TY - JOUR
T1 - Clinically Meaningful Magnetic Resonance Endpoints Sensitive to Preataxic Spinocerebellar Ataxia Types 1 and 3
AU - for the READISCA Consortium
AU - Chandrasekaran, Jayashree
AU - Petit, Emilien
AU - Park, Young Woo
AU - du Montcel, Sophie Tezenas
AU - Joers, James M.
AU - Deelchand, Dinesh K.
AU - Považan, Michal
AU - Banan, Guita
AU - Valabregue, Romain
AU - Ehses, Philipp
AU - Faber, Jennifer
AU - Coupé, Pierrick
AU - Onyike, Chiadi U.
AU - Barker, Peter B.
AU - Schmahmann, Jeremy D.
AU - Ratai, Eva Maria
AU - Subramony, S. H.
AU - Mareci, Thomas H.
AU - Bushara, Khalaf O.
AU - Paulson, Henry
AU - Durr, Alexandra
AU - Klockgether, Thomas
AU - Ashizawa, Tetsuo
AU - Lenglet, Christophe
AU - Öz, Gülin
AU - Rosenthal, Liana
AU - Burns, Matthew
AU - Grobe-Einsler, Marcus
AU - Oender, Demet
AU - Kimmich, Okka
AU - Roy, Nina
AU - Ewenczyk, Claire
AU - Heinzmann, Anna
AU - Lallemant, Pauline
AU - Heide, Solveig
AU - Charles, Perrine
AU - Coarelli, Giulia
AU - Cunha, Paulina
AU - Sayah, Sabrina
AU - Wilmot, George
AU - Scorr, Laura
AU - Opal, Puneet
AU - Sha, Sharon
AU - Santini, Veronica
AU - Sampson, Jacinda
AU - Perlman, Susan
AU - Geschwind, Michael
AU - Nelson, Alexandra
AU - Dietiker, Cameron
AU - Gomez, Christopher
N1 - Publisher Copyright:
© 2022 The Authors. Annals of Neurology published by Wiley Periodicals LLC on behalf of American Neurological Association.
PY - 2023/4
Y1 - 2023/4
N2 - OBJECTIVE: This study was undertaken to identify magnetic resonance (MR) metrics that are most sensitive to early changes in the brain in spinocerebellar ataxia type 1 (SCA1) and type 3 (SCA3) using an advanced multimodal MR imaging (MRI) protocol in the multisite trial setting.METHODS: SCA1 or SCA3 mutation carriers and controls (n = 107) underwent MR scanning in the US-European READISCA study to obtain structural, diffusion MRI, and MR spectroscopy data using an advanced protocol at 3T. Morphometric, microstructural, and neurochemical metrics were analyzed blinded to diagnosis and compared between preataxic SCA (n = 11 SCA1, n = 28 SCA3), ataxic SCA (n = 14 SCA1, n = 37 SCA3), and control (n = 17) groups using nonparametric testing accounting for multiple comparisons. MR metrics that were most sensitive to preataxic abnormalities were identified using receiver operating characteristic (ROC) analyses.RESULTS: Atrophy and microstructural damage in the brainstem and cerebellar peduncles and neurochemical abnormalities in the pons were prominent in both preataxic groups, when patients did not differ from controls clinically. MR metrics were strongly associated with ataxia symptoms, activities of daily living, and estimated ataxia duration. A neurochemical measure was the most sensitive metric to preataxic changes in SCA1 (ROC area under the curve [AUC] = 0.95), and a microstructural metric was the most sensitive metric to preataxic changes in SCA3 (AUC = 0.92).INTERPRETATION: Changes in cerebellar afferent and efferent pathways underlie the earliest symptoms of both SCAs. MR metrics collected with a harmonized advanced protocol in the multisite trial setting allow detection of disease effects in individuals before ataxia onset with potential clinical trial utility for subject stratification. ANN NEUROL 2023;93:686-701.
AB - OBJECTIVE: This study was undertaken to identify magnetic resonance (MR) metrics that are most sensitive to early changes in the brain in spinocerebellar ataxia type 1 (SCA1) and type 3 (SCA3) using an advanced multimodal MR imaging (MRI) protocol in the multisite trial setting.METHODS: SCA1 or SCA3 mutation carriers and controls (n = 107) underwent MR scanning in the US-European READISCA study to obtain structural, diffusion MRI, and MR spectroscopy data using an advanced protocol at 3T. Morphometric, microstructural, and neurochemical metrics were analyzed blinded to diagnosis and compared between preataxic SCA (n = 11 SCA1, n = 28 SCA3), ataxic SCA (n = 14 SCA1, n = 37 SCA3), and control (n = 17) groups using nonparametric testing accounting for multiple comparisons. MR metrics that were most sensitive to preataxic abnormalities were identified using receiver operating characteristic (ROC) analyses.RESULTS: Atrophy and microstructural damage in the brainstem and cerebellar peduncles and neurochemical abnormalities in the pons were prominent in both preataxic groups, when patients did not differ from controls clinically. MR metrics were strongly associated with ataxia symptoms, activities of daily living, and estimated ataxia duration. A neurochemical measure was the most sensitive metric to preataxic changes in SCA1 (ROC area under the curve [AUC] = 0.95), and a microstructural metric was the most sensitive metric to preataxic changes in SCA3 (AUC = 0.92).INTERPRETATION: Changes in cerebellar afferent and efferent pathways underlie the earliest symptoms of both SCAs. MR metrics collected with a harmonized advanced protocol in the multisite trial setting allow detection of disease effects in individuals before ataxia onset with potential clinical trial utility for subject stratification. ANN NEUROL 2023;93:686-701.
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U2 - 10.1002/ana.26573
DO - 10.1002/ana.26573
M3 - Article
C2 - 36511514
AN - SCOPUS:85145382674
SN - 0364-5134
VL - 93
SP - 686
EP - 701
JO - Annals of Neurology
JF - Annals of Neurology
IS - 4
ER -