Diffusion tensor MRI assesses corticospinal tract damage in ALS
- PMID: 10496265
- DOI: 10.1212/wnl.53.5.1051
Diffusion tensor MRI assesses corticospinal tract damage in ALS
Abstract
Background: A number of neurophysiologic and neuroimaging techniques have been evaluated in the research setting to assess upper motor neuron (UMN) damage in ALS. Changes in tissue structure in the CNS modify the diffusional behavior of water molecules, which can be detected by diffusion tensor MRI.
Objectives: To explore the hypothesis that degeneration of the motor fibers in ALS would be reflected by changes in the diffusion characteristics of the white matter fibers in the posterior limb of the internal capsule and that these changes could be detected by diffusion tensor MRI.
Methods: We studied 22 patients with El Escorial definite, probable, or possible ALS-11 with limb onset (mean age 54.5 +/- 10.7 years) and 11 with bulbar onset (mean age 49.6 +/- 11.7 years)-and compared them with 20 healthy, age-matched controls (mean age 46.0 +/- 12.6 years). We assessed central motor conduction time (CMCT), threshold to stimulation, and silent period using transcranial magnetic stimulation. Diffusion tensor MRI was performed using a 1.5-T GE Signa system (Milwaukee, WI) fitted with Advanced NMR hardware and software capable of producing echo planar MR images. Data were acquired from seven coronal slices centered to include the posterior limb of the internal capsule. Maps of the mean diffusivity, fractional anisotropy, and T2-weighted signal intensity were generated.
Results: There were no differences between the subject groups on measures of CMCT, threshold to stimulation, and silent period. However, the CMCT correlated with clinical measures of UMN involvement. We found a significant increase in the mean diffusivity and reduction in fractional anisotropy along the corticospinal tracts between the three subject groups, most marked in the bulbar-onset group. The fractional anisotropy correlated with measures of disease severity and UMN involvement, whereas the mean diffusivity correlated with disease duration.
Conclusion: The results support the use of diffusion tensor MRI in detecting pathology of the corticospinal tracts in ALS.
Similar articles
-
Differential involvement of corticospinal tract (CST) fibers in UMN-predominant ALS patients with or without CST hyperintensity: A diffusion tensor tractography study.Neuroimage Clin. 2017 Feb 22;14:574-579. doi: 10.1016/j.nicl.2017.02.017. eCollection 2017. Neuroimage Clin. 2017. PMID: 28337412 Free PMC article.
-
Diffusion tensor imaging patterns differ in bulbar and limb onset amyotrophic lateral sclerosis.Clin Neurol Neurosurg. 2013 Aug;115(8):1281-7. doi: 10.1016/j.clineuro.2012.11.031. Epub 2012 Dec 23. Clin Neurol Neurosurg. 2013. PMID: 23266262
-
Diffusion tensor MRI of early upper motor neuron involvement in amyotrophic lateral sclerosis.Brain. 2004 Feb;127(Pt 2):340-50. doi: 10.1093/brain/awh041. Epub 2003 Nov 7. Brain. 2004. PMID: 14607785
-
[Objective markers for upper motor neuron involvement in amyotrophic lateral sclerosis].Brain Nerve. 2007 Oct;59(10):1053-64. Brain Nerve. 2007. PMID: 17969345 Review. Japanese.
-
[An autopsy case of amyotrophic lateral screlosis (ALS): magnetic resonance imaging and pathological findings of the pyramidal tract].Rinsho Shinkeigaku. 1997 Sep;37(9):810-6. Rinsho Shinkeigaku. 1997. PMID: 9430996 Review. Japanese.
Cited by
-
Kinetics of neurodegeneration based on a risk-related biomarker in animal model of glaucoma.Mol Neurodegener. 2013 Jan 18;8:4. doi: 10.1186/1750-1326-8-4. Mol Neurodegener. 2013. PMID: 23331478 Free PMC article.
-
Isotropic resolution diffusion tensor imaging with whole brain acquisition in a clinically acceptable time.Hum Brain Mapp. 2002 Apr;15(4):216-30. doi: 10.1002/hbm.10018. Hum Brain Mapp. 2002. PMID: 11835610 Free PMC article.
-
Measures and markers in amyotrophic lateral sclerosis.NeuroRx. 2004 Apr;1(2):273-83. doi: 10.1602/neurorx.1.2.273. NeuroRx. 2004. PMID: 15717028 Free PMC article. Review.
-
Investigation of Neurodegenerative Processes in Amyotrophic Lateral Sclerosis Using White Matter Fiber Density.Clin Neuroradiol. 2019 Sep;29(3):493-503. doi: 10.1007/s00062-018-0670-8. Epub 2018 Feb 19. Clin Neuroradiol. 2019. PMID: 29460142
-
White matter alterations differ in primary lateral sclerosis and amyotrophic lateral sclerosis.Brain. 2011 Sep;134(Pt 9):2642-55. doi: 10.1093/brain/awr178. Epub 2011 Jul 28. Brain. 2011. PMID: 21798965 Free PMC article.
Publication types
MeSH terms
Grants and funding
LinkOut - more resources
Full Text Sources
Medical
Miscellaneous