TY - JOUR
T1 - Half way there
T2 - Theoretical considerations for power laws and sticks in diffusion mri for tissue microstructure
AU - Hall, Matt G.
AU - Ingo, Carson
N1 - Funding Information:
Funding: M.G.H. received funding from NPL’s ISCF Medical Imaging Accelerator programme financed by the U.K. Department for Business, Energy and Industrial Strategy’s Industrial Strategy Challenge Fund. C.I. was funded by National Institutes of Health grant number R03HD094615.
Publisher Copyright:
© 2021 by the authors. Licensee MDPI, Basel, Switzerland.
PY - 2021/8/2
Y1 - 2021/8/2
N2 - In this article, we consider how differing approaches that characterize biological microstructure with diffusion weighted magnetic resonance imaging intersect. Without geometrical boundary assumptions, there are techniques that make use of power law behavior which can be derived from a generalized diffusion equation or intuited heuristically as a time dependent diffusion process. Alternatively, by treating biological microstructure (e.g., myelinated axons) as an amalgam of stick-like geometrical entities, there are approaches that can be derived utilizing convolution-based methods, such as the spherical means technique. Since data acquisition requires that multiple diffusion weighting sensitization conditions or b-values are sampled, this suggests that implicit mutual information may be contained within each technique. The information intersection becomes most apparent when the power law exponent approaches a value of12, whereby the functional form of the power law converges with the explicit stick-like geometric structure by way of confluent hypergeometric functions. While a value of12 is useful for the case of solely impermeable fibers, values that diverge from12 may also reveal deep connections between approaches, and potentially provide insight into the presence of compartmentation, exchange, and permeability within heterogeneous biological microstructures. All together, these disparate approaches provide a unique opportunity to more completely characterize the biological origins of observed changes to the diffusion attenuated signal.
AB - In this article, we consider how differing approaches that characterize biological microstructure with diffusion weighted magnetic resonance imaging intersect. Without geometrical boundary assumptions, there are techniques that make use of power law behavior which can be derived from a generalized diffusion equation or intuited heuristically as a time dependent diffusion process. Alternatively, by treating biological microstructure (e.g., myelinated axons) as an amalgam of stick-like geometrical entities, there are approaches that can be derived utilizing convolution-based methods, such as the spherical means technique. Since data acquisition requires that multiple diffusion weighting sensitization conditions or b-values are sampled, this suggests that implicit mutual information may be contained within each technique. The information intersection becomes most apparent when the power law exponent approaches a value of12, whereby the functional form of the power law converges with the explicit stick-like geometric structure by way of confluent hypergeometric functions. While a value of12 is useful for the case of solely impermeable fibers, values that diverge from12 may also reveal deep connections between approaches, and potentially provide insight into the presence of compartmentation, exchange, and permeability within heterogeneous biological microstructures. All together, these disparate approaches provide a unique opportunity to more completely characterize the biological origins of observed changes to the diffusion attenuated signal.
KW - Anomalous diffusion
KW - Biological microstructure
KW - Diffusion MRI
KW - Fractional calculus
KW - Kurtosis
KW - Multi-shell diffusion MRI
KW - Power law
KW - Spherical deconvolution
KW - Spherical means
KW - Time dependent diffusion
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U2 - 10.3390/math9161871
DO - 10.3390/math9161871
M3 - Article
AN - SCOPUS:85112417657
SN - 2227-7390
VL - 9
JO - Mathematics
JF - Mathematics
IS - 16
M1 - 1871
ER -