Diffusion-Weighted Imaging: Recent Advances and Applications.


Journal

Seminars in ultrasound, CT, and MR
ISSN: 1558-5034
Titre abrégé: Semin Ultrasound CT MR
Pays: United States
ID NLM: 8504689

Informations de publication

Date de publication:
Oct 2021
Historique:
entrez: 19 9 2021
pubmed: 20 9 2021
medline: 29 10 2021
Statut: ppublish

Résumé

Quantitative diffusion imaging techniques enable the characterization of tissue microstructural properties of the human brain "in vivo", and are widely used in neuroscientific and clinical contexts. In this review, we present the basic physical principles behind diffusion imaging and provide an overview of the current diffusion techniques, including standard and advanced techniques as well as their main clinical applications. Standard diffusion tensor imaging (DTI) offers sensitivity to changes in microstructure due to diseases and enables the characterization of single fiber distributions within a voxel as well as diffusion anisotropy. Nonetheless, its inability to represent complex intravoxel fiber topologies and the limited biological specificity of its metrics motivated the development of several advanced diffusion MRI techniques. For example, high-angular resolution diffusion imaging (HARDI) techniques enabled the characterization of fiber crossing areas and other complex fiber topologies in a single voxel and supported the development of higher-order signal representations aiming to decompose the diffusion MRI signal into distinct microstructure compartments. Biophysical models, often known by their acronym (e.g., CHARMED, WMTI, NODDI, DBSI, DIAMOND) contributed to capture the diffusion properties from each of such tissue compartments, enabling the computation of voxel-wise maps of axonal density and/or morphology that hold promise as clinically viable biomarkers in several neurological and neuroscientific applications; for example, to quantify tissue alterations due to disease or healthy processes. Current challenges and limitations of state-of-the-art models are discussed, including validation efforts. Finally, novel diffusion encoding approaches (e.g., b-tensor or double diffusion encoding) may increase the biological specificity of diffusion metrics towards intra-voxel diffusion heterogeneity in clinical settings, holding promise in neurological applications.

Identifiants

pubmed: 34537117
pii: S0887-2171(21)00084-6
doi: 10.1053/j.sult.2021.07.006
pii:
doi:

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

490-506

Informations de copyright

Copyright © 2021 Elsevier Inc. All rights reserved.

Auteurs

Eloy Martinez-Heras (E)

Center of Neuroimmunology, Laboratory of Advanced Imaging in Neuroimmunological Diseases, Hospital Clinic Barcelona, Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS) and Universitat de Barcelona. Barcelona. Spain. Electronic address: emartind@clinic.cat.

Francesco Grussu (F)

Radiomics Group, Vall d'Hebron Institute of Oncology, Vall d'Hebron Barcelona Hospital Campus, Barcelona, Spain; Queen Square MS Center, Queen Square Institute of Neurology, Faculty of Brain Sciences, University College London, London, UK.

Ferran Prados (F)

Queen Square MS Center, Queen Square Institute of Neurology, Faculty of Brain Sciences, University College London, London, UK; Center for Medical Image Computing (CMIC), Department of Medical Physics and Bioengineering, University College London, London, UK; E-health Center, Universitat Oberta de Catalunya. Barcelona. Spain.

Elisabeth Solana (E)

Center of Neuroimmunology, Laboratory of Advanced Imaging in Neuroimmunological Diseases, Hospital Clinic Barcelona, Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS) and Universitat de Barcelona. Barcelona. Spain.

Sara Llufriu (S)

Center of Neuroimmunology, Laboratory of Advanced Imaging in Neuroimmunological Diseases, Hospital Clinic Barcelona, Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS) and Universitat de Barcelona. Barcelona. Spain.

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Classifications MeSH