Corticospinal tract involvement in spinocerebellar ataxia type 3: a diffusion tensor imaging study
Purpose The aim of this study was to evaluate the integrity of the corticospinal tracts (CST) in patients with SCA3 and age- and gender-matched healthy control subjects using diffusion tensor imaging (DTI). We also looked at the clinical correlates of such diffusivity abnormalities. Methods We asses...
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Published in | Neuroradiology Vol. 63; no. 2; pp. 217 - 224 |
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Main Authors | , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Berlin/Heidelberg
Springer Berlin Heidelberg
01.02.2021
Springer Nature B.V |
Subjects | |
Online Access | Get full text |
ISSN | 0028-3940 1432-1920 1432-1920 |
DOI | 10.1007/s00234-020-02528-3 |
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Summary: | Purpose
The aim of this study was to evaluate the integrity of the corticospinal tracts (CST) in patients with SCA3 and age- and gender-matched healthy control subjects using diffusion tensor imaging (DTI). We also looked at the clinical correlates of such diffusivity abnormalities.
Methods
We assessed 2 cohorts from different Brazilian centers: cohort 1 (
n
= 29) scanned in a 1.5 T magnet and cohort 2 (
n
= 91) scanned in a 3.0 T magnet. We used Pearson’s coefficients to assess the correlation of CST DTI parameters and ataxia severity (expressed by SARA scores).
Results
Two different results were obtained. Cohort 1 showed no significant between-group differences in DTI parameters. Cohort 2 showed significant between-group differences in the FA values in the bilateral precentral gyri (
p
< 0.001), bilateral superior corona radiata (
p
< 0.001), bilateral posterior limb of the internal capsule (
p
< 0.001), bilateral cerebral peduncle (
p
< 0.001), and bilateral basis pontis (
p
< 0.001). There was moderate correlation between CST diffusivity parameters and SARA scores in cohort 2 (Pearson correlation coefficient: 0.40–0.59).
Conclusion
DTI particularly at 3 T is able to uncover and quantify CST damage in SCA3. Moreover, CST microstructural damage may contribute with ataxia severity in the disease. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 |
ISSN: | 0028-3940 1432-1920 1432-1920 |
DOI: | 10.1007/s00234-020-02528-3 |