Shunrou Fujiwara1, Kuniaki Ogasawara1, Kohei Chida1, Yosuke Akamatsu1, Takahiro Koji1, Kenya Miyoshi1, Kohki Oikawa1, Jun Yoshida1, Yoshitaka Kubo1, and Yoshichika Yoshioka1
1Iwate Medical University, Yahaba, Japan
Synopsis
Keywords: Neurofluids, Brain
Motivation: Few study has developed the 3-D image like DTI-tractography to show tendency of CSF dynamic through the whole brain.
Goal(s): To develop DWI-fluidography for demonstrating tendency of CSF dynamic through the whole brain.
Approach: DWI with multiple b values and MPGs was scanned, and calculated a statistical variation of DWI signals obtained by different MPGs at each b value. The normalized value of the summation of all variations was defined as a value in a voxel for DWI-fluidography.
Results: The 3-D DWI-fluidography clearly showed differences of CSF dynamics at anatomical spaces filled with CSF, and the fluidography could reflect quantitative results with ADCs.
Impact: The DWI-fluidgraphy has the potential to help us to diagnose/find/investigate CSF-related diseases in the brain. Then, it may open the door to new research area.
Introduction
Diffusion-weighted imaging (DWI) was well-known as
a tool for simultaneously estimating the microcirculation of blood in the
capillary network and molecular water diffusion in brain tissues. In a recent
report, CSF influx and reflux to the brain have been quantified using apparent
diffusion coefficient (ADC) change obtained from DWI between pre- and
post-ischemic stroke in mice.1 On the other hand, a study in humans
demonstrated that diffusion tensor imaging (DTI), which is based on one of DWI
features as multi-directional motion probing gradients (MPG), was used for
analytically assessing the interstitial fluid,2 which is a
type of CSF through the intra-brain.1, 3-5; however, few study has
developed the three-dimensional (3-D) image like DTI-tractography to show
tendency of CSF dynamics through the whole brain, with validating whether the
3-D image can reflect each ADC estimated in each anatomical cavity like the
ventricle, cistern and subarachnoid space. The present study aimed to develop
“DWI-fluidography”, which is based on DWI with multiple b values for
demonstrating tendency of CSF dynamic through the whole brain.Methods
Thirteen healthy subjects participated in this
study from April 2015 to July 2017. All MRI procedures were performed using a
7T-MRI system (Discovery MR950; GE Healthcare, Milwaukee, WI, USA) with a
32-channel head coil. For each subject, a single-shot spin-echo echo-planar
imaging sequence was performed as DWI in the axial
direction from the section showing the fastigium of the fourth ventricle to
that showing both the primary motor area and the central sulcus using the
following parameters: repetition time (TR)/echo time (TE): 5000/76.9 [ms];
matrix: 110 × 110; field of view: 220 × 220 [mm2]; slice
thickness: 2.0 [mm] with no gap; 40 slices; nine b-values: 10, 20, 40, 80, 160,
320, 640, 1000, and 2000 [s/mm2] and non-diffusion-weighted image (b
= 0 [s/mm2]); MPG: three orthogonal directions (1, 0, 0), (0, 1, 0),
(0, 0, 1); number of excitations: 1. Zero-filling interpolation was applied to
each slice, and the final in-plane resolution was 0.86 × 0.86 [mm2].
To clearly represent CSF dynamics on DWI-fluidography, we first calculated a statistical
variation of DWI signals obtained by different MPGs at each b value. Then, all variations
obtained at all b values were summed voxel-by-voxel. The summation value was
normalized, and finally, the normalized value was defined as a value in a voxel
for DWI-fluidography. For quantitative analysis, ADCC and ADCK
were estimated using mono-exponential and kurtosis signal models for
quantifying the CSF dynamics at the following twelve anatomical space: the
subarachnoid space at a section showing the centrum semiovale over the roof of
the lateral ventricle (SAS); anterior horns and trigones of the lateral
ventricle (aLV and tLV, respectively) on the left and right sides; left and
right foramina of Monro (FM); cistern of the velum interpositum (CVI); left and
right Sylvian cisterns (SC); the quadrigeminal cistern (QC); and the fourth
ventricle at the section showing the interpeduncular sulcus (FV). Mann-Whitney U
test was performed with the significant level p<0.05. This prospective, observational study was approved by the Ethics Committee of our institute and all protocols was carried out in
accordance with the approved guidelines and regulations.Results
Each dataset of 10 subjects (10 men; mean age, 31.8
± 3.2 years; range, 28–39 years) was analyzed because three subjects were
excluded due to the susceptibility artifacts. The 3-D DWI-fluidography clearly showed
differences of CSF dynamics at anatomical spaces (Figure 1). In quantitative
analysis, ADCC at SAS and aLV (median, interquartile range: SAS,
2.64, 2.44 – 2.80; aLV, 2.53, 2.41 – 2.83) was significantly lower than that at
FM, CVI, QC, SC and FV (FM, 3.39, 3.26 – 3.56; CVI, 3.20, 3.02 – 3.38; QC,
3.32, 2.97 – 3.43; SC, 3.17, 3.11 – 3.22; FV, 3.23, 3.00 – 3.78), and that at
tLV (2.91, 2.63 – 3.08) was significantly lower than that at FM (3.39, 3.26 –
3.56). Then, ADCK at SAS and aLV (SAS, 3.11, 2.90 – 3.64; aLV, 3.01,
2.96 – 3.16) was significantly lower than that at tLV, FM, CVI, QC and SC (tLV,
3.73, 3.28 – 4.54; FM, 5.98, 5.07 – 7.02; CVI, 3.82, 3.52 – 4.72; QC, 4.29,
3.04 – 4.79; SC, 5.80, 4.62 – 6.15), and that at FV (8.51, 6.93 – 9.96) was
significantly higher than at the other spaces. In addition, ADCK at
FM and SC was significantly higher than that at tLV, CVI and QC. Consequently, the
DWI-fluidography could reflect quantitative results with ADCs.Conclusion
The 3-D DWI-fluidography could demonstrate tendency
of CSF dynamic through the whole brain.Acknowledgements
No acknowledgement found.References
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