Title: High field MRI: clinical applications and safety
 1(No Transcript) 
 2Quantitative methods and investigating BOLD 
mechanisms
Susan Francis 
 3Quantitative Imaging
- Relaxation times, MT, diffusion, perfusion/ blood 
 volume
- Neuroapplications 
- BOLD mechanisms 
- Cortical layering 
- MS etc 
- Cancer
4Quantitative imaging
- Rapid imaging sequences 
- EPI 
- HASTEFISP 
- Appropriate fitting 
5What would we like to measure?
- CBV changes- venous and arterial 
- CBF changes 
- Oxygenation changes
REST
Glucose and O2
Venule
Arteriole
Capillary Bed
Glucose and O2 
 6What do we want to measure?
- CBV changes- venous and arterial 
- CBF changes 
- Oxygenation changes
ACTIVE
Glucose and O2
Arteriole
Venule
Capillary Bed
Glucose and O2 
 7What do we want to measure?
- CBV changes- venous and arterial 
- CBF changes 
- Oxygenation changes
- With a temporal resolution sufficient to test 
 models of HDR
Stimulus
0
30
60
Time (s)
8 s
Time (s)
Post stimulus undershoot
Initial dip 
 8Measuring total DCBV by T2 effect of contrast 
agents
  9Typical R2 timecourse
30
29
28
27
-1
26
R2 / s
25
24
Infusion
23
22
-2
0
2
4
6
8
10
12
14
16
18
Time / min 
 10Understanding the HDR
- Now repeating the study at higher temporal 
 resolution, and shorter paradigm
1st Block
1100
2nd Block
3rd Block
4th Block
600
5th Block
EPI Signal (a.u.)
-5
15
35
55
5
Time (s)
Stimulus
Button press 
 11Measuring Venous Blood Volume using multiecho T2
  12Blood oxygenation effect on T2
p
p
p
p
p
p/2
tcp 
 13Measuring DCBV by T1 effect 
 14Measuring DCBV by T1 effect
- Assuming fast exchange, in the presence of CA, 
 the T1 of a voxel is given by
Schwarzbauer et al., Magn. Res. Med., 1993 
 15ME-LL-EPI sequence
TR
a0
ME-EPI 
ME-EPI 
ME-EPI 
ME-EPI 
TA
TI
TA
TA
Broadening Gradient
Rewind gradient
Signal
T2 decay
TE1
TE2 
 16T1 during an infusion of CA
1.14
1.13
1.12
1.11
Tl (s)
1.1
1.09
Stimulus
1.08
1.07
1.06
0
120
240
360
480
600
720
840
960
time (s)
Washout
CA given 
 17Results 
-  DCBVtot  27 
- Rise times similar, DCBV falls slower than T2 
- Faster changes than observed by Mandeville in 
 anaesthetized rats (T2 method)
50
10
CBV
40
8
T2
30
6
CBV change ()
T2 change ()
20
4
10
2
0
0
80
120
0
20
40
60
100
Time (s)
-10
-2 
 18Combining CBV and CBF measurements 
 19LLEPI-FAIR 
- LL-EPI with alternating selective and 
 non-selective (S/NS) inversion pulses
- Better sensitivity than FAIR 
- Previous models (ITS-FAIR, Turbo-TILT) can be 
 improved
- Did not take account of transit times 
- Starting magnetization different in NS and S 
 cases
- cannot model difference signal 
a0
EPI 
EPI 
EPI 
EPI 
TI
TA 
 20Results
- CBF increases by 85 on activation
21Measuring arterial CBVa 
 22EPI star with diffusion weighting
With and without diffusion weighting which will 
suppress signal from arteries 
 23EPI star with diffusion weighting
With and without diffusion weighting which will 
suppress signal from arteries 
 24CBVa using EPIstar
0.9
0.8
0.7
0.6
 Change
0.5
0.4
0.3
0.2
0.1
0
0
1000
2000
3000
4000
5000
1
0.8
0.6
 Change
0.4
0.2
0
0
1000
2000
3000
4000
5000
Inversion Time (ms)