Abstract
Background
Amyloid-β (Aβ) deposition in mild cognitive impairment (MCI) disrupts interhemispheric homotopic connectivity, yet its longitudinal course is unclear.
Objective
We aim to characterize the longitudinal decay of voxel-mirrored homotopic connectivity (VMHC) in MCI patients, elucidate underlying Aβ-associated mechanisms, and link these processes to cognitive decline.
Methods
Eighty-three ADNI participants (60 MCI, 23 cognitively normal [CN]) underwent baseline and two-year follow-up. MCI cases were stratified by 18F-AV45 PET into Aβ-positive (MCI-Aβ+, n = 44) and Aβ-negative (MCI-Aβ-, n = 16) subgroups. VMHC and corpus-callosum volume were compared across groups (ANOVA). Spearman correlations linked regional VMHC to cognition, cerebrospinal fluid (CSF) biomarkers, and callosal volume. Linear mixed-effects models tested group-by-time interactions; two-year VMHC change was related to parallel cognitive decline.
Results
At baseline, MCI-Aβ- patients showed lower VMHC in the fusiform and postcentral gyri, whereas MCI-Aβ+ patients exhibited additional reductions in the precuneus, superior frontal gyrus, cerebellum, and superior occipital gyrus. Lower VMHC correlated with poorer cognition, corpus-callosum atrophy, and abnormal CSF profiles; callosal volume itself did not differ between groups. Longitudinally, MCI-Aβ+ participants exhibited a slower VMHC decline across the posterior cingulate, cerebellum and thalamus. Two-year cumulative change in VMHC inversely correlated with change in cognitive performance.
Conclusions
Aβ burden shapes distinct trajectories of interhemispheric connectivity loss in MCI. VMHC decline tracks multi-domain cognitive deterioration and may serve as a biomarker of progression toward Alzheimer's disease.
Keywords
Get full access to this article
View all access options for this article.
References
Supplementary Material
Please find the following supplemental material available below.
For Open Access articles published under a Creative Commons License, all supplemental material carries the same license as the article it is associated with.
For non-Open Access articles published, all supplemental material carries a non-exclusive license, and permission requests for re-use of supplemental material or any part of supplemental material shall be sent directly to the copyright owner as specified in the copyright notice associated with the article.
