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. 2025 May 31;24(4):106.
doi: 10.1007/s12311-025-01858-3.

Selection of Clinical Outcome Assessments for Trial Readiness in ARSACS - 2-year Progression and Responsiveness to Change Part 1: Disease Severity, Swallowing, Upper Limb Function, and Participation

Isabelle Lessard  1   2 , Luc J Hébert  2   3   4 , Bernard Brais  5 , Elise Duchesne  2   3   4   6 , Xavier Rodrigue  4   7 , Jean-Denis Brisson  2   8   9   10 , François Routhier  3   4 , Krista Best  3   4 , Isabelle Côté  2 , Cynthia Gagnon  11   12   13   14
Affiliations

Selection of Clinical Outcome Assessments for Trial Readiness in ARSACS - 2-year Progression and Responsiveness to Change Part 1: Disease Severity, Swallowing, Upper Limb Function, and Participation

Isabelle Lessard et al. Cerebellum. .

Abstract

Progress has been made in developing new therapies for certain ataxias. To ensure clinical trial readiness and support the development of robust trial design, it is essential to know the disease progression rate and metrological properties of clinical outcome assessments (COAs), including their responsiveness to change. The objectives of this study were 1) to document over a trial-relevant time frame of two years the progression of disease severity, swallowing, upper limb function, and participation, and 2) to assess the responsiveness to change of related COAs in adults with autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS), one of the most frequent recessive ataxias worldwide. Sixty participants from two neuromuscular clinics (Saguenay and Québec City, Canada) were included. The COAs were the Disease Severity Index for ARSACS (DSI-ARSACS), Scale for the Assessment and Rating of Ataxia (SARA), Swallowing Disturbance Questionnaire, grip and pinch strength, Standardized Finger-to-Nose test, TEMPA, Barthel Index, and Assessment of Life Habits questionnaire. Self-perception of previous-year progression of specific impairments was also documented using a global rating of change scale (GRS). A significant progression in the DSI-ARSACS (-1.5 points), SARA (+ 1.6 points), Barthel Index (-7.4 points), and grip (-2.3 kg) and pinch (-0.25 kg) strength was observed. Only a few COAs were able to specifically detect a difference in participants who reported worsening, with grip strength being the most sensitive COA to assess upper limb function. Since a high proportion of participants reported not having any impairments, the statistical power was limited for responsiveness analyses and further study would be needed.

Keywords: ARSACS; Participation; Responsiveness to change; Swallowing; Upper limb function.

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Conflict of interest statement

Declarations. Ethics Approval: The study was approved by the Ethics Review Board of the Centre intégré universitaire de santé et de services sociaux du Saguenay–Lac-Saint-Jean (#2018–046) and performed in accordance with the ethical standards as laid down in the 1964 Declaration of Helsinki and its later amendments. Consent to Participate: All participants provided written informed consent. Competing Interests: C.G. acted as a consultant at the time of the study for Seelos, and Biogen, all unrelated to the present manuscript. She also conducts academic work for Biogen, Ionis, and Seelos. J.B. received research honoraries from ARTHEx Biotech, Harmony Biosciences, PepGen, Pharnext and Vertex Pharmaceuticals, all unrelated to the present manuscript. He also conducted academic work for Biogen. All other authors have no competing interests to disclose.

References

    1. Engert JC, Berube P, Mercier J, Doré C, Lepage P, Ge B, Bouchard JP, Mathieu J, Melançon SB, Schalling M, Lander ES, Morgan K. Hudson TJ and Richter A ARSACS, a spastic ataxia common in northeastern Quebec, is caused by mutations in a new gene encoding an 115-kb ORF. Nat Genet. 2000;24:120–5. https://doi.org/10.1038/72769 . - DOI - PubMed
    1. Bouchard JP, Richter A, Mathieu J, Brunet D, Hudson TJ, Morgan K, Melançon SB. Autosomal recessive spastic ataxia of Charlevoix-Saguenay. Neuromuscul Disord. 1998;8:474–9. https://doi.org/10.1016/s0960-8966(98)00055-8 . - DOI - PubMed
    1. Bouchard JP, Barbeau A, Bouchard R, Bouchard RW. Autosomal recessive spastic ataxia of Charlevoix-Saguenay. Can J Neurol Sci. 1978;5:61–9. - DOI - PubMed
    1. Briand MM, Rodrigue X, Lessard I, Mathieu J, Brais B, Côté I, Gagnon C. Expanding the clinical description of autosomal recessive spastic ataxia of Charlevoix-Saguenay. J Neurol Sci. 2019;400:39–41. https://doi.org/10.1016/j.jns.2019.03.008 . - DOI - PubMed
    1. Gagnon C, Brais B, Lessard I, Lavoie C, Côté I, Mathieu J. From motor performance to participation: A quantitative descriptive study in adults with Autosomal recessive spastic ataxia of Charlevoix-Saguenay. Orphanet J Rare Dis. 2018;13:165. https://doi.org/10.1186/s13023-018-0898-z . - DOI - PubMed - PMC

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