TY - JOUR
T1 - Cerebellar Volumetry in Ataxias
T2 - Relation to Ataxia Severity and Duration
AU - Ferreira, Mónica
AU - Schaprian, Tamara
AU - Kügler, David
AU - Reuter, Martin
AU - Deike-Hoffmann, Katharina
AU - Timmann, Dagmar
AU - Ernst, Thomas M.
AU - Giunti, Paola
AU - Garcia-Moreno, Hector
AU - van de Warrenburg, Bart
AU - van Gaalen, Judith
AU - de Vries, Jeroen
AU - Jacobi, Heike
AU - Steiner, Katharina Marie
AU - Öz, Gülin
AU - Joers, James M.
AU - Onyike, Chiadi
AU - Povazan, Michal
AU - Reetz, Kathrin
AU - Romanzetti, Sandro
AU - Klockgether, Thomas
AU - Faber, Jennifer
N1 - Publisher Copyright:
© The Author(s) 2024. corrected publication 2024.
PY - 2024/8
Y1 - 2024/8
N2 - Cerebellar atrophy is the neuropathological hallmark of most ataxias. Hence, quantifying the volume of the cerebellar grey and white matter is of great interest. In this study, we aim to identify volume differences in the cerebellum between spinocerebellar ataxia type 1 (SCA1), SCA3 and SCA6 as well as multiple system atrophy of cerebellar type (MSA-C). Our cross-sectional data set comprised mutation carriers of SCA1 (N=12), SCA3 (N=62), SCA6 (N=14), as well as MSA-C patients (N=16). Cerebellar volumes were obtained from T1-weighted magnetic resonance images. To compare the different atrophy patterns, we performed a z-transformation and plotted the intercept of each patient group’s model at the mean of 7 years of ataxia duration as well as at the mean ataxia severity of 14 points in the SARA sum score. In addition, we plotted the extrapolation at ataxia duration of 0 years as well as 0 points in the SARA sum score. Patients with MSA-C demonstrated the most pronounced volume loss, particularly in the cerebellar white matter, at the late time intercept. Patients with SCA6 showed a pronounced volume loss in cerebellar grey matter with increasing ataxia severity compared to all other patient groups. MSA-C, SCA1 and SCA3 showed a prominent atrophy of the cerebellar white matter. Our results (i) confirmed SCA6 being considered as a pure cerebellar grey matter disease, (ii) emphasise the involvement of cerebellar white matter in the neuropathology of SCA1, SCA3 and MSA-C, and (iii) reflect the rapid clinical progression in MSA-C.
AB - Cerebellar atrophy is the neuropathological hallmark of most ataxias. Hence, quantifying the volume of the cerebellar grey and white matter is of great interest. In this study, we aim to identify volume differences in the cerebellum between spinocerebellar ataxia type 1 (SCA1), SCA3 and SCA6 as well as multiple system atrophy of cerebellar type (MSA-C). Our cross-sectional data set comprised mutation carriers of SCA1 (N=12), SCA3 (N=62), SCA6 (N=14), as well as MSA-C patients (N=16). Cerebellar volumes were obtained from T1-weighted magnetic resonance images. To compare the different atrophy patterns, we performed a z-transformation and plotted the intercept of each patient group’s model at the mean of 7 years of ataxia duration as well as at the mean ataxia severity of 14 points in the SARA sum score. In addition, we plotted the extrapolation at ataxia duration of 0 years as well as 0 points in the SARA sum score. Patients with MSA-C demonstrated the most pronounced volume loss, particularly in the cerebellar white matter, at the late time intercept. Patients with SCA6 showed a pronounced volume loss in cerebellar grey matter with increasing ataxia severity compared to all other patient groups. MSA-C, SCA1 and SCA3 showed a prominent atrophy of the cerebellar white matter. Our results (i) confirmed SCA6 being considered as a pure cerebellar grey matter disease, (ii) emphasise the involvement of cerebellar white matter in the neuropathology of SCA1, SCA3 and MSA-C, and (iii) reflect the rapid clinical progression in MSA-C.
KW - Ataxia
KW - Atrophy
KW - Cerebellum
KW - z-scores
UR - http://www.scopus.com/inward/record.url?scp=85185140716&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85185140716&partnerID=8YFLogxK
U2 - 10.1007/s12311-024-01659-0
DO - 10.1007/s12311-024-01659-0
M3 - Article
C2 - 38363498
AN - SCOPUS:85185140716
SN - 1473-4222
VL - 23
SP - 1521
EP - 1529
JO - Cerebellum
JF - Cerebellum
IS - 4
ER -