Real-life gait assessment in degenerative cerebellar ataxia: Toward ecologically valid biomarkers.


Journal

Neurology
ISSN: 1526-632X
Titre abrégé: Neurology
Pays: United States
ID NLM: 0401060

Informations de publication

Date de publication:
01 09 2020
Historique:
received: 30 10 2019
accepted: 02 03 2020
pubmed: 3 7 2020
medline: 27 10 2020
entrez: 3 7 2020
Statut: ppublish

Résumé

With disease-modifying drugs on the horizon for degenerative ataxias, ecologically valid motor biomarkers are highly warranted. In this observational study, we aimed to unravel and validate markers of ataxic gait in real life by using wearable sensors. We assessed gait characteristics of 43 patients with degenerative cerebellar disease (Scale for the Assessment and Rating of Ataxia [SARA] 9.4 ± 3.9) compared with 35 controls by 3 body-worn inertial sensors in 3 conditions: (1) laboratory-based walking; (2) supervised free walking; (3) real-life walking during everyday living (subgroup n = 21). Movement analysis focused on measures of spatiotemporal step variability and movement smoothness. A set of gait variability measures was identified that allowed us to consistently identify ataxic gait changes in all 3 conditions. Lateral step deviation and a compound measure of spatial step variability categorized patients vs controls with a discrimination accuracy of 0.86 in real life. Both were highly correlated with clinical ataxia severity (effect size ρ = 0.76). These measures allowed detecting group differences even for patients who differed only 1 point in the clinical SARA We identified measures of ataxic gait that allowed us not only to capture the gait variability inherent in ataxic gait in real life, but also to demonstrate high sensitivity to small differences in disease severity, with the highest effect sizes in real-life walking. They thus represent promising candidates for motor markers for natural history and treatment trials in ecologically valid contexts. This study provides Class I evidence that a set of gait variability measures, even if accessed in real life, correlated with the clinical severity of ataxia in patients with degenerative cerebellar disease.

Identifiants

pubmed: 32611635
pii: WNL.0000000000010176
doi: 10.1212/WNL.0000000000010176
doi:

Types de publication

Journal Article Observational Study Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e1199-e1210

Informations de copyright

© 2020 American Academy of Neurology.

Auteurs

Winfried Ilg (W)

From the Departments of Cognitive Neurology (W.I., J.S., M.G.) and Neurodegeneration (A.T., L.S.), Hertie Institute for Clinical Brain Research; Centre for Integrative Neuroscience (CIN) (W.I., J.S., M.G.); German Research Center for Neurodegenerative Diseases (DZNE) (A.T., L.S., M.S.), Tübingen; and Department of Neurology (D.T.), University of Duisburg-Essen, Germany. winfried.ilg@uni-tuebingen.de.

Jens Seemann (J)

From the Departments of Cognitive Neurology (W.I., J.S., M.G.) and Neurodegeneration (A.T., L.S.), Hertie Institute for Clinical Brain Research; Centre for Integrative Neuroscience (CIN) (W.I., J.S., M.G.); German Research Center for Neurodegenerative Diseases (DZNE) (A.T., L.S., M.S.), Tübingen; and Department of Neurology (D.T.), University of Duisburg-Essen, Germany.

Martin Giese (M)

From the Departments of Cognitive Neurology (W.I., J.S., M.G.) and Neurodegeneration (A.T., L.S.), Hertie Institute for Clinical Brain Research; Centre for Integrative Neuroscience (CIN) (W.I., J.S., M.G.); German Research Center for Neurodegenerative Diseases (DZNE) (A.T., L.S., M.S.), Tübingen; and Department of Neurology (D.T.), University of Duisburg-Essen, Germany.

Andreas Traschütz (A)

From the Departments of Cognitive Neurology (W.I., J.S., M.G.) and Neurodegeneration (A.T., L.S.), Hertie Institute for Clinical Brain Research; Centre for Integrative Neuroscience (CIN) (W.I., J.S., M.G.); German Research Center for Neurodegenerative Diseases (DZNE) (A.T., L.S., M.S.), Tübingen; and Department of Neurology (D.T.), University of Duisburg-Essen, Germany.

Ludger Schöls (L)

From the Departments of Cognitive Neurology (W.I., J.S., M.G.) and Neurodegeneration (A.T., L.S.), Hertie Institute for Clinical Brain Research; Centre for Integrative Neuroscience (CIN) (W.I., J.S., M.G.); German Research Center for Neurodegenerative Diseases (DZNE) (A.T., L.S., M.S.), Tübingen; and Department of Neurology (D.T.), University of Duisburg-Essen, Germany.

Dagmar Timmann (D)

From the Departments of Cognitive Neurology (W.I., J.S., M.G.) and Neurodegeneration (A.T., L.S.), Hertie Institute for Clinical Brain Research; Centre for Integrative Neuroscience (CIN) (W.I., J.S., M.G.); German Research Center for Neurodegenerative Diseases (DZNE) (A.T., L.S., M.S.), Tübingen; and Department of Neurology (D.T.), University of Duisburg-Essen, Germany.

Matthis Synofzik (M)

From the Departments of Cognitive Neurology (W.I., J.S., M.G.) and Neurodegeneration (A.T., L.S.), Hertie Institute for Clinical Brain Research; Centre for Integrative Neuroscience (CIN) (W.I., J.S., M.G.); German Research Center for Neurodegenerative Diseases (DZNE) (A.T., L.S., M.S.), Tübingen; and Department of Neurology (D.T.), University of Duisburg-Essen, Germany.

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