4.6 Article

Implicit associative learning relates to basal ganglia gray matter microstructure in young and older adults

Journal

BEHAVIOURAL BRAIN RESEARCH
Volume 397, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.bbr.2020.112950

Keywords

Implicit associative learning; Diffusion imaging; Basal ganglia; Hippocampus; Aging

Funding

  1. National Institutes of Health/National Institute on Aging [R00 AG047334, R21 AG054804]

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The study reveals age-related differences in implicit associative learning and microstructural changes in the basal ganglia and hippocampus during the learning process. Restricted diffusion in the caudate is related to early IAL, while hindered diffusion in the globus pallidus is related to late IAL, with these correlations independent of age.
Older adults are impaired at implicit associative learning (IAL), or the learning of relationships between stimuli in the environment without conscious awareness. These age effects have been attributed to differential engagement of the basal ganglia (e.g. caudate, globus pallidus) and hippocampus throughout learning. However, no studies have examined gray matter diffusion relations with IAL, which can reveal microstructural properties that vary with age and contribute to learning. In this study, young (18-29 years) and older (65-87 years) adults completed the Triplet Learning Task, in which participants implicitly learn that the location of cues predict the target location on some trials (high frequency triplets). Diffusion imaging was also acquired and multicompartment diffusion metrics were calculated using neurite orientation dispersion and density imaging (NODDI). As expected, results revealed age deficits in IAL (smaller differences in performance to high versus low frequency triplets in the late learning stage) and age-related differences in basal ganglia and hippocampus free, hindered, and restricted diffusion. Significant correlations were seen between restricted caudate diffusion and early IAL and between hindered globus pallidus diffusion and late IAL, which were not moderated by age group. These findings indicate that individual differences in basal ganglia, but not hippocampal, gray matter microstructure contribute to learning, independent of age, further supporting basal ganglia involvement in IAL.

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