White-matter integrity and working memory: Links to aging and dopamine-related genesVise andre og tillknytning
2022 (engelsk)Inngår i: eNeuro, E-ISSN 2373-2822, Vol. 9, nr 2, artikkel-id 0413-21.2022Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]
Working memory, a core function underlying many higher-level cognitive processes, requires cooperation of multiple brain regions. White matter refers to myelinated axons, which are critical to inter-regional brain communication. Past studies on the association between white-matter integrity and working memory have yielded mixed findings. Using voxel-wise tract-based spatial statistics analysis, we investigated this relationship in a sample of 328 healthy adults from 25 to 80 years of age. Given the important role of dopamine (DA) in working-memory functioning and white matter, we also analyzed the effects of dopamine-related genes on them. There were associations between white-matter integrity and working memory in multiple tracts, indicating that working-memory functioning relies on global connections between different brain areas across the adult lifespan. Moreover, a mediation analysis suggested that white-matter integrity contributes to age-related differences in working memory. Finally, there was an effect of the COMT Val158Met polymorphism on white-matter integrity, such that Val/Val carriers had lower fractional anisotropy (FA) values than any Met carriers in the internal capsule, corona radiata, and posterior thalamic radiation. As this polymorphism has been associated with dopaminergic tone in the prefrontal cortex (PFC), this result provides evidence for a link between DA neurotransmission and white matter. Taken together, the results support a link between white-matter integrity and working memory and provide evidence for its interplay with age and DA-related genes.
sted, utgiver, år, opplag, sider
Society for Neuroscience , 2022. Vol. 9, nr 2, artikkel-id 0413-21.2022
Emneord [en]
Aging, COMT, DTI, Dopamine, White Matter, Working Memory
HSV kategori
Identifikatorer
URN: urn:nbn:se:oru:diva-98328DOI: 10.1523/ENEURO.0413-21.2022ISI: 000789037300003PubMedID: 35346961Scopus ID: 2-s2.0-85128165001OAI: oai:DiVA.org:oru-98328DiVA, id: diva2:1648287
Forskningsfinansiär
Swedish Research Council, 421-20131039The Swedish Brain Foundation, F02014-0224Forte, Swedish Research Council for Health, Working Life and Welfare
Merknad
Funding agency:
Alexander von Humboldt Foundation
2022-03-302022-03-302022-05-18bibliografisk kontrollert