Beeri Michal Schnaider, Rapp Michael, Schmeidler James, Reichenberg Abraham, Purohit Dushyant P, Perl Daniel P, Grossman Hillel T, Prohovnik Isak, Haroutunian Vahram, Silverman Jeremy M
The Mount Sinai School of Medicine, Department of Psychiatry, New York, NY 10029, USA.
Neurobiol Aging. 2009 Aug;30(8):1184-91. doi: 10.1016/j.neurobiolaging.2007.11.011. Epub 2008 Jan 10.
To examine the association between number of born children and neuropathology of Alzheimer's disease (AD).
The brains of 86 subjects with data on the number of biological children born, were studied postmortem. Primary analyses included 73 subjects (average age at death=80; 42 women) devoid of cerebrovascular disease associated lesions (i.e., infarcts) or of non-AD related neuropathology. Women were significantly older at death than men (85.6 vs. 73.4; p<.0005) but did not differ significantly from men in number of children or dementia severity. Secondary analyses included 13 additional subjects who had concomitant cerebrovascular disease. Density of neuritic plaques (NPs) and neurofibrillary tangles (NFTs) in the hippocampus, entorhinal cortex, amygdala and multiple regions of the cerebral cortex, as well as composites of these indices reflecting overall neuropathology, were analyzed. For men and women separately, partial correlations, controlling for age at death and dementia severity, were used to assess the associations of number of children with these neuropathological variables.
Among women, all the partial correlations were positive, with statistical significance for overall neuropathology (r=.37; p=.02), overall NPs (r=.36; p=.02), and for NPs in the amygdala (r=.47; p=.002). Among men, none of the partial correlations were statistically significant. Results of the secondary analyses were similar.
Since the associations between number of children and neuropathology of AD were found for women only, they might reflect sex-specific mechanisms (such as variations in estrogen or luteinizing hormone levels) rather than social, economic, biological or other mechanisms common to both men and women.
研究生育子女数量与阿尔茨海默病(AD)神经病理学之间的关联。
对86名有亲生子女数量数据的受试者的大脑进行了死后研究。主要分析包括73名受试者(平均死亡年龄 = 80岁;42名女性),他们没有脑血管疾病相关病变(即梗死)或非AD相关神经病理学。女性的死亡年龄显著高于男性(85.6岁对73.4岁;p <.0005),但在子女数量或痴呆严重程度方面与男性没有显著差异。次要分析包括另外13名患有伴发脑血管疾病的受试者。分析了海马体、内嗅皮质、杏仁核和大脑皮质多个区域的神经炎性斑块(NP)和神经原纤维缠结(NFT)的密度,以及反映总体神经病理学的这些指标的综合指标。分别对男性和女性,在控制死亡年龄和痴呆严重程度的情况下,使用偏相关分析来评估子女数量与这些神经病理学变量之间的关联。
在女性中,所有偏相关均为正,总体神经病理学(r =.37;p =.02)、总体NP(r =.36;p =.02)以及杏仁核中的NP(r =.47;p =.002)具有统计学意义。在男性中,没有一个偏相关具有统计学意义。次要分析结果相似。
由于仅在女性中发现了子女数量与AD神经病理学之间的关联,它们可能反映了性别特异性机制(如雌激素或促黄体生成素水平的变化),而不是男性和女性共有的社会、经济、生物学或其他机制。