Pasquini Lorenzo, Tonch Annika, Plant Claudia, Zherdin Andrew, Ortner Marion, Kurz Alexander, Förstl Hans, Zimmer Claus, Grimmer Timo, Wohlschäger Afra, Riedl Valentin, Sorg Christian
1 Department of Neuroradiology, Klinikum rechts der Isar, Technische Universität München , Munich, Germany .
Brain Connect. 2014 Jun;4(5):323-36. doi: 10.1089/brain.2013.0213.
In Alzheimer's disease (AD), recent findings suggest that amyloid-β (Aβ)-pathology might start 20-30 years before first cognitive symptoms arise. To account for age as most relevant risk factor for sporadic AD, it has been hypothesized that lifespan intrinsic (i.e., ongoing) activity of hetero-modal brain areas with highest levels of functional connectivity triggers Aβ-pathology. This model induces the simple question whether in older persons without any cognitive symptoms intrinsic activity of hetero-modal areas is more similar to that of symptomatic patients with AD or to that of younger healthy persons. We hypothesize that due to advanced age and therefore potential impact of pre-clinical AD, intrinsic activity of older persons resembles more that of patients than that of younger controls. We tested this hypothesis in younger (ca. 25 years) and older healthy persons (ca. 70 years) and patients with mild cognitive impairment and AD-dementia (ca. 70 years) by the use of resting-state functional magnetic resonance imaging, distinct measures of intrinsic brain activity, and different hierarchical clustering approaches. Independently of applied methods and involved areas, healthy older persons' intrinsic brain activity was consistently more alike that of patients than that of younger controls. Our result provides evidence for larger similarity in intrinsic brain activity between healthy older persons and patients with or at-risk for AD than between older and younger ones, suggesting a significant proportion of pre-clinical AD cases in the group of cognitively normal older people. The observed link of aging and AD with intrinsic brain activity supports the view that lifespan intrinsic activity may contribute critically to the pathogenesis of AD.
在阿尔茨海默病(AD)中,最近的研究结果表明,淀粉样蛋白-β(Aβ)病理可能在首次出现认知症状的20 - 30年前就已开始。为了解释年龄作为散发性AD最相关的风险因素,有人提出假设,即具有最高功能连接水平的异模态脑区的终身内在(即持续的)活动会引发Aβ病理。这个模型引发了一个简单的问题,即在没有任何认知症状的老年人中,异模态脑区的内在活动更类似于有症状的AD患者还是年轻健康人的内在活动。我们假设,由于年龄较大以及因此可能存在的临床前AD的影响,老年人的内在活动更类似于患者而非年轻对照组。我们通过使用静息态功能磁共振成像、不同的内在脑活动测量方法以及不同的层次聚类方法,在年轻(约25岁)和年长(约70岁)的健康人以及患有轻度认知障碍和AD痴呆(约70岁)的患者中测试了这一假设。无论应用何种方法和涉及哪些脑区,健康老年人的内在脑活动始终比年轻对照组更类似于患者。我们的结果为健康老年人与患有AD或有AD风险的患者之间在内在脑活动上的相似性大于老年人与年轻人之间的相似性提供了证据,这表明在认知正常的老年人组中存在相当比例的临床前AD病例。观察到的衰老和AD与内在脑活动之间的联系支持了这样一种观点,即终身内在活动可能对AD的发病机制起关键作用。