About

Log in?

DTU users get better search results including licensed content and discounts on order fees.

Anyone can log in and get personalized features such as favorites, tags and feeds.

Log in as DTU user Log in as non-DTU user No thanks

DTU Findit

Journal article

ActiveAxADD: Toward non-parametric and orientationally invariant axon diameter distribution mapping using PGSE

From

Swiss Federal Institute of Technology Lausanne1

Department of Applied Mathematics and Computer Science, Technical University of Denmark2

Visual Computing, Department of Applied Mathematics and Computer Science, Technical University of Denmark3

Purpose: Non-invasive axon diameter distribution (ADD) mapping using diffusion MRI is an ill-posed problem. Current ADD mapping methods require knowledge of axon orientation before performing the acquisition. Instead, ActiveAx uses a 3D sampling scheme to estimate the orientation from the signal, providing orientationally invariant estimates.

The mean diameter is estimated instead of the distribution for the solution to be tractable. Here, we propose an extension (ActiveAxADD) that provides non-parametric and orientationally invariant estimates of the whole distribution. Theory: The accelerated microstructure imaging with convex optimization (AMICO) framework accelerates mean diameter estimation using a linear formulation combined with Tikhonov regularization to stabilize the solution.

Here, we implement a new formulation (ActiveAxADD) that uses Laplacian regularization to provide robust estimates of the whole ADD. Methods: The performance of ActiveAxADD was evaluated using Monte Carlo simulations on synthetic white matter samples mimicking axon distributions reported in histological studies.

Results: ActiveAxADD provided robust ADD reconstructions when considering the isolated intra-axonal signal. However, our formulation inherited some common microstructure imaging limitations. When accounting for the extra axonal compartment, estimated ADDs showed spurious peaks and increased variability because of the difficulty of disentangling intra and extra axonal contributions.

Conclusion: Laplacian regularization solves the ill-posedness regarding the intra axonal compartment. ActiveAxADD can potentially provide non-parametric and orientationally invariant ADDs from isolated intra-axonal signals. However, further work is required before ActiveAxADD can be applied to real data containing extra-axonal contributions, as disentangling the 2 compartment appears to be an overlooked challenge that affects microstructure imaging methods in general.

Language: English
Year: 2020
Pages: 2322-2330
ISSN: 15222594 and 07403194
Types: Journal article
DOI: 10.1002/mrm.28053
ORCIDs: 0000-0002-8823-9176 , 0000-0001-8557-9223 , 0000-0002-8960-5465 , Dyrby, Tim Bjørn , 0000-0003-2938-9657 and 0000-0002-4677-6678

DTU users get better search results including licensed content and discounts on order fees.

Log in as DTU user

Access

Analysis