白质参考区对Florbetapir PET测量淀粉样斑块沉积与认知能力下降之间关系的影响。

V Bhargava, M Wang, Y Chen, J Luo, M Weiner, S Landau, W Jagust, M Sabbagh, Y Su, E M Reiman, K Chen
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引用次数: 0

摘要

本研究的目的是系统地研究淀粉样蛋白PET示踪剂、Florbetapir (FBP)和认知之间的横断面和纵向关联,当不同的参考区域——整个小脑和白质——被用于淀粉样蛋白沉积的标准化摄取值比(SUVR)半量化时。1238例轻度AD痴呆、轻度认知障碍(MCI)、来自AD神经影像学计划(ADNI)的认知未受损(CU)参与者被用来表征和比较使用脑白质与整个小脑参考区对florbetapir淀粉样斑块沉积SUVR指标与认知或临床衰退测量(ADAS-Cog-13、CDR-Sum Boxes和AVLT-total)在年龄和教育共变后的横截面和纵向关系的影响。在横断面和纵向比较中,florbetapir PET测量的脑白质参考区淀粉样斑块沉积与轻度痴呆、MCI和CU组的认知或临床衰退的每项测量都更密切相关
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Impact of a White Matter Reference Region on the Relationship between Florbetapir PET Measurements of Amyloid Plaque Deposition and Measurements of Cognitive Decline.

The objective of this study was to systematically investigate both cross-sectional and longitudinal associations between amyloid PET tracer, Florbetapir (FBP), and cognition when different reference regions of interest - whole cerebellum versus white matter - are used for Standardized Uptake Value Ratio (SUVR) semi-quantification of amyloid beta deposition. Baseline and 2.2±0.4 year follow-up Florbetapir PET scans from 1,238 mild AD dementia, mild cognitive impairment (MCI), and cognitively unimpaired (CU) participants from AD Neuroimaging Initiative (ADNI) were used to characterize and compare the impact of using a cerebral white matter versus whole cerebellar reference region on cross-sectional and longitudinal relationships between florbetapir SUVR indicators of amyloid plaque deposition and measurements of cognitive or clinical decline (ADAS-Cog-13, CDR-Sum Boxes, and AVLT-total) after covarying for age and education. In both cross-sectional and longitudinal comparisons, florbetapir PET measurements of amyloid plaque deposition using the cerebral white matter reference region were more closely related to each measure of cognitive or clinical decline in the aggregate mild dementia, MCI and CU group (P<1.3E-06). This study supports the potential use of a cerebral white matter reference region in the detection and tracking of amyloid plaque deposition using florbetapir PET. Additional studies are needed to clarify the generalizability of findings to other amyloid PET ligands.

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