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Regional Brain and Spinal Cord Volume Loss in Spinocerebellar Ataxia Type 3

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...

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Autores principales: Faber, Jennifer, Schaprian, Tamara, Berkan, Koyak, Reetz, Kathrin, França, Marcondes Cavalcante, de Rezende, Thiago Junqueira Ribeiro, Hong, Jiang, Liao, Weihua, van de Warrenburg, Bart, van Gaalen, Judith, Durr, Alexandra, Mochel, Fanny, Giunti, Paola, Garcia-Moreno, Hector, Schoels, Ludger, Hengel, Holger, Synofzik, Matthis, Bender, Benjamin, Oz, Gulin, Joers, James, de Vries, Jereon J., Kang, Jun-Suk, Timmann-Braun, Dagmar, Jacobi, Heike, Infante, Jon, Joules, Richard, Romanzetti, Sandro, Diedrichsen, Jorn, Schmid, Matthias, Wolz, Robin, Klockgether, Thomas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9521507/
https://www.ncbi.nlm.nih.gov/pubmed/33951232
http://dx.doi.org/10.1002/mds.28610
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author Faber, Jennifer
Schaprian, Tamara
Berkan, Koyak
Reetz, Kathrin
França, Marcondes Cavalcante
de Rezende, Thiago Junqueira Ribeiro
Hong, Jiang
Liao, Weihua
van de Warrenburg, Bart
van Gaalen, Judith
Durr, Alexandra
Mochel, Fanny
Giunti, Paola
Garcia-Moreno, Hector
Schoels, Ludger
Hengel, Holger
Synofzik, Matthis
Bender, Benjamin
Oz, Gulin
Joers, James
de Vries, Jereon J.
Kang, Jun-Suk
Timmann-Braun, Dagmar
Jacobi, Heike
Infante, Jon
Joules, Richard
Romanzetti, Sandro
Diedrichsen, Jorn
Schmid, Matthias
Wolz, Robin
Klockgether, Thomas
author_facet Faber, Jennifer
Schaprian, Tamara
Berkan, Koyak
Reetz, Kathrin
França, Marcondes Cavalcante
de Rezende, Thiago Junqueira Ribeiro
Hong, Jiang
Liao, Weihua
van de Warrenburg, Bart
van Gaalen, Judith
Durr, Alexandra
Mochel, Fanny
Giunti, Paola
Garcia-Moreno, Hector
Schoels, Ludger
Hengel, Holger
Synofzik, Matthis
Bender, Benjamin
Oz, Gulin
Joers, James
de Vries, Jereon J.
Kang, Jun-Suk
Timmann-Braun, Dagmar
Jacobi, Heike
Infante, Jon
Joules, Richard
Romanzetti, Sandro
Diedrichsen, Jorn
Schmid, Matthias
Wolz, Robin
Klockgether, Thomas
author_sort Faber, Jennifer
collection PubMed
description 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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spelling pubmed-95215072022-09-29 Regional Brain and Spinal Cord Volume Loss in Spinocerebellar Ataxia Type 3 Faber, Jennifer Schaprian, Tamara Berkan, Koyak Reetz, Kathrin França, Marcondes Cavalcante de Rezende, Thiago Junqueira Ribeiro Hong, Jiang Liao, Weihua van de Warrenburg, Bart van Gaalen, Judith Durr, Alexandra Mochel, Fanny Giunti, Paola Garcia-Moreno, Hector Schoels, Ludger Hengel, Holger Synofzik, Matthis Bender, Benjamin Oz, Gulin Joers, James de Vries, Jereon J. Kang, Jun-Suk Timmann-Braun, Dagmar Jacobi, Heike Infante, Jon Joules, Richard Romanzetti, Sandro Diedrichsen, Jorn Schmid, Matthias Wolz, Robin Klockgether, Thomas Mov Disord Article 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. 2021-10 2021-05-05 /pmc/articles/PMC9521507/ /pubmed/33951232 http://dx.doi.org/10.1002/mds.28610 Text en https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the Creative Commons Attribution-NonCommercial (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Article
Faber, Jennifer
Schaprian, Tamara
Berkan, Koyak
Reetz, Kathrin
França, Marcondes Cavalcante
de Rezende, Thiago Junqueira Ribeiro
Hong, Jiang
Liao, Weihua
van de Warrenburg, Bart
van Gaalen, Judith
Durr, Alexandra
Mochel, Fanny
Giunti, Paola
Garcia-Moreno, Hector
Schoels, Ludger
Hengel, Holger
Synofzik, Matthis
Bender, Benjamin
Oz, Gulin
Joers, James
de Vries, Jereon J.
Kang, Jun-Suk
Timmann-Braun, Dagmar
Jacobi, Heike
Infante, Jon
Joules, Richard
Romanzetti, Sandro
Diedrichsen, Jorn
Schmid, Matthias
Wolz, Robin
Klockgether, Thomas
Regional Brain and Spinal Cord Volume Loss in Spinocerebellar Ataxia Type 3
title Regional Brain and Spinal Cord Volume Loss in Spinocerebellar Ataxia Type 3
title_full Regional Brain and Spinal Cord Volume Loss in Spinocerebellar Ataxia Type 3
title_fullStr Regional Brain and Spinal Cord Volume Loss in Spinocerebellar Ataxia Type 3
title_full_unstemmed Regional Brain and Spinal Cord Volume Loss in Spinocerebellar Ataxia Type 3
title_short Regional Brain and Spinal Cord Volume Loss in Spinocerebellar Ataxia Type 3
title_sort regional brain and spinal cord volume loss in spinocerebellar ataxia type 3
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9521507/
https://www.ncbi.nlm.nih.gov/pubmed/33951232
http://dx.doi.org/10.1002/mds.28610
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