Journal Article

DZNE-2026-00212

http://join2-wiki.gsi.de/foswiki/pub/Main/Artwork/join2_logo100x88.png Cognitive impairment in SCA3: A multi-center cohort study with demographic, imaging, and biomarker correlates.

Maas, R. P. P. W. M. ; Garcia-Moreno, H. ; Faber, J.DZNE* ; Gonzalez, C. ; Schöls, L.DZNE* ; de Vries, J. J. ; Bushara, K. ; Reetz, K. ; Onyike, C. U. ; Jacobi, H. ; Erdlenbruch, F. ; Infante, J. ; Santana, M. M. ; Hübener-Schmid, J. ; de Almeida, L. P. ; Lima, M. ; Giunti, P. ; Klockgether, T.DZNE* ; group, E. s. (Collaboration Author) ; van de Warrenburg, B. P. C.

2026
Elsevier [Amsterdam]

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Please use a persistent id in citations: doi:10.1016/j.nbd.2026.107301

Abstract: Cognitive deficits are common in spinocerebellar ataxia type 3 (SCA3), but their neurobiological correlates remain largely unknown.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.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.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.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.

Keyword(s): Humans (MeSH) ; Male (MeSH) ; Female (MeSH) ; Middle Aged (MeSH) ; Cognitive Dysfunction: diagnostic imaging (MeSH) ; Cognitive Dysfunction: etiology (MeSH) ; Cognitive Dysfunction: blood (MeSH) ; Cognitive Dysfunction: psychology (MeSH) ; Adult (MeSH) ; Biomarkers: blood (MeSH) ; Magnetic Resonance Imaging (MeSH) ; Machado-Joseph Disease: complications (MeSH) ; Machado-Joseph Disease: diagnostic imaging (MeSH) ; Machado-Joseph Disease: psychology (MeSH) ; Machado-Joseph Disease: genetics (MeSH) ; Machado-Joseph Disease: blood (MeSH) ; Cohort Studies (MeSH) ; Neurofilament Proteins: blood (MeSH) ; Aged (MeSH) ; Prospective Studies (MeSH) ; Mental Status and Dementia Tests (MeSH) ; Cerebellum ; Cognition ; Machado-Joseph disease ; Spinocerebellar ataxia type 3 ; Biomarkers ; Neurofilament Proteins ; neurofilament protein L

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Contributing Institute(s):

1. Clinical Research Coordination (Clinical Research (Bonn))
2. Clinical Neurogenetics (AG Schöls)
3. Patient Studies (Bonn) (Patient Studies (Bonn))

Research Program(s):

1. 353 - Clinical and Health Care Research (POF4-353) (POF4-353)

Experiment(s):

1. European Spinocerebellar Ataxia Type 3/Machado-Joseph Disease Initiative

Appears in the scientific report 2026

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