Dependence of apparent diffusion coefficients on axonal spacing, membrane permeability, and diffusion time in spinal cord white matter

Citation
Jc. Ford et al., Dependence of apparent diffusion coefficients on axonal spacing, membrane permeability, and diffusion time in spinal cord white matter, J MAGN R I, 8(4), 1998, pp. 775-782
Citations number
13
Categorie Soggetti
Radiology ,Nuclear Medicine & Imaging
Journal title
JMRI-JOURNAL OF MAGNETIC RESONANCE IMAGING
ISSN journal
10531807 → ACNP
Volume
8
Issue
4
Year of publication
1998
Pages
775 - 782
Database
ISI
SICI code
1053-1807(199807/08)8:4<775:DOADCO>2.0.ZU;2-F
Abstract
We used a numerical simulation of water self-diffusion among permeable cyli nders to predict the dependence of MR-based apparent diffusion coefficients in white matter on axonal separation, barrier permeability, and diffusion time (T). The transverse apparent diffusion coefficient (tADC), calculated with simulated diffusion-sensitizing gradients perpendicular to the axon fi bers, remains a function of T down to diffusion times as short as .1 mu sec for a range of diffusion barrier permeability, As the diffusion time lengt hens, the response of tADC depends on axon diameter, with decreases in tADC occurring earliest, and most dramatically, for the smallest fiber diameter simulated (2 mu m). For a given axonal separation, asymptotic values of AD C are determined by permeability alone and are the same for 2-mu m and 11-m u m fibers of equal membrane permeability. The effect of increased relative intracellular volume is manifested primarily in a decrease in tADC at shor t T, Increases in interaxonal spacing increase the tADC at asymptotically l ong diffusion times and reduce the dependence on permeability, However, at the widest plausible axonal separations, permeability remains an important determinant of tADC, These simulations may enhance interpretation of measur ed tADC in the context of the underlying physiologic and structural changes at the cellular level that accompany white-matter disease.