Transcript Chapter 3

Chapter 3
Principles of nuclear magnetic
resonance and MRI
Review
Basic Physics of MRI
• Nuclei line up with magnetic moments either in a parallel or antiparallel configuration.
• In body tissues more line up in parallel creating a small additional
magnetization M in the direction of B0.
Nuclei spin axis not
parallel to B0 field
direction.
Nuclear magnetic
moments precess
about B0.
Basic Physics of MRI
• Frequency of precession of magnetic moments given by
Larmor relationship
f = g x B0
f = Larmor frequency (mHz)
g = Gyromagnetic ratio (mHz/Tesla)
B0 = Magnetic field strength (Tesla)
g ~ 43 mHz/Tesla
Larmor frequencies of RICs MRIs
3T ~ 130 mHZ
7T ~ 300 mHz
11.7T ~ 500 mHz
Basic Physics of MRI
NMRable Nuclei
 Body 1H content is high due to water (>67%)
 Hydrogen protons in mobile water are primary
source of signals in fMRI and aMRI
Basic Physics of MRI
• M is parallel to B0 since
transverse components of
magnetic moments are randomly
oriented.
• The difference between the
numbers of protons in the
parallel (up here) and antiparallel states leads to the net
magnetization (M).
• Proton density relates to the
number of parallel states per unit
volume.
• Signal producing capability
depends on proton density.
B0
Basic Physics of MRI
Frequency of rotation of M
about B1 determined by
the magnitude (strength)
of B1.
Basic RF Pulse Concepts
RF Pulse
strength
duration
RF pulse duration and
strength determine flip
angle
Basic Physics of MRI
FID = Free Induction Decay
• 90° RF pulse rotates M into
transverse (x-y) plane
• Rotation of M within transverse
plane induces signal in receiver
coil at Larmor frequency.
• Magnitude signal dependent on
proton density and Mxy.
FID magnitude decays in an
exponential manner with a
time constant T2. Decay due
to spin-spin relaxation.
t
T2
S (t )  S0e  sin(2ft )
Need for 180° Pulse - Spin
Echo
• FID also diminishes due to local static
magnetic field inhomogeneity
• Some spins precess faster and some
slower than those due to B0
90
°
180°
• 180 ° RF pulse reverses
dephasing at TE (echo time)
• Residual decay due to T2
Spin Echo Signal
Nuclear Magnetic Resonance
(NMR) Signal: Spin Echo (SE)
TR (repetition time) = time between RF excitation pulses
90o
90o
180o
FID
TE/2
Spin Echo
TE/2
TE = time from 90o pulse to center of spin echo
Developing Contrast Using
Weighting
•
•
Contrast = difference in image values between different tissues
T1 weighted example: gray-white contrast is possible because T1 differs between
these two types of tissue
T1 and T2
• T1-Relaxation: Recovery
– Recovery of longitudinal orientation
of M along z-axis.
– ‘T1 time’ refers to time interval for
63% recovery of longitudinal
magnetization.
– Spin-Lattice interactions.
• T2-Relaxation: Dephasing
– Loss of transverse magnetization
Mxy.
– ‘T2 time’ refers to time interval for
37% loss of original transverse
magnetization.
– Spin-spin interactions,and more.
Properties of Body Tissues
Tissue
T1 (ms) T2 (ms)
Grey Matter (GM)
950
100
White Matter (WM)
600
80
Muscle
900
50
Cerebrospinal Fluid (CSF) 4500
2200
Fat
250
60
Blood
1200
100-200
T1 values for B0 ~ 1Tesla.
T2 ~ 1/10th T1 for soft tissues
Basic Physics of MRI: T1 and T2
T1 is shorter in fat (large
molecules) and longer in
CSF (small molecules). T1
contrast is higher for lower
TRs.
T2 is shorter in fat and longer
in CSF. Signal contrast
increased with TE.
• TR determines T1 contrast
• TE determines T2 contrast.
Contrast, Imaging Parameters
T1W
T2W

S(TR,TE)  r1 eTR /T1  eTE /T2
orr1 e

TR /T1
e
TE /T2*


SE
GRE
r - proton density
SE – spin echo imaging
GRE – gradient echo imaging
Short TEs reduce T2W
Long TRs reduce T1W
Making an Image
k-space (frequency domain)
A k-space domain
image is formed using frequency
and phase encoding
Two Spaces
Image space
y
k-space
ky
FT-1
kx
x
FT
Acquired Data
MRI task is to acquire k-space image then
transform to a spatial-domain image. kx is
sampled (read out) in real time to give N
samples. ky is adjusted before each readout.
Final Image
MR image is the magnitude
of the Fourier transform of
the k-space image
The k-space Trajectory
Equations that govern 2D k-space trajectory
kx = g 0t Gx(t) dt
if Gx is constant
kx = gGxt
ky = g 0t’ Gy(t) dt
if Gy is constant
ky = gGyt’
The kx, ky frequency coordinates are established
by durations (t) and strength of gradients (G).
Simple MRI Frequency Encoding:
RF Excitation
Slice
Selection (Gz)
Frequency
Encoding (Gx)
digitizer on
Readout
Exercise drawing k-space manipulation
The k-space Trajectory
Frequency
Encoding
Gradient
(Gx)
Move to left
side of k-space.
(0,0)
ky
Digitizer records N
samples along kx
where ky = 0
kx
Simple MRI Frequency Encoding: Spin
Echo
Excitation
Slice
Selection
Frequency
Encoding (Gx)
digitizer on
Readout
Exercise drawing k-space representation
The K-space Trajectory
180 pulse
Digitizer records N
samples of kx
where ky = 0
Frequency and Phase Encoding for 2D
Spin Echo Imaging
90
180
Excite
Slice
Select
kx
ky
Frequency
Encode
Phase
Encode
digitizer on
Readout
The 2D K-space Trajectory
180 pulse
Digitizer records N
samples of kx and
N samples of ky
Gradient Echo Imaging
• Signal is generated by magnetic field refocusing
mechanism only (the use of negative and
positive gradient)
• Signal intensity is governed by
S = So e-TE/T2*
• Can be used to measure T2* value of the tissue
• R2* = R2 + R2ih +R2ph (R2=1/T2)
• Used in 3D and BOLD fMRI
MRI Pulse Sequence for Gradient
Echo Imaging
E.
Excitation
Slice
Selection
Frequency
Encoding
Phase
Encoding
digitizer on
Readout
Ernst angle (E) for optimum SNR .
 TR
T1
cos(E )  e
FLASH Pulse Sequence
Gz
refocus
TR2
crusher
TR1
crusher
B1
Gy
Gx
acquire
Gy
Gx
Fig. 3.19. Courtesy of Peter Jezzard.
crusher
Gz
TRN/2
TRN
TRN/2
crusher
B1
TRN
TR2
TR1
2D Gradient Echo
RF (10-15 degrees)
Short TR (10-50 msec)
N= 256 (2.5-13 sec per slice)
3D Sequence (Gradient Echo)
read
acq
Gx
phase
Gy
Select
& phase
Gz
RF
B1
kz
kx
Scan time = NyNzTR
Good for high resolution T1W images of brain
ky
3D T1W
brain image
0.8mm spacing
Time = 25 min
2D Echo Planar
Imaging (EPI)
a)
b)
B1
Gz
refocus
Gy
Gx
acquire
Fig. 3.20. Courtesy of Peter Jezzard.
2d Gradient Echo
Entire 2D slice within one TR
64x64 or 128x128
Time per slice (30-50 msec)
Whole volume (2-4 sec)
Good for fMRI studies
FLASH Image T2* Weighted
TE = 30 msec
CSF is bright
Signal loss and distortions due
to local differences in
magnetic field
Sources of Contrast in Brain
- Endogenous - BOLD
- Exogenous - could be
contrast agent (Gd based)
- Other - Susceptibility
R2* = net T2 relaxation rate = 1/T2*
Fig. 3.23 courtesy of Peter Jezzard.
R2* = R2tis + R2ih + R2BOLD + R2suc
Chapter 8
Quantitative Measurements Using
fMRI
Review
T2* fMRI Signal
From Neural Activity to fMRI
Signal
Neural activity
Signalling
Vascular response
Vascular tone (reactivity)
Autoregulation
Synaptic signalling
BOLD signal
Blood flow,
oxygenation
and volume
arteriole
B0 field
glia
Metabolic signalling
End bouton
dendrite
venule
Complex relationship between change in neural activity and change in
blood flow (CBF), oxygen consumption (CMRO2) and volume (CBV).
fMRI Bold Response Model
positive
BOLD response
•
•
•
•
Initial dip
0.5-1sec
Overshoot
peak 5-8 sec
+ BOLD response
2-3%
Final undershoot
variable
3
BOLD response, %
2
initial
dip
overshoot
post stimulus
undershoot
1
Deoxyhemoglobin
BOLD signal
0
time
stimulus
Figure 8.1. from textbook.
Graded BOLD Response
• Graded change in signal for a) BOLD and b) perfusion (CBF).
• 3 minute visual pattern stimulation with different luminance levels.
• Note max BOLD change of 2-3 % and max CBF change of 40-50 %.
Figure 8.2. from textbook. N=12 subjects.
Perfusion vs. Volume Change
•
•
•
•
30 second stimulation
3-second intervals
DCBF rapid
DCBV slow
BOLD volume assessed using
exogenous tracer that remains in
blood.
In rat experiments TC for DCBV similar to that for BOLD overshoot.
Figure 8.4. from textbook.
Mandeville et al., 1999
Measurement of Cerebral Blood Flow
with PET or MRI (Arterial Spin Labeling - ASL)
PET orPET
SPECT
MRI PERFUSION
Ste ady State M ethod
Ste ady State M ethod
Method
keV
511
decay
arterial
labeling
imaging
slice
control
labeling
T1 relaxation
+
511 keV
arterial
spin labeling
15 O infusion
O-15 H 0
2
or inhalation
• Uses magnetically labeled arterial blood water
as an endogenous flow tracer
• Potentially provide quantifiable CBF in
classical units (mL/min per 100 gm of tissue)
Detre et al., 1992
Arterial Spin Labelling
z (=B0)
excitation
y
inversion
slab
blood
x
inversion
imaging
plane
• ASL is an example of a motion contrast
white matter = low
perfusion
Gray matter = high
perfusion
• IMAGEperfusion = IMAGEuninverted – IMAGEinverted
• Perfusion is useful for clinical studies: how much blood is getting to a
region, how long does it take to get there?
www.fmrib.ox.ac.uk/~karla/
Chapter 5
Hardware for MRI
Review
3T Siemens Trio
•
•
•
•
•
•
60 cm patient bore
40 mT/m max gradient amplitude per axis
200 T/m/sec slew rate
2nd order active shimming
~0.30 ppm B0 homogeneity over 40 cm sphere
self shielded
• Shielding
• Shims
• Field Strength
• A helium-cooled superconducting
magnet generates the static field.
– Always on: only quench field in
emergency.
– niobium titanium wire.
• Coils allow us to
– Make static field homogenous
(shims: solenoid coils)
– Briefly adjust magnetic field
(gradients: solenoid coils)
– Transmit, record RF signal (RF
coils: antennas)
MRI Scanner
Anatomy
Superconductor Magnet
Necessary Equipment
3T magnet
Magnet
RF Coil
gradient coils
(inside)
Gradient Coils
RF Coil
Magnet Shielding and Shimming
Iron Shielding
Magnet
Shim coil
Subject
Gradient coil
RF coil
Figure 5.2 from textbook.
Shims
superconducting
static
room temperature
Gradient Coils
Sounds generated during imaging due to mechanical stress within gradient coils.
Current and Gradient Pulse Shape
a
c
d
b
Jerry Allison.
a. gradient current supplied (short rise time induces eddy currents)
b. eddy currents oppose changing field w/o compensation
c. gradient current supplied with eddy current compensation
d. potential field vs time with eddy current compensation
dB/dt Effect (more eddy currents)
Peripheral Nerve Stimulation
• dB/dt -- dE/dt
• dt is gradient
ramp time
• dB/dt largest
near ends of
gradient coils
• spatial gradient
of dE/dt also
important
dB
dt
dB/dt / E-Field
Characteristics of Stimulation
• Not dependent on B0
• Gradients - 40mT/m (larger Bmax for longer coil)
• Gradient Coil Differences - strength (increases dB)
and length (head vs. body determines site)
• Rise Time - shorter rise time means larger shorter dt
and therefore larger dB/dt
• Other
– Disruption of nearby medical electronic devices
– Subject Instructions
• Don’t clasp hands - closed circuit, lower threshold
• Report tingling, muscle twitching, painful sensations
MRI Scanner Components
Schematic of MRI System
Exciter
XMTR
T/R
switch
Synthesizer
RCVR
RF
Coil
Same or different transmit
and receive coil.
Preamp
Network
A/P
Host
RAM
Shim
coils
Pulse
programmer
Synthesizer, A/P
XMTR, RCVR, T/R
Gx, Gy, Gz
Figure 5.1b from textbook.
Amps
Shim
driver
Gradient
coils
A/P - Array Processor
RF, Shim, Gradient Coils inside magnet
All but Host, RAM, and A/P in equipment room
RF Coil
• RF Coils can transmit and receive RF signals (i.e. apply B1
and monitor Mxy)
• A typical coil is a tuned LC circuit and may be considered a
near-field antenna
NSM-P035 Permanent Magnet MRI
Comprehensive Receiving coils
 7 standard configuration:
QD head coil
QD Extremity Coil
QD Neck Coil
Flat Spine Coil
QD Body Coil
Breast Coil
Surface Coils
RF Coil Uniformity and SNR
Surface coil/head coil comparison
1400
17 cm spherical phantom
b
S
N
R
(1)
SNR
1200
1000
2
800
600
(2)
1
400
4
3
200
0
(3)
0
50
100
150
200
250
distance, mm
(4)
B1 directions indicated by color arrows.
(1) two surface coils on opposite sides in phase.
(2) two surface coils out of phase.
(3) single surface coil on right side. (largest SNR)
(4) head coil. (most uniform SNR)
Figure 5.7 from textbook.
Stimulus Presentation / Monitoring
Additional Equipment
E-Prime
• Software
• Time-Line
– Control Stimulus
– Monitor Response
– Synchronize timing
with MRI
fMRI Study Time
• New Design
• Scanning
– Setup
– Scans
– Take down
• Preprocessing
• Statistical
Analysis
4+ hr (one instance)
1-1.5 hr/subject
15-20 min
45 min to 1 hr
15 min
<2 hr/ subject

variable
fMRI Study – All Data
•
•
•
•
•
Raw Data
Motion Correction
Other Corrections
Spatial Normalization
Statistical Analysis
•
•
~200 mBytes
~180 mBytes
~180 mBytes each possibly
~ 30 mBytes
Statistical Parametric Image (128x128x20)
Statistical Parametric Map (2x SPI)
< 1 MByte
> 1 MByte
Total Data per subject can be 0.5-1.0 gBytes
Chapter 7
Spatial and temporal resolution in
fMRI
Review
Typical Paradigm
Behaviour
•
•
Task
•
Behavior
•
Instruction
Presentation
– stimulation
– timing
Processing
– sensing
– decision
Response
– plan
– motor
Presentation Response
Trial #1
Trial #2
Onset and Width of BOLD
response as temporal measures.
---- Not time to peak ---Figure 7.4 from textbook.
fMRI responses
0
time (s)
5
0
5
time (s)
• BOLD signal time course
• presentation (black)
• processing (light grey)
• response (dark grey)
Estimating Neural Processing Time From
BOLD Response Onset
(b)
M1
SMA
V1
D

Figure 7.5 from textbook.
300
BOLD onset difference (ms)
fMRI response ampitude
(a)
time
250
D
200
150

100
50
0
-50
150
200
250
300
kinematic RT (ms)
Task – use joystick to move cursor from start box to target box as rapidly and accurately as
possible (10 trials in multiple subjects).
BOLD response – V1 (primary visual cortex), SMA (supplementary motor area), M1
(primary motor area)
Analysis – D but not  increases with increasing reaction time (RT).
Conclusion – Delay in reaction time from planning rather than execution of movement.
350
Estimating Neural Processing Time From
from BOLD Response Width
(b)
fMRI
(a)
Task
fMRI signal change from
SPL
1. 03
1. 02
Trial B
1. 01
Trial A
1. 00
RT(A) RT(B)
0. 99
0. 9 8
5
10
15
Time after presentation (s)
0
(c)
Normalized width of BOLD response (s)
Task – determine if one object could be rotated to
match a second. Rotation angle varied by design.
Press button yes or no.
BOLD response – Superior Parietal Lobule (SPL)
Analysis – Normalized width of BOLD response
correlated with reaction time (RT).
Conclusion – SPL intimately involved in mental
rotation of object.
20
16
12
8
4
00
4
8
12
Reaction Time(s)
16
Figure 7.6 from textbook.
Chapter 6
Selection of optimal pulse sequences
for fMRI
Review
Advantages
BOLD
Disadvantages
Highest activation contrast 2x-4x over
perfusion
complicated non-quantitative signal
easiest to implement
no baseline information
multislice trivial
susceptibility artifacts
can use very short TR
Perfusion
unique and quantitative information
low activation contrast
baseline information
longer TR required
easy control over observed vasculature
multislice is difficult
non-invasive
slow mapping of baseline information
no susceptibility artifacts
Table 6.1a. Summary of practical advantages and disadvantages of pulse
sequences (derived from textbook)
Time/secs
0
1
2
3
4
Perfusion
Venous outflow
No
Velocity
Nulling
Velocity
Nulling
Arteries
Arterioles Capillaries Venules
Veins
TI
ASL
Figure 6.1a Signal is detected from water spins in the arterial-capillary region of the
vasculature and from water in tissues surrounding the capillaries. Relative sensitivity
controlled by adjusting TI and by incorporating velocity nulling gradients (also known as
diffusion weighting). Nulling and TI~1 sec makes ASL sensitive to capillaries and surrounds.
Time/secs
Arterial inflow
(BOLD TR < 500 ms)
0
1
2
3
4
GE-BOLD
No
Velocity
Nulling
Velocity
Nulling
Arteries
Arterioles Capillaries Venules
Veins
Figure 6.1b Gradient Echo BOLD is sensitive to susceptibility perturbers of all sizes, and
are therefore sensitive to all intravasculature and extravascular effects in the capillaryvenous portions of the vasculature. If a very short TR is used may show signal from arterial
inflow, which can be removed by using a longer TR and/or outer volume saturation.
Time/secs
Arterial inflow
(BOLD TR < 500 ms)
0
1
2
3
4
SE-BOLD
No
Velocity
Nulling
Velocity
Nulling
Arteries
Arterioles Capillaries Venules
Veins
Figure 6.1c Spin Echo BOLD is sensitive to susceptibility perturbers about the size of a red
blood cell or capillary, making it predominantly sensitive to intravascular water spins in vessels
of all sizes and to extravascular (tissue) water surrounding capillaries. Velocity nulling reduces
the signals from larger vessesl.
TI
TI
ASL
pulse
Gradient-echo
TE
90°
ASL
pulse
Spin-echo
180° TE
90°
RF
RF
Gx
Gx
Gy
Gy
Gz
Gz
spin-echo
180°
Figure 6.2 Pulse sequence diagrams of (a)
gradient echo, (b) spin echo, and (c)
asymmetric spin echo EPI. The TE is shown
at the center of 9-line k-space (typically 64
or more lines).  is the offset from center of
k-space to echo. Additional pulses needed
for ASL are indicated schematically.
90°
RF
Gx
Gy
Gz
/2
TE

Chapter 4
Ultrafast fMRI
Review
Effects of Field Homogeneity
R2* = R2 + R2mi +R2ma
• R2 = transverse relaxation rate due to spin-spin
interactions and diffusion through microscopic
gradients
• R2mi = transverse relaxation rate due to
microscopic changes, i.e. deoxyhemoglobin
• R2ma = transverse relaxation rate due to
macroscopic field inhomogeneity
R2*a is relaxation rate during activation
R2*r is relaxation rate at rest
DR 2*  ( R 2 *a  R 2 *r )  ( R 2  R 2 mi  R 2 ma ) a  ( R 2  R 2 mi  R 2 ma ) r
DR 2*  ( R 2  R 2 mi ) a  ( R 2  R 2 mi ) r  ( R 2 a  R 2 r )  ( R 2 mi a  R 2 mi r )
DR 2*  DR 2  DR 2 mi
4x4x4 mm3
2x2x2 mm3
Spin Echo
Gradient Echo EPI
Fig. 4.3 EPI obtained with TE= 60 and TR=3000 msec and 63 and 95 ky lines. Note
recovery of signal loss in d vs c and ghosting in c.
r.f.
TE
readout window
read gradient
rephase
dephase
gradient
echo
dephase
Fig. 4.5 Gradient echo (GE) echo forms at center of readout window where area under
rephasing gradient = area of dephasing gradient. Unlike spin echo dephasing is due to
spatial difference in Larmor frequencies during application of gradients. First half of
readout window is rephasing and second half is dephasing again. This process repeats at the
center of readout window for each ky line in k-space for EPI.
For EPI where is the readout signal largest?
a)
b)
n
Phase
n-1
RF
Slice
n-1
1
Read
2
n
2
Phase
1
Read
Fig. 4.7 GE EPI pulse sequence and k-space organization of samples.
What flip angle is used for EPI?
Effect of system parameters on EPI images for fixed
field of view.
Parameter
Echo
Spacing
Resolution
SNR
Geometric
distortion
Increase gradient slew rate
Reduced
---
---
Reduced
Increase sampling bandwidth
(kx)
Reduced
---
Reduced
Reduced
Increase number of shots
(interleaving ky)
Reduced
---
Increased
Reduced
Use of ramp sampling (similar
to slew rate effect)
Reduced
---
---
Reduced
Increase read matrix (kx)
Increased
Increased
Reduced
Increased
Increase phase matrix (ky)
---
Increased*
Reduced
---
Increase field strength
---
---
Increased
Increased
Table 4.1 from text.
* actual resolution increase less than expected due to smoothing effect of signal decay.
fMRI methods for reduced k-space coverage
• Keyhole
– acquire full k-space as reference
– acquire reduced low-frequency k-space fMRI study
– fill in missing k-space from reference
• Half-Fourier
– acquire 50-60% of k-space starting at highest ky
– theoretical symmetry used to fill in missing ky
fMRI methods for reduced k-space coverage
• Sensitivity encoding (SENSE)
– Multiple RF coils with independent signal for each (parallel imaging)
– Calibration maps from full k-space
– each coil part of k-space
– 2X improvement EPI, 4X for GE
• UNFOLD
– Acquire k-space in sequential time segments
• time 1 acquire lines 1, 5, 9, 13 ...
• time 2 acquire lines 2, 6, 10, 14 ...
• time 3 acquire lines 3, 7, 11, 15 ...
• time 4 acquire lines 4, 8, 12, 16 ...
• reorder into k-space
• 4x faster per segment reduces inter echo distortions