Evidence map›Paper›PMID 28669902›Full record

ArticleNeuroImage2017

Improved tractography using asymmetric fibre orientation distributions.

Matteo Bastiani, Michiel Cottaar, Krikor Dikranian, Aurobrata Ghosh, Hui Zhang, Daniel C Alexander, Timothy E Behrens, Saad Jbabdi, Stamatios N Sotiropoulos

Abstract read
In one paragraph

Article in NeuroImage, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

28 citing papers in PubMed.

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  18. Globally Optimized Super-Resolution of Diffusion MRI Data via Fiber Continuity.Medical image computing and computer-assisted intervention : MICCAI ... International Conference on Medical Image Computing and Computer-Assisted Intervention · 2020
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Matteo BastianiWellcome Centre for Integrative Neuroscience (WIN) - Oxford Centre for Functional Magnetic Resonance Imaging of the Brain (FMRIB), University of Oxford, UK. Electronic address: matteo.bastiani@ndcn.ox.ac.uk.
Michiel CottaarWellcome Centre for Integrative Neuroscience (WIN) - Oxford Centre for Functional Magnetic Resonance Imaging of the Brain (FMRIB), University of Oxford, UK.
Krikor DikranianDepartment of Neuroscience, Washington University, St. Louis, MO, USA.
Aurobrata GhoshDepartment of Computer Science & Centre for Medical Image Computing, University College London, UK.
Hui ZhangDepartment of Computer Science & Centre for Medical Image Computing, University College London, UK.
Daniel C AlexanderDepartment of Computer Science & Centre for Medical Image Computing, University College London, UK.
Timothy E BehrensWellcome Centre for Integrative Neuroscience (WIN) - Oxford Centre for Functional Magnetic Resonance Imaging of the Brain (FMRIB), University of Oxford, UK.
Saad JbabdiWellcome Centre for Integrative Neuroscience (WIN) - Oxford Centre for Functional Magnetic Resonance Imaging of the Brain (FMRIB), University of Oxford, UK.
Stamatios N SotiropoulosWellcome Centre for Integrative Neuroscience (WIN) - Oxford Centre for Functional Magnetic Resonance Imaging of the Brain (FMRIB), University of Oxford, UK; Sir Peter Mansfield Imaging Centre, School of Medicine, University of Nottingham, UK.

Funding

Mapping the Human Connectome: Structure, Function, and HeritabilityU54MH091657 · NIMH · WASHINGTON UNIVERSITY · PI UGURBIL, KAMIL, VAN ESSEN, DAVID C · 2010 to 2014
$34.7M
European Research Council 319456Medical Research Council MR/L009013/1NIMH NIH HHS U54 MH091657Wellcome Trust 203139
6 · The paper itself

Abstract

Diffusion MRI allows us to make inferences on the structural organisation of the brain by mapping water diffusion to white matter microstructure. However, such a mapping is generally ill-defined; for instance, diffusion measurements are antipodally symmetric (diffusion along x and -x are equal), whereas the distribution of fibre orientations within a voxel is generally not symmetric. Therefore, different sub-voxel patterns such as crossing, fanning, or sharp bending, cannot be distinguished by fitting a voxel-wise model to the signal. However, asymmetric fibre patterns can potentially be distinguished once spatial information from neighbouring voxels is taken into account. We propose a neighbourhood-constrained spherical deconvolution approach that is capable of inferring asymmetric fibre orientation distributions (A-fods). Importantly, we further design and implement a tractography algorithm that utilises the estimated A-fods, since the commonly used streamline tractography paradigm cannot directly take advantage of the new information. We assess performance using ultra-high resolution histology data where we can compare true orientation distributions against sub-voxel fibre patterns estimated from down-sampled data. Finally, we explore the benefits of A-fods-based tractography using in vivo data by evaluating agreement of tractography predictions with connectivity estimates made using different in-vivo modalities. The proposed approach can reliably estimate complex fibre patterns such as sharp bending and fanning, which voxel-wise approaches cannot estimate. Moreover, histology-based and in-vivo results show that the new framework allows more accurate tractography and reconstruction of maps quantifying (symmetric and asymmetric) fibre complexity.

Indexed as

Nerve FibersAlgorithmsAnimalsBrainBrain MappingDiffusion Tensor ImagingHumansImage Processing, Computer-AssistedMacacaModels, NeurologicalPattern Recognition, AutomatedAsymmetryConnectomeDiffusion MRIStructural connectivityTractography

Identifiers

PMID28669902
PMCPMC6318223

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.