4.6 Article

Structural and Functional Brain Connectivity Uniquely Contribute to Episodic Memory Performance in Older Adults

Journal

FRONTIERS IN AGING NEUROSCIENCE
Volume 14, Issue -, Pages -

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fnagi.2022.951076

Keywords

multimodal neuroimaging; individual differences; diffusion tensor imaging; resting state functional connectivity; episodic memory

Funding

  1. Alzheimer's Association Grant [AARF-20-685267]
  2. National Institutes of Health [U19-AG033655, P30-AG066507, P41-EB031771]

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In this study, the independent contributions of structural and functional connectivity markers to individual differences in episodic memory performance in cognitively normal older adults were examined. The results showed that fornix RD, hippocampal cingulum RD, and salience network functional connectivity were significant predictors of memory performance. These findings demonstrated that a combination of structural and functional connectivity markers best accounted for individual variability in episodic memory function in cognitively normal older adults.
In this study, we examined the independent contributions of structural and functional connectivity markers to individual differences in episodic memory performance in 107 cognitively normal older adults from the BIOCARD study. Structural connectivity, defined by the diffusion tensor imaging (DTI) measure of radial diffusivity (RD), was obtained from two medial temporal lobe white matter tracts: the fornix and hippocampal cingulum, while functional connectivity markers were derived from network-based resting state functional magnetic resonance imaging (rsfMRI) of five large-scale brain networks: the control, default, limbic, dorsal attention, and salience/ventral attention networks. Hierarchical and stepwise linear regression methods were utilized to directly compare the relative contributions of the connectivity modalities to individual variability in a composite delayed episodic memory score, while also accounting for age, sex, cerebrospinal fluid (CSF) biomarkers of amyloid and tau pathology (i.e., A beta(42)/A beta(40) and p-tau(181)), and gray matter volumes of the entorhinal cortex and hippocampus. Results revealed that fornix RD, hippocampal cingulum RD, and salience network functional connectivity were each significant independent predictors of memory performance, while CSF markers and gray matter volumes were not. Moreover, in the stepwise model, the addition of sex, fornix RD, hippocampal cingulum RD, and salience network functional connectivity each significantly improved the overall predictive value of the model. These findings demonstrate that both DTI and rsfMRI connectivity measures uniquely contributed to the model and that the combination of structural and functional connectivity markers best accounted for individual variability in episodic memory function in cognitively normal older adults.

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