Magn Reson Mater Phy
DOI 10.1007/s10334-008-0104-8
RESEARCH ARTICLE
Water proton T
1
measurements in brain tissue at 7, 3, and 1.5 T
using IR-EPI, IR-TSE, and MPRAGE: results and optimization
P. J. Wright · O. E. Mougin · J. J. Totman · A. M. Peters ·
M. J. Brookes · R. Coxon · P. E. Morris · M. Clemence ·
S. T. Francis · R. W. Bowtell · P. A. Gowland
Received: 9 July 2007 / Revised: 17 December 2007 / Accepted: 7 January 2008
© ESMRMB 2008
Abstract
Method This paper presents methods of measuring the lon-
gitudinal relaxation time using inversion recovery turbo spin
echo (IR-TSE) and magnetization-prepared rapid gradient
echo (MPRAGE) sequences, comparing and optimizing these
sequences, reporting T
1
values for water protons measured
from brain tissue at 1.5, 3, and 7T. T
1
was measured in
cortical grey matter and white matter using the IR-TSE,
MPRAGE, and inversion recovery echo planar imaging
(IR-EPI) pulse sequences.
Results In four subjects the T
1
of white and grey matter were
found to be 646 ± 32 and 1,197 ± 134ms at 1.5T, 838 ± 50
and 1,607 ± 112 ms at 3 T, and 1,126 ± 97, and 1,939 ± 149 ms
at 7T with the MPRAGE sequence. The T
1
of the putamen
was found to be 1,084 ± 63 ms at 1.5 T, 1,332 ± 68 ms at 3 T,
and 1,644 ± 167ms at 7T. The T
1
of the caudate head was
found to be 1,109 ± 66 ms at 1.5 T, 1,395 ± 49 ms at 3 T, and
1,684 ± 76 ms at 7 T.
Discussion There was a trend for the IR-TSE sequence to
underestimate T
1
in vivo. The sequence parameters for the
IR-TSE and MPRAGE sequences were also optimized in
terms of the signal-to-noise ratio (SNR) in the fitted T
1
. The
optimal sequence for IR-TSE in terms of SNR in the fitted T
1
P. J. Wright · O. E. Mougin · A. M. Peters · M. J. Brookes ·
R. Coxon · P. E. Morris · S. T. Francis · R. W. Bowtell ·
P. A. Gowland (B )
Sir Peter Mansfield Magnetic Resonance Centre,
School of Physics and Astronomy, University of Nottingham,
Nottingham, UK
e-mail: Penny.gowland@nottingham.ac.uk
J. J. Totman
The Brain and Body Centre, University of Nottingham,
Nottingham, UK
M. Clemence
Philips Medical Systems, Reigate Surrey, UK
was found to have five readouts at TIs of 120, 260, 563, 1,221,
2,647, 5,736 ms and TR of 7 s. The optimal pulse sequence
for MPRAGE with readout flip angle = 8
◦
was found to have
five readouts at TIs of 160, 398, 988, 2,455, and 6,102 ms and
a TR of 9 s. Further optimization including the readout flip
angle suggests that the flip angle should be increased, beyond
levels that are acceptable in terms of power deposition and
point-spread function.
Keywords High field · Relaxometry · Pulse sequences ·
Optimization
Introduction
Relaxation times provide a more reliable marker of tissue
state than MRI signal intensities, which depend on the exact
RF field, the sensitivity profile of the receiver coil, and other
factors such as receiver gain and the competing effects of
different relaxation times. If relaxation time measurements
could be made with adequate sensitivity and accuracy, then
they could provide an improved method for studying dis-
ease progression and for characterizing normal tissue types,
for instance in neurodevelopment [1, 2]. Furthermore,
knowledge of the tissue relaxation times is important for opti-
mizing sequences to provide maximum image contrast, opti-
mizing contrast agent dose, and for optimizing quantitative
sequences for measurements of other important parameters
such as perfusion. It is expected that longitudinal relaxation
times increase as the field strength is increased and that val-
ues obtained from different tissues converge [3]. At present
there are only a few reported in vivo measurements of longi-
tudinal relaxation times in human brain at 7 T, although there
has been one study considering the change in water proton
relaxation times at fields from 0.2 to 7 T [4].
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