Ning HUA1, Mitchell Horn1, Adam Aakil1, Stephan Anderson2, and Hernan Jara1
1Boston University, Boston, MA, United States, 2Boston Medical Center, Boston, MA, United States
Synopsis
Purpose:
To evaluate the effect of inherent and incidental magnetization transfer (MT)
on T1 and T2 measurements when using the mixed turbo spin echo sequence (mixed-TSE).
Methods: mixed-TSE was
applied to a phantom of 1-5% agarose gel. The levels of the MT effects were induced
and controlled by varying the number of slices per acquisition package. Results:
T1 values were underestimated in multi-slice mixed-TSE. No obvious trend was
observed for T2 measurements. Conclusion:
mixed-TSE is powerful and efficient tool for qMRI, yet caution should be taken
when interpreting the derived T1 values because of MT effects.
Introduction
Mixed turbo
spin echo (mixed-TSE) acquisition is time efficient, and can be utilized to generate
quantitative T1 and T2 maps 1, 2, which permits direct inter-subject
comparison. To
maximize efficiency, multi-slice acquisition is often adopted in TSE based
sequences. However, incidental magnetic transfer (MT) is a well-known
phenomenon caused by multi-slice imaging 3. The off-resonance radio
frequency (RF) deposition, originated from pulses targeting adjacent slices, saturates
protons bounded to macromolecules, and subsequently transfers the saturation to
mobile ones. The incidental magnetization transfer inevitably exists in all
images acquired at four time-points (Figure 1), yet its net effect on T1
and T2 quantification is still unknown. The purpose of this work was to evaluate
the MT effects of the mixed-TSE sequence in T1 and T2 measurements.Methods and Materials
As shown in Figure
1, Mixed-TSE consists of an initial inversion recovery pulse (IR), and after a delay
(TI), is followed by two 90⁰ excitation pulses with the same
repetition time (TR). The total TR would be TI+2TR. After each 90⁰ excitation pulses, images are
acquired at both echo times, TE1 and TE2, using TSE. All scans were performed
at a 3T system (Achieva, Philips Healthcare, Best, The Netherlands). Key parameters
were: TI=1000ms, total TR=19000ms, each train length= 12, TE1=12.858ms, TE2=90,
voxel dimensions = 0.5 x 0.5mm3, slice thickness=2mm NEX=1, and acquisition
package=2. The incidental MT effects were introduced by varying slice number
per acquisition package. The number of slices varied between 2 to 20, with an
interval of 2. The resulting slice per package was from 1 to 10, with an
interval of one. Two slices located at the central remained at the same location
across all acquisition volumes with various slice number, and was used for
later T1/T2 comparison. The matching T1, and T2 mapping algorithms were
programmed in Matlab (version R2017a, Mathworks, MA). The phantom used in this
study consisted of 1%, 2%, 3%, 4% and 5% agarose gel, solidified in 15ml Falcon
tubes. Manual contours were drawn in ImageJ (NIH) to obtain the mean and the
standard deviation for each sample with various slice/package. Results
The measure
T1 and T2 values are listed in Table 1.
To facilitate comparison between different concentrations of agarose gels, all
the T1 andT2 values were normalized to the corresponding mean values measured at
1 slice/package (Figure 2). With the increase of agarose concentration, the
portion of protons bounded to macro-molecules increases, and we observed an
expected decrease of T1, and shortening of T2 (Table 1). As more protons bounded to macro-molecules, an increased
MT effects was expected, and a corresponding increased underestimation of T1
was observed (Figure 2): for 1% agarose, there is a maximum of 6.2% T1
decrease; 2% agarose, 8.1% T1 decrease; 3% agarose, 8.8% T1 decrease; 4%
agarose, 11.9% T1 decrease; 5% agarose, 12.2% T1 decrease. Among the 5 agarose
samples, in 3 the maximum decrease of T1 were observed when there was 7 slices/package,
and the other 2 at 8 slices/package. There is no obvious trend of T2 changes
was observed upon MT influence.Discussion
With the
advent of faster MRI pulse sequences and image processing techniques,
quantitative MRI is now possible in routine clinical practice. The derived
metrics may enable several post-processing applications such as Synthetic MRI,
Structural qMRI, and most importantly, it can enhance diagnostic accuracy by
allowing direct intra-patient and inter-patient comparisons. However, multi-slice
acquisition causes incidental MT, and results an underestimation of T1 values,
but no obvious effects was observed on T2 measurements. The fact that the
amount of T1 decrease peaked around 7~8 slices/package suggests that, in this
agarose gel phantom, the range of off-resonance saturation covers a territory
of ±2mmx7 or 8 (±14 to 16mm).Conclusion
The
incidental MT effects in multi-slice mixed-TSE may lead to an underestimation
of T1 values. The extent of this underestimation is directly related to the
number of adjacent slices in the acquisition package that may exert
off-resonance saturation. However, there is no obvious MT effect on T2
measures.Acknowledgements
No acknowledgement found.References
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