Davis School of Gerontology, University of Southern California, Los Angeles, CA 90089, USA.
Neurobiol Aging. 2011 Apr;32(4):604-13. doi: 10.1016/j.neurobiolaging.2009.04.008. Epub 2009 May 9.
We examined the relationships between normal aging, Alzheimer's disease (AD), and brain levels of sex steroid hormones in men and women. In postmortem brain tissue from neuropathologically normal, postmenopausal women, we found no age-related changes in brain levels of either androgens or estrogens. In comparing women with and without AD at different ages, brain levels of estrogens and androgens were lower in AD cases aged 80 years and older but not significantly different in the 60-79 year age range. In male brains, we observed that normal aging was associated with significant decreases in androgens but not estrogens. Further, in men aged 60-79 years, brain levels of testosterone but not estrogens were lower in cases with mild neuropathological changes as well as those with advanced AD neuropathology. In male cases over age 80, brain levels hormones did not significantly vary by neuropathological status. To begin investigating the relationships between hormone levels and indices of AD neuropathology, we measured brain levels of soluble β-amyloid (Aβ). In male cases with mild neuropathological changes, we found an inverse relationship between brain levels of testosterone and soluble Aβ. Collectively, these findings demonstrate sex-specific relationships between normal, age-related depletion of androgens and estrogens in men and women, which may be relevant to development of AD.
我们研究了正常衰老、阿尔茨海默病(AD)以及男性和女性大脑中性类固醇激素水平之间的关系。在绝经后女性的神经病理学正常的脑组织中,我们没有发现大脑中雄激素或雌激素水平与年龄相关的变化。在比较不同年龄患有和不患有 AD 的女性时,80 岁及以上 AD 患者的雌激素和雄激素水平较低,但在 60-79 岁年龄范围内没有显著差异。在男性大脑中,我们观察到正常衰老与雄激素水平显著下降有关,但雌激素水平没有显著下降。此外,在 60-79 岁的男性中,患有轻度神经病理学变化以及患有晚期 AD 神经病理学变化的患者的睾丸激素水平(而非雌激素水平)较低。在 80 岁以上的男性病例中,激素水平与神经病理学状态无关。为了开始研究激素水平与 AD 神经病理学指标之间的关系,我们测量了大脑中可溶性β-淀粉样蛋白(Aβ)的水平。在轻度神经病理学变化的男性病例中,我们发现大脑中睾丸激素水平与可溶性 Aβ之间存在反比关系。综上所述,这些发现表明,男性和女性大脑中性激素水平的正常、与年龄相关的雄激素和雌激素的消耗与 AD 的发展具有性别特异性关系。