4.7 Article

Dissociable diffusion MRI patterns of white matter microstructure and connectivity in Alzheimer's disease spectrum

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SCIENTIFIC REPORTS
卷 7, 期 -, 页码 -

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NATURE PORTFOLIO
DOI: 10.1038/srep45131

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  1. European Commission's 7th Framework Programme [602450]
  2. Research Council of Norway [213837, 223273, 204966/F20, 249795/F20]
  3. South-Eastern Norway Regional Health Authority [2013123, 2014097, 2015073, 2016083]
  4. National Association for Public Health's Dementia Research Program of Norway
  5. KG Jebsen Foundation

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Recent efforts using diffusion tensor imaging (DTI) have documented white matter (WM) alterations in Alzheimer's disease (AD). The full potential of whole-brain DTI, however, has not been fully exploited as studies have focused on individual microstructural indices independently. In patients with AD (n =79), mild (MCI, n =55) and subjective (SCI, n =30) cognitive impairment, we applied linked independent component analysis (LICA) to model inter-subject variability across five complementary DTI measures (fractional anisotropy (FA), axial/radial/mean diffusivity, diffusion tensor mode), two crossing fiber measures estimated using a multi-compartment crossing-fiber model reflecting the volume fraction of the dominant (f1) and non-dominant (f2) diffusion orientation, and finally, connectivity density obtained from full-brain probabilistic tractography. The LICA component explaining the largest data variance was highly sensitive to disease severity (AD < MCI < SCI) and revealed widespread coordinated decreases in FA and f1 with increases in all diffusivity measures in AD. Additionally, it reflected regional coordinated decreases and increases in f2, mode and connectivity density, implicating bidirectional alterations of crossing fibers in the fornix, uncinate fasciculi, corpus callosum and major sensorimotor pathways. LICA yielded improved diagnostic classification performance compared to univariate regionof-interest features. Our results document coordinated WM microstructural and connectivity alterations in line with disease severity across the AD continuum.

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