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. Author manuscript; available in PMC: 2022 Jun 30.
Published in final edited form as: NMR Biomed. 2019 Dec 9;34(5):e4196. doi: 10.1002/nbm.4196

Table 2.

SNR comparisons between PRESS and MRSF, in both the phantom and in-vivo, based on numerical 3D Bloch spin simulations. Simulations were run for each singlet (NAA, Cr, Cho), using its mean measured T1 and T2 values, and averaged over all singlets. Note that, on average, T1 values in the phantom are shorter than in-vivo, while T2 values are longer. The SNR per unit time of the TR=1500 ms PRESS was normalized to one. The table demonstrates that using just the short echo time (TE=35 ms) scans of MRSF for metabolite quantification yields approximately 60% of the optimal PRESS SNR. However, since T1 is often unknown in-vivo, acquisitions with prolonged TRs are preferred, such as a PRESS with TR=5000 ms; relative to such an acquisition, the TE=35 MRSF scans yield approximately 0.61/0.78≈80% of the SNR.

Normalized Voxel Volume Weighted Voxel Volume SNR per unit time
Phantom (average over all singlets)
PRESS (TR/TE=1500/35 ms) 0.87 0.48 1.00
PRESS (TR/TE=5000/35 ms) 0.87 0.54 0.59
MRSF (All TEs) 0.67 0.34 0.70
MRSF (TE=35 ms) 0.64 0.32 0.57
In-vivo (average over all singlets)
PRESS (TR/TE=1500/35 ms) 0.87 0.48 1.00
PRESS (TR/TE=5000/35 ms) 0.87 0.68 0.78
MRSF (All TEs) 0.67 0.31 0.67
MRSF (TE=35 ms) 0.64 0.32 0.61