Xue Fei, Michels Karin B
Obstetrics and Gynecology Epidemiology Center, Department of Obstetrics, Gynecology and Reproductive Biology, Brigham and Women's Hospital, Harvard Medical School, and Department of Epidemiology, Harvard School of Public Health, Boston, MA, USA.
Obstetrics and Gynecology Epidemiology Center, Department of Obstetrics, Gynecology and Reproductive Biology, Brigham and Women's Hospital, Harvard Medical School, and Department of Epidemiology, Harvard School of Public Health, Boston, MA, USA.
Lancet Oncol. 2007 Dec;8(12):1088-1100. doi: 10.1016/S1470-2045(07)70377-7.
Emerging evidence suggests an association between female prenatal experience and her subsequent risk of developing breast cancer. Potential underlying mechanisms include variation in amounts of maternal endogenous sex hormones and growth hormones, germ-cell mutations, formation of cancer stem-cells, and other genetic or epigenetic events. We reviewed and summarised quantitatively the available data on intrauterine exposures and risk of breast cancer.
We systematically searched for studies that assessed association between perinatal factors and risk of breast cancer. We reviewed separately each of the perinatal factors, including birthweight, birth length, parental age at delivery, gestational age, intrauterine exposure to diethylstilbestrol, twin membership, maternal pre-eclampsia or eclampsia, and other factors.
We identified 57 studies published between Oct 1, 1980, and June 21, 2007. Increased risk of breast cancer was noted with increased birthweight (relative risk [RR] 1.15 [95% CI 1.09-1.21]), birth length (1.28 [1.11-1.48]), higher maternal age (1.13 [1.02-1.25]), and paternal age (1.12 [1.05-1.19]). Decreased risk of breast cancer was noted for maternal pre-eclampsia and eclampsia (0.48 [0.30-0.78]) and twin membership (0.93 [0.87-1.00]). No association was noted between risk of breast cancer and gestational age at birth (0.95 [0.71-1.26]) or maternal diethylstilbestrol treatment (1.40 [0.86-2.28]).
The intrauterine environment contributes to the predisposition of women to breast cancer in adulthood. The in-utero mechanisms responsible for such predisposition need to be elucidated.
新出现的证据表明,女性产前经历与其随后患乳腺癌的风险之间存在关联。潜在的潜在机制包括母体内源性激素和生长激素量的变化、生殖细胞突变、癌症干细胞的形成以及其他遗传或表观遗传事件。我们对宫内暴露与乳腺癌风险的现有数据进行了综述和定量总结。
我们系统地搜索了评估围产期因素与乳腺癌风险之间关联的研究。我们分别审查了每个围产期因素,包括出生体重、出生身长、父母分娩年龄、孕周、宫内暴露于己烯雌酚、双胞胎身份、母亲先兆子痫或子痫以及其他因素。
我们确定了1980年10月1日至2007年6月21日期间发表的57项研究。出生体重增加(相对风险[RR]1.15[95%CI 1.09 - 1.21])、出生身长增加(1.28[1.11 - 1.48])、母亲年龄较大(1.13[1.02 - 1.25])和父亲年龄较大(1.12[1.05 - 1.19])时,乳腺癌风险增加。母亲先兆子痫和子痫(0.48[0.30 - 0.78])以及双胞胎身份(0.93[0.87 - 1.00])时,乳腺癌风险降低。未发现乳腺癌风险与出生时的孕周(0.95[0.71 - 1.26])或母亲己烯雌酚治疗(1.40[0.86 - 2.28])之间存在关联。
子宫内环境导致女性成年后患乳腺癌的易感性。需要阐明导致这种易感性的宫内机制。