Vannini Patrizia, Almkvist Ove, Dierks Thomas, Lehmann Christoph, Wahlund Lars-Olof
Department of Neurobiology, Care Sciences and Society, Division of Clinical Geriatrics, Karolinska Institutet, Karolinska University Hospital, Huddinge, 141 86 Stockholm, Sweden.
Psychiatry Res. 2007 Oct 15;156(1):43-57. doi: 10.1016/j.pscychresns.2007.02.003. Epub 2007 Aug 23.
Mild cognitive impairment (MCI) often refers to the preclinical stage of dementia, where the majority develop Alzheimer's disease (AD). Given that neurodegenerative burden and compensatory mechanisms might exist before accepted clinical symptoms of AD are noticeable, the current prospective study aimed to investigate the functioning of brain regions in the visuospatial networks responsible for preclinical symptoms in AD using event-related functional magnetic resonance imaging (fMRI). Eighteen MCI patients were evaluated and clinically followed for approximately 3 years. Five progressed to AD (PMCI) and eight remained stable (SMCI). Thirteen age-, gender- and education-matched controls also participated. An angle discrimination task with varying task demands was used. Brain activation patterns as well as task demand-dependent and -independent signal changes between the groups were investigated by using an extended general linear model including individual performance (reaction time [RT]) of each single trial. Similar behavioral (RT and accuracy) responses were observed between MCI patients and controls. A network of bilateral activations, e.g. dorsal pathway, which increased linearly with increasing task demand, was engaged in all subjects. Compared with SMCI patients and controls, PMCI patients showed a stronger relation between task demand and brain activity in left superior parietal lobules (SPL) as well as a general task demand-independent increased activation in left precuneus. Altered brain function can be detected at a group level in individuals that progress to AD before changes occur at the behavioral level. Increased parietal activation in PMCI could reflect a reduced neuronal efficacy due to accumulating AD pathology and might predict future clinical decline in patients with MCI.
轻度认知障碍(MCI)通常指痴呆的临床前期,其中大多数人会发展为阿尔茨海默病(AD)。鉴于在AD公认的临床症状出现之前可能就已存在神经退行性负担和代偿机制,当前的前瞻性研究旨在使用事件相关功能磁共振成像(fMRI)来研究负责AD临床前期症状的视觉空间网络中脑区的功能。对18名MCI患者进行了评估,并进行了约3年的临床随访。其中5人进展为AD(进展性MCI,PMCI),8人病情保持稳定(稳定型MCI,SMCI)。13名年龄、性别和教育程度匹配的对照者也参与了研究。采用了一种具有不同任务要求的角度辨别任务。通过使用包括每个单次试验的个体表现(反应时间[RT])的扩展通用线性模型,研究了各组之间的脑激活模式以及任务需求依赖性和非依赖性信号变化。MCI患者和对照者之间观察到了相似的行为(RT和准确性)反应。所有受试者都参与了一个双侧激活网络,例如背侧通路,其随着任务要求的增加而线性增加。与SMCI患者和对照者相比,PMCI患者在左顶上小叶(SPL)中任务需求与脑活动之间的关系更强,并且在左楔前叶中存在一般任务需求非依赖性的激活增加。在进展为AD的个体中,在行为水平发生变化之前,可以在群体水平上检测到脑功能的改变。PMCI中顶叶激活增加可能反映了由于AD病理学积累导致的神经元效能降低,并可能预测MCI患者未来的临床衰退。