4.7 Article

Diffusion MRI microstructural models in the cervical spinal cord - Application, normative values, and correlations with histological analysis

期刊

NEUROIMAGE
卷 201, 期 -, 页码 -

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.neuroimage.2019.116026

关键词

Spinal cord; Diffusion MRI; Microstructure; Validation; Multi-compartment model; Signal model

资金

  1. National Institutes of Health [R21 NS087465-01, R01 EY023240, R01EB017230, T32EB001628]
  2. National Multiple Sclerosis Society [RG-1501-02840]
  3. Department of Defense [W81XWH13-0073]
  4. National Center for Research Resources [UL1 RR024975-0]

向作者/读者索取更多资源

Multi-compartment tissue modeling using diffusion magnetic resonance imaging has proven valuable in the brain, offering novel indices sensitive to the tissue microstructural environment in vivo on clinical MRI scanners. However, application, characterization, and validation of these models in the spinal cord remain relatively understudied. In this study, we apply a diffusion signal model (diffusion tensor imaging, DTI) and two commonly implemented microstructural models (neurite orientation dispersion and density imaging, NODDI; spherical mean technique, SMT) in the human cervical spinal cord of twenty-one healthy controls. We first provide normative values of DTI, SMT, and NODDI indices in a number of white matter ascending and descending pathways, as well as various gray matter regions. We then aim to validate the sensitivity and specificity of these diffusion-derived contrasts by relating these measures to indices of the tissue microenvironment provided by a histological template. We find that DTI indices are sensitive to a number of microstructural features, but lack specificity. The microstructural models also show sensitivity to a number of microstructure features; however, they do not capture the specific microstructural features explicitly modelled. Although often regarded as a simple extension of the brain in the central nervous system, it may be necessary to re-envision, or specifically adapt, diffusion microstructural models for application to the human spinal cord with clinically feasible acquisitions - specifically, adjusting, adapting, and re-validating the modeling as it relates to both theory (i.e. relevant biology, assumptions, and signal regimes) and parameter estimation (for example challenges of acquisition, artifacts, and processing).

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