O3-07-02: WHITE MATTER BURDEN IN CLINICALLY NORMAL OLDER ADULTS MEDIATES THE RELATIONSHIP BETWEEN AMYLOID BURDEN AND MEMORY FREE RECALL BUT NOT CUED RECALL

2014 ◽  
Vol 10 ◽  
pp. P221-P222
Author(s):  
Kate Papp ◽  
Dorene M. Rentz ◽  
Rebecca England Amariglio ◽  
Trey Hedden ◽  
Alexander Dagley ◽  
...  
Author(s):  
Breton M. Asken ◽  
William G. Mantyh ◽  
Renaud La Joie ◽  
Amelia Strom ◽  
Kaitlin B. Casaletto ◽  
...  

2013 ◽  
Vol 9 ◽  
pp. P700-P700
Author(s):  
Seon Young Ryu ◽  
Jean-Philippe Coutu ◽  
H. Diana Rosas ◽  
David Salat

2009 ◽  
Vol 29 (40) ◽  
pp. 12686-12694 ◽  
Author(s):  
T. Hedden ◽  
K. R. A. Van Dijk ◽  
J. A. Becker ◽  
A. Mehta ◽  
R. A. Sperling ◽  
...  

2017 ◽  
Vol 13 (7) ◽  
pp. P917
Author(s):  
Irina Orlovsky ◽  
Beth C. Mormino ◽  
Willem Huijbers ◽  
Aaron P. Schultz ◽  
Dorene M. Rentz ◽  
...  

Cortex ◽  
2017 ◽  
Vol 95 ◽  
pp. 92-103 ◽  
Author(s):  
Sarah E. MacPherson ◽  
Simon R. Cox ◽  
David A. Dickie ◽  
Sherif Karama ◽  
John M. Starr ◽  
...  

Neurology ◽  
2017 ◽  
Vol 88 (15) ◽  
pp. 1431-1438 ◽  
Author(s):  
Kathryn V. Papp ◽  
Dorene M. Rentz ◽  
Elizabeth C. Mormino ◽  
Aaron P. Schultz ◽  
Rebecca E. Amariglio ◽  
...  

Objective:To determine whether a decline in cued recall is observable in the preclinical stage of Alzheimer disease (AD) in clinically normal older adults with elevated β-amyloid (Aβ) burden on PET imaging.Methods:Clinically normal older adults underwent baseline neuroimaging (PET to assess Aβ+/− status and MRI) and annual neuropsychological testing. Cox proportional hazards models were used to assess the relative risk of cued memory decline (drop of 1, 2, 3, or 4 points on the total score of the Free and Cued Selective Reminding Test) in relation to neuroimaging measures, functional status, age, sex, and education.Results:A total of 276 older adults (Clinical Dementia Rating = 0, mean Mini-Mental State Examination score = 29 ± 1.06) were followed up for a mean of 3.6 ± 1.2 years. Despite the infrequency of cued memory decline (only 19% of participants scored ≤46/48 in total recall by year 3), Aβ+ participants were 3.55 times (95% confidence interval = 1.77–7.12) more likely to exhibit decline in total recall (≤46/48) compared with their Aβ− peers. Furthermore, Aβ+ participants who scored ≤46/48 had smaller hippocampal volumes (t = 3.37, p = 0.001) and evidence of early functional decline, i.e., greater risk of progression to global Clinical Dementia Rating of 0.5 (χ2 = 14.30, p < 0.001), compared with their Aβ+ peers with intact total recall.Conclusions:Cued memory decline in healthy older adults may be particularly indicative of Aβ-related decline during the preclinical stage of AD and useful for identifying Aβ+ clinically normal individuals at greatest risk of short-term clinical progression.


2012 ◽  
Vol 32 (46) ◽  
pp. 16233-16242 ◽  
Author(s):  
T. Hedden ◽  
E. C. Mormino ◽  
R. E. Amariglio ◽  
A. P. Younger ◽  
A. P. Schultz ◽  
...  

Author(s):  
Irina Orlovsky ◽  
Willem Huijbers ◽  
Bernard J. Hanseeuw ◽  
Elizabeth C. Mormino ◽  
Trey Hedden ◽  
...  

Author(s):  
Lauren E. Oberlin ◽  
Matteo Respino ◽  
Lindsay Victoria ◽  
Lila Abreu ◽  
Matthew J. Hoptman ◽  
...  

AbstractNeuroimaging features of small vessel disease (SVD) are highly prevalent in older adulthood and associated with significant variability in clinical symptoms, yet the factors predicting these symptom disparities are poorly understood. We employed a novel metric of SVD, peak width of skeletonized mean diffusivity (PSMD), to elucidate the relationship of late-life depression (LLD) to the cognitive presentation of vascular pathology. A total of 109 older adults without a diagnosis of a neurocognitive disorder were enrolled in the study; 44 with major depressive disorder and 65 age-matched controls. Subjects completed neuropsychological testing and magnetic resonance imaging including FLAIR and diffusion tensor imaging sequences, from which white matter hyperintensity volume and diffusion metrics (fractional anisotropy, mean diffusivity, PSMD) were quantified. In hierarchical models, the relationship between vascular burden and cognitive performance varied as a function of diagnostic status, such that the negative association between PSMD and processing speed was significantly stronger in participants with LLD compared to controls. Greater PSMD also predicted poorer performance on delayed memory and executive function tasks specifically among those with LLD, while there were no associations between PSMD and task performance among controls. PSMD outperformed conventional SVD and diffusion markers in predicting cognitive performance and dysexecutive behaviors in participants with LLD. These data suggest that LLD may confer a vulnerability to the cognitive manifestations of white matter abnormalities in older adulthood. PSMD, a novel biomarker of diffuse microstructural changes in SVD, may be a more sensitive marker of subtle cognitive deficits stemming from vascular pathology in LLD.


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