Esra Abaci Turk1, Jeffrey N. Stout1, Borjan Gagoski1, Mary Katherine Manhard2, Elfar Adalsteinsson3,4,5, Kawin Setsompop2, Polina Golland3,6, Drucilla J. Roberts7, William H. Barth Jr8, and P. Ellen Grant1
1Fetal-Neonatal Neuroimaging & Developmental Science Center, Boston Children's Hospital, Boston, MA, United States, 2Athinoula A. Martinos Center for Biomedical Imaging, Massachusetts General Hospital, Charlestown, MA, United States, 3Department of Electrical Engineering and Computer Science, Massachusetts Institute of Technology, Cambridge, MA, United States, 4Harvard-MIT Health Sciences and Technology, Massachusetts Institute of Technology, Cambridge, MA, United States, 5Institute for Medical Engineering and Science, Massachusetts Institute of Technology, Cambridge, MA, United States, 6Computer Science and Artificial Intelligence Laboratory (CSAIL), Massachusetts Institute of Technology, Cambridge, MA, United States, 7Pathology, Massachusetts General Hospital, Boston, MA, United States, 8Maternal-Fetal Medicine, Massachusetts General Hospital, Boston, MA, United States
Synopsis
T2*
relaxometry has been proposed as a semi-quantitative measure for placental
oxygen transport. However, to use T2* as a diagnostic tool, it is necessary to
define the normal range of results and factors that influence those results. In
this study we investigated the effect of maternal position, breath-holds and oxygen
state on placental T2*. We observed lower T2* with breath-hold protocol
compared to no breath-hold protocol in left lateral position. Additionally,
lower T2* was measured in supine position during normoxic episode compared to
left lateral position with no breath-hold protocol. Further studies are needed
to understand these factors better.
Purpose:
The
ultimate goal of placental MRI is to improve individual patient care by accurately
characterizing individual placental function. T2* relaxometry has been proposed
as a semi-quantitative measure of the spatiotemporal patterns of placental
oxygen delivery and transport between the mother and the fetus, which may
enable us to better understand the function of the placenta and to detect
placental insufficiency.1-5 To use T2* measurements as a diagnostic
tool, the initial phase requires defining the normal range of T2* values and
factors that influence placental T2* maps. In this study, we investigated the
effect of maternal position, breath holds and oxygen state on placental T2*
measurements. Methods:
Subjects: 8 subjects, 7 with normal singleton pregnancies and
1with high-risk pregnancy (gestational age: 25-38 weeks) were included. Acquisitions:
Scans were performed on a 3T Skyra scanner (Siemens Healthcare, Erlangen,
Germany). 4 of the subjects were asked to switch position (supine to left
lateral or vice versa) during the scan and the same MRI protocol was applied in
both positions to compare the effect of maternal positioning on T2*
measurements. For the remainder (3 normal pregnancies and 1 high risk pregnancy), data were collected only in the left lateral position. Time
course, no breath-hold, T2* were obtained using a multi-echo (TEs: 18, 47.8, 77.5ms)
GRE EPI sequence (TR: 4.2s, in-plane resolution of 3.1mm×3.1mm, a slice thickness of
3mm, 70 slices, GRAPPA 2, SMS 2) during an initial normoxic
episode (room air, 21% O2, 5min), followed by a hyperoxic episode (100% FiO2,
3min). Single time point breath-hold T2* measurements were obtained just before
the time course above using a multi-echo (TEs: 18, 47.8, 77.5ms) GRE MRI
sequence (TR: 384ms, in-plane
resolution of 3mm×3mm, a slice thickness of 3mm with 7.5mm slice gap, 12 slices, GRAPPA 2, total acquisition time: 2.3min with 6 breath-holds 13s each).
For 4 subjects participating single position protocol, another breath-hold T2*
measurement was collected at the end of hyperoxic episode. Processing and
Analysis: We corrected signal non-uniformity and motion in the dynamic multi-echo
GRE EPI series using our previously reported computational pipeline.6 Voxel-wise T2* maps were
calculated by fitting a mono exponential decay model to the measured
intensities and their corresponding echo times. We employed
the Student t-test for group comparisons between T2* values collected during
normoxic episode in left lateral and supine positions and also
between T2* values collected with and without breath-hold acquisitions during
normoxic and hyperoxic episodes.Results and Discussion:
Data from 2 normal subjects
participated in the positioning protocol were excluded due to the extreme fetal
motion. The other 6 data sets were successfully analyzed. Figure 1 demonstrates the results of 4
subjects participating the single position protocol. We observed significantly lower
placental T2* values with breath-hold (p=0.038). Higher contrast between periphery
and center of cotyledon structures was observed in breath-hold protocol
compared to no breath-hold protocol as shown with single slice T2* maps. Note
that for subject 2, at the end of hyperoxic episode we observed a non-labor
uterine contraction not reported by the mother resulting in a decrease in T2*
estimate (i.e. average T2* = 30.5ms) lower than the baseline measurement (i.e. average
T2* = 31.5ms). For subject 4, high risk pregnancy, we observed lower T2* values
both in breath-hold and no breath-hold protocols compared to the control
subjects at the similar gestation age (i.e. 32weeks).
Figure 2 shows the average
T2* plots for two normal subjects in two different maternal positions. For both
subjects we observed lower T2* estimates in supine position compared to the
left lateral position during normoxic episode when no breath hold protocol was
used. Increase in T2* estimates during hyperoxic episode was higher in supine
position (i.e. For subject 5 ΔT2*supine=12.7ms, ΔT2*left =
8.2ms; For subject 6 ΔT2*supine= 8.2 ms, ΔT2*left =
6.6ms). In the left lateral position T2* estimates were lower with the breath-hold
protocol, but in the supine position we observed very similar values with both
protocols such that for subject 5 (with positioning order as supine first, and
left lateral second) T2* with breath-hold was higher than no breath-hold and
for subject 6 (with positioning order as left lateral first, and supine second)
estimates were similar. This can be also related with the duration spent in
each position and the order of the positioning. Further studies and more
subjects are needed to better understand these factors. Conclusion:
We show
that placental T2* measures vary with maternal position, breath-hold and oxygen
state. In addition, occult contractions contribute to T2* variability. In order
to develop T2* mapping as a diagnostic tool and decrease variance in placental
T2* measures, the impact of these factors needs to be well characterized in both
healthy and pathologic placentas.Acknowledgements
NIH
U01 HD087211, NIH R01 EB017337, NIH P41 EB015902. References
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