metab. 2017 Oct 1;102(10):3739-3748. doi: 10.1210/jc.2016-3476.
Full-term pregnancy is associated with a transient increase and life-time decrease in maternal breast cancer risk. Estrone (E1), estradiol (E2), and estriol (E3) are in high concentration during the third trimester. E1 and E2 metabolism produces carcinogenic intermediaries, and E3 metabolism does not.
We tested the hypothesis that higher E3 in pregnancy is protective while higher E1 plus E2 increases risk.
Prospective case-cohort study (n = 620; 204 cases) nested in a 38-year follow-up of 15,528 pregnant women in the Child Health and Development Studies. We measured E1, E2, and E3 in archived third trimester serum and estimated associations with breast cancer.
Northern California Kaiser members receiving obstetric care from 1959 to 1967.
Breast cancer diagnosed through 1997.
Doubling of E1+E2 was associated with greater risk [hazard ratio (HR), 1.7; 95% confidence interval (CI), 1.2 to 2.4]. In contrast, doubling of E3 or the E3/E1+E2 ratio was associated with protection (HR, 0.7; 95% CI, 0.5 to 1.0; HR, 0.6; 95% CI, 0.4 to 0.8, respectively). Associations were stronger for diagnoses within 15 years after delivery compared with 16 to 38 years (Pinteraction = 0.0002) for gravidas >27 years at delivery vs ≤27 (Pinteraction = 0.01) and for primiparas vs multiparas (Pinteraction = 0.02).
Relatively high third trimester E3 levels might protect parous women from breast cancer and E1 and E2 might enhance the risk. If findings are confirmed, third trimester pregnancy estrogens could help explain how parity affects breast cancer.
足月妊娠与母亲患乳腺癌风险的短暂增加及终生降低有关。在妊娠晚期,雌酮(E1)、雌二醇(E2)和雌三醇(E3)浓度较高。E1和E2的代谢会产生致癌中间体,而E3的代谢则不会。
我们检验了这样一种假设,即孕期较高的E3具有保护作用,而较高的E1加E2会增加风险。
前瞻性病例队列研究(n = 620;204例病例),嵌套于对儿童健康与发育研究中15528名孕妇进行的38年随访研究。我们测量了存档的妊娠晚期血清中的E1、E2和E3,并估计了与乳腺癌的关联。
1959年至1967年期间接受产科护理的北加利福尼亚凯撒会员。
截至1997年诊断出的乳腺癌。
E1 + E2翻倍与更高的风险相关[风险比(HR),1.7;95%置信区间(CI),1.2至2.4]。相比之下,E3或E3/E1 + E2比值翻倍与保护作用相关(HR分别为0.7;95%CI,0.5至1.0;HR为0.6;95%CI,0.4至0.8)。与分娩后16至38年相比,分娩后15年内诊断出的关联更强(P交互作用 = 0.0002),分娩时年龄>27岁与≤27岁的孕妇相比(P交互作用 = 0.01),初产妇与经产妇相比(P交互作用 = 0.02)。
妊娠晚期相对较高的E3水平可能会保护经产妇免受乳腺癌侵害,而E1和E2可能会增加风险。如果研究结果得到证实,妊娠晚期的孕期雌激素可能有助于解释产次如何影响乳腺癌。