Purpose
To develop and validate a T1âcorrected chemicalâshift encoded MRI (CSEâMRI) method to improve noise performance and reduce bias for quantification of tissue proton density fatâfraction (PDFF).
Methods
A variable flip angle (VFA)âCSEâMRI method using jointâfit reconstruction was developed and implemented. In computer simulations and phantom experiments, sources of bias measured using VFAâCSEâMRI were investigated. The effect of tissue T1 on bias using low flip angle (LFA)âCSEâMRI was also evaluated. The noise performance of VFAâCSEâMRI was compared to LFAâCSEâMRI for liver fat quantification. Finally, a prospective pilot study in patients undergoing gadoxetic acidâenhanced MRI of the liver to evaluate the ability of the proposed method to quantify liver PDFF before and after contrast.
Results
VFAâCSEâMRI was accurate and insensitive to transmit B1 inhomogeneities in phantom experiments and computer simulations. With high flip angles, phase errors because of RF spoiling required modification of the CSE signal model. For relaxation parameters commonly observed in liver, the jointâfit reconstruction improved the noise performance marginally, compared to LFAâCSEâMRI, but eliminated T1ârelated bias. A total of 25 patients were successfully recruited and analyzed for the pilot study. Strong correlation and good agreement between PDFF measured with VFAâCSEâMRI and LFAâCSEâMRI (preâcontrast) was observed before (R2 = 0.97; slope = 0.88, 0.81â0.94 95% confidence interval [CI]; intercept = 1.34, â0.77â1.92 95% CI) and after (R2 = 0.93; slope = 0.88, 0.78â0.98 95% CI; intercept = 1.90, 1.01â2.79 95% CI) contrast.
Conclusion
Jointâfit VFAâCSEâMRI is feasible for T1âcorrected PDFF quantification in liver, is insensitive to B1 inhomogeneities, and can eliminate T1 bias, but with only marginal SNR advantage for T1 values observed in the liver.