Flote Vidar G, Frydenberg Hanne, Ursin Giske, Iversen Anita, Fagerland Morten W, Ellison Peter T, Wist Erik A, Egeland Thore, Wilsgaard Tom, McTiernan Anne, Furberg Anne-Sofie, Thune Inger
The Cancer Centre, Oslo University Hospital, Oslo, Norway.
Cancer Registry of Norway, Majorstuen, Oslo, Norway.
Cancer Prev Res (Phila). 2015 Jun;8(6):535-44. doi: 10.1158/1940-6207.CAPR-14-0267. Epub 2015 Mar 24.
High-density lipoprotein-cholesterol (HDL-C) may influence the proliferation of breast tumor cells, but it is unclear whether low HDL-C levels, alone or in combination with cyclic estrogen and progesterone, are associated with mammographic density, a strong predictor of breast cancer development. Fasting morning serum concentrations of HDL-C were assessed in 202 premenopausal women, 25 to 35 years of age, participating in the Norwegian Energy Balance and Breast Cancer Aspects (EBBA) I study. Estrogen and progesterone were measured both in serum, and daily in saliva, throughout an entire menstrual cycle. Absolute and percent mammographic density was assessed by a computer-assisted method (Madena), from digitized mammograms (days 7-12). Multivariable models were used to study the associations between HDL-C, estrogen and progesterone, and mammographic density phenotypes. We observed a positive association between HDL-C and percent mammographic density after adjustments (P = 0.030). When combining HDL-C, estradiol, and progesterone, we observed among women with low HDL-C (<1.39 mmol/L), a linear association between salivary 17β-estradiol, progesterone, and percent and absolute mammographic density. Furthermore, in women with low HDL-C, each one SD increase of salivary mid-menstrual 17β-estradiol was associated with an OR of 4.12 (95% confidence intervals; CI, 1.30-13.0) of having above-median percent (28.5%), and an OR of 2.5 (95% CI, 1.13-5.50) of having above-median absolute mammographic density (32.4 cm(2)). On the basis of plausible biologic mechanisms linking HDL-C to breast cancer development, our findings suggest a role of HDL-C, alone or in combination with estrogen, in breast cancer development. However, our small hypothesis generating study requires confirmation in larger studies.
高密度脂蛋白胆固醇(HDL-C)可能影响乳腺肿瘤细胞的增殖,但目前尚不清楚低HDL-C水平单独或与循环雌激素和孕激素联合是否与乳房X线密度有关,乳房X线密度是乳腺癌发生的一个强有力的预测指标。在参与挪威能量平衡与乳腺癌相关因素(EBBA)I研究的202名25至35岁的绝经前女性中,评估了空腹早晨血清HDL-C浓度。在整个月经周期中,同时测定血清以及每日唾液中的雌激素和孕激素。通过计算机辅助方法(Madena),从数字化乳房X线照片(第7 - 12天)评估绝对和百分比乳房X线密度。使用多变量模型研究HDL-C、雌激素和孕激素与乳房X线密度表型之间的关联。调整后,我们观察到HDL-C与百分比乳房X线密度之间存在正相关(P = 0.030)。当将HDL-C、雌二醇和孕激素结合起来时,我们在HDL-C水平低(<1.39 mmol/L)的女性中观察到,唾液中17β-雌二醇、孕激素与百分比和绝对乳房X线密度之间存在线性关联。此外,在HDL-C水平低的女性中,唾液中月经中期17β-雌二醇每增加一个标准差,百分比高于中位数(28.5%)的优势比为4.12(95%置信区间;CI,1.30 - 13.0),绝对乳房X线密度高于中位数(32.4 cm²)的优势比为2.5(95% CI,1.13 - 5.50)。基于将HDL-C与乳腺癌发生联系起来的合理生物学机制,我们的研究结果表明HDL-C单独或与雌激素联合在乳腺癌发生中起作用。然而,我们这项小型的探索性研究需要在更大规模的研究中得到证实。