4.7 Article

Searching for the neurite density with diffusion MRI: Challenges for biophysical modeling

期刊

HUMAN BRAIN MAPPING
卷 40, 期 8, 页码 2529-2545

出版社

WILEY
DOI: 10.1002/hbm.24542

关键词

anisotropy; axons; dendrites; diffusion MRI; myelin; neurites

资金

  1. Stiftelsen for Strategisk Forskning [AM13-0090]
  2. Vetenskapsradet [2016-03443, 349-2007-869]
  3. National Institutes of Health [P41EB015898, P41EB015902, R01MH074794]
  4. Random Walk Imaging [MN15]
  5. Swedish Foundation for Strategic Research (SSF) [AM13-0090] Funding Source: Swedish Foundation for Strategic Research (SSF)
  6. Swedish Research Council [2016-03443] Funding Source: Swedish Research Council

向作者/读者索取更多资源

In vivo mapping of the neurite density with diffusion MRI (dMRI) is a high but challenging aim. First, it is unknown whether all neurites exhibit completely anisotropic (stick-like) diffusion. Second, the density of tissue components may be confounded by non-diffusion properties such as T2 relaxation. Third, the domain of validity for the estimated parameters to serve as indices of neurite density is incompletely explored. We investigated these challenges by acquiring data with b-tensor encoding and multiple echo times in brain regions with low orientation coherence and in white matter lesions. Results showed that microscopic anisotropy from b-tensor data is associated with myelinated axons but not with dendrites. Furthermore, b-tensor data together with data acquired for multiple echo times showed that unbiased density estimates in white matter lesions require data-driven estimates of compartment-specific T2 values. Finally, the stick fractions of different biophysical models could generally not serve as neurite density indices across the healthy brain and white matter lesions, where outcomes of comparisons depended on the choice of constraints. In particular, constraining compartment-specific T2 values was ambiguous in the healthy brain and had a large impact on estimated values. In summary, estimating neurite density generally requires accounting for different diffusion and/or T2 properties between axons and dendrites. Constrained index parameters could be valid within limited domains that should be delineated by future studies.

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