Regional brain and spinal cord volume Loss in spinocerebellar ataxia type 3
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Identificadores
URI: http://hdl.handle.net/10902/24040DOI: 10.1002/mds.28610
ISSN: 0885-3185
ISSN: 1531-8257
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Faber, Jennifer; Schaprian, Tamara; Berkan, Koyak; Reetz, Kathrin; França, Marcondes Cavalcante; Rezende, Thiago Junqueira Ribeiro de; Jiang Hong; Weihua Liao; Warrenburg, Bart van de; Gaalen, Judith van; Durr, Alexandra; Mochel, Fanny; Giunti, Paola; Garcia-Moreno, Hector; Schoels, Ludger; Hengel, Holger; Synofzik, Matthis; Bender, Benjamin; Oz, Gulin; [et al.]Fecha
2021-10Derechos
This is an open access article under the terms of the Creative
Commons Attribution-NonCommercial License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes
Publicado en
Movement Disorders, 2021, 36(10), 2021
Editorial
John Wiley and Sons Inc.
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Palabras clave
Spinocerebellar ataxia
MRI
Volumetry
Biomarker
Resumen/Abstract
Background:
Given that new therapeutic options for spinocerebellar ataxias are on the horizon, there is a need for markers that reflect disease-related alterations, in particular, in the preataxic stage, in which clinical scales are lacking sensitivity.
Objective:
The objective of this study was to quantify regional brain volumes and upper cervical spinal cord areas in spinocerebellar ataxia type 3 in vivo across the entire time course of the disease.
Methods:
We applied a brain segmentation approach that included a lobular subsegmentation of the cerebellum to magnetic resonance images of 210 ataxic and 48 preataxic spinocerebellar ataxia type 3 mutation carriers and 63 healthy controls. In addition, cervical cord cross-sectional areas were determined at 2 levels.
Results:
The metrics of cervical spinal cord segments C3 and C2, medulla oblongata, pons, and pallidum, and the cerebellar anterior lobe were reduced in preataxic mutation carriers compared with controls. Those of cervical spinal cord segments C2 and C3, medulla oblongata, pons, midbrain, cerebellar lobules crus II and X, cerebellar white matter, and pallidum were reduced in ataxic compared with nonataxic carriers. Of all metrics studied, pontine volume showed the steepest decline across the disease course. It covaried with ataxia severity, CAG repeat length, and age. The multivariate model derived from this analysis explained 46.33% of the variance of pontine volume.
Conclusion:
Regional brain and spinal cord tissue loss in spinocerebellar ataxia type 3 starts before ataxia onset. Pontine volume appears to be the most promising imaging biomarker candidate for interventional trials that aim at slowing the progression of spinocerebellar ataxia type 3.
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