4.7 Article

Tissue magnetic susceptibility mapping as a marker of tau pathology in Alzheimer's disease

期刊

NEUROIMAGE
卷 159, 期 -, 页码 334-345

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.neuroimage.2017.08.003

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资金

  1. UK Medical Research Council [MR/J500422/1, MR/G09002073/1]
  2. NC3Rs studentship [NC/K500276/1]
  3. Wellcome Trust
  4. Royal Society [204624/Z/16/Z]
  5. EPSRC [EP/N034864/1]
  6. Medical Research Council [MR/J013110/1]
  7. King's College London
  8. UCL Comprehensive Cancer Imaging Centre CR-UK EPSRC
  9. MRC (England)
  10. DoH (England)
  11. UK Regenerative Medicine Platform Safety Hub (MRC) [MR/K026739/1]
  12. Eli Lilly and Company
  13. MRC [MR/K026739/1, MR/J013110/1] Funding Source: UKRI
  14. Medical Research Council [MR/K026739/1, MR/J013110/1] Funding Source: researchfish
  15. National Centre for the Replacement, Refinement and Reduction of Animals in Research (NC3Rs) [NC/K500276/1] Funding Source: researchfish

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Alzheimer's disease is connected to a number of other neurodegenerative conditions, known collectively as 'tauopathies', by the presence of aggregated tau protein in the brain. Neuroinflammation and oxidative stress in AD are associated with tau pathology and both the breakdown of axonal sheaths in white matter tracts and excess iron accumulation grey matter brain regions. Despite the identification of myelin and iron concentration as major sources of contrast in quantitative susceptibility maps of the brain, the sensitivity of this technique to tau pathology has yet to be explored. In this study, we perform Quantitative Susceptibility Mapping (QSM) and T2* mapping in the rTg4510, a mouse model of tauopathy, both in vivo and ex vivo. Significant correlations were observed between histological measures of myelin content and both mean regional magnetic susceptibility and T2* values. These results suggest that magnetic susceptibility is sensitive to tissue myelin concentrations across different regions of the brain. Differences in magnetic susceptibility were detected in the corpus callosum, striatum, hippocampus and thalamus of the rTg4510 mice relative to wild type controls. The concentration of neurofibrillary tangles was found to be low to intermediate in these brain regions indicating that QSM may be a useful biomarker for early stage detection of tau pathology in neurodegenerative diseases.

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