期刊
NEUROIMAGE-CLINICAL
卷 26, 期 -, 页码 -出版社
ELSEVIER SCI LTD
DOI: 10.1016/j.nicl.2020.102203
关键词
Alzheimer's disease; Diffusion tensor imaging; White matter; Brain regions; CELF1; Immune response; Gene expression; Multiscale embedded gene coexpression network analysis
类别
资金
- National Institutes of Health/National Institute on Aging [U01AG046170, RF1AG054014, RF1AG057440, R01AG057907, F32AG064904]
Introduction: Microstructural abnormalities in white matter (WM) are often reported in Alzheimer's disease (AD). However, it is unclear which brain regions have the strongest WM changes in presymptomatic AD and what biological processes underlie WM abnormality during disease progression. Methods: We developed a systems biology framework to integrate matched diffusion tensor imaging (DTI), genetic and transcriptomic data to investigate regional vulnerability to AD and identify genetic risk factors and gene subnetworks underlying WM abnormality in AD. Results: We quantified regional WM abnormality and identified most vulnerable brain regions. A SNP rs2203712 in CELF1 was most significantly associated with several DTI-derived features in the hippocampus, the top ranked brain region. An immune response gene subnetwork in the blood was most correlated with DTI features across all the brain regions. Discussion: Incorporation of image analysis with gene network analysis enhances our understanding of disease progression and facilitates identification of novel therapeutic strategies for AD.
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