KyungPyo Hong1,2 and Daniel Kim1
1Radiology, UCAIR, University of Utah, Salt Lake City, UT, United States, 2Bioengineering, University of Utah, Salt Lake City, UT, United States
Synopsis
Patients
with end-stage heart failure (HF) often require advanced therapeutics, but
current clinical profiles and biomarkers are not adequate for predicting
outcomes. Myocardial perfusion reserve may be an important predictor, but it is
technically challenging to perform perfusion MRI in patients with end-stage HF
because they often have implantable cardioverter defibrillator (ICD), which
generates significant image artifacts. We developed a novel cardiac perfusion
pulse sequence using a wideband saturation pulse. Compared with standard
perfusion MRI, wideband perfusion MRI suppresses image artifacts induced by
ICD. Introduction
Patients
with end-stage heart failure (HF) may require advanced therapeutics to recover
their failing heart. However, current clinical profiles and biomarkers do not
adequately predict which therapeutic is appropriate. Myocardial perfusion
reserve and fibrosis, which can be measured with MRI, may be important
predictors for guiding advanced therapeutics. However, patients with end-stage
HF often have implantable cardioverter defibrillators (ICD), which induces
severe image artifacts that render standard perfusion MRI useless. We had developed
a novel cardiac T1 mapping method [1] using BISTRO [2] as a wideband saturation
pulse for measuring diffuse myocardial fibrosis in patients with ICD. In this
study, we implemented BISTRO as a wideband saturation pulse to enable
first-pass myocardial perfusion MRI in patients with end-stage HF.
Methods
Pulse Sequence: We implemented optimized BISTRO as a
train of 4 adiabatic hyperbolic secant pulses (each pulse duration = 2.82 ms,
net frequency bandwidth = 9.2 kHz) into a cardiac perfusion MRI pulse sequence
using TurboFLASH readout. For convenience, we call this method wideband
perfusion MRI. We then compared the performance between wideband and standard
cardiac perfusion MRI in 4 human subjects (see below for more details).
Conventional perfusion MRI sequence utilized a train of three 90˚ rectangular
pulses as the saturation pulse (net frequency bandwidth = 2.9 kHz). Both pulse
sequences used identical image parameters, including: FOV = 360 mm x 270 mm
(PE), slice thickness = 8 mm, acquisition matrix = 192 x 144 (PE), TE = 1.3 ms,
TR = 2.7 ms, readout duration = 194 ms, receiver bandwidth = 1000 Hz/pixel,
flip angle = 12˚, acceleration factor (GRAPPA) = 2, linear k-space ordering,
inversion time = 106 ms.
Subject: We recruited four healthy volunteers
(two males; age = 32.7 ± 6.7 yrs). To mimic a realistic situation, we taped an ICD
(VITALITY AVT, Boston Scientific) on the left breast, approximately 5-10 cm
away from heart [1,3]. All subjects provided written informed consent.
MR Imaging: We imaged 4 subjects on a 3T MRI
system (Prisma, Siemens). (Residual Mz
after saturation pulse) Prior to Gd-BOPTA administration, we performed
saturation-no-recovery experiment to calculate residual longitudinal
magnetization (Mz) after wideband and standard saturation pulses, as previously
described [4]. This experiment was conducted in a 2-chamber plane, as the image
artifact is often seen in the anterior wall. (First-pass Perfusion MRI) Each subject underwent two perfusion MRIs
with 30 min delay between the first and second perfusion MRI acquisitions,
where each perfusion MRI was conducted with 0.075 mmol/kg of Gd-BOPTA. The
pulse sequence order was randomized to minimize potential bias.
Image Analysis: We calculated residual Mz by dividing
the T1-weighted image by the proton density image (i.e., equilibrium
magnetization). We calculated mean residual Mz for seven myocardial segments in
a 2-chamber view [5]. For perfusion MRI, to compare signal intensities between
different segments, we normalized the T1-weighted images by a proton density
weighted image. This process corrects for surface coil inhomogeneity.
Results
Figure 1 shows severe image artifacts using a standard perfusion MRI sequence. Note
that the same artifacts disappear with a wideband perfusion MRI pulse sequence.
Averaging the results over 4 subjects (Figure 2), for each segment, the mean residual
Mz values were higher for standard than
wideband pulse sequences. Figure 3 shows perfusion images pre-contrast, at peak
blood enhancement, and at peak wall enhancement. Note that artifacts are
visible in standard images, whereas they are suppressed in wideband images. Normalized
signal-time curves of artifact-affected and remote zones illustrate this
difference (see Figure 4). Figure 5 shows standard and wideband perfusion
images at peak blood enhancement for subjects 2-4. In all four cases, standard
perfusion MRI produced image artifacts, whereas wideband perfusion MRI
suppressed image artifacts.
Discussions
This study demonstrated feasibility of
wideband cardiac perfusion MRI for assessment of perfusion reserve in patients
implanted with ICD. This new perfusion MRI sequence, in conjunction with
wideband late gadolinium-enhanced (LGE) MRI [3] and wideband cardiac T1 mapping
[1], may enable comprehensive assessment of cardiac health in patients with
end-stage HF for guiding advanced therapeutics. .
Acknowledgements
This work was supported in part by the following
grants:
NIH-5R01HL116895-02
and AHA-14GRNT18350028
References
[1] Hong K, et al., MRM 2015;
74:336-345.
[2] Luo Y, et al., MRM 2001;
45(6):1095-1102.
[3] Rashid S, et al., Radiology 2014;
270(1):269-274.
[4] Kim D,
et al., MRM 2009; 62:1368-1378.
[5] Cerqueira MD, et al., Circulation
2002; 105:539-542.