4.7 Article

One diffusion acquisition and different white matter models: How does microstructure change in human early development based on WMTI and NODDI?

期刊

NEUROIMAGE
卷 107, 期 -, 页码 242-256

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.neuroimage.2014.12.009

关键词

Diffusion MRI; White matter; Brain development; DKI; Modeling; Microstructure

资金

  1. National Institutes of Health [R01-NS088040, R21-NS081230]
  2. Raymond and Beverly Sackler Laboratories for Convergence of Physical, Engineering, and Biomedical Sciences
  3. Litwin Foundation for Alzheimer's Research
  4. Alzheimer Drug Discovery Foundation
  5. Interuniversity Attraction Poles Program [P7/11]
  6. Belgian Science Policy Office
  7. King Baudouin Foundation
  8. Belgian American Educational Foundation

向作者/读者索取更多资源

White matter microstructural changes during the first three years of healthy brain development are characterized using two different models developed for limited clinical diffusion data: White Matter Tract Integrity (WMTI) metrics from Diffusional Kurtosis Imaging (DKI) and Neurite Orientation Dispersion and Density Imaging (NODDI). Both models reveal a non-linear increase in intra-axonal water fraction and in tortuosity of the extra-axonal space as a function of age, in the genu and splenium of the corpus callosum and the posterior limb of the internal capsule. The changes are consistent with expected behavior related to myelination and asynchrony of fiber development. The intra-and extracellular axial diffusivities as estimated with WMTI do not change appreciably in normal brain development. The quantitative differences in parameter estimates between models are examined and explained in the light of each model's assumptions and consequent biases, as highlighted in simulations. Finally, we discuss the feasibility of a model with fewer assumptions. (C) 2014 Elsevier Inc. All rights reserved.

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