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Sensitivity of Advanced Magnetic Resonance Imaging to Progression over Six Months in Early Spinocerebellar Ataxia.
Rezende, Thiago J R; Petit, Emilien; Park, Young Woo; Tezenas du Montcel, Sophie; Joers, James M; DuBois, Jonathan M; Moore Arnold, H; Povazan, Michal; Banan, Guita; Valabregue, Romain; Ehses, Philipp; Faber, Jennifer; Coupé, Pierrick; Onyike, Chiadi U; Barker, Peter B; Schmahmann, Jeremy D; Ratai, Eva-Maria; Subramony, Sub H; Mareci, Thomas H; Bushara, Khalaf O; Paulson, Henry; Klockgether, Thomas; Durr, Alexandra; Ashizawa, Tetsuo; Lenglet, Christophe; Öz, Gülin.
Afiliação
  • Rezende TJR; Department of Neurology, School of Medical Sciences, University of Campinas, Campinas, Brazil.
  • Petit E; Sorbonne Université, Paris Brain Institute, Inserm, INRIA, CNRS, APHP, Paris, France.
  • Park YW; Department of Radiology, Center for Magnetic Resonance Research, University of Minnesota, Minneapolis, Minnesota, USA.
  • Tezenas du Montcel S; Sorbonne Université, Paris Brain Institute, Inserm, INRIA, CNRS, APHP, Paris, France.
  • Joers JM; Department of Radiology, Center for Magnetic Resonance Research, University of Minnesota, Minneapolis, Minnesota, USA.
  • DuBois JM; Biogen, Cambridge, Massachusetts, USA.
  • Moore Arnold H; Biogen, Cambridge, Massachusetts, USA.
  • Povazan M; Department of Radiology, Johns Hopkins University, School of Medicine, Baltimore, Maryland, USA.
  • Banan G; Norman Fixel Center for Neurological Disorders, College of Medicine, University of Florida, Gainesville, Florida, USA.
  • Valabregue R; Sorbonne Université, Paris Brain Institute, Inserm, INRIA, CNRS, APHP, Paris, France.
  • Ehses P; German Center for Neurodegenerative Diseases (DZNE), Bonn, Germany.
  • Faber J; German Center for Neurodegenerative Diseases (DZNE), Bonn, Germany.
  • Coupé P; Department of Neurology, University Hospital Bonn, Bonn, Germany.
  • Onyike CU; Laboratoire Bordelais de Recherche en Informatique, Université de Bordeaux, Talence, France.
  • Barker PB; Department of Radiology, Johns Hopkins University, School of Medicine, Baltimore, Maryland, USA.
  • Schmahmann JD; Department of Radiology, Johns Hopkins University, School of Medicine, Baltimore, Maryland, USA.
  • Ratai EM; Laboratory for Neuroanatomy and Cerebellar Neurobiology, Department of Neurology, Ataxia Center, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts, USA.
  • Subramony SH; A. A. Martinos Center for Biomedical Imaging, Massachusetts General Hospital, Department of Radiology, Harvard Medical School, Boston, Massachusetts, USA.
  • Mareci TH; Norman Fixel Center for Neurological Disorders, College of Medicine, University of Florida, Gainesville, Florida, USA.
  • Bushara KO; Norman Fixel Center for Neurological Disorders, College of Medicine, University of Florida, Gainesville, Florida, USA.
  • Paulson H; Department of Radiology, Center for Magnetic Resonance Research, University of Minnesota, Minneapolis, Minnesota, USA.
  • Klockgether T; Department of Neurology, University of Michigan, Ann Arbor, Michigan, USA.
  • Durr A; German Center for Neurodegenerative Diseases (DZNE), Bonn, Germany.
  • Ashizawa T; Department of Neurology, University Hospital Bonn, Bonn, Germany.
  • Lenglet C; Sorbonne Université, Paris Brain Institute, Inserm, INRIA, CNRS, APHP, Paris, France.
  • Öz G; Department of Neurology, The Houston Methodist Research Institute, Houston, Texas, USA.
Mov Disord ; 2024 Jul 26.
Article em En | MEDLINE | ID: mdl-39056163
ABSTRACT

BACKGROUND:

Clinical trials for upcoming disease-modifying therapies of spinocerebellar ataxias (SCA), a group of rare movement disorders, lack endpoints sensitive to early disease progression, when therapeutics will be most effective. In addition, regulatory agencies emphasize the importance of biological outcomes.

OBJECTIVES:

READISCA, a transatlantic clinical trial readiness consortium, investigated whether advanced multimodal magnetic resonance imaging (MRI) detects pathology progression over 6 months in preataxic and early ataxic carriers of SCA mutations.

METHODS:

A total of 44 participants (10 SCA1, 25 SCA3, and 9 controls) prospectively underwent 3-T MR scanning at baseline and a median [interquartile range] follow-up of 6.2 [5.9-6.7] months; 44% of SCA participants were preataxic. Blinded analyses of annual changes in structural, diffusion MRI, MR spectroscopy, and the Scale for Assessment and Rating of Ataxia (SARA) were compared between groups using nonparametric testing. Sample sizes were estimated for 6-month interventional trials with 50% to 100% treatment effect size, leveraging existing large cohort data (186 SCA1, 272 SCA3) for the SARA estimate.

RESULTS:

Rate of change in microstructural integrity (decrease in fractional anisotropy, increase in diffusivities) in the middle cerebellar peduncle, corona radiata, and superior longitudinal fasciculus significantly differed in SCAs from controls (P < 0.005), with high effect sizes (Cohen's d = 1-2) and moderate-to-high responsiveness (|standardized response mean| = 0.6-0.9) in SCAs. SARA scores did not change, and their rate of change did not differ between groups.

CONCLUSIONS:

Diffusion MRI is sensitive to disease progression at very early-stage SCA1 and SCA3 and may provide a >5-fold reduction in sample sizes relative to SARA as endpoint for 6-month-long trials. © 2024 The Author(s). Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article