Celone Kim A, Calhoun Vince D, Dickerson Bradford C, Atri Alireza, Chua Elizabeth F, Miller Saul L, DePeau Kristina, Rentz Doreen M, Selkoe Dennis J, Blacker Deborah, Albert Marilyn S, Sperling Reisa A
Memory Disorders Unit, Department of Neurology, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts 02115, USA.
J Neurosci. 2006 Oct 4;26(40):10222-31. doi: 10.1523/JNEUROSCI.2250-06.2006.
Memory function is likely subserved by multiple distributed neural networks, which are disrupted by the pathophysiological process of Alzheimer's disease (AD). In this study, we used multivariate analytic techniques to investigate memory-related functional magnetic resonance imaging (fMRI) activity in 52 individuals across the continuum of normal aging, mild cognitive impairment (MCI), and mild AD. Independent component analyses revealed specific memory-related networks that activated or deactivated during an associative memory paradigm. Across all subjects, hippocampal activation and parietal deactivation demonstrated a strong reciprocal relationship. Furthermore, we found evidence of a nonlinear trajectory of fMRI activation across the continuum of impairment. Less impaired MCI subjects showed paradoxical hyperactivation in the hippocampus compared with controls, whereas more impaired MCI subjects demonstrated significant hypoactivation, similar to the levels observed in the mild AD subjects. We found a remarkably parallel curve in the pattern of memory-related deactivation in medial and lateral parietal regions with greater deactivation in less-impaired MCI and loss of deactivation in more impaired MCI and mild AD subjects. Interestingly, the failure of deactivation in these regions was also associated with increased positive activity in a neocortical attentional network in MCI and AD. Our findings suggest that loss of functional integrity of the hippocampal-based memory systems is directly related to alterations of neural activity in parietal regions seen over the course of MCI and AD. These data may also provide functional evidence of the interaction between neocortical and medial temporal lobe pathology in early AD.
记忆功能可能由多个分布式神经网络来维持,而这些网络会被阿尔茨海默病(AD)的病理生理过程所破坏。在本研究中,我们使用多变量分析技术来研究52名处于正常衰老、轻度认知障碍(MCI)和轻度AD连续体中的个体的记忆相关功能磁共振成像(fMRI)活动。独立成分分析揭示了在联想记忆范式期间激活或失活的特定记忆相关网络。在所有受试者中,海马激活和顶叶失活表现出强烈的相互关系。此外,我们发现了fMRI激活在损伤连续体中的非线性轨迹的证据。与对照组相比,受损较轻的MCI受试者海马出现反常的过度激活,而受损较重的MCI受试者则表现出明显的激活不足,类似于轻度AD受试者中观察到的水平。我们在内侧和外侧顶叶区域的记忆相关失活模式中发现了一条非常相似的曲线,在受损较轻的MCI中失活程度更大,而在受损较重的MCI和轻度AD受试者中失活消失。有趣的是,这些区域失活的失败也与MCI和AD中新皮质注意力网络中阳性活动的增加有关。我们的研究结果表明,基于海马的记忆系统功能完整性的丧失与在MCI和AD过程中观察到的顶叶区域神经活动的改变直接相关。这些数据也可能为早期AD中新皮质和内侧颞叶病理之间的相互作用提供功能证据。