4.4 Article

Double diffusion encoding and applications for biomedical imaging

期刊

JOURNAL OF NEUROSCIENCE METHODS
卷 348, 期 -, 页码 -

出版社

ELSEVIER
DOI: 10.1016/j.jneumeth.2020.108989

关键词

Diffusion MRI; tissue microstructure; double diffusion encoding; microscopic anisotropy; magnetic resonance spectroscopy; diffusion correlation tensor; exchange

资金

  1. European Union's Horizon 2020 research and innovation programme under the Marie Sklodowska-Curie grant [101003390]
  2. European Research Council (ERC) [679058]
  3. Engineering and Physical Sciences Research Council [EPSRC EP/N018702/1]
  4. UKRI Future Leaders Fellowship [MR/T020296/1]
  5. Danish National Research Foundation (CFIN)
  6. Danish Ministry of Science, Innovation, and Education (MINDLab)
  7. H2020 European Research Council [804746]
  8. Danish Council for Independent Research [4093-00280B]
  9. Champalimaud Centre for the Unknown, Lisbon (Portugal)
  10. EPSRC [EP/N018702/1] Funding Source: UKRI
  11. UKRI [MR/T020296/1] Funding Source: UKRI
  12. European Research Council (ERC) [804746] Funding Source: European Research Council (ERC)

向作者/读者索取更多资源

Diffusion Magnetic Resonance Imaging (dMRI) is a crucial non-invasive technique for probing tissue structure, with double diffusion encoding (DDE) being an advanced method that provides specific diffusion correlations information and is versatile for different applications. DDE measurements can help improve biophysical models, study intra-cellular diffusion, and enhance contrast in preclinical and clinical settings.
Diffusion Magnetic Resonance Imaging (dMRI) is one of the most important contemporary non-invasive modalities for probing tissue structure at the microscopic scale. The majority of dMRI techniques employ standard single diffusion encoding (SDE) measurements, covering different sequence parameter ranges depending on the complexity of the method. Although many signal representations and biophysical models have been proposed for SDE data, they are intrinsically limited by a lack of specificity. Advanced dMRI methods have been proposed to provide additional microstructural information beyond what can be inferred from SDE. These enhanced contrasts can play important roles in characterizing biological tissues, for instance upon diseases (e.g. neurodegenerative, cancer, stroke), aging, learning, and development. In this review we focus on double diffusion encoding (DDE), which stands out among other advanced acquisitions for its versatility, ability to probe more specific diffusion correlations, and feasibility for preclinical and clinical applications. Various DDE methodologies have been employed to probe compartment sizes (Section 3), decouple the effects of microscopic diffusion anisotropy from orientation dispersion (Section 4), probe displacement correlations, study exchange, or suppress fast diffusing compartments (Section 6). DDE measurements can also be used to improve the robustness of biophysical models (Section 5) and study intra-cellular diffusion via magnetic resonance spectroscopy of metabolites (Section 7). This review discusses all these topics as well as important practical aspects related to the implementation and contrast in preclinical and clinical settings (Section 9) and aims to provide the readers a guide for deciding on the right DDE acquisition for their specific application.

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