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Functional maintenance in the multiple demand network characterizes superior fluid intelligence in aging
Umeå universitet, Medicinska fakulteten, Umeå centrum för funktionell hjärnavbildning (UFBI). Umeå universitet, Medicinska fakulteten, Institutionen för integrativ medicinsk biologi (IMB). Umeå universitet, Medicinska fakulteten, Wallenberg centrum för molekylär medicin vid Umeå universitet (WCMM).
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2020 (engelsk)Inngår i: Neurobiology of Aging, ISSN 0197-4580, E-ISSN 1558-1497, Vol. 85, s. 145-153Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]

The multiple demand network (MDN) is conceptualized as the core processing system for multi-tasking. Increasing evidence also provides strong support for the involvement of the MDN in fluid intelligence (gF), that is, the ability to solve new problems. However, the underlying neural mechanisms of declining intelligence in old age are poorly explored, particularly whether maintenance of the functional architecture of the MDN can characterize superior intelligence in successful aging. Here, we used eigenvector centrality (EC) to explore the resting-state functional architecture of the MDN in terms of its communication across the entire brain. We found gF to be negatively associated with age and that the MDN EC competitively mediated age-related decline in gF over the aging lifespan, suggesting that excessive cross-talk from the MDN is deleterious for intelligence. Critically, older individuals with comparable MDN EC as younger individuals exhibited superior gF compared with their age-matched counterparts. Taken together, these data provide support for the maintenance of youth-like functional architecture of the MDN and its implication for superior intelligence in successful aging. 

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Elsevier, 2020. Vol. 85, s. 145-153
Emneord [en]
Functional MRI (fMRI), Functional centrality, Brain maintenance, Aging lifespan, Fluid intelligence
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Identifikatorer
URN: urn:nbn:se:umu:diva-166827DOI: 10.1016/j.neurobiolaging.2019.09.006ISI: 000501333500015PubMedID: 31718925Scopus ID: 2-s2.0-85075521472OAI: oai:DiVA.org:umu-166827DiVA, id: diva2:1382467
Tilgjengelig fra: 2020-01-03 Laget: 2020-01-03 Sist oppdatert: 2023-03-23bibliografisk kontrollert

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Salami, Alireza

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