Service de Neurologie and Neuropsychologie, Pôle de neurosciences cliniques, AP-HM Timone, INSERM U751, Université de la Méditerranée, Marseille, France.
J Alzheimers Dis. 2011;27(1):11-22. doi: 10.3233/JAD-2011-110557.
Diagnosis of Alzheimer's disease (AD) in its earliest stages becomes increasingly important as disease modifying agents are being developed. In this area of research, many clinical and neuroimaging studies focus on markers of hippocampal dysfunction. However, during the "transentorhinal stage" of AD, neurofibrillary tangles (NFT), related to tau protein pathology, develop in the anterior subhippocampal (perirhinal/entorhinal) cortex before the hippocampus. NFT are tightly correlated with clinical symptoms. Therefore, an accurate understanding of the behavioral correlate of transentorhinal dysfunction could critically contribute to the early diagnosis of the disease. Recent findings from studies in animals and human brain-damaged patients suggest that the anterior subhippocampal region, functionally integrated into an anterior mesiotemporal network, is involved in object based context-free memory. In this article, we evaluate the hypothesis according to which tau deposition in the anterior subhippocampal region during the earliest stages of the most common form of AD, with predominant MTL dysfunction, will lead to dysfunction of neural networks implicated in context-free memory. We challenge the view that impaired episodic memory is the hallmark of early AD. Instead, a model that integrates the localization and temporal sequence of NFT within the mesial temporal lobe (MTL) is proposed. Paralleling the development of NFT in anterior subhippocampal areas, impaired context-free, object-based, memory could be the first detectable sign in AD. In a subsequent, "hippocampal" stage, context-rich, episodic and spatial memory, becomes altered as well. The question as to the "episodic" nature of "episodic memory tasks" is also addressed.
阿尔茨海默病(AD)的早期诊断变得越来越重要,因为目前正在开发能够改变疾病进程的药物。在这个研究领域,许多临床和神经影像学研究都集中在海马功能障碍的标志物上。然而,在 AD 的“transentorhinal 阶段”,与 tau 蛋白病理学相关的神经原纤维缠结(NFT)在前海马(旁海马/内嗅皮层)中发展,而海马则在其之前。NFT 与临床症状密切相关。因此,准确理解 transentorhinal 功能障碍的行为相关性可以为疾病的早期诊断提供关键信息。动物和人脑损伤患者的研究最近发现表明,前海马区域与内侧颞叶网络功能整合,参与基于物体的无上下文记忆。在本文中,我们根据以下假设进行评估:在最常见的 AD 形式(以 MTL 功能障碍为主)的早期阶段,tau 在海马前区的沉积将导致无上下文记忆所涉及的神经网络功能障碍。我们挑战这样一种观点,即情景记忆障碍是 AD 早期的标志。相反,提出了一个整合内侧颞叶(MTL)内 NFT 定位和时间序列的模型。NFT 在海马前区的发展平行,无上下文、基于物体的记忆障碍可能是 AD 最早可检测到的迹象。在随后的“海马”阶段,情景丰富、情景和空间记忆也会发生改变。关于“情景记忆任务”的“情景”性质的问题也得到了探讨。