Low amyloid-β deposition correlates with high education in cognitively normal older adults: a pilot study

2014 ◽  
Vol 30 (9) ◽  
pp. 919-926 ◽  
Author(s):  
Fumihiko Yasuno ◽  
Hiroaki Kazui ◽  
Naomi Morita ◽  
Katsufumi Kajimoto ◽  
Masafumi Ihara ◽  
...  
2019 ◽  
Vol 70 (2) ◽  
pp. 553-562 ◽  
Author(s):  
Chinedu T. Udeh-Momoh ◽  
Bowen Su ◽  
Stephanie Evans ◽  
Bang Zheng ◽  
Shireen Sindi ◽  
...  

2015 ◽  
Vol 48 (s1) ◽  
pp. S151-S159 ◽  
Author(s):  
Beth E. Snitz ◽  
Oscar L. Lopez ◽  
Eric McDade ◽  
James T. Becker ◽  
Ann D. Cohen ◽  
...  

2019 ◽  
Vol 27 (11) ◽  
pp. 1247-1256 ◽  
Author(s):  
Kelsey D. Biddle ◽  
Federico d'Oleire Uquillas ◽  
Heidi I.L. Jacobs ◽  
Benjamin Zide ◽  
Dylan R. Kirn ◽  
...  

2018 ◽  
Vol 29 (5) ◽  
pp. 1997-2009 ◽  
Author(s):  
Jenna N Adams ◽  
Samuel N Lockhart ◽  
Lexin Li ◽  
William J Jagust

Abstract Tau is associated with hypometabolism in patients with Alzheimer’s disease. In normal aging, the association between tau and glucose metabolism is not fully characterized. We used [18F] AV-1451, [18F] Fluorodeoxyglucose, and [11C] Pittsburgh Compound-B (PiB) PET to measure associations between tau and glucose metabolism in cognitively normal older adults (N = 49). Participants were divided into amyloid-negative (PiB–, n = 28) and amyloid-positive (PiB+, n = 21) groups to determine effects of amyloid-β. We assessed both local and across-brain regional tau–glucose metabolism associations separately in PiB–/PiB+ groups using correlation matrices and sparse canonical correlations. Relationships between tau and glucose metabolism differed by amyloid status, and were primarily spatially distinct. In PiB– subjects, tau was associated with broad regions of increased glucose metabolism. In PiB+ subjects, medial temporal lobe tau was associated with widespread hypometabolism, while tau outside of the medial temporal lobe was associated with decreased and increased glucose metabolism. We further found that regions with earlier tau spread were associated with stronger negative correlations with glucose metabolism. Our findings indicate that in normal aging, low levels of tau are associated with a phase of increased metabolism, while high levels of tau in the presence of amyloid-β are associated with hypometabolism at downstream sites.


2013 ◽  
Vol 70 (5) ◽  
pp. 594 ◽  
Author(s):  
Maureen Handoko ◽  
Marianne Grant ◽  
Michael Kuskowski ◽  
Kathleen R. Zahs ◽  
Anders Wallin ◽  
...  

2006 ◽  
Vol 14 (7S_Part_11) ◽  
pp. P640-P640
Author(s):  
Kelsey D. Biddle ◽  
Federico d'Oleire Uquillas ◽  
Benjamin Zide ◽  
Dylan Kirn ◽  
Keith A. Johnson ◽  
...  

2021 ◽  
Vol 5 (1) ◽  
pp. 111-120
Author(s):  
Shane Fernandez ◽  
Samantha C. Burnham ◽  
Lidija Milicic ◽  
Greg Savage ◽  
Paul Maruff ◽  
...  

Abstract. Background: Genetic variation in Spondin-1, specifically rs11023139, has been associated with reduced rates of cognitive decline in individuals with Alzheimer’s disease. Objective: The aim of this study was to assess whether the association was present in cognitively normal older adults. Methods: Longitudinal cognitive decline was investigated using linear mixed modelling in a cohort of 590 cognitively normal older adults enrolled in the Australian Imaging, Biomarkers and Lifestyle Study. Results: No independent effect of Spondin-1 rs11023139 on cognitive decline was observed. However, significant associations were observed for the interaction between Apolipoprotein E (APOE) ɛ4 and rs11023139 in individuals with high amyloid-β burden. APOE ɛ4/rs11023139-A carriers declined significantly faster than APOE ɛ4/rs11023139-G_G carriers in measures of global cognition (p = 0.011) and verbal episodic memory (p = 0.020). Conclusion: These results suggest that carriage of the Spondin-1 rs11023139-A allele significantly contributes to a worsening of cognitive performance in APOE ɛ4 cognitively normal older adults with a high neocortical amyloid-β burden.


2020 ◽  
Vol 1 (1) ◽  
Author(s):  
Chris A Chou ◽  
Cristina D Toedebusch ◽  
Tiara Redrick ◽  
David Freund ◽  
Jennifer S McLeland ◽  
...  

Abstract Study Objectives Multiple methods for monitoring sleep-wake activity have identified sleep disturbances as risk factors for Alzheimer disease (AD). In order to identify the level of agreement between different methods, we compared sleep parameters derived from single-channel EEG (scEEG), actigraphy, and sleep diaries in cognitively normal and mildly impaired older adults. Methods Two hundred ninety-three participants were monitored at home for up to six nights with scEEG, actigraphy, and sleep diaries. Total sleep time (TST), sleep efficiency (SE), sleep onset latency (SOL), and wake after sleep onset (WASO) were calculated using each of these methods. In 109 of the 293 participants, the ratio of cerebrospinal fluid concentrations of phosphorylated tau (p-tau) and amyloid-β-42 (Aβ42) was used as a biomarker for AD pathology. Results Agreement was highest for TST across instruments, especially in cognitively normal older adults. Overall, scEEG and actigraphy appeared to have greater agreement for multiple sleep parameters than for scEEG and diary or actigraphy and diary. Levels of agreement between scEEG and actigraphy overall decreased in mildly impaired participants and those with biomarker evidence of AD pathology, especially for measurements of TST. Conclusions Caution should be exercised when comparing scEEG and actigraphy in individuals with mild cognitive impairment or with AD pathology. Sleep diaries may capture different aspects of sleep compared to scEEG and actigraphy. Additional studies comparing different methods of measuring sleep-wake activity in older adults are necessary to allow for comparison between studies using different methods.


2017 ◽  
Vol 59 (3) ◽  
pp. 975-985 ◽  
Author(s):  
Jennifer R. Gatchel ◽  
Nancy J. Donovan ◽  
Joseph J. Locascio ◽  
Aaron P. Schultz ◽  
J. Alex Becker ◽  
...  

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