Iacono D, Markesbery W R, Gross M, Pletnikova O, Rudow G, Zandi P, Troncoso J C
Division of Neuropathology, Department of Pathology, Johns Hopkins University, School of Medicine, Ross Building 558, 720 Rutland Avenue, Baltimore, MD 21205, USA.
Neurology. 2009 Sep 1;73(9):665-73. doi: 10.1212/WNL.0b013e3181b01077. Epub 2009 Jul 8.
It is common to find substantial Alzheimer disease (AD) lesions, i.e., neuritic beta-amyloid plaques and neurofibrillary tangles, in the autopsied brains of elderly subjects with normal cognition assessed shortly before death. We have termed this status asymptomatic AD (ASYMAD). We assessed the morphologic substrate of ASYMAD compared to mild cognitive impairment (MCI) in subjects from the Nun Study. In addition, possible correlations between linguistic abilities in early life and the presence of AD pathology with and without clinical manifestations in late life were considered.
Design-based stereology was used to measure the volumes of neuronal cell bodies, nuclei, and nucleoli in the CA1 region of hippocampus (CA1). Four groups of subjects were compared: ASYMAD (n = 10), MCI (n = 5), AD (n = 10), and age-matched controls (n = 13). Linguistic ability assessed in early life was compared among all groups.
A significant hypertrophy of the cell bodies (+44.9%), nuclei (+59.7%), and nucleoli (+80.2%) in the CA1 neurons was found in ASYMAD compared with MCI. Similar differences were observed with controls. Furthermore, significant higher idea density scores in early life were observed in controls and ASYMAD group compared to MCI and AD groups.
在死亡前不久认知功能正常的老年受试者尸检大脑中,常常发现大量阿尔茨海默病(AD)病变,即神经炎性β-淀粉样斑块和神经原纤维缠结。我们将这种状态称为无症状AD(ASYMAD)。我们在修女研究的受试者中,评估了ASYMAD与轻度认知障碍(MCI)相比的形态学基础。此外,还考虑了早年语言能力与晚年有无临床表现的AD病理学之间的可能相关性。
采用基于设计的体视学方法测量海马CA1区神经元细胞体、细胞核和核仁的体积。比较了四组受试者:ASYMAD(n = 10)、MCI(n = 5)、AD(n = 10)和年龄匹配的对照组(n = 13)。比较了所有组早年评估的语言能力。
与MCI相比,ASYMAD中CA1神经元的细胞体(+44.9%)、细胞核(+59.7%)和核仁(+80.2%)显著肥大。与对照组也观察到类似差异。此外,与MCI组和AD组相比,对照组和ASYMAD组早年的观念密度得分显著更高。
1)神经元肥大可能是对阿尔茨海默病(AD)病理学的早期细胞反应,或反映了尽管存在大量AD病变但仍能防止认知障碍的代偿机制;2)尽管存在AD病变,但早年较高的观念密度得分与晚年认知功能完整有关。