Michael Langham1, Benoit Desjardins1, Erin Englund1, Emile R Mohler, III2, Thomas Floyd3, Jamal J Derakshan1, and Felix W Wehrli1
1Department of Radiology, University of Pennsylvania, Philadelphia, PA, United States, 2Department of Medicine, University of Pennsylvania, Philadelphia, PA, United States, 3Department of Anesthesiology, SUNY Stony Brook, Stony Brook, NY, United States
Synopsis
An alternative unenhanced structural and
functional evaluation (SaFE-MRI) MRI is proposed and described for assessing
peripheral artery disease (PAD). The
SaFE-MRI protocol interleaves 3D double-echo steady-state (DESS) acquisition
and velocity mapping at each station. In SaFE-MRI velocity maps in all major conduit arteries (from
abdominal aorta to runoff arteries) serve as a “road map” for locating hemodynamically
significant stenoses and gray- and black-blood images are used to grade stenoses
and detect vascular calcium. Initial results in patients with PAD agree with
the finding from CTA and CE-MRA examinations as well as pressure volume
recordings. Introduction and Motivation
Contrast-enhanced
angiographic evaluations of MRI and CT are the reference standards for
assessing peripheral artery disease (PAD). Because PAD and diabetes often
co-exist the prevalence of renal insufficiency is a major challenge to
contrast-based angiography [1]. We introduce and describe an alternative
unenhanced MRI method to assess PAD by integrating
structural (high resolution gray- and black-blood images with
double-echo steady-state (DESS) [2])
and
functional (velocity waveforms in all of the major conduit arteries)
evaluations, which we refer to as
SaFE-MRI.
Methods
All studies were performed on a 3T
system (Siemens TIM Trio) with the manufacturer’s peripheral artery coil system
coupled with a body matrix coil. The SaFE-MRI protocol interleaves 3D DESS
acquisition and velocity mapping at each station.
Simultaneous structural gray- and
black-blood (GB, BB) imaging with water-selective 3D DESS
The water-selective 3D DESS pulse
sequence that acquires two Fourier modes of unbalanced SSFP signal, also known
as SSFP-FID and SSFP-Echo (Fig 1a). The
unbalanced gradient pulse (crusher in Fig
1a) prevents mutual interference of FID
and Echo signals. The same crusher also acts as a flow-sensitizing (signal
attenuates for moving spins) gradient. As described previously [2] the blood
signal is moderate or “gray,” (Fig 1b)
on FID images, whereas on Echo images the blood signal is completely suppressed
or ”black-blood” (Fig 1c), thereby
providing complementary information on vessel patency and lesion characteristics.
Ungated time-resolved
blood flow velocity quantification with velocity-encoded projections
Previously developed ungated1D PC-MRI
[3] is able to resolve velocity waveforms bilaterally without gating in a fraction
of time that is required for cine 2D
PC-MRI. Method allows velocity waveforms in all of the major conduit arteries in
successive slices spaced 45mm apart, from abdominal aorta down to
infrapopliteal arteries in approximately 10 minutes. The basic design principle
rests on collection of velocity-encoded projections that are free of background
tissue signal (see [3]).
Human Subject Study
After acquiring 3D DESS images and
velocity waveforms of the peripheral arteries in healthy subjects, SaFE-MRI was
performed on two patients with PAD recently having undergone angiographic
evaluation with CTA and CE-MRA, respectively.
3D
DESS flip angle 8o+8o,
TEFID/TEEcho/TR=2.2/7.8/10.6ms, bandwidth=744Hz/voxel
(FID), 223 Hz/voxel (Echo), FOV=352×192×360mm3, spatial
resolution=0.78×0.78×3mm3 zero-padded to 0.39×0.39×1.5mm3 , acquisition time (TA)=5.2mins for one station (typically three are needed).
1D PC-MRI flip
angle 15o, TE/TR=5.2/10ms, bandwidth=142 Hz/voxel, FOV=352×192×10mm3,
spatial resolution=1×1×10mm3, TA~15s/slice.
Results
Fig
2 shows the typical triphasic velocity
waveforms in the major segments of peripheral arteries of a healthy subject; in
practice the velocity waveform is “recorded” every 45 mm. In contrast, severe
PAD leads to monophasic waveforms with reduced peak forward velocity and
absence of retrograde and late forward flow (
Fig 3). The bilateral monophasic velocity waveforms in the distal
external iliac arteries (
Fig 3a) suggest
hemodynamically significant proximal stenosis even though CTA report states
only moderate atherosclerosis within abdominal aorta and minimal narrowing of
the distal external iliac artery. However, according to the pulse volume
recordings (PVR) report, the pressure waveforms at proximal thigh are abnormal
bilaterally, a hallmark of aorto-iliac occlusive disease, thus give credence to
the monophasic velocity waveforms.
Figs
3b and
c show the probable cause
of the undetectable blood flow in distal right SFA.
Fig
4 further demonstrates the potential
clinical utility of velocity waveform analysis. In this patient normal
waveforms are observed except for runoff vessels. Absence of flow in ATA and
PTA is consistent CE-MRA findings (single run-off bilaterally) and PVR (abnormal
at the bilateral ankles).
In
Fig
5a, the signal void within SFA on BB image suggests partially patent lumen but
the same ROI is also hypointense on GB image (
Fig 5b), i.e. calcium, which is invisible on MRA, is detectable
with DESS as confirmed by CTA,
Fig 5c.
Conclusions
SaFE-MRI is a new method for integrated
structural and functional assessment of the peripheral vascular system comprising:
· Velocity maps serving as a “road
map” for identifying and grading hemodynamically significant stenoses
visualized on GB and BB images.
· Unlike cuff-based PVR velocity
waveforms above the groin (aortoiliac arteries) and arteries with incompressible medial calcification can also be recorded.
· Method allows detection of vessel-wall
calcification (Fig 5) and diagnostic quality images even in the presence of stents [2].
· Obviates both contrast material and
exposure to ionizing radiation.
Acknowledgements
This work was supported by NIH Grants K25
HL111422, R01 HL075649, RO1 HL109545, EE received support from AHA pre-doctoral
fellowship and JJD gratefully acknowledges research support from NIH T32
EB004311 Research Track Radiology Residency.References
[1]
Paraskevas et al., Annals of vascular surgery 2009.
[2] Langham et al, ISMRM
2015, p. 559.
[3] Langham et al, MRM 2010.