𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Water diffusion anisotropy in white and gray matter of the human spinal cord

✍ Scribed by Cristina Rossi; Andreas Boss; Günter Steidle; Petros Martirosian; Uwe Klose; Silvia Capuani; Bruno Maraviglia; Claus D. Claussen; Fritz Schick


Publisher
John Wiley and Sons
Year
2008
Tongue
English
Weight
1002 KB
Volume
27
Category
Article
ISSN
1053-1807

No coin nor oath required. For personal study only.

✦ Synopsis


Abstract

Purpose

To develop a reliable technique for diffusion imaging of the human spinal cord at 1.5 Tesla and to assess potential differences in diffusion anisotropy in cross‐sectional images.

Materials and Methods

A single‐shot echo‐planar imaging sequence with double spin‐echo diffusion preparation was optimized regarding cerebrospinal fluid artifacts, effective resolution, and contrast‐to‐noise ratios. Eleven healthy volunteers participated in the study for quantitative characterization of diffusion anisotropy in white matter (WM) and gray matter (GM) by means of two diffusion encoding schemes: octahedral‐six‐directions for fractional anisotropy (FA) evaluation and orthogonal‐three‐directions for anisotropy index (AI) calculation.

Results

Pulse‐trigger gated sequences with optimal matrix size (read × phase = 64 × 32) and b‐value (700 s/mm^2^) allowed the acquisition of high‐resolved images (voxel size = 0.9 × 0.9 × 5.0 mm^3^). The GM butterfly shape was recognizable in both AI and FA maps. Both encoding schemes yielded high diffusion anisotropy in dorsal WM (FA = 0.79 ± 0.07; AI = 0.39 ± 0.04). Lateral WM showed slightly lower anisotropy (FA = 0.69 ± 0.08; AI = 0.35 ± 0.03) than dorsal WM. Clearly smaller anisotropy was found in regions containing GM (FA = 0.45 ± 0.06; AI = 0.21 ± 0.05).

Conclusion

Diffusion anisotropy data of the spinal cord can be obtained in a clinical setting. Its application seems promising for the assessment of neurological disorders. J. Magn. Reson. Imaging 2008. © 2008 Wiley‐Liss, Inc.


📜 SIMILAR VOLUMES


A regional volumetric study of the gray
✍ A. M. Lassek; G. L. Rasmussen 📂 Article 📅 1939 🏛 John Wiley and Sons 🌐 English ⚖ 886 KB

Department of Anatomy, Medical College of tlae State of 8011th Carolina, Charlestoit EIGHT FIQURES Little investigative work has been done on the prenatal growth of the gray and white matter of the human spinal cord. This is especially true of late fetal cords. Miller ('13) studied quantitatively t

Dependence of apparent diffusion coeffic
✍ J. Chetley Ford; David B. Hackney; Ehud Lavi; Micheal Phillips; Upen Patel 📂 Article 📅 1998 🏛 John Wiley and Sons 🌐 English ⚖ 887 KB

## Abstract We used a numerical simulation of water self‐diffusion among permeable cylinders 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)

Propriospinal fibers in the white matter
✍ Dr. Kyungsoon Chung; Richard E. Coggeshall 📂 Article 📅 1988 🏛 John Wiley and Sons 🌐 English ⚖ 697 KB

The propriospinal system, which consists of those neurons completely contained within the spinal cord, is important because it underlies much spinal behavior. To provide quantitative data on this system, the present study determines numbers of axons in the isolated S2 cat spinal cord and compares th

Astrocytic hypertrophy in dysmyelination
✍ Laura A. Harsan; Patrick Poulet; Blandine Guignard; Nathalie Parizel; Robert P. 📂 Article 📅 2007 🏛 John Wiley and Sons 🌐 English ⚖ 646 KB

## Abstract The effect of a proteolipid protein (PLP) mutation on the developing white matter anisotropy was examined by diffusion tensor magnetic resonance imaging (DT‐MRI) in a noninvasive study of a mouse model of Pelizaeus‐Merzbacher disease (PMD). The jimpy PLP mutation in mice produces an irr

Developmental apoptosis in the spinal co
✍ A.J.A. De Louw; W.D.J. Van De Berg; J. De Vente; C.E. Blanco; A.W.D. Gavilanes; 📂 Article 📅 2001 🏛 John Wiley and Sons 🌐 English ⚖ 204 KB

## Abstract We investigated developmental apoptosis in the white matter of the cervical spinal cord at postnatal days 2, 5, and 8. Apoptotic cells were labeled using TUNEL and caspase‐3 immunostaining. Apoptotic cells were diffusely distributed throughout the white matter of the spinal cord. The to