Jie Li1, Xiao Ling1, Tao Wen1, Rui Wang1, Zhongping Zhang2, Kai Ai3, and Jing Zhang1
1Lanzhou University second hospital, Lanzhou, China, 2Philips Healthcare, Guangzhou, China, 3Philips Healthcare, Xi'an, China
Synopsis
Estimating
placental function is highly desirable, as impaired placental function is
associated with FGR and poor neonatal outcome. This study evaluated variations
of T2* after oxygen inhalation of 8 pregnant women in the second and third trimesters
using quantitative mDixon-Quant imaging. The hyperoxic T2* after oxygen inhalation was significantly higher
than baseline T2* which defined as before oxygen inhalation. The change of baseline
T2* and hyperoxic
T2* was significantly negative correlated with gestational age.
The result showed that |△T2*| was correlated with placental function.
We speculate T2* based mDixon-Quant imaging is useful in noninvasive assessment
of placental function.
Introduction
Impairment of
placental function increases the risk of fetal growth restriction (FGR). FGR is
easy to cause fetal hypoxia, postpartum death and cerebral palsy and other
related diseases. However, due to the special situation of gestational woman, it
is difficult to evaluate placental function comprehensively. Previous studies
focus on morphology rather than function of placenta by using Ultrasound[1,2]. As a noninvasive radiation-free examination with high resolution and
contrast, magnetic resonance imaging (MRI) can provide
a complementary information to assess the function of the placenta[3].
The
aim of this study is to use mDixon-Quant imaging based transverse relaxation
time (T2*) to estimate placental condition in normal pregnancies and in pregnancies
complicated by FGR. Our hypothesis is that both normal pregnancy and
pregnancy with FGR will have higher T2* after oxygen inhalation. And compared
with FGR, normal pregnancy will have higher T2*.Methods
Eight pregnant women (5
normal pregnancies, 3 pregnancies with FGR) were included in this prospective
study from July to December 2020. All subjects
underwent MRI examination with a 3.0T scanner (Ingenia
CX, Philips Healthcare, the Netherlands). mDixon-Quant imaging was performed before
and after breathing 60% oxygen (7 L/min) via a face mask for 7 minutes,
respectively. Regions of interest (ROIs) were drawn at three slices which covering the entire
placenta by two independent radiologist whom had over 8 years
of experience. To compare the ability of the placental oxygen transport, we defined
unit gestational age T2* as |△T2*|
= {(hyperoxic T2*- baseline T2*)/Gestational age}. Finally, independent two sample t-tests were used to
detect changes of T2* between two
groups . P-value
< 0.05 was considered as statistically significant.Results
The result shows baseline T2* and hyperoxic T2* decreased
with gestational age, see Figure 1 and 2. Compared with the control
group, the baseline T2* and hyperoxic T2* were lower in the pregnancies with
FGR (P<0.05). The |△T2*| was no difference between
the two groups (P>0.05), see Figure 3.Discussion
The placenta
matures and the oxygen transport capacity decreases gradually during whole pregnancy. The baseline T2*
and hyperoxic T2* decreased with the increase of gestational age. In addition,
the hyperoxic T2* is higher than
baseline T2* both in normal and FGR pregnancy. A possible explaination is that the increment of oxygen inhaled leads to increased
newly bound oxygenated hemoglobin in the placenta [4]. This study
demonstrated that the baseline T2* and hyperoxic T2* of placenta are lower in
pregnancies accompanied by FGR than normal pregnancies. It may be caused by the decrease of the oxygen transport
capacity in the FGR placenta, which has few villi , blood vessels stenosis or even occlusion. Although there was no significant difference in
the |△T2*| between the two
groups, we found that the |△T2*| in normal pregnancies is higher
than pregnancies with FGR. This may be caused by the small sample size and the control
group has large individual difference. Despite this, we speculate that the |△T2*| in normal pregnancies is higher than pregnancies with FGR. Further
studies will include a large sample size to get the consistent conclusion.Conclusion
Our study utilized
mDIXON-Quant imaging to provide the pathophysiological information of placenta
in pregnancy. This could be used as an objective and quantitative method to
evaluate the placental function hence offering a timely adjustment for treatment scheme with dysfunction
placenta.Acknowledgements
No acknowledgement found.References
1. Baschat,
A. A., Neurodevelopment following fetal growth restriction and its relationship
with antepartum parameters of placental dysfunction. Ultrasound Obstet.
Gynecol. 2011, 37:501–514.
2. Srensen A , Hutter
J , Seed M , et al., T2*‐weighted placental MRI: basic research tool
or emerging clinical test for placental dysfunction?. Ultrasound in Obstetrics
& Gynecology, 2020, 55(3):293-302.
3. Bernstein I. M., J. D. Horbar, G. J. Badger, et al., Morbidity and mortality among very-low-birth-weight neonates
with intrauterine growth restriction. The Vermont Oxford Network. Am. J.
Obstet. Gynecol. 2000, 182:198–206.
4. S.
Aimot-Macron, L.J. Salomon, B. Deloison, et al. In vivo MRI assessment of placental and foetal oxygenation changes in a
rat model of growth restriction using blood oxygen level-dependent (BOLD)
magnetic resonance imaging. Eur. Radiol. 2013, 23:1335e1342.
5. Ingram E , Morris D , Naish J , et al., MR Imaging Measurements of Altered Placental Oxygenation in Pregnancies Complicated by Fetal Growth Restriction. Radiology, 2017, 285(3):162385.