[18F]AV-1451 PET IMAGING OF TAU PATHOLOGY PREDICTS WHITE MATTER HYPERINTENSITIES IN HEALTHY AGING, MILD COGNITIVE IMPAIRMENT AND ALZHEIMER'S DISEASE: THE NIMROD STUDY

2017 ◽  
Vol 13 (7) ◽  
pp. P1236-P1237
Author(s):  
Silvy Gabel ◽  
Elijah Mak ◽  
Simon Cervenka ◽  
P Simon Jones ◽  
Ajenthan Surendranathan ◽  
...  
2002 ◽  
Vol 51 (2) ◽  
pp. 182-189 ◽  
Author(s):  
Thomas W. Mitchell ◽  
Elliott J. Mufson ◽  
Julie A. Schneider ◽  
Elizabeth J. Cochran ◽  
Jonathan Nissanov ◽  
...  

2019 ◽  
Vol 75 (7) ◽  
pp. 1382-1392 ◽  
Author(s):  
Marie Caillaud ◽  
Carol Hudon ◽  
Benjamin Boller ◽  
Simona Brambati ◽  
Simon Duchesne ◽  
...  

Abstract Objective The concepts of mild cognitive impairment (MCI) and subjective cognitive decline (SCD) have been proposed to identify individuals in the early stages of Alzheimer’s disease (AD), or other neurodegenerative diseases. One approach to validate these concepts is to investigate the relationship between pathological brain markers and cognition in those individuals. Method We included 126 participants from the Consortium for the Early Identification of Alzheimer’s disease-Quebec (CIMA-Q) cohort (67 SCD, 29 MCI, and 30 cognitively healthy controls [CH]). All participants underwent a complete cognitive assessment and structural magnetic resonance imaging. Group comparisons were done using cognitive data, and then correlated with hippocampal volumes and white matter hyperintensities (WMHs). Results Significant differences were found between participants with MCI and CH on episodic and executive tasks, but no differences were found when comparing SCD and CH. Scores on episodic memory tests correlated with hippocampal volumes in both MCI and SCD, whereas performance on executive tests correlated with WMH in all of our groups. Discussion As expected, the SCD group was shown to be cognitively healthy on tasks where MCI participants showed impairment. However, SCD’s hippocampal volume related to episodic memory performances, and WMH to executive functions. Thus, SCD represents a valid research concept and should be used, alongside MCI, to better understand the preclinical/prodromal phase of AD.


2018 ◽  
Vol 63 (2) ◽  
pp. 515-527 ◽  
Author(s):  
Esther van den Berg ◽  
Mirjam I. Geerlings ◽  
Geert Jan Biessels ◽  
Paul J. Nederkoorn ◽  
Raoul P. Kloppenborg

2009 ◽  
Vol 5 (4S_Part_12) ◽  
pp. P358-P358
Author(s):  
Suzuka Ataka ◽  
Hiroyuki Shimada ◽  
Jun Takeuchi ◽  
Joji Kawabe ◽  
Makoto Shigematsu ◽  
...  

2019 ◽  
Author(s):  
Karen Misquitta ◽  
Mahsa Dadar ◽  
D. Louis Collins ◽  
Maria Carmela Tartaglia ◽  

AbstractBackground and Purpose: Neuropsychiatric symptoms (NPS) are frequently encountered in patients with Alzheimer’s disease (AD). Focal grey matter atrophy has been linked to NPS development. Cerebrovascular disease can cause focal lesions and is common among AD patients. As cerebrovascular disease can be detected on MRI as white matter hyperintensities (WMH), this study evaluated WMH burden in mild cognitive impairment (MCI), AD and normal controls and determined their relationship with NPS. Methods: NPS were assessed using the Neuropsychiatric Inventory and grouped into subsyndromes. WMH were measured using an automatic segmentation technique and mean deformation-based morphometry was used to measure atrophy of grey matter regions. Results: WMHs and grey matter atrophy both contributed significantly to NPS subsyndromes in MCI and AD subjects, however, WMH burden played a greater role. Conclusions: This study could provide a better understanding of the pathophysiology of NPS in AD.


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