Fiber ball imaging (FBI) is a recently proposed diffusion MRI (dMRI) method for estimating fiber orientation density functions together with specific microstructural parameters in white matter. The theory underlying FBI predicts the b-value dependence for the dMRI harmonic power of any given degree as long as the b-value is sufficiently large. Good agreement between theory and experiment has been previously demonstrated for the zero-degree harmonic power. Here the predicted functional forms for higher degree harmonics are shown to also agree well with experimental measurements, providing additional support for the validity of FBI.
The spherical harmonic expansion for the dMRI signal can be written as S(b,n)=S0∞∑l=0l∑m=−lamlYml(θ,ϕ), where S0 is the signal for the b=0, Yml are the spherical harmonics, (θ,ϕ) are the spherical angles for n, and aml are the expansion coefficients of degree l and order m. The harmonic power for each degree may then be defined as
pl≡12l+1l∑m=−l|aml|2.
All odd degree harmonics vanish by reflection symmetry, S(b,−n)=S(b,n), implying pl>0 for even degree harmonics only. Neglecting extra-axonal contributions, the theory underlying FBI predicts1
pl≈ulb[gl(bDa)]2,
for even degrees when b≥4000 s/mm2 where ul is a scaling factor independent of b, and
gl(x)=(l2)!xl+12Γ(l+32)1F1(l+12;l+32;−x), for l=0, 2, 4, 6,...
with 1F1 being the confluent hypergeometric function and Γ indicating the gamma function. Equation (3) implies p0≈u0/b for large b, which is equivalent to the observed b−12 decay of the direction-averaged signal. However, for higher even degrees, Equation (3) predicts that the harmonic power has a peak for finite b-values. Thus, one finds
bl=νlDa,
where bl is the b-value for the harmonic power peak of degree l and νl is a constant. The first few values of νl are found numerically to be ν2≈3.969, ν4≈11.040, ν6≈22.023, and ν8≈37.014.
For one adult volunteer, HARDI data were gathered on a Siemens 3T Prisma with b-values ranging from 1000 to 10,000 s/mm2 with 64 diffusion-encoding directions and 11 b=0 s/mm2 per b-value shell. Other acquisition parameters were TE=110ms, TR=4400ms, FOV=222 x222mm2, and voxel size = (3mm)3.
Image processing included denoising,5 Gibbs ringing removal,6 and Rician noise bias correction.7 In-house MATLAB scripts were used to calculate the spherical harmonic expansion of the dMRI signal up to l=6, as well as the corresponding pl for each harmonic using Equation (2). Additionally, several diffusion and microstructural parameters were estimated from the data by applying diffusional kurtosis imaging and the fiber ball WM (FBWM) model.8,9 In a WM mask defined as all brain voxels with mean kurtosis>1.0 and mean diffusivity<1.5 μm2/ms,10 excluding the cerebellum, the harmonic powers were either averaged over all voxels within the mask or within an individual anatomical slice of the mask.
A quadratic fit to p4 at b=3000,4000 and 5000 s/mm2 estimated b4 which was used in Equation (5) to calculate Da. This value for Da was fixed in Equation (3) and the harmonic power of each degree for b=0−10,000 s/mm2 was calculated. Normalization was done for each pl by p2 at b=1000 s/mm2 (p∗2) and the scale factor ul was set so that theory and experiment coincided at b=6000 s/mm2. Thus, for the full dataset, only four adjustable parameters were used.
1. Jensen JH, Russell Glenn G, Helpern JA. Fiber ball imaging. Neuroimage. 2016;124(Pt A):824-833.
2. Tuch DS, Reese TG, Wiegell MR, Makris N, Belliveau JW, Wedeen VJ. High angular resolution diffusion imaging reveals intravoxel white matter fiber heterogeneity. Magn Reson Med. 2002;48(4):577-582.
3. McKinnon ET, Jensen JH, Glenn GR, Helpern JA. Dependence on b-value of the direction-averaged diffusion-weighted imaging signal in brain. Magn Reson Imaging. 2017;36:121-127.
4. Veraart J, Fieremans E, Novikov DS. On the scaling behavior of water diffusion in human brain white matter. Neuroimage. 2018;185:379-387.
5. Veraart J, Novikov DS, Christiaens D, Ades-Aron B, Sijbers J, Fieremans E. Denoising of diffusion MRI using random matrix theory. Neuroimage. 2016;142:394-406.
6. Kellner E, Dhital B, Kiselev VG, Reisert M. Gibbs-ringing artifact removal based on local subvoxel-shifts. Magn Reson Med. 2016;76(5):1574-1581.
7. Gudbjartsson H, Patz S. The Rician distribution of noisy MRI data. Magn Reson Med. 1995;34(6):910-914.
8. Jensen JH, Helpern JA. MRI quantification of non-Gaussian water diffusion by kurtosis analysis. NMR Biomed. 2010;23(7):698-710.
9. McKinnon ET, Helpern JA, Jensen JH. Modeling white matter microstructure with fiber ball imaging. Neuroimage. 2018;176:11-21.
10. Yang AW, Jensen JH, Hu CC, Tabesh A, Falangola MF, Helpern JA. Effect of cerebral spinal fluid suppression for diffusional kurtosis imaging. J Magn Reson Imaging. 2013;37(2):365-371.
11. Kaden E, Kelm ND, Carson RP, Does MD, Alexander DC. Multi-compartment microscopic diffusion imaging. Neuroimage. 2016;139:346-359.
12. Veraart J, Novikov DS, Fieremans E. TE dependent Diffusion Imaging (TEdDI) distinguishes between compartmental T2 relaxation times. Neuroimage. 2018;182:360-369.
13. Dhital B, Reisert M, Kellner E, Kiselev VG. Intra-axonal diffusivity in brain white matter arXiv preprint arXiv:1712.04565