Stage‐Dependent Biomarker Changes in Spinocerebellar Ataxia Type 3

Spinocerebellar ataxia type 3/Machado–Joseph disease is the most common autosomal dominant ataxia. In view of the development of targeted therapies, knowledge of early biomarker changes is needed. We analyzed cross‐sectional data of 292 spinocerebellar ataxia type 3/Machado–Joseph disease mutation c...

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Published inAnnals of neurology Vol. 95; no. 2; pp. 400 - 406
Main Authors Faber, Jennifer, Berger, Moritz, Wilke, Carlo, Hubener‐Schmid, Jeannette, Schaprian, Tamara, Santana, Magda M., Grobe‐Einsler, Marcus, Onder, Demet, Koyak, Berkan, Giunti, Paola, Garcia‐Moreno, Hector, Gonzalez‐Robles, Cristina, Lima, Manuela, Raposo, Mafalda, Melo, Ana Rosa Vieira, Almeida, Luís Pereira, Silva, Patrick, Pinto, Maria M., Warrenburg, Bart P., Gaalen, Judith, Vries, Jeroen, Oz, Gulin, Joers, James M., Synofzik, Matthis, Schols, Ludger, Riess, Olaf, Infante, Jon, Manrique, Leire, Timmann, Dagmar, Thieme, Andreas, Jacobi, Heike, Reetz, Kathrin, Dogan, Imis, Onyike, Chiadikaobi, Povazan, Michal, Schmahmann, Jeremy, Ratai, Eva‐Maria, Schmid, Matthias, Klockgether, Thomas
Format Journal Article
LanguageEnglish
Published Hoboken, USA John Wiley & Sons, Inc 01.02.2024
Wiley Subscription Services, Inc
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Summary:Spinocerebellar ataxia type 3/Machado–Joseph disease is the most common autosomal dominant ataxia. In view of the development of targeted therapies, knowledge of early biomarker changes is needed. We analyzed cross‐sectional data of 292 spinocerebellar ataxia type 3/Machado–Joseph disease mutation carriers. Blood concentrations of mutant ATXN3 were high before and after ataxia onset, whereas neurofilament light deviated from normal 13.3 years before onset. Pons and cerebellar white matter volumes decreased and deviated from normal 2.2 years and 0.6 years before ataxia onset. We propose a staging model of spinocerebellar ataxia type 3/Machado–Joseph disease that includes a biomarker stage characterized by objective indicators of neurodegeneration before ataxia onset. ANN NEUROL 2024;95:400–406
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ISSN:0364-5134
1531-8249
DOI:10.1002/ana.26824