Aocai Yang1 and Guolin Ma2
1Department of Radiology, China–Japan Friendship Hospital, Beijing, China, 2China–Japan Friendship Hospital, Beijing, China
Synopsis
Keywords: Alzheimer's Disease, Alzheimer's Disease
Motivation: Associations between abnormal quantitative susceptibility mapping (QSM), brain atrophy, and altered brain connectome in AD remain unclear.
Goal(s): We aim to examine imaging markers from various MRI modalities, with a focus on their spatial correlations, to enhance our understanding of AD pathology.
Approach: By combining multi-contrast MRI techniques, our study provides new insights into the overlapping relationships among brain atrophy, altered regional QSM, and brain connectome.
Results: We observed a remarkable overlap between reduced cortical thickness and abnormal QSM in seven distinct brain regions. In AD patients, we identified specific regional correlations between cortical thickness and network topology from these overlapping brain regions.
Impact: Our
study provides new insights into the complex relationships among iron
accumulation, brain atrophy, and brain connectome in Alzheimer's disease.
INTRODUCTION
Susceptibility
ron abnormality and brain network disconnections are observed in Alzheimer's
disease (AD), with disrupted iron homeostasis hypothesized to be linked to AD
pathology and neuron loss. However, associations between abnormal quantitative
susceptibility mapping (QSM), brain atrophy, and altered brain connectome in AD
remain unclear.METHODS
This
study utilized multi-modal MRI techniques to explore overlapped regions between
cortical atrophy and increased susceptibility and investigate relationships
between structural and functional brain connectome, gray matter volumes, and
regional QSM on 30 AD patients and 26 healthy controls enrolled at China-Japan
Friendship Hospital. We calculated the QSM signal and cortical thickness in 246
brain regions and identified the overlapped regions. The structural and
functional connectomes were constructed based on diffusion MRI tractography and
functional connectivity, respectively. The network topology was quantified
using graph theory analyses. RESULTS
We
revealed seven brain regions with both reduced cortical thickness and abnormal QSM,
including right superior frontal gyrus, left superior temporal gyrus, right
fusiform gyrus, left superior parietal lobule, right superior parietal lobule,
left inferior parietal lobule, and left precuneus. Unique correlations between
cortical thickness and network topology specific to the AD group were observed
in five of these regions, with stronger associations in functional compared to
structural topology. Decreased spatial covariance of QSM and global efficiency
of the structural network was also found in AD patients. CONCLUSION
Our
study provides new insights into the complex relationships among iron
accumulation, brain atrophy, and brain connectome in Alzheimer's disease (AD).
By combining multi-contrast MRI techniques, we observed distinct coupling
patterns between brain connectivity and cortical iron deposition in AD,
highlighting the potential role of iron in neurodegeneration. Our findings
contribute to a better understanding of the underlying mechanisms involved in
AD pathology. Further research is needed to validate and expand upon these
findings, with the aim of identifying potential therapeutic targets for AD.Acknowledgements
The authors thank Dr. Lizhi Xie from GE Healthcare for help in solving MR technical problems.References
No reference found.