West Mark J, Kawas Claudia H, Stewart Walter F, Rudow Gay L, Troncoso Juan C
Department of Neurobiology, Institute of Anatomy, Building 234, University Park, Aarhus 8000, Denmark.
Neurobiol Aging. 2004 Oct;25(9):1205-12. doi: 10.1016/j.neurobiolaging.2003.12.005.
In a previous study of hippocampal neurons in aging and AD [Lancet 344 (1994) 769], we demonstrated that the loss of neurons in the CA1 region was disease-specific and not related to aging. In the present study, we examined for loss of hippocampal neurons in preclinical AD, a period during which there are abundant amyloid deposits in the brain but no evidence of cognitive decline. We examined the postmortem brains of 33 subjects from the Baltimore Longitudinal Study of Aging and the Johns Hopkins Alzheimer's Disease Research Center. Using unbiased stereology, we estimated the total number of neurons in the granule cell layer, hilus, CA3-2, CA1, and subiculum of AD (n = 14) preclinical AD (n = 8), and age-matched control subjects (n = 11). The results from the present study confirm our previous finding of significant neuronal losses in the CA1 (48%), hilus (14%), and subiculum (24%) in AD [Lancet 344 (1994) 769]. However, we did not observe a significant loss of neurons in CA1 or any of the other subdivisions of the hippocampus in preclinical AD.
在之前一项关于衰老和阿尔茨海默病(AD)中海马神经元的研究[《柳叶刀》344卷(1994年)第769页]中,我们证明了CA1区神经元的丧失是疾病特异性的,与衰老无关。在本研究中,我们检查了临床前AD阶段海马神经元的丧失情况,在此期间大脑中有大量淀粉样蛋白沉积,但没有认知能力下降的证据。我们检查了来自巴尔的摩衰老纵向研究和约翰霍普金斯阿尔茨海默病研究中心 的33名受试者的死后大脑。使用无偏倚的体视学方法,我们估计了AD患者(n = 14)、临床前AD患者(n = 8)和年龄匹配的对照受试者(n = 11)颗粒细胞层、齿状回门、CA3-2、CA1和下托中的神经元总数。本研究结果证实了我们之前的发现,即AD患者的CA1区(48%)、齿状回门(14%)和下托(24%)存在显著的神经元损失[《柳叶刀》344卷(1994年)第769页]。然而,我们在临床前AD患者的CA1区或海马体的任何其他亚区均未观察到显著的神经元损失。