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7/31/2019 MRS Demo ACRN 6684 3Dsiemens Final
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ACRIN-6684ACRIN-6684
-- MRS data acquisition and Raw Data
Handling Instructions
For Siemens Data
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In vivoIn vivo MR SpectroscopyMR Spectroscopy
Representative MRS of a normal human brain@3T
NAA
Glu/Gln
Cho Cr
MI
Lipids,macromolecules
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Proton MRS is able to detect the following metabolites:
N-Acetyl Aspartate (NAA) at 2 ppm: Marker of
neuronal density and viability Creatine (Cr) at 3 ppm: Energy metabolism, generation
of ATP
Choline (Cho) at 3.2 ppm: Pathological alterations in
membrane turnover, increased in tumors
Lipids (Lip) between 0.8 1.5 ppm: Breakdown of
tissue, elevated in brain tumors - lipids indicate necrosis
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Lactate (Lac) at 1.3 ppm, inverted at 144ms:
produced by an anaerobic metabolism, found in
tumor containing zones of necrosis
1000 950 900 850 800
-1.00E+008
0.00E+000
1.00E+008
2.00E+008
3.00E+008
Y
AxisTitle
X Axis Title
fft(real)
/ ppm
1000
950 900 850 800
-1.00E+008
0.00E+000
1.00E+008
2.00E+008
3.00E+008
Y
AxisTitle
X Axis Title
fft(real)
/ ppm
Lac
NAA
Cr
Cho
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The SequenceThe Sequence
3D chemical shift imaging using aPoint-resolved spectroscopy(PRESS) excitation pulse
sequence.
3D Volumetric Spectroscopypreferred 2D CSI Spectroscopy is
acceptable
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Optimal Voxel PlacementOptimal Voxel Placement
The ROI will be placed at the center ofthe enhancing tumor covering thelesion and the normal brain as much aspossible but excluding thesubcutaneous fat and sinuses.
b i l l
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Suboptimal VoxelSuboptimal Voxel
PlacementPlacement Proximity to sinuses can result in signal
broadening and susceptibility artifacts Proximity to scull can result in contaminating
lipid signal
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3D MRSI Parameters3D MRSI ParametersTE 144 ms, TR 1140 ms,
FOV > 160 mm2,
Phase encoding arrays 12 x 12 x 8
Numbers of Acquisitions: 1
Spatial zero-filling to 16 x 16 x 8 phaseencoding arrays will result in an individualvoxel size of 1 x 1 x 1 cm3.
Approximate imaging time: ~6 min utilizingelliptical k-space sampling k-space sampling
Manual shimming is recommended before theacquisition to obtain the best magnetic field
homogeneity.
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ShimmingShimming
Shimming = adjusting the magnetic field to make it
more homogeneous 1.5T: Signal line width or full width at half maximum
(FWHM):
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Shimming on SiemensShimming on Siemens
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Manual Shimming onManual Shimming on
SiemensSiemens
Hit the Show tabThen Invalidate AllAdjust AllWait a couple of minutesuntil it says
Adjustments finished
Hit the Show tabThen Invalidate AllAdjust AllWait a couple of minutesuntil it says
Adjustments finished
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Hit the Interactive Shim tabThen hit Measure (1)Numbers will begin to scroll on theabove white box (2)
You can alter the shim by changing Z,then Y, then X. Do this slowly, only acouple of increments at a time, thenstart with z again Stop (3) and Apply (4)
1.
2.
3.
4.
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Saturation BandsSaturation BandsClick SAT and place up to 10 SAT bands around
the voxel to suppress signals from lipid/fat
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Saving the Data in .rdaSaving the Data in .rda
formatformat
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The spectrum appears inone of the quadrantsNote: if another window
appears asking you to selecta protocol for the spectrum,
just select any of theprotocols listed and click OK.
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Go to the top of thescreen Click on
PatientDropdown menu willappearSave data
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Select first option, Selected
results and 3 referenceimages (shown above)This will save the spectrum
and corresponding images in
a DICOM format
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Go to a difference slice and
repeat the process
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In order to use a different
slice:Right click on the ImageA scroll down window willappearSelect 3D CSI Selection
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Under 3D CSI Selection:Choose Plane number
Sav ng t e Data n r aav ng t e ata n r a
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Sav ng t e Data n .r aav ng t e ata n .r aformatformat
Click on Options export raw data (shownabove).
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