Ana E RodrÃguez-Soto1, Michael C Langham1, and Felix W Wehrli1
1Department of Radiology, University of Pennsylvania, Philadelphia, PA, United States
Synopsis
Susceptometry-based oximetry is a
well-established, robust method for quantifying hemoglobin oxygen saturation
(HbO2) in vivo; but the
method is somewhat limited by the orientation of the vessel of interest
relative to Bo. T2-based oximetry, based on the dependence
of blood water T2 on HbO2, provides greater flexibility
with respect to vessel geometry. However, the measured T2 critically
depends on Bo and sequence-specific imaging parameters. Here, a T2-prepared
bSSFP sequence and appropriate calibration curve were used to extract HbO2
at the superior sagittal sinus and the results were compared to susceptometry-based
oximetry. The agreement between both methods was excellent with 2% bias.
PURPOSE
Susceptometry-based
oximetry is a well-established, robust method that exploits the intrinsic
susceptibility of deoxyhemoglobin for quantification of whole-blood oxygen
saturation (HbO2). However, the accuracy of the
underlying model is limited to vessels oriented <30° from Bo. An
alternative method, is based on the
dependence of blood water T2 on HbO2, which does not
depend on vessel geometry.3 Whole-blood T2, is a function of
field strength, inter-refocusing pulse interval of the T2
preparation and sequence-specific parameters, which demand the relationship
between T2 and HbO2 to be determined upfront for the particular
pulse sequence used. We have recently generated a calibration curve at 1.5T ex
vivo for a T2-prepared bSSFP sequence, which offers rapid imaging
time, high in-plane resolution and SNR efficiency. Here, we used this setup to
measure HbO2 in vivo at
the superior sagittal sinus (SSS) and compared these results to those obtained
with susceptometry-based oximetry.METHODS
Human
volunteers were scanned in a
1.5T scanner (Siemens Avanto) with a 10-channel head coil. Single-slice
T2-prepared bSSFP (Fig. 1)
were acquired at the SSS to estimate T2 of blood. Imaging parameters: TR=3900ms, T2-preparation
TEs=0,48,96,144,192ms, bSSFP TR/TE=3.8/1.9ms, Tsat=3000ms,
FOV=128×128mm2, voxel
size=1.25×1.25×5mm3, FA=60°, 5 averages, ramp up linear signal stabilization and 14
reference lines prior to half-Fourier acquisition and inter-refocusing pulse
interval (τ180) of 12ms. T2
was obtained via a 3-parameter fit to account for the fact that bSSFP transient
signal approaches non-zero amplitude.4 Furthermore, TEs were
corrected for the time during which the magnetization is stored along z during the
composite refocusing pulses (Fig. 1).5
The T2 of blood was then converted to HbO2 using the
Luz-Meiboom model as described by Wright et al 6.
Constants T2o and K were previously determined in our laboratory for
this T2-prepared bSSFP with the above imaging parameters. Extracted
HbO2 values were then compared against those from susceptometry-based
oximetry: $$$ HbO_2=[1-\frac{(2|Δφ|}{(γ χ_{do} ΔTE B_o (cos^2 θ-1/3) Hct))}] $$$.1 Here, is the average phase difference between
intravascular blood and the surrounding tissue,7
is the susceptibility difference (in cgs units) between fully deoxygenated and
fully oxygenated erythrocytes, is the inter-echo spacing of the gradient-echo
sequence used,1 is the angle of the SSS with respect to Bo
and Hct is the hematocrit. T2-based HbO2
values were then compared against those estimated via susceptometry-derived HbO2
as the independent variable. Imaging parameters: TR=50ms, TE1=6.4ms,
TE2=11.9ms, FOV=128×128mm2,
voxel size=1×1×5mm3, FA=17°. Furthermore, in order to examine the robustness
of T2-prepared bSSFP to blood flow velocity in vivo, the latter was measured in the SSS with MRI
phase-contrast. Imaging parameters: TR=21.1ms, TE=6.5ms, FOV=200×200mm2, voxel size=0.625×0.625×5mm3,
VENC = 30cm/s, and FA=15°. Intraclass correlation coefficient (ICC), Bland-Altman
and paired t-tests were used to evaluate the agreement between both oximetry
methods.RESULTS
Seven healthy young volunteers (39.8±3.1 years old, 4 male)
participated in this study. The
values of T2o and K used were
169ms and 17.6Hz, respectively. Average HbO2 at the SSS was 65±4% and 67±4% via T2-and susceptometry-based oximetry, respectively (Fig. 2). In Fig. 3A the data from the two methods are plotted
against each other. We notice that all T2-based SvO2
values are below the line of identity suggesting a slight bias. The latter is confirmed by the Bland-Altman
plot (Fig. 3B), which yielded a mean difference (SvO2T2 – SvO2Susc)
of -2.0% (±1.7%). Nevertheless,
the ICC of 0.935 (p=0.001) suggests
remarkable agreement between the two oximetric methods.
DISCUSSION AND CONCLUSIONs
Good agreement was found between T2-prepared
bSSFP oximetry and susceptometry-based oximetry in the SSS. This vessel was
selected because it is relatively straight and runs roughly parallel to Bo
with participants supine in the MRI scanner. Further, the model had previously
been evaluated both experimentally2 and numerically.8 However,
cerebral oxygen metabolism is tightly regulated, which limits the range of baseline
SvO2 values. Nonetheless, results suggest that T2-prepared
bSSFF is a reliable and accurate technique to extract HbO2 in vivo. Further work is required to examine
the performance of the method over a wider range of oxygen saturations at
anatomic locations where susceptometry is not practical. Acknowledgements
NIH
grants U01-HD087180 and K25 HL111422.References
1.
Fernandez-Seara MA, Techawiboonwong A, Detre JA, Wehrli FW. MR susceptometry for
measuring global brain oxygen extraction. Magn Reson Med. 2006;55:967-73.
2. Jain V, Langham MC, Wehrli FW. MRI
estimation of global brain oxygen consumption rate. J Cereb Blood Flow Metab.
2010;30:1598-607.
3. Thulborn KR, Waterton JC, Matthews PM,
Radda GK. Oxygenation dependence of the transverse relaxation time of water
protons in whole blood at high field. Biochim Biophys Acta. 1982;714(2):265-70.
4. Akçakaya M, Basha TA, Weingärtner S,
Roujol S, Berg S, Nezafat R. Improved quantitative myocardial T2
mapping: impact of the fitting model. Magn Reson Med. 2015;74:93-105.
5. Foltz WD, Stainsby JA, Wright GA. T2 accuracy on a
whole-body imager. Magn
Reson Med.
1997;38:759-68.
6. Wright G, Hu B, Macovski A. Estimating
oxygen saturation of blood in vivo with MR imaging at 1.5T. Magn Reson Med. 1991;1:275-83.
7.
Jain V, Abdulmalik O, Propert KJ, Wehrli FW. Investigating the magnetic
susceptibility properties of fresh human blood for non invasive oxygen
saturation quantification. Magn Reson Med. 2011;86:863-67.
8.
Li C., Langham MC, Epstein CL, Magland JF, Wu J, Gee J, Wehrli FW. Accuracy of
the cylinder approximation for susceptometric measurement of intravascular oxygen
saturation. Magn Reson Med. 2012; 67:808-13.