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Amyloid burden cortical thickness and cognitive function in the Wisconsin Registry for Alzheimers Prevention

机译:威斯康星州注册表中的淀粉样蛋白负荷皮质厚度和认知功能可预防老年痴呆

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摘要

There is a growing interest in understanding how amyloid β (Aβ) accumulation in preclinical Alzheimer's disease relates to brain morphometric measures and cognition. Existing investigations in this area have been primarily conducted in older cognitively normal (CN) individuals. Therefore, not much is known about the associations between Aβ burden, cortical thickness, and cognition in midlife. We examined this question in 109, CN, late to middle-aged adults (mean age = 60.72 ± 5.65 years) from the Wisconsin Registry for Alzheimer's Prevention. They underwent Pittsburgh Compound B (PiB) and anatomical magnetic resonance (MR) imaging, and a comprehensive cognitive examination. Blinded visual rating of the PiB scans was used to classify the participants as Aβ+ or Aβ−. Cortical thickness measurements were derived from the MR images. The Aβ+ group exhibited significant thinning of the entorhinal cortex and accelerated age-associated thinning of the parahippocampal gyrus compared with the Aβ− group. The Aβ+ group also had numerically lower, but nonsignificant, test scores on all cognitive measures, and significantly faster age-associated cognitive decline on measures of Speed & Flexibility, Verbal Ability, and Visuospatial Ability. Our findings suggest that early Aβ aggregation is associated with deleterious changes in brain structure and cognitive function, even in midlife, and that the temporal lag between Aβ deposition and the inception of neurodegenerative/cognitive changes might be narrower than currently thought.
机译:人们越来越了解临床前阿尔茨海默氏病中淀粉样蛋白β(Aβ)的积累如何与大脑形态测量和认知有关。该领域的现有研究主要在认知能力正常的老年人中进行。因此,关于Aβ负担,皮层厚度和中年认知之间的关联知之甚少。我们在威斯康星州预防老年痴呆症登记处的109名CN中晚期至中年成年人(平均年龄= 60.72±5.65岁)中研究了这个问题。他们接受了匹兹堡化合物B(PiB)和解剖磁共振(MR)成像以及全面的认知检查。 PiB扫描的盲目等级用于将参与者分类为Aβ+或Aβ-。皮质厚度测量值是从MR图像得出的。与Aβ-组相比,Aβ+组的内嗅皮层明显变薄,海马旁回生的年龄相关的变薄加速。 Aβ+组在所有认知指标上的得分均在数值上较低,但意义不重大,而在速度和柔韧性,言语能力和视觉空间能力指标上,与年龄相关的认知能力下降明显更快。我们的发现表明,即使在中年,早期Aβ聚集也与大脑结构和认知功能的有害变化有关,并且Aβ沉积和神经退行性/认知变化开始之间的时间滞后可能比当前的想法更窄。

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