Abstract

AbstractBackgroundSubjective Cognitive Decline (SCD) may increase the risk of Alzheimer’s Disease and related dementias (ADRD). Brain network changes may occur at both the functional and structural levels in SCD. To better understand these network changes, diffusional kurtosis imaging (DKI) and functional connectome (FC) measures were examined in SCD and healthy controls (HC). We hypothesized that DKI and FC measures in the medial temporal lobe would be sensitive to differences between SCD and healthy controls (HC).MethodSCD classification was determined by clinician evaluation or Everyday Cognition average item score > 1.6, with objectively healthy cognitive performance (Montreal Cognitive Assessment score > 22). DKI and fMRI images were acquired on a Siemens PRISMA scanner in 33 SCD subjects and 33 age/sex matched HCs (mean age=69.1 yr). DSI Studio’s Automatic fiber tracking extracted the DKI measure mean kurtosis (MK) in 3 bilateral white matter bundles associated with ADRD: inferior longitudinal fasciculus (ILF), cingulum‐parahippocampus (CP), and uncinate fasciculus (UF). FC measure eigenvector centrality (Evc) was calculated in 19 medial temporal nodes using the Brain Connectivity Toolbox. Generalized Linear Models were conducted for each bundle to determine whether EVC in the left ventrolateral amygdala (LAMG) was predicted by MK, Diagnosis or the MK*Diagnosis interaction.ResultIn the left ILF, the effect of MK approached significance (p = .054) as did the MK*Diagnosis interaction (p = .059). Lower MK was associated with higher LAMG EVC in HC (r = ‐.40) but there was no association between MK and EVC for SCD. In the left UF, effect of MK was significant (p = .003), but no effect of Diagnosis and no interaction. Lower MK was associated with higher LAMG EVC (r = ‐.359) in both SCD and HC.ConclusionThis preliminary study showed that in HC, white matter integrity of the ILF was associated with LAMG functional connectivity, but this association was absent in SCD. While present results should be interpreted with caution due to small sample sizes, these findings indicate that healthy aging structural‐functional associations are disrupted in SCD, but future studies should determine whether this is a reliable marker of brain organization changes.

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