4.7 Article

T1 relaxometry of crossing fibres in the human brain

Journal

NEUROIMAGE
Volume 141, Issue -, Pages 133-142

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.neuroimage.2016.07.037

Keywords

Inversion recovery; DTI; Myelination; T-1

Funding

  1. Wellcome Trust through a Sir Henry Wellcome Postdoctoral Fellowship [061447, 21341]
  2. Wellcome Trust through New Investigator Award
  3. European Research Council through an ERC Starting Grant (MULTICONNECT) [639938]
  4. Netherlands Organisation for Scientific Research through a VIDI grant [14637]
  5. European Research Council (ERC) [639938] Funding Source: European Research Council (ERC)

Ask authors/readers for more resources

A comprehensive tract-based characterisation of white matter should include the ability to quantify myelin and axonal attributes irrespective of the complexity of fibre organisation within the voxel. Recently, a new experimental framework that combines inversion recovery and diffusion MRI, called inversion recovery diffusion tensor imaging (IR-DTI), was introduced and applied in an animal study. IR-DTI provides the ability to assign to each unique fibre population within a voxel a specific value of the longitudinal relaxation time, T-1, which is a proxy for myelin content. Here, we apply the IR-DTI approach to the human brain in vivo on 7 healthy subjects for the first time. We demonstrate that the approach is able to measure differential tract properties in crossing fibre areas, reflecting the different myelination of tracts. We also show that tract-specific T-1 has less inter-subject variability compared to conventional T-1 in areas of crossing fibres, suggesting increased specificity to distinct fibre populations. Finally we show in simulations that changes in myelination selectively affecting one fibre bundle in crossing fibre areas can potentially be detected earlier using IR-DTI. (C) 2016 The Authors. Published by Elsevier Inc. This is an open access article under the CC BY license.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.7
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available