Anne-Sophie van Schelt1, Nienke P.M. Wassenaar1, Eric M. Schrauben1, Jules L. Nelissen1, Jing Guo2, Ingolf Sack2, Jaap Stoker1, Aart J. Nederveen1, and Jurgen H. Runge1
1Radiology and Nuclear Medicine, Amsterdam UMC location AMC, Amsterdam, Netherlands, 2Department of Radiology, Charité – Universitätsmedizin Berlin, Berlin, Germany
Synopsis
Pancreas magnetic resonance elastography (MRE)
allows non-invasice estimation of tissue stiffness for multiple pathophysiological
diseases. MRE reproducibility and the effect of bowel-preparation (butylscopolaminebromide
and drinking water) for increased MRE data quality were assessed for the
pancreas. Shear wave speed and MRE quality were determined for the pancreas,
liver and kidneys. Intrasession and
intersession reproducibility showed a coefficient-of-variation of 6.59%
and 13.10%. Repeated measures ANOVA showed no significant difference in SWS of
all organs (f=3/11,p>0.05). Bowel-preparation methods for pancreatic MRE do
not increase MRE quality. Drinking water increases the MRE quality for kidneys
and liver whilst not altering the measured SWS.
Introduction
Magnetic resonance elastography
(MRE) in the pancreas has the potential to elucidate
multiple pancreatic pathologies[1], such as pancreatic adenocarcinoma. To
characterize tumor microenvironment and estimate stromal disposition in the
pancreas a high quality and reproducible MRE is imperative. However, its
central abdominal location presents two potential issues as bowel movement may
interfere with the shear wave resulting in low quality MRE data while the
presence of gas in the gastrointestinal tract surrounding the pancreas inhibits
shear wave propagation.
To address these challenges, we hypothesize
the effects of two MRE patient preparation methods: 1) drinking 0.5L of water decreases
the amount of air in the stomach and increases wave penetration, and 2) using butylscopolaminebromide
(Buscopan:20mg/ml,Eureco-PharmaB.V) increases MRE quality through inhibition of
smooth-muscle contraction. The aim of this study was to assess test-retest of
reproducibility of non-prepared pancreatic MRE and to see if patient
preparation improves MRE quality.Methods
MRE
reproducibility of the pancreas was studied in a group of 10 healthy volunteers
(♀=6,mean age=26±3years). Both
intrasession and intersession reproducibility were investigated (figure.1a). Different subject preparations were
evaluated in 15 healthy volunteers (♀=7,mean age=41±16years), following the preparation steps as indicated in Figure 1b; No
preparation (TOMO1), Buscopan (TOMO2), water (TOMO3), water and Buscopan (TOMO4).
Buscopan was injected via IV to temporarily (~4min) decrease bowel movement.
All scanning was performed at 3.0T (Ingenia,Philips,Best,Netherlands)
in combination with body transmit, anterior, and posterior receive coils. Volunteers
were positioned prone, head first. Four compressed-air driven MRE-transducers were
placed on the lower thoracic cage, two anterior and two posterior (figure.1d)[2].
Elastography images were acquired with a multi-frequency free-breathing SE-EPI
sequence at four frequencies (MREfreq=30,40,50,60Hz)[2]. Sequence
parameters were: nslices=29, voxelsize=2.7x2.7x5mm3, SENSE=2.5, TE/TR=55/2400ms,
number of MRE-offsets=8, MEGdir=3, and acquisition-time≈4 min. All
subjects fasted four hours prior to scanning.
Postprocessing was accomplished using the kMDEV inversion algorithm resulting in
shear-wave-speed (SWS) maps of the abdomen[3]. Volumes-of-interest were manually
drawn on the mean magnitude images to assess the mean pancreatic SWS, along
with the kidneys and liver to assess influence on other organs. Strain-SNR and
attenuation of the shear wave were evaluated as quality parameters[4].
The reproducibility and repeatability of
TOMO1 was assessed by Bland-Altman plots. Repeated measures ANOVA and pairwise
comparison (p<.05) were used to determine intra-subject variability for all
parameters for the preparation methods (SPSS,Statistics,Version26,IBM,USA). The
differences in pancreatic SWS throughout preparation methods were compared to
the within- and between-session reproducibility.Results
Intrasession
and intersession reproducibility are shown using
Bland-Altman plots in Figure 2, with an mean SWS of 1.10±0.10m/s overall and
coefficient-of-variation: CVintrasession=6.59% and CVintersession=13.10%.
Figure 3 shows magnitude images and corresponding elastograms for a single
volunteer over all preparation scans. Repeated
measures ANOVA showed no significant difference for SWS of all organs (f=3/11,p>.05). However, exploratory pairwise comparison for the pancreas showed
significant difference between TOMO1 and TOMO2 (p=.005). Mean SWS of the pancreas were 1.13±0.26, 1.19±0.28, 1.15±0.27 and 1.18±0.27m/s for TOMO1,2,3 and 4,
respectively (figure.4). Strain-SNR
and attenuation showed no significant differences between different scans
for the pancreas (figure.5). However, there is a difference between before and
after drinking water in the kidneys and liver, with the exception between TOMO2
and TOMO4 in the liver. There was no significant difference in attenuation of
the shear wave for all scans.Discussion
Mean SWS in the pancreas were in line with
previously published literature[2]. Pairwise comparison showed that there is a
significant difference between the SWS in the pancreas of TOMO1 and TOMO2.
Buscopan injection increases the mean SWS of the pancreas compared to nonprepared-MRE.
However, this difference was not observed between other preparation scans
or in the kidneys and liver. The pancreas is surrounded by the hepatopancreatic
ampulla, which is a smooth-muscle sphincter controlling inflow and inhibiting
reflux of duodenal substances into the ampulla. Buscopan could have an
influence on the ductal pressure and thereby apparent SWS, because it inhibits spontaneous smooth-muscle activity and thereby the
hepatopancreatic ampulla. Nevertheless, the difference observed between the nonprepared-MRE
and Buscopan SWS is within the limits of the repeatability, indicating that
this effect is negligible.
Quality parameters showed no significant difference in the pancreas, suggesting
that there is no increased wave penetration when drinking 0.5L of water or decrease of shear-wave interference using Buscopan. However, there is an observed difference in the strain-SNR in the
kidney and liver. For the kidneys there seems a difference between before and
after drinking water, with an increase in strain-SNR after drinking water. In
the liver this is also observed, except between TOMO2 and TOMO4. Previous work showed
similar results for the mean SWS in the pancreas (1.20±0.12m/s) and no change
in SWS of the pancreas, liver and kidney at different hydration states (an hour
after drinking water)[2].Conclusion
Bowel-preparation methods for pancreatic
MRE does not increase MRE quality. Repeated measures ANOVA showed no significant
difference in SWS for all organs(f=3/11,p>0.05). Exploratory pairwise
comparison for the pancreas showed significant difference between TOMO1 and
TOMO2(p=.005). This could be due to Buscopan having an effect on the
hepatopancreatic ampulla. However, this effect is within the limits of the
repeatability of the nonprepared-MRE and therefore clinically irrelevant. Drinking
water increases the MRE quality for kidneys and liver whilst not altering the
measured SWS.Acknowledgements
This research was funded by KWF Kankerbestrijding. References
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