It is demonstrated that Frequency-dependent multidimensional MRI can reveal the spatial and microstructural heterogeneity associated with amyloid pathology and provide a more comprehensive characterization of AD-related tissue alterations.
Abstract
Alzheimer’s disease (AD) pathology involves amyloid deposition, reactive gliosis, and localized tissue alterations that coexist within the same brain regions, creating heterogeneous microstructural environments within individual imaging voxels. Conventional diffusion MRI averages these environments into aggregate measures, potentially obscuring their distinct contributions. Frequency-dependent multidimensional MRI (ωMD-MRI) resolves distributions of water components with different diffusion length scales, anisotropies, and relaxation properties, providing sensitivity to microstructural restriction, heterogeneity, and shape-size correlations within a voxel. Whether these measurements reveal microstructural complexity associated with AD pathology remains unclear. Here, we performed ωMD-MRI on ex vivo brain specimens from approximately 8-month-old 5xFAD and wild-type mice and interpreted the imaging findings alongside complementary histology. ωMD-MRI revealed widespread but spatially nonuniform differences between 5xFAD and wild-type brains. Measurements sensitive to microstructural restriction, heterogeneity, and shape-size correlations consistently indicated greater microstructural heterogeneity in 5xFAD brains, with the most prominent differences in the hippocampal formation and major cerebral white matter tracts. Complementary qualitative histology demonstrated extensive amyloid deposition and glial activation in affected regions, while overall cytoarchitecture and myelin organization remained largely preserved. Thus, the ωMD-MRI abnormalities occurred in tissue characterized by multiple coexisting pathological and relatively preserved microstructural environments rather than widespread structural degeneration. These findings demonstrate that ωMD-MRI can reveal the spatial and microstructural heterogeneity associated with amyloid pathology and provide a more comprehensive characterization of AD-related tissue alterations.
DTI and MRS demonstrate complementary WM microstructural and neurochemical alterations in MS and examine the reported associations between DTI-derived diffusion metrics and MRS-derived metabolic markers.
Dheeraj Kumar, Shivam Agrawal, Rajul Rastogi et al.· The Egyptian Journal of Neur...· 0 citations
The proposed intravoxel diffusivity probability distribution (IDPD) model enables noninvasive cellular-level microstructure imaging, offering a promising avenue to evaluate living cell functions in vivo.
Xiao-Dong Li, Jing Zhao, Bao-Lan Lu et al.· 0 citations
BACKGROUND AND PURPOSE
Neurodegeneration is a key component of clinical disability in multiple sclerosis (MS). However, the underlying mechanism of localized gray matter (GM) atrophy in MS remains unknown. More recently, a network-based etiology has been postulated, which may be associated with clinical progression. Th...
Florence L. Chiang, Eva A. Krijnen, Diana A. Hobbs et al.· AJNR. American journal of ne...· 0 citations
Lesion composition may offer a more informative framework than global WMH burden for understanding cerebrovascular contributions to aging and neurodegeneration, with potential implications for risk stratification, clinical interpretation, and targeted interventions.
Raúl González-Gómez, Enzo Tagliazuchi, C. G. Campo et al.· Neurology· 0 citations
Background/Objectives: Cerebral small vessel disease (SVD) is a heterogeneous condition in which similar conventional MRI findings may be associated with different clinical manifestations and pathogenetic mechanisms. Previously, hierarchical clustering of structural MRI features in patients with severe white matter hyp...
E. Kremneva, L. Dobrynina, K. Shamtieva et al.· Diagnostics· 0 citations
Brain aging reflects heterogeneous vascular-metabolic and neurodegenerative processes, yet brain age is often reduced to a gray matter (GM)-dominant estimate. Emerging evidence suggests that subtle “dirty-appearing” T2-FLAIR abnormalities may mark diffuse white matter (WM) vulnerability that precedes or extends beyond...
Hosung Kim, Cong Zang, Jin-Soo Lee et al.· Research Square· 0 citations
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