@article{10902/26672,
year = {2022},
url = {https://hdl.handle.net/10902/26672},
abstract = {Background: Disease severity in spinocerebellar ataxia type 3 (SCA3) is commonly defined by the Scale for the Assessment and Rating of Ataxia (SARA) sum score, but little is known about the contributions and progression patterns of individual items.

Objectives: To investigate the temporal dynamics of SARA item scores in SCA3 patients and evaluate if clinical and demographic factors are differentially associated with evolution of axial and appendicular ataxia.
Methods: In a prospective, multinational cohort study involving 11 European and 2 US sites, SARA scores were determined longitudinally in 223 SCA3 patients with a follow-up assessment after 1 year.
Results: An increase in SARA score from 10 to 20 points was mainly driven by axial and speech items, with a markedly smaller contribution of appendicular items. Finger chase and nose-finger test scores not only showed the lowest variability at baseline, but also the least deterioration at follow-up. Compared with the full set of SARA items, omission of both tests would result in lower sample size requirements for therapeutic trials. Sex was associated with change in SARA sum score and appendicular, but not axial, subscore, with a significantly faster progression in men. Despite considerable interindividual variability, the average annual progression rate of SARA score was approximately three times higher in subjects with a disease duration over 10 years than in those within 10 years from onset.
Conclusion: Our findings provide evidence for a difference in temporal dynamics between axial and appendicular ataxia in SCA3 patients, which will help inform the design of clinical trials and development of new (etiology-specific) outcome measures.},
organization = {Funding agencies: This publication is an outcome of ESMI, an EU Joint Programme — Neurodegenerative Disease Research (JPND) Project (www.jpnd.eu). The project is supported through the following funding
organizations under the aegis of JPND: Germany, Federal Ministry of Education and Research (BMBF; funding codes 01ED1602A/B); Netherlands, The Netherlands Organization for Health Research and
Development; Portugal, Foundation for Science and Technology and Regional Fund for Science and Technology of the Azores; United Kingdom, Medical Research Council. This project has received funding from the European Union’s Horizon 2020 research and innovation programme under grant agreement no. 643417. At the United States sites this work was in part supported by the National Ataxia Foundation.},
publisher = {John Wiley and Sons Inc.},
publisher = {Movement Disorders, 2022, 37(9), 1850-1860},
title = {Differential temporal dynamics of axial and appendicular ataxia in SCA3},
author = {Maas, Roderick P. P. W. M. and Teerenstra, Steven and Lima, Manuela and Pires, Paula and Pereira de Almeida, Luís and Gaalen, Judith van and Timmann, Dagmar and Infante Ceberio, Jon and Onyike, Chiadi and Bushara, Khalaf and Jacobi, Heike and Reetz, Kathrin and Santana, Magda M. and Afonso Ribeiro, Joana and Hübener-Schmid, Jeannette and Vries, Jeroen J. de and Synofzik, Matthis and Schöls, Ludger and García-Moreno, Héctor and Giunti, Paola},
}