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基于正电子发射断层扫描(PET)的阿尔茨海默病tau蛋白积累Braak分期中的言语记忆形成

Verbal memory formation across PET-based Braak stages of tau accumulation in Alzheimer's disease.

作者信息

Fernández Arias Jaime, Therriault Joseph, Thomas Emilie, Lussier Firoza Z, Bezgin Gleb, Tissot Cécile, Servaes Stijn, Mathotaarachchi Sulantha S, Schoemaker Dorothée, Stevenson Jenna, Rahmouni Nesrine, Kang Min Su, Pallen Vanessa, Poltronetti Nina Margherita, Wang Yi-Ting, Kunach Peter, Chamoun Mira, Quispialaya S Kely M, Vitali Paolo, Massarweh Gassan, Gauthier Serge, Rajah Maria N, Pascoal Tharick, Rosa-Neto Pedro

机构信息

Faculty of Medicine, McGill University, Montreal, QC H3G 2M1, Canada.

Department of Neurology and Neurosurger, McGill University Research Centre for Studies in Aging, Verdun, QC H4H 1R3, Canada.

出版信息

Brain Commun. 2023 May 18;5(3):fcad146. doi: 10.1093/braincomms/fcad146. eCollection 2023.

Abstract

A classical early sign of typical Alzheimer's disease is memory decline, which has been linked to the aggregation of tau in the medial temporal lobe. Verbal delayed free recall and recognition tests have consistently probed useful to detect early memory decline, and there is substantial debate on how performance, particularly in recognition tests, is differentially affected through health and disease in older adults. Using PET-Braak staging, we investigated delayed recall and recognition memory dysfunction across the Alzheimer's disease spectrum. Our cross-sectional study included 144 cognitively unimpaired elderly, 39 amyloid-β+ individuals with mild cognitive impairment and 29 amyloid-β+ Alzheimer's disease patients from the Translational Biomarkers in Aging and Dementia cohort, who underwent [F]MK6240 tau and [F]AZD4694 amyloid PET imaging, structural MRI and memory assessments. We applied non-parametric comparisons, correlation analyses, regression models and voxel-wise analyses. In comparison with PET-Braak Stage 0, we found that reduced, but not clinically significant, delayed recall starts at PET-Braak Stage II (adjusted < 0.0015), and that recognition (adjusted = 0.011) displayed a significant decline starting at PET-Braak Stage IV. While performance in both delayed recall and recognition related to tau in nearly the same cortical areas, further analyses showed that delayed recall rendered stronger associations in areas of early tau accumulation, whereas recognition displayed stronger correlations in mostly posterior neocortical regions. Our results support the notion that delayed recall and recognition deficits are predominantly associated with tau load in allocortical and neocortical areas, respectively. Overall, delayed recall seems to be more dependent on the integrity of anterior medial temporal lobe structures, while recognition appears to be more affected by tau accumulation in cortices beyond medial temporal regions.

摘要

典型阿尔茨海默病的一个经典早期迹象是记忆衰退,这与内侧颞叶中tau蛋白的聚集有关。言语延迟自由回忆和识别测试一直被证明有助于检测早期记忆衰退,并且对于老年人的健康和疾病如何不同地影响测试表现,尤其是识别测试的表现,存在大量争论。我们使用PET-Braak分期,研究了阿尔茨海默病谱系中延迟回忆和识别记忆功能障碍。我们的横断面研究纳入了144名认知未受损的老年人、39名患有轻度认知障碍的淀粉样蛋白β阳性个体以及29名来自衰老与痴呆转化生物标志物队列的淀粉样蛋白β阳性阿尔茨海默病患者,他们接受了[F]MK6240 tau和[F]AZD4694淀粉样蛋白PET成像、结构MRI和记忆评估。我们应用了非参数比较、相关分析、回归模型和体素分析。与PET-Braak 0期相比,我们发现延迟回忆在PET-Braak II期开始下降,但无临床显著意义(校正后<0.0015),而识别(校正后=0.011)在PET-Braak IV期开始出现显著下降。虽然延迟回忆和识别表现与tau蛋白在几乎相同的皮质区域相关,但进一步分析表明,延迟回忆在早期tau蛋白积累区域的关联更强,而识别在大多数后新皮质区域的相关性更强。我们的结果支持这样一种观点,即延迟回忆和识别缺陷分别主要与异皮质和新皮质区域的tau蛋白负荷相关。总体而言,延迟回忆似乎更依赖于前内侧颞叶结构的完整性,而识别似乎更受内侧颞叶区域以外皮质中tau蛋白积累的影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec05/10213301/b985d3e2a8d7/fcad146_ga1.jpg

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