Department of Clinical and Experimental Medicine, University of Pisa, Pisa, Italy.
Laboratoire MAP 5 (UMR CNRS 8145), Université de Paris, Paris, France.
Breast Cancer Res. 2021 Apr 17;23(1):47. doi: 10.1186/s13058-021-01425-8.
Menopausal hormone therapy (MHT) is a risk factor for breast cancer (BC). Evidence suggests that its effect on BC risk could be partly mediated by mammographic density. The aim of this study was to investigate the relationship between MHT, mammographic density and BC risk using data from a prospective study.
We used data from a case-control study nested within the French cohort E3N including 453 cases and 453 matched controls. Measures of mammographic density, history of MHT use during follow-up and information on potential confounders were available for all women. The association between MHT and mammographic density was evaluated by linear regression models. We applied mediation modelling techniques to estimate, under the hypothesis of a causal model, the proportion of the effect of MHT on BC risk mediated by percent mammographic density (PMD) for BC overall and by hormone receptor status.
Among MHT users, 4.2% used exclusively oestrogen alone compared with 68.3% who used exclusively oestrogens plus progestogens. Mammographic density was higher in current users (for a 60-year-old woman, mean PMD 33%; 95% CI 31 to 35%) than in past (29%; 27 to 31%) and never users (24%; 22 to 26%). No statistically significant association was observed between duration of MHT and mammographic density. In past MHT users, mammographic density was negatively associated with time since last use; values similar to those of never users were observed in women who had stopped MHT at least 8 years earlier. The odds ratio of BC for current versus never MHT users, adjusted for age, year of birth, menopausal status at baseline and BMI, was 1.67 (95% CI, 1.04 to 2.68). The proportion of effect mediated by PMD was 34% for any BC and became 48% when the correlation between BMI and PMD was accounted for. These effects were limited to hormone receptor-positive BC.
Our results suggest that, under a causal model, nearly half of the effect of MHT on hormone receptor-positive BC risk is mediated by mammographic density, which appears to be modified by MHT for up to 8 years after MHT termination.
绝经激素治疗(MHT)是乳腺癌(BC)的一个风险因素。有证据表明,其对 BC 风险的影响可能部分通过乳腺 X 线摄影密度来介导。本研究旨在使用前瞻性研究的数据来探讨 MHT、乳腺 X 线摄影密度和 BC 风险之间的关系。
我们使用了法国队列 E3N 中的病例对照研究嵌套的数据,其中包括 453 例病例和 453 例匹配对照。所有女性均有乳腺 X 线摄影密度、随访期间 MHT 使用史以及潜在混杂因素的信息。通过线性回归模型评估 MHT 与乳腺 X 线摄影密度之间的关系。我们应用中介模型技术,根据因果模型的假设,估计 MHT 对整体 BC 风险的影响中,通过 PMD (BC 激素受体状态的比例)介导的比例。
在 MHT 使用者中,仅使用雌激素的比例为 4.2%,而仅使用雌激素加孕激素的比例为 68.3%。当前使用者的乳腺 X 线摄影密度更高(对于 60 岁的女性,平均 PMD 为 33%;95%CI 为 31%至 35%),而非过去(29%;27%至 31%)和从不使用的女性(24%;22%至 26%)。MHT 使用时间与乳腺 X 线摄影密度之间未观察到统计学显著关联。在过去的 MHT 使用者中,乳腺 X 线摄影密度与末次使用后时间呈负相关;在至少 8 年前停止 MHT 的女性中,观察到与从不使用的女性相似的数值。当前 MHT 使用者与从不使用的 BC 患者相比,BC 的比值比(OR)为 1.67(95%CI,1.04 至 2.68)。PMD 介导的效应比例为任何 BC 的 34%,当考虑 BMI 和 PMD 之间的相关性时,该比例增加到 48%。这些影响仅限于激素受体阳性 BC。
根据因果模型,MHT 对激素受体阳性 BC 风险的影响近一半是由乳腺 X 线摄影密度介导的,这似乎在 MHT 终止后长达 8 年受到 MHT 的影响。