White matter dysfunction in Alzheimer’s disease is associated with disease-related transcriptomic signatures

While anatomical white matter (WM) alterations in Alzheimer's disease (AD) are well-established, functional WM dysregulation remains rarely investigated. The current study examines WM functional connectivity and network properties alterations in AD and mild cognitive impairment (MCI) and further describes their spatially correlated genes. AD and MCI shared decreased functional connectivity, clustering coefficient, and local efficiency within WM regions involved in impaired sensory-motor, visual-spatial, language, or memory functions. AD-specific dysfunction (i.e., AD vs. MCI and cognitively unimpaired participants) was predominantly located in WM, including anterior and posterior limb of internal capsule, corona radiata, and left tapetum. This WM dysfunction spatially correlates with specific genes, which are enriched in multiple biological processes related to synaptic function and development, and are mostly active in neurons and astrocytes. These findings may contribute to understanding molecular, cellular, and functional signatures associated with WM damage in AD.

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Publication Details

Journal
Communications Biology
Published
2025-05-28
DOI
https://doi.org/10.1038/s42003-025-08177-7
Citations
5
Primary Topic
Alzheimer's disease research and treatments
Type
article
Field-Weighted Citation Impact
5.82

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article

White matter dysfunction in Alzheimer’s disease is associated with disease-related transcriptomic signatures

Yasser Iturria‐Medina, Fanyu Zhang, Bharat B. Biswal, Yilu Li et al.
5 citations
Communications Biology
Alzheimer's disease research and treatments
5.82
article

White matter dysfunction in Alzheimer’s disease is associated with disease-related transcriptomic signatures

Yasser Iturria‐Medina, Fanyu Zhang, Bharat B. Biswal, Yilu Li, Guanyu Zhou, Pan Wang, Lin Liu, Dezhong Yao, Jinzhong Peng
article en
5 citations

Abstract

While anatomical white matter (WM) alterations in Alzheimer's disease (AD) are well-established, functional WM dysregulation remains rarely investigated. The current study examines WM functional connectivity and network properties alterations in AD and mild cognitive impairment (MCI) and further describes their spatially correlated genes. AD and MCI shared decreased functional connectivity, clustering coefficient, and local efficiency within WM regions involved in impaired sensory-motor, visual-spatial, language, or memory functions. AD-specific dysfunction (i.e., AD vs. MCI and cognitively unimpaired participants) was predominantly located in WM, including anterior and posterior limb of internal capsule, corona radiata, and left tapetum. This WM dysfunction spatially correlates with specific genes, which are enriched in multiple biological processes related to synaptic function and development, and are mostly active in neurons and astrocytes. These findings may contribute to understanding molecular, cellular, and functional signatures associated with WM damage in AD.

Communications BiologyVol. 8(1)
New Jersey Institute of Technology (US), Montreal Neurological Institute and Hospital (CA), University of Electronic Science and Technology of China (CN), McGill University (CA)
U.S. Department of Defense, Alzheimer's Association, Bristol-Myers Squibb, Eli Lilly and Company, Pfizer, Biogen, University of Southern California, Meso Scale Diagnostics, BioClinica, Novartis Pharmaceuticals Corporation, Northern California Institute for Research and Education, National Natural Science Foundation of China, Eisai, Servier, H. Lundbeck A/S, IXICO, National Institutes of Health, Genentech, Avid Radiopharmaceuticals, Canadian Institutes of Health Research
Openalex Percentile: Top 4%
Alzheimer's disease research and treatments
5.82
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White matter dysfunction in Alzheimer’s disease is associated with disease-related transcriptomic signatures — Yasser Iturria‐Medina, Fanyu Zhang, et al. · Communications Biology (2025) | TGRS Research Map | TGRS