Biophysical modeling lies at the core of evaluating tissue cellular structure using diffusion-weighted MRI, albeit with shortcomings. The challenges lie not only in the complexity of the diffusion phenomenon, but also in the need to know the diffusion-specific properties of diverse cellular compartments in vivo. The likelihood function obtained from the commonly acquired Stejskal-Tanner diffusion-weighted MRI data is degenerate with different parameter constellations explaining the signal equally well, thereby hindering an unambiguous parameter estimation. The aim of this study is to measure the intra-axonal water diffusivity which is one of the central parameters of white matter models. Estimating intra-axonal diffusivity is complicated by (i) the presence of other compartments, and (ii) the orientation dispersion of axons. Our measurement involves an efficient signal suppression of water in extra-axonal space and all cellular processes oriented outside a narrow cone around the principal fiber direction. This is achieved using a planar water mobility filter that suppresses signal from all molecules that are mobile in the plane transverse to the fiber bundle. After the planar filter, the diffusivity of the remaining intra-axonal signal is measured using linear and spherical diffusion encoding. We find the average intra-axonal diffusivity D=2.25±0.03μm/ms for the timing of the applied gradients, which gives D≈2.0μm/ms when extrapolated to infinite diffusion time. The result imposes a strong limitation on the parameter selection for biophysical modeling of diffusion-weighted MRI.
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http://dx.doi.org/10.1016/j.neuroimage.2019.01.015 | DOI Listing |
Diagnostics (Basel)
August 2024
Department of Health and Functioning, Western Norway University of Applied Sciences (HVL), 5063 Bergen, Norway.
Unlabelled: The cerebral small vessel disease (cSVD) is one of the main causes of vascular and mixed cognitive impairment (CI), and it is associated, in particular, with brain ageing. An understanding of structural tissue changes in an intact cerebral white matter in cSVD might allow one to develop the sensitive biomarkers for early diagnosis and monitoring of disease progression.
Purpose Of The Study: to evaluate microstructural changes in the corpus callosum (CC) using diffusion MRI (D-MRI) approaches in cSVD patients with different severity of CI and reveal the most sensitive correlations of diffusion metrics with CI.
Neurology
August 2024
From the Cardiff University Brain Research Imaging Centre (C.L.M., D.J., K.G., A.D., C.M.W.T.), Cardiff University; Neuroscience and Mental Health Research Institute (C.L.M., K.J.P.), Division of Psychological Medicine and Clinical Neurosciences, Cardiff University School of Medicine; North Bristol NHS Trust (K.S.-K.), United Kingdom; and Image Sciences Institute (C.M.W.T.), University Medical Center Utrecht, the Netherlands.
Axon diameter and myelin thickness are closely related microstructural tissue properties that affect the conduction velocity of action potentials in the nervous system. Imaging them non-invasively with MRI-based methods is thus valuable for studying brain microstructure and function. However, the relationship between MRI-based axon diameter and myelination measures has not been investigated across the brain, mainly due to methodological limitations in estimating axon diameters.
View Article and Find Full Text PDFInvest Ophthalmol Vis Sci
July 2024
Department of Ophthalmology, New York University Grossman School of Medicine, New York, New York, United States.
Purpose: To investigate the contributions of the microstructural and metabolic brain environment to glaucoma and their association with visual field (VF) loss patterns by using advanced diffusion magnetic resonance imaging (dMRI), proton magnetic resonance spectroscopy (MRS), and clinical ophthalmic measures.
Methods: Sixty-nine glaucoma and healthy subjects underwent dMRI and/or MRS at 3 Tesla. Ophthalmic data were collected from VF perimetry and optical coherence tomography.
Neurooncol Adv
June 2024
Department of Neuroradiology, Medical Center-University of Freiburg, University of Freiburg, Freiburg, Germany.
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