Roberta Catania1, Amir A. Borhani1, Camila Lopes Vendrami1, Roger C Grimm2, Bradley D. Bolster3, and Frank Miller1
1Northwestern University Feinberg School of Medicine, Chicago, IL, United States, 2Mayo Clinic, Rochester, MN, United States, 3Siemens Medical Solutions USA, Inc., Salt Lake City, UT, United States
Synopsis
3D MRE allows volumetric assessment of liver
stiffness. Performance of this method as compared to 2D techniques (GRE and seEPI),
was evaluated, with respect to the ROI areas per slice, stiffness values, and
presence of artifacts. The 3D MRE provided larger area of liver and was less
prone to artifacts. Liver Stiffness Measures (LSM) based on 3D technique were
lower than 2D technique. 3D MRE exhibits less susceptibility to artifacts and provides
larger measurable areas of liver. LSM based on 3D MRE however were lower than
2D techniques.
Introduction
The purpose of this study was to evaluate performance
of 3D magnetic resonance
elastography (MRE) using spin-echo echo-planar imaging (seEPI) for assessment
of liver
stiffness compared with 2D
seEPI and 2D gradient recalled echo (GRE) sequences.Materials and Methods
The study was approved by IRB. Imaging studies of patients who underwent
liver MRE in a single institution between September 2020 and December 2020 were
analyzed retrospectively. All studies were performed using the same 1.5T scanner
(MAGNETOM Aera, Siemens Healthcare, Erlangen, Germany) and included 2D GRE MRE
and prototype 2D and 3D seEPI MRE sequences. Liver stiffness maps (elastograms)
were generated using a 2D and 3D multi-modal direct inversion algorithm,
respectively (Mayo Clinic, Rochester MN).
The output of these inversions includes a confidence mask that excludes
areas determined by the algorithm to be unreliable measurements. Four axial slices
were obtained through the liver for GRE and 2D seEPI techniques while 26 slices
were generated by 3D seEPI MRE. Elastograms with confidence masks were used for
quantitative assessment. A polygonal region of interest (ROI) was manually
drawn on each slice, using the magnitude images as the anatomic reference, in
order to include the largest cross section of liver while carefully avoiding
the liver edge, major vessels, gallbladder fossa, and areas of wave
interferences ¹,².
A separate “non-curated” ROI was also drawn simply to include the largest cross
section of liver within the confidence mask (irrespective of presence of wave
interference) to assess the contribution of artifacts. Mean and standard
deviation of stiffness (in kPa) was recorded for each measurement, as well as the
corresponding ROI area. Liver stiffness measure (LSM) was calculated as the
arithmetic mean of individual stiffness values for the acquired slices for each
MRE technique. For 3D MRE technique, the 4 slices with the largest cross
section were also used for calculation of LSM (so called “abbreviated LSM”). LSMs
were categorically classified as advanced (≥4 kPa), significant (≥3.5 kPa), and
non-significant (<3.5 kPa)³. Failure of MRE was defined as lack of
propagation of waves through the liver and/or complete exclusion of liver on
confidence mask. Two-tailed paired t-test, Pearson correlation coefficient, and
intraclass coefficient correlation (ICC) were used to assess the concordance
and intra-patient variations between LSMs calculated by different pulse
sequences and different methods of ROI placement. The magnitude of discordance
was evaluated by Bland-Altman plots. A p-value <0.05 was set as a statistically
significant difference.
Results
33 patients (17 males, mean age 55 ± 12.6, mean BMI 33.6 ± 8.1) were included in the study. Except for single
case of failure with GRE technique, all the MREs were deemed diagnostic. The
total area of the curated ROIs (based on 4 slices) were 5601 mm² (± 3597), 9358
mm² (± 4132), and 12131 mm² (± 11383) for GRE, 2D seEPI, and 3D MREs,
respectively. The curated ROIs based on 3D technique were significantly larger
than the ones by GRE technique (p<0.002). Although there was a trend for
increased size, the ROIs derived from 3D MRE were not significantly different
from 2D seEPI based on paired statistics (p=0.17). While the LSMs based on
curated and non-curated ROIs were significantly different for GRE and 2D seEPI
(p<0.002 and p<0.001), these 2 methods of segmentation were not
significantly different for 3D MRE (p=0.943). Abbreviated 3D LSM (based on 4
slices) had excellent correlation with 3D LSM (based on all slices) (r=0.932;
p<0.001) and the LSM based on these 2 approaches were not significantly
different (p=0.459). LSM based on 3D technique ranged between 1.92 and 6.7 (mean
3.17 ± 1.16). 3D LSM had excellent correlation with both 2D techniques (r=0.941
and r=0.932 for GRE 2D and seEPI 2D, p<0.001). Notably, 3D LSM was generally
lower than its 2D counterparts which was statistically different from GRE LSM
(p<0.001) but did not reach statistical significance when compared to 2D seEPI
LSM (p=0.058). In 9 patients, there were >0.5 kPa difference between the 3D
LSM and 2D seEPI LSM. In 8 patients, the 2D and 3D LSMs resulted in allocation
to different fibrosis categories. Most of these cases had small liver area on
the 2D confidence map which could have resulted in less accurate measurements. Conclusions
3D seEPI MRE is a robust technique providing larger cross section of liver
for measurement (both per slice and in total) and hence a better representation
the global liver stiffness. Our preliminary results showed this technique to be
less prone to wave interference artifacts, which can translate into more
accurate and more reproducible measurement of liver stiffness. Our study also
showed that the need for curated ROI placement (which requires higher level of experience)
is less crucial for 3D technique which makes this technique more robust and a
better option for automated segmentation. While the LSM values based on the 3D
technique had excellent correlation with 2D methods, the individual values were
slightly lower which reached statistical significance when compared to GRE
technique. This difference, which could be attributed to less incidence of “hot
spots” on 3D technique, suggests the need for further calibration and
definition of new fibrosis classification threshold values for this emerging technique.Acknowledgements
No acknowledgement found.References
1. Idilman IS, Li J, Yin
M, Venkatesh SK. MR elastography of liver: current status and future
perspectives. Abdom Radiol (NY). 2020 Nov;45(11):3444-3462. doi:
10.1007/s00261-020-02656-7. Epub 2020 Jul 23. PMID: 32705312.
2. Venkatesh SK, Wells ML, Miller FH, Jhaveri KS,
Silva AC, Taouli B, Ehman RL. Magnetic resonance elastography: beyond liver
fibrosis-a case-based pictorial review. Abdom Radiol (NY). 2018 Jul;43(7):1590-1611.
doi: 10.1007/s00261-017-1383-1.
3. Venkatesh SK, Ehman RL. Magnetic resonance elastography
of liver. Magn Reson Imaging Clin N Am. 2014 Aug;22(3):433-46. doi:
10.1016/j.mric.2014.05.001.