
Searching for the neurite density with diffusion MRI: Challenges for biophysical modeling
Author(s) -
Lampinen Björn,
Szczepankiewicz Filip,
Novén Mikael,
Westen Danielle,
Hansson Oskar,
Englund Elisabet,
Mårtensson Johan,
Westin CarlFredrik,
Nilsson Markus
Publication year - 2019
Publication title -
human brain mapping
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.005
H-Index - 191
eISSN - 1097-0193
pISSN - 1065-9471
DOI - 10.1002/hbm.24542
Subject(s) - neurite , white matter , diffusion mri , fractional anisotropy , neuroscience , anisotropy , connectomics , connectome , nuclear magnetic resonance , biological system , physics , chemistry , functional connectivity , biology , magnetic resonance imaging , medicine , optics , radiology , biochemistry , in vitro
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.