Afis Ajala1,2, Jiming Zhang3, Erick Buko4, Janie Swaab3, Melissa Dotson3, Benjamin Cheong3, Pei-Herng Hor4, and Raja Muthupillai3
1Physics, University of Houston [Main Campus], Houston, TX, United States, 2Department of Diagnostic and Interventional Radiology, Baylor St. Luke's Medical Center, Houston, TX, United States, 3Baylor St. Luke's Medical Center, Houston, TX, United States, 4University of Houston [Main Campus], Houston, TX, United States
Synopsis
A common clinical index of left ventricular (LV)
diastolic function is the ratio of peak trans-mitral blood velocity (E) to mitral annular velocities (Em) during early diastole. Here, we provide clinical validation of a single
TR, dual-echo approach wherein the first and second echoes are velocity
sensitized to encode E and Em respectively.
Introduction
More people die of heart disease than any other
world-wide extracting a tremendous human and economic toll on society. As nearly one of two heart failure patients
have preserved ejection fraction (HFpEF), there is an increased interest in the
estimation of diastolic function. A widely
used echocardiographic metric for evaluating LV diastolic function is the ratio
of transmitral velocity (E) to mitral
annular velocity (Em)
during the early filling phase of diastole. Measuring E/Em, using conventional phase contrast MRI (PC-MRI) is
challenging. As Em is several fold lower than E, it is challenging to simultaneously measure both velocities with
adequate sensitivity with a single velocity sensitivity (VENC value), e.g., the
traditional approach of setting VENC slightly above the maximum
velocity (e.g., E in this instance)
will have sub-optimal velocity to noise ratio (VNR) for estimating Em [1]. To
circumvent this, traditional PC-MRI approaches measure E and Em,
independently over the course of two repetition times (TRs), at the cost of
prolonged scan time. We have previously
described a dual echo PC-MRI approach, in which the first and second echoes are
sensitized to velocities in the range of E
and Em respectively[2].
Purpose: (1) To demonstrate
the clinical feasibility of a dual echo PC-MRI technique with velocity
sensitivities suitable to encode transmitral blood velocities with the first
echo, and mitral annular velocities with the second echo. (2) To compare the performance of the
dual-echo dual velocity (DEDV) phase contrast MRI in the measurement of E/Em in normal and clinical
subjects.Materials and Methods:
Subjects:
6 asymptomatic subjects (5 males, age: 49 $$$\pm$$$ 13 yrs), and 8 clinical patients (details summarized in Table 1) were imaged on a commercial 3T MR imager (Ingenia,
Philips Healthcare) with VCG gating. A 32
element thoracic phased array coil was used for signal reception. All subjects
provided written informed consent.
MRI acquisition: A custom dual echo pulse
sequence that allowed the prescription of different VENC values for a dual echo
scan was created (Figure 1) for a free-breathing segmented k-space PC-MRI
sequence. PC-MRI of the short axis slice
positioned below and parallel to the mitral valve plane was acquired with the
DEDV pulse sequence with velocity sensitivity for the first and the second
echoes set at: 150 cm/s and 20 cm/s; acquired voxel size: 2 x 2 x 8 mm$$$^3$$$;
temporal resolution: 20 ms. The same slice
was acquired with conventional SEDV technique with VENC values set at 150 cm/s
and 20 cm/s in two separate scans. All other parameters, such as prescribed
FOV, acquired voxel size, flip angle (15$$$^\circ$$$), and NSA (2), were kept identical
for both the SEDV and DEDV scans.
Data Analysis: Trans-mitral
blood and myocardial tissue velocities were estimated from regions of interest
(ROIs) circumscribing LV blood and myocardium (Figure 2), from PC-MRI acquired with high
and low velocity sensitivities respectively. Myocardial region was further
subdivided into equiangular segments to extract Em of septal, inferior, lateral, and anterior
walls. E/Em was calculated for each segment using both
techniques as indicated in Figure 2 (C and D) for symptomatic and clinical subjects. The positive axis of velocity was defined as tissue motion towards
the apex of the heart. For classification purposes, E/Em ratio greater than 15 (or greater than 12) in the
septal region (or lateral) is indicative of elevated LV pressure[3].Results
The mean scan time for SEDV and DEDV techniques were: 7.2$$$\pm$$$2.4 min versus 4.5$$$\pm$$$2.3 min, respectively. Representative mean velocity versus time curves derived from phase contrast images acquired
using the DEDV and conventional SEDV methods for asymptomatic and clinical subjects are shown
in Figure 2 (C and D). Figure 2B shows a magnitude image obtained at peak diastole, with a wall thickness of about 15.7 mm (> 11 mm normal threshold), which may be associated with the lower peak early diastolic filling velocity seen in the myocardium (Figure 2D). 7 out of 8 clinical subjects had preserved ejection fraction. E/Em ratios estimated using the SEDV and DEDV methods were
highly correlated (Figure 3), and showed elevated estimates in the septal (and lateral) region of the myocardium for 50% (and 37.5%) of the clinical subjects. E/Em obtained in the anterior and lateral walls of the myocardium were mostly in the normal or intermediate zone, except for a single subject that showed E/Em ratio as high as 37.5 in the inferior wall. 3 clinical subjects had E/Em ratios in the normal range, and were diagnosed to be normal as well. All asymptomatic volunteers showed E/Em in the normal zone or in the lower intermediate zone.Discussion
(a) Imparting two velocity sensitivities within one TR reduces scan time by sharing the temporal overhead associated with slice excitation, spoiling, etc, and can be relevant for dual VENC 4D flow MRI for improved VNR.
(b) The DEDV
method can be used to estimate E/Em that is comparable to that obtained with the conventional SEDV method in asymptomatic and clinical subjects.
(c) The estimated E/Em ratios are useful for evaluating diastolic function, but more diastolic indices such as deceleration time (DT), E/DT will improve diagnosis of diastolic dysfunction[4].
(d) The results obtained need to be confirmed in a larger clinical study.Acknowledgements
No acknowledgement found.References
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