Neurite orientation dispersion and density imaging (NODDI) is a widely used tool for modeling microstructure using diffusion MRI, but its computational cost can be prohibitively expensive. This work investigates the efficacy of integrating the spherical mean technique (SMT) into a non-linear optimization framework to improve NODDI parameter estimation. Through quantitative simulation, comparative, and reliability analyses, we found that integrating SMT into more traditional non-linear optimization enables rapid, accurate, and reliable estimation of neurite density and dispersion compared to other approaches.
Neurite orientation dispersion and density imaging (NODDI) is a multi-compartment modeling technique for deriving microstructural parameters from multi-shell diffusion MRI1. It has been widely adopted due to its simplicity and improved biophysical specificity compared to other techniques, such as diffusion tensor modeling2,3; however, its computational cost can be prohibitive when datasets are large or the available compute resources are limited. While a variety of approximate accelerated fitting methods have been proposed, faster non-linear fitting approaches remain attractive due to their accuracy and flexibility for setting study specific diffusivity and incorporating priors.
The spherical mean technique (SMT) is a mathematical tool for obtaining orientationally-invariant parameters of multi-compartment models using powder averaging of the diffusion signal within each shell of the gradient encoding4. SMT has been previously used for neurite density estimation5 but it has been neither systematically evaluated nor combined with dispersion estimation. Because its use may provide computational advantages, we investigated such a multi-stage approach for estimating the complete set of NODDI parameters by integrating the SMT into a typical non-linear optimization framework (NODDI-SMT). We evaluated this approach through simulation experiments, quantitative comparisons with other techniques using in vivo data, and a scan-rescan analysis of reliability across a typical population.
Datasets: Our experiments used the in vivo human scan with 1.875x1.875x2.5 mm3 voxels and b=0,700,2000 s/mm2 released on NITRC with the NODDI toolbox6 and 44 pairs of test-retest in vivo human scans with 1.25 mm isotropic voxels and b=0,1000,2000,3000 s/mm2 from the Human Connectome Project7 (HCP).
Fitting: We incorporated SMT into NODDI fitting using the following multi-stage approach: first, the neurite density index (NDI) and isotropic volume fraction (FISO) were estimated using powder averaged signals with the SMT, then the orientation dispersion index (ODI) and NDI were obtained using Powell's BOBYQA non-linear optimization algorithm8 with the SMT parameters as initial conditions. We compared the performance of SMT fitting with two reference fitting techniques: Accelerated Microstructure Imaging via Convex Optimization9 (AMICO), implemented using the publicly available Python code10 and non-linear least squares (NLLS) using BOBYQA with fixed initial conditions.
Experiments: We evaluated this technique using three experiments. First, we evaluated the accuracy of NLLS and SMT fitting across several levels of Rician noise (Fig 1). We simulated diffusion MR signals from a variety of typical NODDI parameter sets and assessed the error from NLLS and SMT fitting. Second, we evaluated consistency among AMICO, NLLS, and SMT-based fitting approaches by comparing their runtimes, parameter estimates, and residual fitting errors with NITRC data (Figs. 2,3), and excluded voxels that were mostly free water from the analysis. Third, we evaluated scan-rescan reliability using the coefficient of variation (CV) and intra-class correlation (ICC) with HCP data (Figs. 4,5) using averages from regions-of-interest from the Johns Hopkins and Desikan-Killiany white matter atlases coregistered using DTI-TK11.
[1] Zhang, H., Schneider, T., Wheeler-Kingshott, C. A., & Alexander, D. C. (2012). NODDI: practical in vivo neurite orientation dispersion and density imaging of the human brain. Neuroimage, 61(4), 1000-1016.
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[6] https://www.nitrc.org/projects/noddi_toolbox
[7] Sotiropoulos, S. N., Jbabdi, S., Xu, J., Andersson, J. L., Moeller, S.,Auerbach, E. J., ... & Feinberg, D. A. (2013). Advances in diffusion MRI acquisition and processing in the Human Connectome Project. Neuroimage, 80,125-143.
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[9] Daducci, A., Canales-Rodríguez, E. J., Zhang, H., Dyrby, T. B., Alexander, D. C., & Thiran, J. P. (2015). Accelerated microstructure imaging via convex optimization (AMICO) from diffusion MRI data. NeuroImage, 105, 32-44.
[10] https://github.com/daducci/AMICO
[11] Zhang, H., Yushkevich, P. A., Alexander, D. C., & Gee, J. C. (2006). Deformable registration of diffusion tensor MR images with explicit orientation optimization. Medical image analysis, 10(5), 764-785.
[12] Cabeen, R. P., Laidlaw, D. H., Toga, A. W., (2018). Quantitative ImagingToolkit: Software for Interactive 3D Visualization, Processing, and Analysis ofNeuroimaging Datasets. ISMRM 2018, Abstract 2854
[13] http://cabeen.io/
[14] http://resource.loni.usc.edu/resources/downloads/