Spatial Imaging-Transcriptomic analysis reveals the Molecular Basis of diffusion MRI signature in mouse model of Alzheimer’s Disease
Motivation: While numerous studies noted the reduction of fractional anisotropy (FA) from diffusion MRI as a sensitive marker in Alzheimer's disease, the underlying biology remained elusive. Goal(s): We aimed to explore biological basis of DTI metrics by integrating diffusion MRI with spatial transcriptomic data from the same individual. Approach: We performed voxelwise correlation between the co-registered transcriptomic and MRI data and downstream enrichment analysis. Results: We revealed links to myelin, oligodendrocytes, and Alzheimer's-associated biological processes.These findings enhanced our understanding of changes of diffusion MRI in Alzheimer's disease. Impact: Spatial imaging-transcriptomic provides a certain level of biological evidence for the molecular processes underlying DTI signatures of Alzheimer’s disease. Similar approach can be applied to other types of MRI markers in different neurodegenerative diseases.
Authors
- Yiqi Shen (ORCID: https://orcid.org/0009-0008-5195-5129)
- Vicky Yao (ORCID: https://orcid.org/0000-0002-3201-9983)
- Zhiyong Zhao (ORCID: https://orcid.org/0000-0002-1432-0430)
- Zuozhen Cao (ORCID: https://orcid.org/0000-0001-8119-6436)
- Sihui Li (ORCID: https://orcid.org/0009-0007-2442-9783)
- Qinfeng Zhu (ORCID: https://orcid.org/0000-0001-8038-0274)
- Dan Wu (ORCID: https://orcid.org/0000-0002-9303-5821)
- Menglei Wang (ORCID: https://orcid.org/0000-0003-3305-4817)
- Guojun Xu (ORCID: https://orcid.org/0000-0002-8526-9281)
Publication Details
- Journal
- Proceedings on CD-ROM - International Society for Magnetic Resonance in Medicine. Scientific Meeting and Exhibition/Proceedings of the International Society for Magnetic Resonance in Medicine, Scientific Meeting and Exhibition
- Published
- 2024-11-26
- DOI
- https://doi.org/10.58530/2024/0962
- Primary Topic
- Alzheimer's disease research and treatments
- Type
- article
- Field-Weighted Citation Impact
- 0.00