Harvey Jennifer A, Santen Richard J, Petroni Gina R, Bovbjerg Viktor E, Smolkin Mark E, Sheriff Fathima S, Russo Jose
Department of Radiology, University of Virginia, Charlottesville, VA 22908, USA.
Menopause. 2008 Jan-Feb;15(1):67-73. doi: 10.1097/gme.0b013e318054e29a.
This retrospective study systematically compared mammographic density with histology in women receiving or not receiving menopausal hormone therapy (HT).
This study was approved by the institutional review board. Twenty-eight postmenopausal women using HT were matched with 28 postmenopausal women not using HT at the time of breast cancer diagnosis. Noncancerous tissue from mastectomy specimens was examined histologically to quantitate the content of fibrous stroma, ducts, and lobule types 1, 2, and 3. Tissue samples were also evaluated for estrogen receptor, progesterone receptor, and Ki67 activity in the ducts and lobules. Breast density was quantified by digitizing the contralateral mammogram and computer-assisted interactive thresholding.
High breast density in women using HT was correlated with greater fibrous stroma (P = 0.020) and lobule type 1 (P = 0.016). Breast density also correlated with Ki67 activity in the ducts (P = 0.031) and lobules (P= 0.023) for both groups combined. Estrogen and progesterone receptors did not correlate with either breast density or HT use.
Increased fibrous stroma and lobule type 1 are associated with increasing mammographic density in women using HT, independent of estrogen and progesterone receptor up-regulation. These findings suggest that increased breast density may be mediated through a paracrine effect. The increase in breast cancer risk with HT use may be due to an increase in target lobule type 1 cells.
这项回顾性研究系统地比较了接受或未接受绝经激素治疗(HT)的女性的乳房X线密度与组织学情况。
本研究经机构审查委员会批准。28名使用HT的绝经后女性与28名在乳腺癌诊断时未使用HT的绝经后女性进行匹配。对乳房切除标本中的非癌组织进行组织学检查,以定量纤维基质、导管以及1型、2型和3型小叶的含量。还对导管和小叶中的雌激素受体、孕激素受体和Ki67活性进行了组织样本评估。通过对侧乳房X线照片数字化和计算机辅助交互式阈值化来量化乳房密度。
使用HT的女性乳房密度高与纤维基质增加(P = 0.020)和1型小叶增加(P = 0.016)相关。两组综合来看,乳房密度还与导管(P = 0.031)和小叶(P = 0.023)中的Ki67活性相关。雌激素和孕激素受体与乳房密度或HT使用均无关联。
在使用HT的女性中,纤维基质增加和1型小叶增加与乳房X线密度增加相关,与雌激素和孕激素受体上调无关。这些发现表明,乳房密度增加可能通过旁分泌效应介导。使用HT导致乳腺癌风险增加可能是由于1型目标小叶细胞增加。