Reduced Hippocampal-Striatal Interactions during Formation of Durable Episodic Memories in Aging. (28th September 2021)

• Record Type: Journal Article
• Authors: Ness, Hedda T; Folvik, Line; Sneve, Markus H; Vidal-Piñeiro, Didac; Raud, Liisa; Geier, Oliver M; Nyberg, Lars; Walhovd, Kristine B; Fjell, Anders M
• Is Part Of: Cerebral cortex. Volume 32:Number 11(2022)
• Page Start: 2358
• Page End: 2372
• Publication Date: 2021-09-28
• Subjects: aging -- durable memory encoding -- fMRI -- functional connectivity -- long-term memory; Cerebral cortex -- Periodicals; Brain -- Periodicals; 612.825
• DOI: 10.1093/cercor/bhab331
• Languages: English
• ISSNs: 1047-3211

Abstract

Abstract: Encoding of durable episodic memories requires cross-talk between the hippocampus and multiple brain regions. Changes in these hippocampal interactions could contribute to age-related declines in the ability to form memories that can be retrieved after extended time intervals. Here we tested whether hippocampal–neocortical– and subcortical functional connectivity (FC) observed during encoding of durable episodic memories differed between younger and older adults. About 48 younger (20–38 years; 25 females) and 43 older (60–80 years; 25 females) adults were scanned with fMRI while performing an associative memory encoding task. Source memory was tested ~20 min and ~6 days postencoding. Associations recalled after 20 min but later forgotten were classified as transient, whereas memories retained after long delays were classified as durable. Results demonstrated that older adults showed a reduced ability to form durable memories and reduced hippocampal–caudate FC during encoding of durable memories. There was also a positive relationship between hippocampal–caudate FC and higher memory performance among the older adults. No reliable age group differences in durable memory–encoding activity or hippocampal–neocortical connectivity were observed. These results support the classic theory of striatal alterations as one cause of cognitive decline in aging and highlight that age-related changes in episodic memory extend beyond hippocampal–neocortical connections.