Back to Search Start Over

Corticospinal tract degeneration and possible pathogenesis in ALS evaluated by MR diffusion tensor imaging.

Authors :
Karlsborg, Merete
Rosenbaum, Sverre
Wiegell, Mette R.
Simonsen, Helle
Larsson, Henrik B.W.
Werdelin, Lene M.
Gredal, Ole
Source :
Amyotrophic Lateral Sclerosis & Other Motor Neuron Disorders. Sep2004, Vol. 5 Issue 3, p136-140. 5p.
Publication Year :
2004

Abstract

BACKGROUND: MR diffusion tensor imaging (DTI) appears to be a powerful method to investigate the neuronal and axonal fibre distribution in the human brain. Changes in diffusion characteristics of water molecules in the white matter can be estimated as the apparent diffusion coefficient (ADC) and the fractional anisotropy index (FA). OBJECTIVES: To characterize DTI changes at three different levels in the corticospinal tract (CST) (corona radiata, internal capsule and pons) in order to elucidate if pathogenesis of ALS is due to an anterograde or retrograde axonal degeneration. METHODS: We studied eight ALS patients with clinical signs of upper motor neuron involvement. The patients were compared with 11 healthy age-matched controls. RESULTS: ADC was significantly increased in the CST in ALS patients at the level of the internal capsule and also increased in the pons, but without statistical significance. ADC was unchanged at the level of the corona radiata. FA was significantly reduced at the lowest level (pons), only tended to be reduced in the internal capsule, but was also unchanged in the corona radiata. CONCLUSIONS: Segmentation of the CST into three regions supports the hypothesis of a 'dying back' mechanism in ALS and suggests that ADC is a more sensitive measure than FA to detect pathological changes in ALS. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
14660822
Volume :
5
Issue :
3
Database :
Academic Search Index
Journal :
Amyotrophic Lateral Sclerosis & Other Motor Neuron Disorders
Publication Type :
Academic Journal
Accession number :
14574121
Full Text :
https://doi.org/10.1080/14660820410018982