Malek I MAKKI1,2, Barbara EU Burkhardt3, and Emanuela Valsangiacomo3
1MRI Research, University Children Hospital, Zurich, Switzerland, 2BioFlow, University Picardie Jules Verne, Amiens, France, 3Cardiology, University Children Hospital, Zurich, Switzerland
Synopsis
SMART1Map sequence was performed on 6 phantoms
with different T1 values. Sixteen schemes were prescribed: 4 heart
rates (60, 80,
100, 120 bpm),
2 spatial resolutions (FOV = 30 cm and FOV = 48 cm) and 2 cardiac phases
(systole and diastole). The results show that SMART1Map underestimates long T1
(native T1 myocardium) at any scheme. We also found an increase in
error with reduced FOV (all other parameters being identical), and an influence of the cardiac phases on T1 at
the levels of native and post-contrast blood and myocardium
Introduction
SMART1Map (Saturation Method using Adaptive
Recovery Times for cardiac T1 Mapping) is a single-point saturation-recovery balanced
SSFP technique [1] that directly measures true T1. Native T1
changes reflect myocardial pathologies related to excess of deposition of T1-altering
substances, including water, protein,
lipid, or iron [2]. The
extracellular volume (ECV) can be calculated from T1 values and is a frequently
used parameter to estimate the degree of myocardial alteration [3]. The
accuracy of T1-mapping have been reported for different T1 values [4].
No study has investigated the influence of imaging parameters
on these measures. This study aimed to assess the accuracy of SMART1Map by using different acquisition parameters
(spatial resolution, heart rate, time delay),
and to describe
their
influence on the measured T1 values.Material and Methods
Six phantoms (P0,
P1, P2,
P3, P4,
P5, 500 mL each) were filled with
water plus a dose of Gadolinium (0.5 mmol/mL) at respectively 0.0, 0.1,
0.2, 0.3,
0.4, 0.5 mL. All images were
acquired on a GE450W 1.5T scanner and 32 channel cardiac coil. The T1
values were measured using standard FSE-IR and 35 different TI values (range
100 ms to 2500ms) by fitting the curve [SI vs TI, T1= TI/Ln(2)]. The imaging parameters were axial
slice (isocenter), thickness 8 mm, TR = 15000ms,
16 ETL (180°), Xres=192, Yres=128,
pFOV=75%. In addition, ten SMART1Map
measurements were performed (time interval between 2 consecutive exams ranges from
1 day to 1 week). The imaging parameters matched the FSE-IR: axial image,
8mm thickness, flip angle 65°, Xres = 192,
Yres=128, BW=100 kHz, pFOV=75%,
TE = min full (1.4 ms). Accuracy and reproducibility were tested with 16
different acquisition schemes: Two time delays (systole and diastole), two spatial resolutions (FOV= 30 and 48 cm), and 4 different heart rates (60, 80, 100, and 120 bpm). The saturation-recovery curve-fits for SMART1Map were carried out using Medis software (Leiden, the Netherlands).Results
The reference T1 values (FSE-IR) of
the phantoms ranged between 2550 ms for pure water (P0,
no Gd), and 376 ms for P5 = 500 mL
water + 0.5 mL Gd (Table 1). Inter-sequence comparison proved that at short T1
(range 750, ±17 to 376±7; P2-P5)
SMART1Map measures accurate and reproducible values at any heart rate, FOV or cardiac-phase. . In contrast for long T1 (2550 ± 50
ms, and 1350 ± 40 ms for P1), SMART1Map systematically underestimates the T1
values (respectively 1985 ± 73 ms and 1240 ± 21 ms) regardless of the heart rate
(60, 80,
100, 120 bpm),
spatial resolution (FOV=30 or 48 cm),
or cardiac phases (systole, diastole).
Whisker curves analysis (Figure 1) shows that SMART1Map results matches quite well with myocardium
native (T1 = 1350ms) and post contrast (T1 = 376 ms). Calculation
of the standard errors of mean (SEM) demonstrated an important influence of the
spatial resolution on the accuracy of the T1 measurements on all
phantoms, regardless of the cardiac phases
and the heart rate (Figure 2). For a smaller FOV (30 vs 48 cm, all other parameters equal) increases the T1
SEM values, on average, from 26ms to 39ms at long T1 = 1240 ms (pre
contrast), and from 7 ms to 15 ms at
short T1 = 376ms (post contrast). In addition,
the acquisition phase (diastole vs systole) influences the accuracy of the T1
measurements. At short T1 (post-contrast),
the SEM is smaller in diastole than in systole, all other parameters equal. (Figure 3). At long T1
(native values), the SEM is smaller
in systole than in diastole. Heart rate has no influence on the accuracy of the
SMART1Map measures.Discussion and Conclusion
The reported normal pre and post contrast T1
values of the myocardium at 1.5T are around 1100 ms and 300 ms, respectively. We demonstrated that SMART1Map provides
accurate measures of post-contrast T1 of the myocardium, but it systematically underestimates native pre-contrast
T1 values (5 to 10%). These errors can be reduced by prescribing
larger FOV and acquiring pre-contrast images during systole and post-contrast
images during diastole. Although the effect of these under-estimations is lower
on the ECV values (due to the ratio myocardium T1 / blood T1), performing SMART1Map using optimized imaging
parameters improves the accuracy of T1-mapping and may lead to improved
clinical diagnosis of disease severity.Acknowledgements
No acknowledgement found.References
[1] Slavin,
Proc. ISMRM, (2012), p.1244.
[2] Riesenkampff et al., Circ Cardiovasc Imaging.
(2015).
[3] Moon et al., JCMR, (2013).
[4] Kellman and Hansen JCMR, (2014)