scholarly journals Using diffusion MRI data acquired with ultra-high gradient strength to improve tractography in routine-quality data

NeuroImage ◽  
2021 ◽  
pp. 118706
Author(s):  
C. Maffei ◽  
C. Lee ◽  
M. Planich ◽  
M. Ramprasad ◽  
N. Ravi ◽  
...  
2021 ◽  
Author(s):  
Chiara Maffei ◽  
Christine Lee ◽  
Michael Planich ◽  
Manisha Ramprasad ◽  
Nivedita Ravi ◽  
...  

The development of scanners with ultra-high gradients, spearheaded by the Human Connectome Project, has led to dramatic improvements in the spatial, angular, and diffusion resolution that is feasible for in vivo diffusion MRI acquisitions. The improved quality of the data can be exploited to achieve higher accuracy in the inference of both microstructural and macrostructural anatomy. However, such high-quality data can only be acquired on a handful of Connectom MRI scanners worldwide, while remaining prohibitive in clinical settings because of the constraints imposed by hardware and scanning time. In this study, we first update the classical protocols for tractography-based, manual annotation of major white-matter pathways, to adapt them to the much greater volume and variability of the streamlines that can be produced from today's state-of-the-art diffusion MRI data. We then use these protocols to annotate 42 major pathways manually in data from a Connectom scanner. Finally, we show that, when we use these manually annotated pathways as training data for global probabilistic tractography with anatomical neighborhood priors, we can perform highly accurate, automated reconstruction of the same pathways in much lower-quality, more widely available diffusion MRI data. The outcomes of this work include both a new, comprehensive atlas of WM pathways from Connectom data, and an updated version of our tractography toolbox, TRActs Constrained by UnderLying Anatomy (TRACULA), which is trained on data from this atlas. Both the atlas and TRACULA are distributed publicly as part of FreeSurfer. We present the first comprehensive comparison of TRACULA to the more conventional, multi-region-of-interest approach to automated tractography, and the first demonstration of training TRACULA on high-quality, Connectom data to benefit studies that use more modest acquisition protocols.


2017 ◽  
Vol 35 (15_suppl) ◽  
pp. 2050-2050
Author(s):  
Ina Ly ◽  
Barbara Wichtmann ◽  
Susie Yi Huang ◽  
Aapo Nummenmaa ◽  
Ovidiu Andronesi ◽  
...  

2050 Background: The infiltrating nature of gliomas, particularly into the peritumoral area, is a major barrier to improving clinical outcome as microscopic disease remains even after apparent gross total resection. Conventional T1 post-contrast and T2/FLAIR MRI do not capture full tumor extent. A better imaging biomarker is needed to improve differentiation between tumor, peritumoral area and normal brain. Methods: 4 pre-surgical patients with non-enhancing, FLAIR-hyperintense lesions suspicious for glioma underwent ultra-high gradient diffusion MRI on the Connectome MRI scanner, a unique scanner with maximum gradient strength of 300 mT/m enabling mapping of cellular microstructures on a micron-level scale. The FLAIR area was defined as the tumor region of interest (ROI). Radiographically normal appearing brain up to 1 cm around the FLAIR area was defined as the peritumoral ROI. Using a novel 3 compartment diffusion model (Linear Multiscale Model), the volume fraction of water (VFW) was calculated within restricted (intracellular), hindered (extracellular) and free (CSF) spaces. VFW in the tumor, peritumoral ROI, contralateral normal white matter (WM) and cortex were compared. Results: Within the tumor ROI, the median VFW in the restricted compartment was decreased vs. the peritumoral ROI (↓ 34%), WM (↓ 46%) and cortex (↓ 18%) while median VFW in the hindered compartment was increased vs. the peritumoral ROI (↑ 26%), WM (↑ 54%) and cortex (↑ 25%). Within the peritumoral ROI, median VFW in the hindered compartment was increased compared to WM (↑ 23%). 3 patients had available histopathology revealing isocitrate dehydrogenase-mutant gliomas. Conclusions: Using ultra-high gradient diffusion MRI and a novel diffusion model, we detected distinct diffusion patterns in the tumor and peritumoral area not seen on conventional MRI. Lower VFW in the restricted compartment within the tumor may reflect decreased intracellular water mobility due to enlarged nuclei. Higher VFW in the hindered compartment in the tumor and peritumoral area may reflect higher degree of tissue permeability and edema. MRI-pathology and larger cohort validation studies are underway to elucidate microenvironment changes in response to treatment.


Langmuir ◽  
2008 ◽  
Vol 24 (14) ◽  
pp. 7365-7370 ◽  
Author(s):  
Konstantin Ulrich ◽  
Monica Sanders ◽  
Farida Grinberg ◽  
Petrik Galvosas ◽  
Sergey Vasenkov

2017 ◽  
Vol 19 (suppl_6) ◽  
pp. vi144-vi144
Author(s):  
Ina Ly ◽  
Barbara Wichtmann ◽  
Susie Huang ◽  
Aapo Nummenmaa ◽  
Ovidiu Andronesi ◽  
...  

2007 ◽  
Vol 25 (4) ◽  
pp. 493-496 ◽  
Author(s):  
Konstantin Ulrich ◽  
Monica Sanders ◽  
Sergey Vasenkov

NeuroImage ◽  
2015 ◽  
Vol 106 ◽  
pp. 464-472 ◽  
Author(s):  
Susie Y. Huang ◽  
Aapo Nummenmaa ◽  
Thomas Witzel ◽  
Tanguy Duval ◽  
Julien Cohen-Adad ◽  
...  

NeuroImage ◽  
2020 ◽  
Vol 222 ◽  
pp. 117197 ◽  
Author(s):  
Qiuyun Fan ◽  
Aapo Nummenmaa ◽  
Thomas Witzel ◽  
Ned Ohringer ◽  
Qiyuan Tian ◽  
...  

2019 ◽  
Vol 225 (4) ◽  
pp. 1277-1291 ◽  
Author(s):  
Susie Y. Huang ◽  
Qiyuan Tian ◽  
Qiuyun Fan ◽  
Thomas Witzel ◽  
Barbara Wichtmann ◽  
...  

2019 ◽  
Author(s):  
J-Donald Tournier ◽  
Daan Christiaens ◽  
Jana Hutter ◽  
Anthony N. Price ◽  
Lucilio Cordero-Grande ◽  
...  

AbstractDiffusion MRI has the potential to provide important information about the connectivity and microstructure of the human brain during normal and abnormal development, non-invasively and in vivo. Recent developments in MRI hardware and reconstruction methods now permit the acquisition of large amounts of data within relatively short scan times. This makes it possible to acquire more informative multi-shell data, with diffusion-sensitisation applied along many directions over multiple b-value shells. Such schemes are characterised by the number of shells acquired, and the specific b-value and number of directions sampled for each shell. However, there is currently no clear consensus as to how to optimise these parameters. In this work, we propose a means of optimising multi-shell acquisition schemes by estimating the information content of the diffusion MRI signal, and optimising the acquisition parameters for sensitivity to the observed effects, in a manner agnostic to any particular diffusion analysis method that might subsequently be applied to the data. This method was used to design the acquisition scheme for the neonatal diffusion MRI sequence used in the developing Human Connectome Project, which aims to acquire high quality data and make it freely available to the research community. The final protocol selected by the algorithm, and currently in use within the dHCP, consists of b = 0, 400, 1000, 2600 s/mm2 with 20, 64, 88 & 128 DW directions per shell respectively.HighlightsA data driven method is presented to design multi-shell diffusion MRI acquisition schemes (b-values and no. directions).This method optimises the multi-shell scheme for maximum sensitivity to the information content in the signal.When applied in neonates, the data suggest that a b=0 + 3 shell strategy is appropriate


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