Neuroimaging Laboratories, Washington University School of Medicine, St. Louis, MO, USA; Mallinckrodt Institute of Radiology, Washington University School of Medicine, St. Louis, MO, USA; Department of Neurology, Washington University School of Medicine, St. Louis, MO, USA; Knight Alzheimer's Disease Research Center, Washington University School of Medicine, St. Louis, MO, USA.
Neuroimaging Laboratories, Washington University School of Medicine, St. Louis, MO, USA; Mallinckrodt Institute of Radiology, Washington University School of Medicine, St. Louis, MO, USA; Knight Alzheimer's Disease Research Center, Washington University School of Medicine, St. Louis, MO, USA.
Neurobiol Aging. 2020 Dec;96:165-175. doi: 10.1016/j.neurobiolaging.2020.08.019. Epub 2020 Sep 1.
In Alzheimer's disease, brain amyloid deposition has a distinct topography that correlates with aerobic glycolysis (AG), that is, the use of glucose beyond that predicted by oxygen consumption. The causes for this relationship remain unclear but might provide crucialinsight into how amyloid deposition begins. Here we develop methods to study the earliest topography of amyloid deposition based on amyloid imaging and investigate its spatiotemporal evolution with respect to the topography of AG in adults. We find that the spatiotemporal dynamics of amyloid deposition are largely explained by 1 factor, defined here as the amyloid topography dissimilarity index (ATDI). ATDI is bimodal, more highly dynamic during early amyloid accumulation, and predicts which individuals will cross a conservative quantitative threshold at least 3-5 years in advance. Using ATDI, we demonstrate that subthreshold amyloid accumulates primarily in regions that have high AG during early adulthood. Our findings suggest that early on-target subthreshold amyloid deposition mirrors its later regional pattern, which best corresponds to the topography of young adult brain AG.
在阿尔茨海默病中,脑淀粉样蛋白沉积具有独特的地形分布,与有氧糖酵解(AG)相关,即葡萄糖的消耗超过了氧消耗的预测值。这种关系的原因尚不清楚,但可能为淀粉样蛋白沉积的起始方式提供重要线索。在这里,我们开发了基于淀粉样蛋白成像的方法来研究淀粉样蛋白沉积的最早地形,并研究其与成年人 AG 地形的时空演化。我们发现,淀粉样蛋白沉积的时空动态主要由一个因素来解释,我们在这里将其定义为淀粉样蛋白地形差异指数(ATDI)。ATDI 呈双峰分布,在淀粉样蛋白早期积累期间更具动态性,并可预测哪些个体将至少提前 3-5 年跨越保守的定量阈值。使用 ATDI,我们证明了亚阈值淀粉样蛋白主要在成年早期 AG 较高的区域积累。我们的研究结果表明,早期靶向亚阈值淀粉样蛋白沉积与其后来的区域模式相吻合,与年轻成人脑 AG 的地形最相符。