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Cognitive impairment in SCA3: A multi-center cohort study with demographic, imaging, and biomarker correlates

Title: Cognitive impairment in SCA3: A multi-center cohort study with demographic, imaging, and biomarker correlates
Authors: Maas, Roderick PPWM; Garcia-Moreno, Hector; Faber, Jennifer; Gonzalez, Carlos; Schöls, Ludger; de Vries, Jeroen J; Bushara, Khalaf; Reetz, Kathrin; Onyike, Chiadi U; Jacobi, Heike; Erdlenbruch, Friedrich; Infante, Jon; Santana, Magda M; Hübener-Schmid, Jeannette; de Almeida, Luís Pereira; Lima, Manuela; Giunti, Paola; Klockgether, Thomas; ESMI study group; van de Warrenburg, Bart PC
Source: Neurobiology of Disease , 220 , Article 107301. (2026)
Publication Year: 2026
Collection: University College London: UCL Discovery
Subject Terms: Cerebellum; Cognition; Machado-Joseph disease; Spinocerebellar ataxia type 3
Description: BACKGROUND: Cognitive deficits are common in spinocerebellar ataxia type 3 (SCA3), but their neurobiological correlates remain largely unknown. OBJECTIVES: To investigate cognitive performance in a large international cohort of SCA3 mutation carriers covering the entire disease course and to explore associations with posterior cerebellar volumes, basal ganglia and thalamus volumes, and plasma neurofilament light chain (NfL) concentration. METHODS: The Montreal Cognitive Assessment (MoCA) was used to evaluate cognitive impairment in this prospective, observational cohort study involving 13 ataxia referral centers. Standardized motor assessments, brain MR imaging, and peripheral blood biosampling were also performed. RESULTS: MoCA data were collected from 61 pre-ataxic SCA3 mutation carriers, 231 ataxic SCA3 patients, and 111 healthy controls. After adjustments for educational level and age, there were significant differences in MoCA total score, as well as visuospatial/executive, attention, language, and abstraction subscores, between healthy controls and ataxic, but not pre-ataxic individuals. MoCA scores declined with ataxia severity, especially in patients with a lower educational level. Patients with a MoCA score < 26 had lower pallidal volumes and higher plasma NfL concentrations than those with a score ≥ 26. However, only the interaction term between ataxia severity and educational level was independently associated with cognitive performance in multivariable regression analyses containing demographic, clinical, volumetric, and biochemical parameters. CONCLUSION: Cognitive deficits in SCA3 generally appear after clinical ataxia onset and progress in parallel with ataxia severity, especially in patients with a lower cognitive reserve. Other measured biochemical and imaging parameters did not have a significant additional contribution.
Document Type: article in journal/newspaper
File Description: text
Language: English
Relation: https://discovery.ucl.ac.uk/id/eprint/10221818/
Availability: https://discovery.ucl.ac.uk/id/eprint/10221818/1/1-s2.0-S0969996126000458-main.pdf; https://discovery.ucl.ac.uk/id/eprint/10221818/
Rights: open
Accession Number: edsbas.C8BACA6E
Database: BASE