Laura Saunders1, Andy Swift1, David Capener1, and James Wild1
1Academic Radiology, University of Sheffield, Sheffield, United Kingdom
Synopsis
Release of
breath hold results in misalignment of the myocardium during cardiac T1
mapping. Several registration methods have been developed to overcome this [1][2][3],
however, it has not been established whether the process of respiration effects
myocardial T1 when mapped with dynamic MOLLI sequences. 10 healthy volunteers
underwent 1.5T MOLLI T1 mapping during both breath hold and free breathing
acquisition. Images were registered using synthetic images created via a
combined inversion recovery and respiratory signal modulation model, which was
verified using Dice Similarity Coefficient. Myocardial T1 was found to be
higher in healthy volunteers when acquired during free breathing, when compared
to inspiration.
Background
For
patients with cardiac or pulmonary disease, breath holds can be difficult or
unachievable. Release of breath hold will result in misalignment of the
myocardium during cardiac T1 mapping. Several registration methods have been
developed to overcome this, however, it has not been established whether the
process of respiration affects the measured myocardial T1.Purpose
To present a method of image registration and T1
mapping for free-breathing MOLLI images and evaluate whether free breathing
images show significantly different T1 when compared to breath hold myocardial
T1.Methods
Free breathing images were
registered using synthetic images which are created using a combined inversion recovery
and respiratory signal-modulation model, which describes the signal intensity
of a group of pixels over time as the combination of inversion recovery and
respiratory motion, see Figure 1. The model uses signal intensity from a group
of pixels within the images to determine respiratory rate. Respiratory rate is
then used to select images from the same respiratory state from which to create
a set of spatially aligned synthetic images. Myocardial and blood T1 values
were calculated using two methods: 1) drawing regions of interest on the
myocardial septum on each image, and calculating T1 from the mean signal of
each region, and 2) drawing regions of interest onto registered T1 maps in the
myocardial septum. T1s calculated using each method were compared for consistency.
Myocardial alignment was determined by segmenting the left ventricle and
calculating Dice Similarity Coefficient for each set of images before and after
registration. 10 healthy volunteers underwent MOLLI T1 mapping acquisitions at 1.5T in both inspiration breath hold and during
free breathing. T1
mapping was performed using a 2D 3-3-5 MOLLI sequence in a single short axis slice. Flip
angle: 35◦;
image dimensions: 128x128; TR: 3.20ms; TE: 1.41ms; parallel imaging using
sensitivity encoding with acceleration factor 2; FOV: 400mm; slice thickness:
5.1mm.Results
DSC
was significantly increased after image registration, p<0.001, see Figure 2
and Table 1. DSC was improved in all patients, with an unregistered DSC range
of 0.55-0.75 and a registered DSC range of 0.60-0.78. There were no significant
differences between myocardial septal T1 values measured from T1 maps when compared to myocardial septal T1 values measured from mean signal
calculated from individual regions of interest drawn on MOLLI images (p=0.903).
In breath hold, myocardial septal T1 = 910±120ms was significantly lower than in free
breathing T1 = 990±160ms (p=0.002). Blood T1 was not significantly higher
during free breathing.Discussion and conclusion
Myocardial
alignment was significantly increased due to image registration, and resulted
in myocardial T1 values consistent with those
determined from mean signal from ROIs drawn on each image. This indicates that the
registration and respiratory model did not lead to erroneous T1 values. Myocardial T1
was found to be significantly higher during free breathing. The predominant
limitation of this method is that it does not compensate for out-of-plane
motion. It is likely that the imaging plane will include images where some of
the protons from another imaging plane with a different magnetization history,
including non-inverted protons. However, the mixing of non-inverted spins into
the imaging plane, would be expected to shorten resultant T1, and our findings are that free-breathing acquisition
resulted in a longer T1. It is not clear what the mechanism of the
observed increase in T1 during respiration is, however,
it is known that myocardial perfusion and oxygenation change with breathing
manoeuvres and this may be the cause of the differences seen in myocardial T1.Acknowledgements
No acknowledgement found.References
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Xue, S. et al., (2012). “Motion correction for myocardial T1 mapping using image
registration with synthetic image estimation,” Magnetic
Resonance in Medicine, 67:644-655
[2]
H. Xue, et al., (2013). “Phase-sensitive inversion recovery for myocardial t1 mapping
with motion correction and parametric fitting,” Magnetic
Resonance in Medicine, 69:1408–20
[3]
Q. Tao, et al., (2018)“Robust motion correction for myocardial t1 and extracellular
volume mapping by principle component analysis-based groupwise image
registration,”, Journal of Magnetic Resonance Imaging, 47:1397–1405