All data were transferred to an
AW4.6 Workstation (GE Healthcare) and analyzed using its Functool software. The raw data were first organized into the Z-spectrum. Then, the Z-spectrum was fitted on a pixel-by-pixel basis according to the procedure described previously (16 (
link)21 (
link)), and the B
0 inhomogeneity map was created. The original Z-spectrum was then corrected for the B
0 inhomogeneity effect through interpolation and centering of the Z-spectrum.
CEST contrast of hydroxyl metabolites was quantified at +1.2 ppm using interpolation method and MTR asymmetry analysis with respect to the water frequency (20 (
link)).
Where S (Δω) and S (−Δω) were the signals at positive offset and its counterpart at negative offset, respectively.
The MT effect from immobile macromolecules was calculated at +15.6 ppm saturation offset (16 (
link)).
The cortical and medullary regions of interest (ROIs) were manually segmented based on the original saturated images at 15.6 ppm that showed the best contrast between the cortex and the medulla. The same ROIs were propagated to the reconstructed MTR
asym(1.2ppm) and MTR maps, and parameter values for each kidney cortex and medulla were obtained.
Li A., Xu C., Liang P., Hu Y., Shen Y., Hu D., Li Z, & Kamel I.R. (2020). Role of Chemical Exchange Saturation Transfer and Magnetization Transfer MRI in Detecting Metabolic and Structural Changes of Renal Fibrosis in an Animal Model at 3T. Korean Journal of Radiology, 21(5), 588-597.