4.7 Article

Diffusion kurtosis imaging probes cortical alterations and white matter pathology following cuprizone induced demyelination and spontaneous remyelination

期刊

NEUROIMAGE
卷 125, 期 -, 页码 363-377

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.neuroimage.2015.10.052

关键词

Diffusion; Kurtosis; White matter; Grey matter; Cuprizone; Demyelination

资金

  1. European Union Seventh Framework Programme [278850]
  2. Molecular Imaging of Brain Pathophysiology (BRAINPATH) within the Marie Curie Actions-Industry-Academia Partnerships and Pathways (IAPP) programme [612360]
  3. Hercules funding [AUHA/012]
  4. Flemish Impulse [42/FA010100/1230]
  5. Research Foundation Flanders (FWO Vlaanderen, Belgium) [G.0130.11, G.0136.11]
  6. ICON project Super MRI
  7. Interuniversity Attraction Poles Programme [P7/11]
  8. Belgian Science Policy Office
  9. IWT (Institute for the Promotion of Innovation through Science and Technology in Flanders (IWT-Vlaanderen) [IWT 2012-2016]
  10. Fund for Scientific Research-Flanders (FWO) [12S1615N]
  11. National Institutes of Health [R21-NS081230, R01NS088040]

向作者/读者索取更多资源

Although MRI is the gold standard for the diagnosis and monitoring of multiple sclerosis (MS), current conventional MRI techniques often fail to detect cortical alterations and provide little information about gliosis, axonal damage and myelin status of lesioned areas. Diffusion tensor imaging (DTI) and diffusion kurtosis imaging (DKI) provide sensitive and complementary measures of the neural tissue microstructure. Additionally, specific white matter tract integrity (WMTI) metrics modelling the diffusion in white matter were recently derived. In the current study we used the well-characterized cuprizone mouse model of central nervous system demyelination to assess the temporal evolution of diffusion tensor (DT), diffusion kurtosis tensor (DK) and WMTI-derived metrics following acute inflammatory demyelination and spontaneous remyelination. While DT-derived metrics were unable to detect cuprizone induced cortical alterations, the mean kurtosis (MK) and radial kurtosis (RK) were found decreased under cuprizone administration, as compared to age-matched controls, in both the motor and somatosensory cortices. The MK remained decreased in the motor cortices at the end of the recovery period, reflecting long lasting impairment of myelination. In white matter, DT, DK and WMTI-derived metrics enabled the detection of cuprizone induced changes differentially according to the stage and the severity of the lesion. More specifically, the MK, the RK and the axonal water fraction (AWF) were the most sensitive for the detection of cuprizone induced changes in the genu of the corpus callosum, a region less affected by cuprizone administration. Additionally, microgliosis was associated with an increase of MK and RK during the acute inflammatory demyelination phase. In regions undergoing severe demyelination, namely the body and splenium of the corpus callosum, DT-derived metrics, notably the mean diffusion (MD) and radial diffusion (RD), were among the best discriminators between cuprizone and control groups, hence highlighting their ability to detect both acute and long lasting changes. Interestingly, WMTI-derived metrics showed the aptitude to distinguish between the different stages of the disease. Both the intraaxonal diffusivity (D-a) and the AWF were found to be decreased in the cuprizone treated group, Da specifically decreased during the acute inflammatory demyelinating phase whereas the AWF decrease was associated to the spontaneous remyelination and the recovery period. Altogether our results demonstrate that DKI is sensitive to alterations of cortical areas and provides, along with WMTI metrics, information that is complementary to DT-derived metrics for the characterization of demyelination in both white and grey matter and subsequent inflammatory processes associated with a demyelinating event. (C) 2015 Published by Elsevier Inc.

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