Gitanjali Chhetri1, Kelly C McPhee1, and Alan H Wilman1
1Biomedical Engineering, University of Alberta, Edmonton, AB, Canada
Synopsis
Differences
in pulse sequences between vendors can result in variation in T2 mapping, if
not accounted for. We show that Bloch
simulation based Indirect and Stimulated Echo Compensation minimizes these
differences in T2 maps across different scanners. In contrast, standard exponential fitting
results in highly variable T2 values across MR systems even if echo and
repetition times are identical. By overcoming errors in T2 quantification
through sequence modelling, T2 mapping can be applied in studies across
multiple sites and vendors.
Introduction
The
combination and comparison of data across multiple sites and vendors is
essential for large group MRI studies, and for testing the robustness of
clinical methods. However, the reliability of data derived from multiple sites
relies on pulse sequence equivalence. In particular, standard T2 mapping from
multiple spin-echoes is highly dependent on the refocusing flip angles and transmit field homogeneity, when an
exponential fit is used. However, modelling of the pulse sequence with
knowledge of the refocusing angles can yield accurate T2 values by accounting
for the effects of stimulated
echoes.1 A common approach to T2
mapping is the use of a dual-echo proton density (PD) and T2-weighted imaging
sequence. However, inter-site studies have noted systematic differences between
vendors in T2 maps calculated from exponential fitting.2 Indirect and Stimulated Echo Compensation (ISEC) using
Bloch simulation of Fast
Spin Echo sequences has been shown to produce robust T2, when flip angles are
known.3 Here we examine T2
mapping variation for a multi-site brain MRI study using both standard
exponential fitting and Bloch-ISEC modelling.Methods
Data: Brain
MRI datasets acquired at 3T on 12 healthy controls were obtained
retrospectively from ADNI-1 (Alzheimer's Disease Neuroimaging Initiative) with
six each from two major manufacturers: Siemens Medical Systems and General
Electric (GE) Healthcare, matched for age and sex (mean age 74 years). All
studies used a 2D dual-echo fast/turbo spin echo sequence with parameters: TE1eff=10.0–12.8ms,
TE2eff=95–103 ms, TR 3000ms, echo train length 14-16, echo spacing 10.0–12.8 ms, 48 slices,
voxel size 3.0 x 0.94 x 0.94 mm3, and acquisition time 5 min. Although
most parameters were very similar, Siemens used a train of 165°-150°-150°...,
while GE used either constant 125° refocusing train, or a variable flip refocusing angle train.
The ADNI-1 study also
included a 3D calibration scan using the body coil for transmitting and
receiving, enabling an approximation of B1+ shape. Scan parameters
were: TEeff 1.0ms, TR 3.3ms, voxel size 2.5 x 2.3 x 2.3 mm3, flip
angle 2°, and acquisition time 42 sec. ADNI-1 calibration scans were replicated on a Siemens 3T for three additional
subjects to compare the extracted B1+ shape to rigorous B1+ mapping
using the Bloch-Siegert approach acquired in the same session.
Predicting B1+ maps from calibration data: Ignoring
proton density and minimal T1 relaxation effects, and noting the small 2° flip angle, signal intensity S of the calibration scan
using body coil transmit (B1+) and body coil receive (B1-)
is proportional to S ∝ B1- * B1+. Further simplification can be made by assuming B1- = B1+ in the brain at 3T, hence the B1+ shape
can be estimated simply by √S ∝ B1+.
B1+ shapes
calculated from the calibration scan of the three validation subjects were
scaled and compared against their respective Bloch-Siegert B1+ maps.
The resulting scaling factor was applied to all B1+ shapes obtained
from each ADNI subject. B1+ shapes and Bloch-Siegert B1+
maps were co-registered and resliced to FSE’s native space using SPM12.
T2 mapping
and Analysis: T2
maps were generated by applying Bloch-ISEC fitting using the dual-echo PD and
T2-weighted images and the estimated B1+ maps, as previously described.3 T2 maps were also generated by fitting the dual-echo data directly with an
exponential decay function. All simulations and fitting methods were performed
using in-house MATLAB (R2016b, 64 bit) code. T2 maps were compared between
methods using whole brain histograms.Results
Comparison of normalized
Bloch-Siegert B1+ map to the scaled B1+ shape map (Figure 1) demonstrates that the shape maps
estimate the actual B1+ maps. Example scaled B1+ shape maps for
Siemens and GE subjects are illustrated in Figure 2.
Whole brain histograms of T2
values from exponential fitting (Figure 3) show considerable variation between
vendors. Bloch-ISEC fitting of the same
data (Figure 4) results in histograms with much less variation, and narrower
widths, suggesting recovery of correct T2 values across areas with RF
inhomogeneity, and reduction of bias due to pulse sequence differences. Example T2 maps from each manufacturer using Bloch-ISEC and exponential fitting are compared in Figure 5.Discussion
Bloch-ISEC
fitting produced similar T2 histograms across vendors and across sites,
provided the refocusing angles were known. The rapid low flip angle calibration
scan in the ADNI-1 data set enabled estimation of the B1+ shape,
which was validated in comparison to actual
measurements of Bloch-Siegert B1+ maps. Further
improvements could account for the proton density variation in the calibration
maps. Conclusion
T2 maps computed via exponential fitting of PD
and T2-weighted images led to striking biases between vendors and sites, owing
to differences in refocusing flip angle trains. These biases in T2 measurements
were removed via modelling of the pulse sequences, using known flip angles and
B1+ shape to account for RF inhomogeneity. Use of PD and T2-weighted images
enables quantitative T2 measurement at the same spatial resolution as standard
weighted images. By accounting for differences in pulse sequences, sequence
modelling allows for T2 mapping in studies across multiple sites and vendors.Acknowledgements
Data collection and sharing was funded by the Alzheimer's Disease Neuroimaging Initiative (ADNI). Contract grant sponsorship is provided by the Canadian Institutes of Health research.
References
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