Spatiotemporal Gait Differences before and after Botulinum Toxin in People with Focal Dystonia: A Pilot Study.

blepharospam botulinum toxin cervical dystonia dystonia gait

Journal

Movement disorders clinical practice
ISSN: 2330-1619
Titre abrégé: Mov Disord Clin Pract
Pays: United States
ID NLM: 101630279

Informations de publication

Date de publication:
Feb 2024
Historique:
revised: 13 10 2023
received: 23 02 2023
accepted: 05 11 2023
medline: 22 2 2024
pubmed: 22 2 2024
entrez: 22 2 2024
Statut: ppublish

Résumé

The impact of focal dystonia on gait has attracted little attention and remains elusive. Considering the importance of both visual and head control in gait, blepharospasm and cervical dystonia should affect gait. Improvement of cervical/eyelid control following botulinum toxin (BTX) injections would translate into gait changes. To assess gait differences in people with focal dystonia before and after BTX treatment. Ten patients with blepharospasm, 10 patients with cervical dystonia, and 20 healthy age- and gender-matched controls were included. Gait was assessed before and 1-month after BTX injections using Biodex Gait Trainer™ 3. Gait velocity, cadence, step length, step asymmetry, and variability of step length were compared between patients and controls, and between the two time-points using non-parametric statistics. At baseline, compared to controls, cervical dystonia patients showed reduced gait velocity, step length, and cadence. After BTX injections, while gait velocity and step length were significantly increased and step length variability reduced, gait parameters still differed between patients and controls. In blepharospasm patients, baseline gait velocity and step length were significantly smaller than in controls. After BTX injections, these gait parameters were significantly increased and variability decreased, so that patients no longer differed from controls. Gait differences exist between patients with focal dystonia not directly affecting the lower limbs and healthy controls. These gait abnormalities were improved differently by BTX treatment according to the type of dystonia. These disparities suggest different pathophysiological mechanisms and support the need for changes in rehabilitation routines in cervical dystonia.

Sections du résumé

BACKGROUND BACKGROUND
The impact of focal dystonia on gait has attracted little attention and remains elusive. Considering the importance of both visual and head control in gait, blepharospasm and cervical dystonia should affect gait. Improvement of cervical/eyelid control following botulinum toxin (BTX) injections would translate into gait changes.
OBJECTIVES OBJECTIVE
To assess gait differences in people with focal dystonia before and after BTX treatment.
METHODS METHODS
Ten patients with blepharospasm, 10 patients with cervical dystonia, and 20 healthy age- and gender-matched controls were included. Gait was assessed before and 1-month after BTX injections using Biodex Gait Trainer™ 3. Gait velocity, cadence, step length, step asymmetry, and variability of step length were compared between patients and controls, and between the two time-points using non-parametric statistics.
RESULTS RESULTS
At baseline, compared to controls, cervical dystonia patients showed reduced gait velocity, step length, and cadence. After BTX injections, while gait velocity and step length were significantly increased and step length variability reduced, gait parameters still differed between patients and controls. In blepharospasm patients, baseline gait velocity and step length were significantly smaller than in controls. After BTX injections, these gait parameters were significantly increased and variability decreased, so that patients no longer differed from controls.
CONCLUSION CONCLUSIONS
Gait differences exist between patients with focal dystonia not directly affecting the lower limbs and healthy controls. These gait abnormalities were improved differently by BTX treatment according to the type of dystonia. These disparities suggest different pathophysiological mechanisms and support the need for changes in rehabilitation routines in cervical dystonia.

Identifiants

pubmed: 38386480
doi: 10.1002/mdc3.13944
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

143-151

Subventions

Organisme : IPSEN Fund

Informations de copyright

© 2023 International Parkinson and Movement Disorder Society.

Références

Albanese A, Bhatia K, Bressman SB, et al. Phenomenology and classification of dystonia: a consensus update. Mov Disord 2013;28:863-873. https://doi.org/10.1002/mds.25475.
Kaji R, Bhatia K, Graybiel AM. Pathogenesis of dystonia: is it of cerebellar or basal ganglia origin? J Neurol Neurosurg Psychiatry 2018;89:488-492. https://doi.org/10.1136/jnnp-2017-316250.
Fischer P, Piña-Fuentes D, Kassavetis P, Sadnicka A. Physiology od dystonia. Int Rev Neurobiol 2023;169:137-162. https://doi.org/10.1016/bs.irn.2023.05.007.
Morgante F, Klein C. Dystonia. Continuum 2013;19:1225-1241. https://doi.org/10.1212/01.CON.0000436154.08791.67.
Bologna M, Valls-Solè J, Kamble N, et al. Dystonia, chorea, hemiballismus and other dyskinesias. Clin Neurophysiol 2022;140:110-125. https://doi.org/10.1016/j.clinph.2022.05.014.
Contarino MF, Van Den Dool J, Balash Y, et al. Clinical practice: evidence-based recommendations for the treatment of cervical dystonia with botulinum toxin. Front Neurol 2017;8:35. https://doi.org/10.3389/fneur.2017.00035.
Albanese A, Bathia KP, Cardoso F, et al. Isolated cervical dystonia: diagnosis and classification. Mov Disord 2023;38:1367-1378. https://doi.org/10.1002/mds.29387.
Medina A, Nilles C, Martino D, Pelletier D, Pringsheim T. The prevalence of idiopathic or inherited isolated dystonia: a systematic review and meta-analysis. Mov Disord Clin Pract 2022;9:860-868. https://doi.org/10.1002/mdc3.13524.
Kongsaengdao S, Maneeton N, Maneeton B. Long-term quality of life in cervical dystonia after treatment with abobotulinum toxin a: a 2-year prospective study. Neuropsychiatr Dis Treat 2018;14:1119-1124. https://doi.org/10.2147/NDT.S152252.
Jost WH, Tatu L. Selection of muscles for botulinum toxin injections in cervical dystonia. Mov Disord Clin Pract 2015;2:224-226. https://doi.org/10.1002/mdc3.12172.
Simpson DM, Hallett M, Ashman EJ, et al. Practice guideline update summary: botulinum neurotoxin for the treatment of blepharospasm, cervical dystonia, adult spasticity, and headache: report of the guideline development Subcommittee of the American Academy of Neurology. Neurology 2016;86:1818-1826. https://doi.org/10.1212/WNL.0000000000002560.
Meoni S, Zurowski M, Lozano AM, et al. Long-term neuropsychiatric outcomes after pallidal stimulation in primary and secondary dystonia. Neurology 2015;85:433-440. https://doi.org/10.1212/WNL.0000000000001811.
De Pauw J, Van der Velden K, Meirte J, et al. The effectiveness of physiotherapy for cervical dystonia: a systematic literature review. J Neurol 2014;261:1857-1865.
Prudente CN, Zetterberg L, Bring A, Bradnam L, Kimberley TJ. Systematic review of rehabilitation in Focal Dystonias: classification and recommendations. Mov Disord Clin Pract 2018;5(3):237-245. https://doi.org/10.1002/mdc3.125.
Bledsoe IO, Viser AC, San LM. Treatment of dystonia: medications, neurotoxins, neuromodulation, and rehabilitation. Neurotherapeutics 2020;17(4):1622-1644. https://doi.org/10.1007/s13311-020-00944-0.
Meoni S, Macerollo A, Moro E. Sex differences in movement disorders. Nat Rev Neurol 2020;16:84-96. https://doi.org/10.1038/s41582-019-0294-x.
Hassell TJW, Charles D. Treatment of Blepharospasm and Oromandibular dystonia with botulinum toxins. Toxins 2020;12:269. https://doi.org/10.3390/toxins12040269.
Scorr LM, Cho HJ, Kilic-Berkmen G, et al. Clinical features and evolution of Blepharospasm: a multicenter international cohort and systematic literature review. Dystonia 2022;1:10359. https://doi.org/10.3389/dyst.2022.10359.
Romano M, Bagnato S, Altavista MC, et al. Diagnostic and therapeutic recommendations in adult dystonia: a joint document by the Italian Society of Neurology, the Italian Academy for the Study of Parkinson's Disease and Movement Disorders, and the Italian Network on Botulinum Toxin. Neurol Sci 2022;43:6929-6945. https://doi.org/10.1007/s10072-022-06424-x.
Barr C, Barnard R, Edwards L, Lennon S, Bradnam L. Impairments of balance, stepping reactions and gait in people with cervical dystonia. Gait Posture 2017;55:55-61. https://doi.org/10.1016/j.gaitpost.2017.04.004.
Patla AE. Understanding the roles of vision in the control of human locomotion. Gait Posture 1997;5:54-69. https://doi.org/10.1016/S0966-6362(96)01109-5.
Esposito M, Dubbioso R, Peluso S, et al. Cervical dystonia patients display subclinical gait changes. Parkinsonism Relat Disord 2017;43:97-100. https://doi.org/10.1016/j.parkreldis.2017.07.005.
Hoffland BS, Veugen LC, Janssen MMHP, Pasman JW, Weerdesteyn V, van de Warrenburg BP. A gait paradigm reveals different patterns of abnormal cerebellar motor learning in primary focal dystonias. The Cerebellum 2014;13:760-766. https://doi.org/10.1007/s12311-014-0594-z.
Wass E, Taylor NF, Matsas A. Familiarisation to treadmill walking in unimpaired older people. Gait Posture 2005;21:72-79. https://doi.org/10.1016/j.gaitpost.2004.01.003.
Van de Putte M, Hagemeister N, St-Onge N, Parent G, de Guise JA. Habituation to treadmill walking. Biomed Mater Eng 2006;16(1):43-52.
Consky ES, Lang AE. Clinical assessment of patients with cervical dystonia. In: Jankovic J, Hallet M, eds. Ther Botulinum Toxin. New York, NY: Marcel Dekker; 1994:211-237.
Jankovic J, Kenney C, Grafe S, Goertelmeyer R, Comes G. Relationship between various clinical outcome assessments in patients with blepharospasm. Mov Disord 2009;24:407-413. https://doi.org/10.1002/mds.22368.
Boynton AM, Carrier DR. The human neck is part of the musculoskeletal core: cervical muscles help stabilize the pelvis during running and jumping. Integr Org Biol 2022;4(1):obac021. https://doi.org/10.1093/iob/obac021.
Magnani RM, Bruijn SM, van Dieën JH, Vieira MF. Head orientation and gait stability in young adults, dancers and older adults. Gait Posture 2020;80:68-73. https://doi.org/10.1016/j.gaitpost.2020.05.035.
Pozzo T, Berthoz A, Lefort L. Head stabilization during various locomotor tasks in humans. I. normal subjects. Exp Brain Res 1990;82:97-106. https://doi.org/10.1007/BF00230842.
Salatino A, Poncini M, George MS, Ricci R. Hunting for right and left parietal hot spots using single-pulse TMS: modulation of visuospatial perception during line bisection judgment in the healthy brain. Front Psychol 2014;5:1238. https://doi.org/10.3389/fpsyg.2014.01238.
Chillemi G, Formica C, Salatino A, et al. Biased visuospatial attention in cervical dystonia. J Int Neuropsychol 2018;24:22-32. https://doi.org/10.1017/S135561771700073X.
Williams L, Butler JS, Thirkettle M, et al. Slowed luminance reaction times in cervical dystonia: disordered superior colliculus processing. Mov Disord 2020;35:877-880. https://doi.org/10.1002/mds.27975.
Gilio F, Currà A, Lorenzano C, Modugno N, Manfredi M, Berardelli A. Effects of botulinum toxin type A on intracortical inhibition in patients with dystonia. Ann Neurol 2020;48:20-26.
Patla AE, Vickers JN. How far ahead do we look when required to step on specific locations in the travel path during locomotion? Exp Brain Res 2003;148:133-138. https://doi.org/10.1007/s00221-002-1246-y.
Perception of Space and Motion. San Diego: Academic Press; 1995.
Hallemans A, Ortibus E, Meire F, Aerts P. Low vision affects dynamic stability of gait. Gait Posture 2010;32:547-551. https://doi.org/10.1016/j.gaitpost.2010.07.018.
Leat SJ, Lovie-Kitchin J. Visual impairment and the useful field of vision. Ophthalmic Physiol Opt 2006;26:392-403. https://doi.org/10.1111/j.1475-1313.2006.00383.x.
Hallemans A, Beccu S, Van Loock K, Ortibus E, Truijen S, Aerts P. Visual deprivation leads to gait adaptations that are age- and context-specific: I. Step-time parameters. Gait Posture 2009;30:55-59. https://doi.org/10.1016/j.gaitpost.2009.02.018.
Studenski S, Perera S, Patel K, et al. Gait speed and survival in older adults. JAMA 2011;305:50-58. https://doi.org/10.1001/jama.2010.1923.

Auteurs

Justine Cuinat (J)

Division of Neurology, CHU of Grenoble, Grenoble, France.

Bettina Debû (B)

University Grenoble Alpes, Grenoble Institute of Neuroscience, INSERM 1216, Grenoble, France.

Sara Meoni (S)

Division of Neurology, CHU of Grenoble, Grenoble, France.
University Grenoble Alpes, Grenoble Institute of Neuroscience, INSERM 1216, Grenoble, France.

Pierre Pelissier (P)

Division of Neurology, CHU of Grenoble, Grenoble, France.

Anna Castrioto (A)

Division of Neurology, CHU of Grenoble, Grenoble, France.
University Grenoble Alpes, Grenoble Institute of Neuroscience, INSERM 1216, Grenoble, France.

Valérie Fraix (V)

Division of Neurology, CHU of Grenoble, Grenoble, France.
University Grenoble Alpes, Grenoble Institute of Neuroscience, INSERM 1216, Grenoble, France.

Elena Moro (E)

Division of Neurology, CHU of Grenoble, Grenoble, France.
University Grenoble Alpes, Grenoble Institute of Neuroscience, INSERM 1216, Grenoble, France.

Classifications MeSH