Cargando…

Robotic and clinical evaluation of upper limb motor performance in patients with Friedreich’s Ataxia: an observational study

BACKGROUND: Friedreich’s ataxia (FRDA) is the most common hereditary autosomal recessive form of ataxia. In this disease there is early manifestation of gait ataxia, and dysmetria of the arms and legs which causes impairment in daily activities that require fine manual dexterity. To date there is no...

Descripción completa

Detalles Bibliográficos
Autores principales: Germanotta, Marco, Vasco, Gessica, Petrarca, Maurizio, Rossi, Stefano, Carniel, Sacha, Bertini, Enrico, Cappa, Paolo, Castelli, Enrico
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4448881/
https://www.ncbi.nlm.nih.gov/pubmed/25900021
http://dx.doi.org/10.1186/s12984-015-0032-6
_version_ 1782373781945188352
author Germanotta, Marco
Vasco, Gessica
Petrarca, Maurizio
Rossi, Stefano
Carniel, Sacha
Bertini, Enrico
Cappa, Paolo
Castelli, Enrico
author_facet Germanotta, Marco
Vasco, Gessica
Petrarca, Maurizio
Rossi, Stefano
Carniel, Sacha
Bertini, Enrico
Cappa, Paolo
Castelli, Enrico
author_sort Germanotta, Marco
collection PubMed
description BACKGROUND: Friedreich’s ataxia (FRDA) is the most common hereditary autosomal recessive form of ataxia. In this disease there is early manifestation of gait ataxia, and dysmetria of the arms and legs which causes impairment in daily activities that require fine manual dexterity. To date there is no cure for this disease. Some novel therapeutic approaches are ongoing in different steps of clinical trial. Development of sensitive outcome measures is crucial to prove therapeutic effectiveness. The aim of the study was to assess the reliability and sensitivity of quantitative and objective assessment of upper limb performance computed by means of the robotic device and to evaluate the correlation with clinical and functional markers of the disease severity. METHODS: Here we assess upper limb performances by means of the InMotion Arm Robot, a robot designed for clinical neurological applications, in a cohort of 14 children and young adults affected by FRDA, matched for age and gender with 18 healthy subjects. We focused on the analysis of kinematics, accuracy, smoothness, and submovements of the upper limb while reaching movements were performed. The robotic evaluation of upper limb performance consisted of planar reaching movements performed with the robotic system. The motors of the robot were turned off, so that the device worked as a measurement tool. The status of the disease was scored using the Scale for the Assessment and Rating of Ataxia (SARA). Relationships between robotic indices and a range of clinical and disease characteristics were examined. RESULTS: All our robotic indices were significantly different between the two cohorts except for two, and were highly and reliably discriminative between healthy and subjects with FRDA. In particular, subjects with FRDA exhibited slower movements as well as loss of accuracy and smoothness, which are typical of the disease. Duration of Movement, Normalized Jerk, and Number of Submovements were the best discriminative indices, as they were directly and easily measurable and correlated with the status of the disease, as measured by SARA. CONCLUSIONS: Our results suggest that outcome measures obtained by means of robotic devices can improve the sensitivity of clinical evaluations of patients’ dexterity and can accurately and efficiently quantify changes over time in clinical trials, particularly when functional scales appear to be no longer sensitive.
format Online
Article
Text
id pubmed-4448881
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-44488812015-05-30 Robotic and clinical evaluation of upper limb motor performance in patients with Friedreich’s Ataxia: an observational study Germanotta, Marco Vasco, Gessica Petrarca, Maurizio Rossi, Stefano Carniel, Sacha Bertini, Enrico Cappa, Paolo Castelli, Enrico J Neuroeng Rehabil Research BACKGROUND: Friedreich’s ataxia (FRDA) is the most common hereditary autosomal recessive form of ataxia. In this disease there is early manifestation of gait ataxia, and dysmetria of the arms and legs which causes impairment in daily activities that require fine manual dexterity. To date there is no cure for this disease. Some novel therapeutic approaches are ongoing in different steps of clinical trial. Development of sensitive outcome measures is crucial to prove therapeutic effectiveness. The aim of the study was to assess the reliability and sensitivity of quantitative and objective assessment of upper limb performance computed by means of the robotic device and to evaluate the correlation with clinical and functional markers of the disease severity. METHODS: Here we assess upper limb performances by means of the InMotion Arm Robot, a robot designed for clinical neurological applications, in a cohort of 14 children and young adults affected by FRDA, matched for age and gender with 18 healthy subjects. We focused on the analysis of kinematics, accuracy, smoothness, and submovements of the upper limb while reaching movements were performed. The robotic evaluation of upper limb performance consisted of planar reaching movements performed with the robotic system. The motors of the robot were turned off, so that the device worked as a measurement tool. The status of the disease was scored using the Scale for the Assessment and Rating of Ataxia (SARA). Relationships between robotic indices and a range of clinical and disease characteristics were examined. RESULTS: All our robotic indices were significantly different between the two cohorts except for two, and were highly and reliably discriminative between healthy and subjects with FRDA. In particular, subjects with FRDA exhibited slower movements as well as loss of accuracy and smoothness, which are typical of the disease. Duration of Movement, Normalized Jerk, and Number of Submovements were the best discriminative indices, as they were directly and easily measurable and correlated with the status of the disease, as measured by SARA. CONCLUSIONS: Our results suggest that outcome measures obtained by means of robotic devices can improve the sensitivity of clinical evaluations of patients’ dexterity and can accurately and efficiently quantify changes over time in clinical trials, particularly when functional scales appear to be no longer sensitive. BioMed Central 2015-04-23 /pmc/articles/PMC4448881/ /pubmed/25900021 http://dx.doi.org/10.1186/s12984-015-0032-6 Text en © Germanotta et al.; licensee BioMed Central. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Germanotta, Marco
Vasco, Gessica
Petrarca, Maurizio
Rossi, Stefano
Carniel, Sacha
Bertini, Enrico
Cappa, Paolo
Castelli, Enrico
Robotic and clinical evaluation of upper limb motor performance in patients with Friedreich’s Ataxia: an observational study
title Robotic and clinical evaluation of upper limb motor performance in patients with Friedreich’s Ataxia: an observational study
title_full Robotic and clinical evaluation of upper limb motor performance in patients with Friedreich’s Ataxia: an observational study
title_fullStr Robotic and clinical evaluation of upper limb motor performance in patients with Friedreich’s Ataxia: an observational study
title_full_unstemmed Robotic and clinical evaluation of upper limb motor performance in patients with Friedreich’s Ataxia: an observational study
title_short Robotic and clinical evaluation of upper limb motor performance in patients with Friedreich’s Ataxia: an observational study
title_sort robotic and clinical evaluation of upper limb motor performance in patients with friedreich’s ataxia: an observational study
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4448881/
https://www.ncbi.nlm.nih.gov/pubmed/25900021
http://dx.doi.org/10.1186/s12984-015-0032-6
work_keys_str_mv AT germanottamarco roboticandclinicalevaluationofupperlimbmotorperformanceinpatientswithfriedreichsataxiaanobservationalstudy
AT vascogessica roboticandclinicalevaluationofupperlimbmotorperformanceinpatientswithfriedreichsataxiaanobservationalstudy
AT petrarcamaurizio roboticandclinicalevaluationofupperlimbmotorperformanceinpatientswithfriedreichsataxiaanobservationalstudy
AT rossistefano roboticandclinicalevaluationofupperlimbmotorperformanceinpatientswithfriedreichsataxiaanobservationalstudy
AT carnielsacha roboticandclinicalevaluationofupperlimbmotorperformanceinpatientswithfriedreichsataxiaanobservationalstudy
AT bertinienrico roboticandclinicalevaluationofupperlimbmotorperformanceinpatientswithfriedreichsataxiaanobservationalstudy
AT cappapaolo roboticandclinicalevaluationofupperlimbmotorperformanceinpatientswithfriedreichsataxiaanobservationalstudy
AT castellienrico roboticandclinicalevaluationofupperlimbmotorperformanceinpatientswithfriedreichsataxiaanobservationalstudy