scholarly journals Depressive Symptoms and Tau Accumulation in the Inferior Temporal Lobe and Entorhinal Cortex in Cognitively Normal Older Adults: A Pilot Study

2017 ◽  
Vol 59 (3) ◽  
pp. 975-985 ◽  
Author(s):  
Jennifer R. Gatchel ◽  
Nancy J. Donovan ◽  
Joseph J. Locascio ◽  
Aaron P. Schultz ◽  
J. Alex Becker ◽  
...  
2018 ◽  
Vol 101 (4) ◽  
pp. 665-671 ◽  
Author(s):  
Jin Hui Joo ◽  
Seungyoung Hwang ◽  
Joseph J. Gallo ◽  
Debra L. Roter

2014 ◽  
Vol 30 (9) ◽  
pp. 919-926 ◽  
Author(s):  
Fumihiko Yasuno ◽  
Hiroaki Kazui ◽  
Naomi Morita ◽  
Katsufumi Kajimoto ◽  
Masafumi Ihara ◽  
...  

2006 ◽  
Vol 14 (7S_Part_2) ◽  
pp. P109-P110
Author(s):  
Laura Wisse ◽  
Mohamad Habes ◽  
Sandhitsu R. Das ◽  
Paul Yushkevich ◽  
David A. Wolk

2021 ◽  
Vol 17 (S1) ◽  
Author(s):  
Anika Wuestefeld ◽  
David Berron ◽  
Danielle van Westen ◽  
Erik Stomrud ◽  
Niklas Mattsson‐Carlgren ◽  
...  

2017 ◽  
Author(s):  
Zachariah M. Reagh ◽  
Jessica A. Noche ◽  
Nicholas J. Tustison ◽  
Derek Delisle ◽  
Elizabeth A. Murray ◽  
...  

AbstractThe entorhinal cortex (EC) is among the earliest brain areas to deteriorate in Alzheimer’s disease (AD). However, the extent to which functional properties of the EC are altered in the aging brain, even in the absence of clinical symptoms, is not understood. Recent human fMRI studies have identified a functional dissociation within the EC, similar to what is found in rodents. Here, we used high-resolution fMRI to identify a specific hypoactivity in the anterolateral EC (alEC) commensurate with major behavioral deficits on an object pattern separation task in asymptomatic older adults. Only subtle deficits were found in a comparable spatial condition, with no associated differences in posteromedial EC between young and older adults. We additionally link this condition to previously reported dentate/CA3 hyperactivity, both of which were associated with object mnemonic discrimination impairment. These results provide novel evidence of alEC-dentate/CA3 circuit dysfunction in cognitively normal aged humans.


2015 ◽  
Vol 46 (1) ◽  
pp. 63-73 ◽  
Author(s):  
Nancy J. Donovan ◽  
David C. Hsu ◽  
Alexander S. Dagley ◽  
Aaron P. Schultz ◽  
Rebecca E. Amariglio ◽  
...  

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.


2018 ◽  
Vol 75 (4) ◽  
pp. 783-791 ◽  
Author(s):  
Nikki L Hill ◽  
Jacqueline Mogle ◽  
Sakshi Bhargava ◽  
Emily Whitaker ◽  
Iris Bhang ◽  
...  

Abstract Objective To test whether race (specifically Black or White) moderates the relationship between memory complaints and depressive symptoms in cognitively normal older adults, and if these relationships vary by memory complaint characteristics. Methods Data from Black (n = 551) and White (n = 1,158) cognitively intact participants (Mage = 77.1, SD = 7.5; 76.6% female) in the Minority Aging Research Study and the Rush Memory and Aging Project were used. Participants completed annual clinical evaluations, including the Center for Epidemiologic Studies Depression scale and two memory complaint questions, over periods of up to 18 years. Ordinal mixed effects models were used to examine within-person relationships between memory complaints and depressive symptoms over time, as well as whether race moderated these associations. Results Reports of greater memory change over time were associated with more depressive symptoms for both Black and White older adults. However, reports of greater frequency of memory problems were related to depressive symptoms for Black older adults only. Conclusion Findings suggest differential associations between memory complaints and depressive symptoms in cognitively normal Black and White older adults and call for future research to examine the influence of race and related factors on memory complaints and depressive symptoms.


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