TY - JOUR
T1 - Effects of biological tissue structural anisotropy and anisotropy of magnetic susceptibility on the gradient echo MRI signal phase
T2 - theoretical background
AU - Yablonskiy, Dmitriy A.
AU - Sukstanskii, Alexander L.
N1 - Publisher Copyright:
Copyright © 2016 John Wiley & Sons, Ltd.
PY - 2017/4/1
Y1 - 2017/4/1
N2 - Quantitative susceptibility mapping is a potentially powerful technique for mapping tissue magnetic susceptibility from gradient recalled echo (GRE) MRI signal phase. In this review, we present up-to-date theoretical developments in analyzing the relationships between GRE signal phase and the underlying tissue microstructure and magnetic susceptibility at the cellular level. Two important phenomena contributing to the GRE signal phase are at the focus of this review – tissue structural anisotropy (e.g. cylindrical axonal bundles in white matter) and magnetic susceptibility anisotropy. One of the most intriguing and challenging problems in this field is calculating the so-called Lorentzian contribution to the phase shift induced by the local environment – magnetized tissue structures that have dimensions smaller than the imaging voxel (e.g. cells, cellular components, blood capillaries). In this review, we briefly discuss a “standard” approach to this problem, based on introduction of an imaginary Lorentzian cavity, as well as a more recent method – the generalized Lorentzian tensor approach (GLTA) – that is based on a statistical approach and a direct solution of the magnetostatic Maxwell equations. The latter adequately accounts for both types of anisotropy: the anisotropy of magnetic susceptibility and the structural tissue anisotropy. In the GLTA the frequency shift due to the local environment is characterized by the Lorentzian tensor (Formula presented.), which has a substantially different structure than the susceptibility tensor (Formula presented.). While the components of (Formula presented.) are compartmental susceptibilities “weighted” by their volume fractions, the components of (Formula presented.) are weighted by specific numerical factors depending on tissue geometrical microsymmetry. In multi-compartment structures, the components of the Lorentzian tensor also depend on the compartmental relaxation properties, hence the MR pulse sequence settings.
AB - Quantitative susceptibility mapping is a potentially powerful technique for mapping tissue magnetic susceptibility from gradient recalled echo (GRE) MRI signal phase. In this review, we present up-to-date theoretical developments in analyzing the relationships between GRE signal phase and the underlying tissue microstructure and magnetic susceptibility at the cellular level. Two important phenomena contributing to the GRE signal phase are at the focus of this review – tissue structural anisotropy (e.g. cylindrical axonal bundles in white matter) and magnetic susceptibility anisotropy. One of the most intriguing and challenging problems in this field is calculating the so-called Lorentzian contribution to the phase shift induced by the local environment – magnetized tissue structures that have dimensions smaller than the imaging voxel (e.g. cells, cellular components, blood capillaries). In this review, we briefly discuss a “standard” approach to this problem, based on introduction of an imaginary Lorentzian cavity, as well as a more recent method – the generalized Lorentzian tensor approach (GLTA) – that is based on a statistical approach and a direct solution of the magnetostatic Maxwell equations. The latter adequately accounts for both types of anisotropy: the anisotropy of magnetic susceptibility and the structural tissue anisotropy. In the GLTA the frequency shift due to the local environment is characterized by the Lorentzian tensor (Formula presented.), which has a substantially different structure than the susceptibility tensor (Formula presented.). While the components of (Formula presented.) are compartmental susceptibilities “weighted” by their volume fractions, the components of (Formula presented.) are weighted by specific numerical factors depending on tissue geometrical microsymmetry. In multi-compartment structures, the components of the Lorentzian tensor also depend on the compartmental relaxation properties, hence the MR pulse sequence settings.
KW - generalized Lorentzian tensor approach
KW - magnetic susceptibility
KW - phase contrast
KW - quantitative susceptibility mapping
KW - white matter
UR - http://www.scopus.com/inward/record.url?scp=85003674264&partnerID=8YFLogxK
U2 - 10.1002/nbm.3655
DO - 10.1002/nbm.3655
M3 - Review article
C2 - 27862452
AN - SCOPUS:85003674264
SN - 0952-3480
VL - 30
JO - NMR in biomedicine
JF - NMR in biomedicine
IS - 4
M1 - e3655
ER -