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Association of deficits in short-term learning and Aβ and hippocampal volume in cognitively normal adults. | LitMetric

Association of deficits in short-term learning and Aβ and hippocampal volume in cognitively normal adults.

Neurology

From Florey Institute of Neuroscience and Mental Health (Y.Y.L., J.E.B., A.M., C.F., C.L.M., P.M.), Parkville; Turner Institute for Brain and Mental Health (Y.Y.L., A.M.), School of Psychological Sciences, Monash University, Clayton; School of Computing and Information Systems (L.B.), The University of Melbourne, Parkville, Victoria; CSIRO Health and Biosecurity (J.F.), Australian e-Health Research Centre, Brisbane; Centre of Excellence for Alzheimer's Disease Research and Care (S.R.R.-S.), School of Medical Sciences, Edith Cowan University; Sir James McCusker Alzheimer's Disease Research Unit (Hollywood Private Hospital) (S.R.R.-S.), Perth; National Ageing Research Institute (D.A.), Parkville, Victoria; Academic Unit for Psychiatry of Old Age, Department of Psychiatry (D.A.), The University of Melbourne, St. George's Hospital, Kew; and Cogstate Ltd. (P.M.), Melbourne, Victoria, Australia.

Published: November 2020

Objective: To determine the extent to which deficits in learning over 6 days are associated with β-amyloid-positive (Aβ+) and hippocampal volume in cognitively normal (CN) adults.

Methods: Eighty CN older adults who had undergone PET neuroimaging to determine Aβ status (n = 42 Aβ- and 38 Aβ+), MRI to determine hippocampal and ventricular volume, and repeated assessment of memory were recruited from the Australian Imaging, Biomarkers and Lifestyle (AIBL) study. Participants completed the Online Repeatable Cognitive Assessment-Language Learning Test (ORCA-LLT), which required they learn associations between 50 Chinese characters and their English language equivalents over 6 days. ORCA-LLT assessments were supervised on the first day and were completed remotely online for all remaining days.

Results: Learning curves in the Aβ+ CN participants were significantly worse than those in matched Aβ- CN participants, with the magnitude of this difference very large ( [95% confidence interval (CI)] 2.22 [1.64-2.75], < 0.001), and greater than differences between these groups for memory decline since their enrollment in AIBL ( [95% CI] 0.52 [0.07-0.96], = 0.021), or memory impairment at their most recent visit. In Aβ+ CN adults, slower rates of learning were associated with smaller hippocampal and larger ventricular volumes.

Conclusions: These results suggest that in CN participants, Aβ+ is associated more strongly with a deficit in learning than any aspect of memory dysfunction. Slower rates of learning in Aβ+ CN participants were associated with hippocampal volume loss. Considered together, these data suggest that the primary cognitive consequence of Aβ+ is a failure to benefit from experience when exposed to novel stimuli, even over very short periods.

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Source
http://dx.doi.org/10.1212/WNL.0000000000010728DOI Listing

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