151. Increased functional homotopy of the prefrontal cortex is associated with corpus callosum degeneration and working memory decline.
- Author
-
Avelar-Pereira B, Bäckman L, Wåhlin A, Nyberg L, and Salami A
- Subjects
- Aged, Aged, 80 and over, Corpus Callosum diagnostic imaging, Corpus Callosum physiology, Female, Humans, Magnetic Resonance Imaging, Male, Memory Disorders diagnostic imaging, Memory Disorders psychology, Nerve Degeneration diagnostic imaging, Nerve Degeneration pathology, Prefrontal Cortex diagnostic imaging, White Matter diagnostic imaging, White Matter pathology, White Matter physiology, Aging pathology, Aging psychology, Corpus Callosum pathology, Memory Disorders etiology, Memory Disorders pathology, Memory, Short-Term physiology, Nerve Degeneration etiology, Prefrontal Cortex pathology
- Abstract
Functional homotopy reflects the link between spontaneous activity in a voxel and its counterpart in the opposite hemisphere. Alterations in homotopic functional connectivity (FC) are seen in normal aging, with highest and lowest homotopy being present in sensory-motor and higher-order regions, respectively. Homotopic FC relates to underlying structural connections, but its neurobiological underpinnings remain unclear. The genu of the corpus callosum joins symmetrical parts of the prefrontal cortex (PFC) and is susceptible to age-related degeneration, suggesting that PFC homotopic connectivity is linked to changes in white-matter integrity. We investigated homotopic connectivity changes and whether these were associated with white-matter integrity in 338 individuals. In addition, we examined whether PFC homotopic FC was related to changes in the genu over 10 years and working memory over 5 years. There were increases and decreases in functional homotopy, with the former being prevalent in subcortical and frontal regions. Increased PFC homotopic FC was partially driven by structural degeneration and negatively associated with working memory, suggesting that it reflects detrimental age-related changes., (Copyright © 2020 The Author(s). Published by Elsevier Inc. All rights reserved.)
- Published
- 2020
- Full Text
- View/download PDF