Karthikeyan Subramanian1, Pavan Kumar Jella1, Feifei Qu1, Tinnakorn Chaiworapongsa2,3, and Mark E Haacke1
1Department of Radiology, Wayne State University, Detroit, MI, United States, 2Perinatology Research Branch, NICHD/NIH/DHHS, Detroit, MI, United States, 3Department of Obstetrics and Gynecology, Wayne State University, Detroit, MI, United States
Synopsis
Keywords: Segmentation, Fetus
Mapping the
vasculature, flow and tissue properties of the placenta and umbilical cord can
serve as a means to study placental and fetal health. The goal of this work is
to use a rapid, multi-echo, interleaved GRE sequence
to minimize motion artifacts and cover the entire abdomen of the mother in a
few minutes. To better map out the vasculature, we propose to both separate the
arteries and veins in the umbilical cord using an R2* mapping thresholding
technique and use vessel tracking to create 3D renderings. We have successfully
done this in a series of 10 fetuses.
Introduction
The placenta
plays a vital role in providing nutrients and oxygen to the fetus. The exchange
process within the cotyledon is driven by the in-flow and out-flow of blood
from both the maternal and fetal sides. Prohibition of this exchange process
leads to placental dysfunction which is considered to be the leading factor for
conditions like fetal growth restriction (FGR) and preeclampsia1-4. It has also
been shown that reduced flow in the umbilical cord is a risk factor for
premature birth. Hence, the use of MR angiographic (MRA) imaging in pregnancy
can not only help in evaluating the normal developing vasculature of the human
fetus and placenta but may also help in identifying abnormal development5. In this study,
we propose a technique for overcoming motion artifacts using an interleaved
gradient recalled echo (GRE) sequence that allows us to acquire time-of-flight (TOF) like
images, T2*, T1 and spin density maps. We also propose to separate the arteries
and veins in the umbilical cord and visualize the chorionic, fetal and
umbilical vessels in 3D using the oxygen saturation effects in the vessels as
visualized with T2* maps.Methods
We used a 2D
interleaved, multi-echo, GRE imaging sequence with both a low flip angle (proton density weighted) and a high flip angle (T1 weighted with a TOF like effect) within the
same sequence in roughly 5 seconds per slice. This makes it possible to
quantify tissue characteristics and help separate arteries from veins. Five pregnant
women suspected of fetal growth restriction were scanned during their second
and third trimester (24 – 37 weeks of gestation) using a 3.0T Siemens Verio
scanner. The following imaging parameters were used6: TR = 35-40
ms, TE = 7.5/27.5 ms, FAs = 8°/40°, voxel size = 1×1 mm2
and slice thickness = 3 mm. In order to extract the vascular information, a Frangi
vesselness filter7 was applied to the
data. The vesselness results were then manually cropped using SPIN (Signal
processing in NMR, SpinTech, Detroit, MI) software and added to the high pass
filtered magnitude image to obtain an image with higher SNR and improved
vascular information. The vessels were then tracked using an automated vessel
extraction tool in SPIN software which uses an adaptive thresholding algorithm.
The tracked result is then visualized in 3D space using Volview 2.0 software.
The vessel extraction process is depicted in Figure 1.
Arteries and
veins were distinguished using a thresholding method on the R2* maps computed
from the two magnitude images (TE 7.5 and 27.5 ms) for each FA (8° and 40°).
These two R2* maps were then averaged. A threshold of 30/s-40/s was applied to
suppress the umbilical artery signal (deoxygenated blood). The thresholded
image was then subtracted from the original image to produce a venous map of
the umbilical cord carrying oxygenated blood. The artery-vein separation
process is shown in Figure 2.Results
The interleaved sequence provided images showing
the usual TOF effect from the high FA interleaved images that were then
compared with the conventional TOF sequences acquired with the same resolution.
The vessel tracking approach was applied to different regions of the fetal and
placental vasculature. Due to the simultaneous acquisition of the multi-echo
interleaved GRE data using two FAs, we were able to create high quality R2*
maps, to aid in differentiating veins
from arteries. When the MRA was acquired covering the entire abdomen of the
mother, we were able to visualize the following vascular territories: blood
supply of the mother’s uterine arteries; endometrial vessels feeding the
placenta; the umbilical cord penetrating the chorionic plate; and the fetal
vessels. Figure 3 shows the extraction of fetal vessels including the heart,
inferior vena cava, aortic arch, subclavian artery, carotid arteries, jugular
veins, and the ductus venosus.Discussion
Using this sequence, we can map the vessels (maternal,
fetal and placental), quantify tissue properties using STAGE in just 5 to 10
minutes also alleviating most motion artifacts. Future applications include fully
automated vessel extraction in other anatomical regions, monitoring oxygen
saturation and study placental health using quantitative susceptibility maps (QSM)
maps and T2* data in fetal growth restricted subjects using just one powerful
imaging sequence.Conclusion
In this study, we presented a non-invasive
approach for acquiring and processing the interleaved multi-echo GRE data that
helps in the visualization and quantification of the placental-fetal vascular
territory. Acknowledgements
No acknowledgement found.References
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