Please use this identifier to cite or link to this item: https://doi.org/10.1002/mrm.27463
DC FieldValue
dc.titleRelevance of time-dependence for clinically viable diffusion imaging of the spinal cord
dc.contributor.authorGrussu F.
dc.contributor.authorIanuş A.
dc.contributor.authorTur C.
dc.contributor.authorPrados F.
dc.contributor.authorSchneider T.
dc.contributor.authorKaden E.
dc.contributor.authorOurselin S.
dc.contributor.authorDrobnjak I.
dc.contributor.authorZhang H.
dc.contributor.authorAlexander D.C.
dc.contributor.authorGandini Wheeler-Kingshott C.A.M.
dc.date.accessioned2019-03-06T07:51:59Z
dc.date.available2019-03-06T07:51:59Z
dc.date.issued2018
dc.identifier.citationGrussu F., Ianuş A., Tur C., Prados F., Schneider T., Kaden E., Ourselin S., Drobnjak I., Zhang H., Alexander D.C., Gandini Wheeler-Kingshott C.A.M. (2018). Relevance of time-dependence for clinically viable diffusion imaging of the spinal cord. Magnetic Resonance in Medicine. ScholarBank@NUS Repository. https://doi.org/10.1002/mrm.27463
dc.identifier.issn07403194
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/152047
dc.description.abstractPurpose: Time-dependence is a key feature of the diffusion-weighted (DW) signal, knowledge of which informs biophysical modelling. Here, we study time-dependence in the human spinal cord, as its axonal structure is specific and different from the brain. Theory and Methods: We run Monte Carlo simulations using a synthetic model of spinal cord white matter (WM) (large axons), and of brain WM (smaller axons). Furthermore, we study clinically feasible multi-shell DW scans of the cervical spinal cord (b = 0; b = 711 s mm-2; b = 2855 s mm-2), obtained using three diffusion times (Δ of 29, 52 and 76 ms) from three volunteers. Results: Both intra-/extra-axonal perpendicular diffusivities and kurtosis excess show time-dependence in our synthetic spinal cord model. This time-dependence is reflected mostly in the intra-axonal perpendicular DW signal, which also exhibits strong decay, unlike our brain model. Time-dependence of the total DW signal appears detectable in the presence of noise in our synthetic spinal cord model, but not in the brain. In WM in vivo, we observe time-dependent macroscopic and microscopic diffusivities and diffusion kurtosis, NODDI and two-compartment SMT metrics. Accounting for large axon calibers improves fitting of multi-compartment models to a minor extent. Conclusions: Time-dependence of clinically viable DW MRI metrics can be detected in vivo in spinal cord WM, thus providing new opportunities for the non-invasive estimation of microstructural properties. The time-dependence of the perpendicular DW signal may feature strong intra-axonal contributions due to large spinal axon caliber. Hence, a popular model known as “stick” (zero-radius cylinder) may be sub-optimal to describe signals from the largest spinal axons. © 2018 International Society for Magnetic Resonance in Medicine
dc.publisherJohn Wiley and Sons Inc.
dc.sourceScopus
dc.subjectdiffusion time
dc.subjectmicrostructure
dc.subjectMonte Carlo simulations
dc.subjectspinal cord
dc.subjectwhite matter
dc.typeArticle
dc.contributor.departmentDEPT OF MEDICINE
dc.description.doi10.1002/mrm.27463
dc.description.sourcetitleMagnetic Resonance in Medicine
dc.grant.fundingagencyHorizon 2020
dc.grant.fundingagencyFramework Programme CDS?QuaMRI grant
dc.grant.fundingagencyEngineering and Physical Sciences Research Council
Appears in Collections:Staff Publications
Elements

Show simple item record
Files in This Item:
File Description SizeFormatAccess SettingsVersion 
mrm.27463.pdf1.37 MBAdobe PDF

OPEN

NoneView/Download

SCOPUSTM   
Citations

2
checked on Jul 19, 2019

Page view(s)

42
checked on Jul 18, 2019

Download(s)

3
checked on Jul 18, 2019

Google ScholarTM

Check

Altmetric


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.