Full-text resources of PSJD and other databases are now available in the new Library of Science.
Visit https://bibliotekanauki.pl

PL EN


Preferences help
enabled [disable] Abstract
Number of results
2017 | 17 | 2 | 69–75

Article title

Visual control improves the accuracy of hand positioning in Huntington’s disease

Content

Title variants

PL
Kontrola wzrokowa zwiększa precyzję ułożenia dłoni w chorobie Huntingtona

Languages of publication

EN

Abstracts

EN
Background: The study aimed at demonstrating dependence of visual feedback during hand and finger positioning task performance among Huntington’s disease patients in comparison to patients with Parkinson’s disease and cervical dystonia. Material and methods: Eighty-nine patients participated in the study (23 with Huntington’s disease, 25 with Parkinson’s disease with dyskinesias, 21 with Parkinson’s disease without dyskinesias, and 20 with cervical dystonia), scoring ≥20 points on Mini-Mental State Examination in order to assure comprehension of task instructions. Neurological examination comprised of the motor section from the Unified Huntington’s Disease Rating Scale for Huntington’s disease, the Unified Parkinson’s Disease Rating Scale Part II–IV for Parkinson’s disease and the Toronto Western Spasmodic Torticollis Rating Scale for cervical dystonia. In order to compare hand position accuracy under visually controlled and blindfolded conditions, the patient imitated each of the 10 examiner’s hand postures twice, once under the visual control condition and once with no visual feedback provided. Results: Huntington’s disease patients imitated examiner’s hand positions less accurately under blindfolded condition in comparison to Parkinson’s disease without dyskinesias and cervical dystonia participants. Under visually controlled condition there were no significant inter-group differences. Conclusions: Huntington’s disease patients exhibit higher dependence on visual feedback while performing motor tasks than Parkinson’s disease and cervical dystonia patients. Possible improvement of movement precision in Huntington’s disease with the use of visual cues could be potentially useful in the patients’ rehabilitation.
PL
Wprowadzenie: Badanie miało na celu ukazanie wpływu wzrokowego sprzężenia zwrotnego na poziom wykonania prób ułożenia dłoni oraz palców wśród pacjentów z chorobą Huntingtona w porównaniu z pacjentami z chorobą Parkinsona i dystonią szyjną. Materiał i metody: W badaniu wzięło udział 89 pacjentów (23 z chorobą Huntingtona, 25 z chorobą Parkinsona i dyskinezami, 21 z chorobą Parkinsona bez dyskinez i 20 z dystonią szyjną), z wynikiem ≥20 punktów w MiniMental State Examination, co zapewniało rozumienie instrukcji testowych. Badanie neurologiczne obejmowało podskale ruchowe z Ujednoliconej Skali Oceny Choroby Huntingtona, Ujednoliconej Skali Oceny Choroby Parkinsona – części II–IV oraz Skalę Oceny Dystonii Szyjnej z Toronto. W celu porównania precyzji ułożenia ręki w warunkach pod kontrolą wzrokową oraz bez niej pacjent odtwarzał dwukrotnie 10 pozycji prezentowanych przez badającego – jeden raz w każdym z powyższych warunków. Wyniki: Pacjenci z chorobą Huntingtona wykazali się mniejszą precyzją w próbach naśladowania ułożenia ręki badającego w warunkach bez kontroli wzrokowej w porównaniu z uczestnikami z chorobą Parkinsona bez dyskinez i dystonią szyjną. W przypadku prób z kontrolą wzrokową nie wystąpiły istotne różnice między grupami. Wnioski: Pacjenci z chorobą Huntingtona wykazują większą zależność od wzrokowego sprzężenia zwrotnego przy wykonywaniu zadań ruchowych niż pacjenci z chorobą Parkinsona i dystonią szyjną. Możliwość uzyskania poprawy precyzji ruchów po dostarczeniu wskazówek wzrokowych u pacjentów z chorobą Huntingtona można wykorzystać w rehabilitacji tej grupy chorych.

Discipline

Year

Volume

17

Issue

2

Pages

69–75

Physical description

Contributors

  • Department of Neurological and Psychiatric Nursing, Medical University of Gdansk, Gdansk, Poland; Department of Neurology, St. Adalbert Hospital, Copernicus PL Ltd., Gdansk, Poland
  • Department of Neurology, St. Adalbert Hospital, Copernicus PL Ltd., Gdansk, Poland
  • Department of Neurological and Psychiatric Nursing, Medical University of Gdansk, Gdansk, Poland; Department of Neurology, St. Adalbert Hospital, Copernicus PL Ltd., Gdansk, Poland
  • Department of Rehabilitation, Medical University of Gdansk, Gdansk, Poland
  • Department of Neurology, St. Adalbert Hospital, Copernicus PL Ltd., Gdansk, Poland
  • Department of Neurology, St. Adalbert Hospital, Copernicus PL Ltd., Gdansk, Poland
  • Department of Neurological and Psychiatric Nursing, Medical University of Gdansk, Gdansk, Poland; Department of Neurology, St. Adalbert Hospital, Copernicus PL Ltd., Gdansk, Poland

References

  • Anderson TJ: Spasmodic torticollis. In: Moore P (ed.): Handbook of Botulinum Toxin Treatment. Blackwell Science, Oxford 1995: 103–130.
  • Ariani G, Wurm MF, Lingnau A: Decoding internally and externally driven movement plans. J Neurosci 2015; 35: 14160–14171.
  • Bilney B, Morris ME, Denisenko S: Physiotherapy for people with movement disorders arising from basal ganglia dysfunction. N Z J Physiother 2003a; 31: 94–100.
  • Bilney B, Morris ME, Perry A: Effectiveness of physiotherapy, occupational therapy, and speech pathology for people with Huntington’s disease: a systematic review. Neurorehabil Neural Repair 2003b; 17: 12–24.
  • Boulet C, Lemay M, Bédard MA et al.: Early Huntington’s disease affects movements in transformed sensorimotor mappings. Brain Cogn 2005; 57: 236–243.
  • Carella F, Bressanelli M, Piacentini S et al.: A study of arm movements in Huntington’s disease under visually controlled and blindfolded conditions. Neurol Sci 2003; 23: 287–293.
  • Ciancarelli I, Tozzi Ciancarelli MG, Carolei A: Effectiveness of intensive neurorehabilitation in patients with Huntington’s disease. Eur J Phys Rehabil Med 2013; 49: 189–195.
  • Consky ES, Basinski A, Belle L et al.: The Toronto Western Spasmodic Torticollis Rating Scale (TWSTRS): assessment of validity and inter-rater reliability. Neurology 1990; 40 (Suppl 1): 445.
  • Despard J, Ternes AM, Dimech-Betancourt B et al.: Characterising upper limb movements in Huntington’s disease and the Impact of restricted visual cues. PLoS One 2015; 10: e0133709.
  • Deuschl G, Lücking CH, Schenck E: Hand muscle reflexes following electrical stimulation in choreatic movement disorders. J Neurol Neurosurg Psychiatry 1989; 52: 755–762.
  • Folstein MF, Folstein SE, McHugh PR: “Mini-mental state.” A practical method for grading the cognitive state of patients for the clinician. J Psychiatr Res 1975; 12: 189–198.
  • García Ruiz PJ, Hernández J, Cantarero S et al.: Bradykinesia in Huntington’s disease. A prospective, follow-up study. J Neurol 2002; 249: 437–440.
  • Gaveau V, Pisella L, Priot AE et al.: Automatic online control of motor adjustments in reaching and grasping. Neuropsychologia 2014; 55: 25–40.
  • Gündel H, Wolf A, Xidara V et al.: High psychiatric comorbidity in spasmodic torticollis: a controlled study. J Nerv Ment Dis 2003; 191: 465–473.
  • Huntington Study Group: Unified Huntington’s Disease Rating Scale: reliability and consistency. Mov Disord 1996; 11: 136–142.
  • Kądzielawa D, Mroziak J, Bolewska A et al. (eds.): Podręcznik do Baterii Testów Neuropsychologicznych Halsteada-Reitana [The Halstead-Reitan Test Battery Manual]. Laboratorium Technik Diagnostycznych Wydziału Psychologii UW, Warszawa 1990. Lemay M, Chouinard S, Richer F et al.: Huntington’s disease affects movement termination. Behav Brain Res 2008; 187: 153–158.
  • Lemay M, Fimbel E, Beuter A et al.: Sensorimotor mapping affects movement correction deficits in early Huntington’s disease. Exp Brain Res 2005; 165: 454–460.
  • Noth J, Podoll K, Friedemann HH: Long-loop reflexes in small hand muscles studied in normal subjects and in patients with Huntington’s disease. Brain 1985; 108: 65–80.
  • Papadelis C, Arfeller C, Erla S et al.: Inferior frontal gyrus links visual and motor cortices during a visuomotor precision grip force task. Brain Res 2016; 1650: 252–266.
  • Paulson HL, Stern MB: Clinical manifestations of Parkinson’s disease. In: Watts LR, Koller WC (eds.): Movement Disorders: Neurologic Principles and Practice. McGraw-Hill, New York 1997: 183–199.
  • Poudel GR, Stout JC, Domínguez D JF et al.: Longitudinal change in white matter microstructure in Huntington’s disease: the IMAGE-HD study. Neurobiol Dis 2015; 74: 406–412.
  • Quinn L, Busse M: Physiotherapy clinical guidelines for Huntington’s disease. Neurodegener Dis Manag 2012; 2: 21–31.
  • Quinn L, Busse M, Dal Bello-Haas V: Management of upper extremity dysfunction in people with Parkinson disease and Huntington disease: facilitating outcomes across the disease lifespan. J Hand Ther 2013a; 26: 148–154.
  • Quinn L, Rosser A, Busse M: Critical features in the development of exercise-based interventions for people with Huntington’s disease. Eur Neurol Rev 2013b; 8: 10–13.
  • Rao AK, Marder KS, Uddin J et al.: Variability in interval production is due to timing-dependent deficits in Huntington’s disease. Mov Disord 2014; 29: 1516–1522.
  • Ross CA, Aylward EH, Wild EJ et al.: Huntington disease: natural history, biomarkers and prospects for therapeutics. Nat Rev Neurol 2014; 10: 204–2016.
  • Say MJ, Jones R, Scahill RI et al.: Visuomotor integration deficits precede clinical onset in Huntington’s disease. Neuropsychologia 2011; 49: 264–270.
  • Schaefer RS: Auditory rhythmic cueing in movement rehabilitation: findings and possible mechanisms. Philos Trans R Soc Lond B Biol Sci 2014; 369: 20130402.
  • Seegelke C, Güldenpenning I, Dettling J et al.: Visuomotor priming of action preparation and motor programming is similar in visually guided and memory-guided actions. Neuropsychologia 2016; 91: 1–8.
  • Seiss E, Praamstra P, Hesse CW et al.: Proprioceptive sensory function in Parkinson’s disease and Huntington’s disease: evidence from proprioception-related EEG potentials. Exp Brain Res 2003; 148: 308–319.
  • Shaffer JJ, Ghayoor A, Long JD et al.: Longitudinal diffusion changes in prodromal and early HD: Evidence of white-matter tract deterioration. Hum Brain Mapp 2017; 38: 1460–1477.
  • Sitek EJ, Sołtan W, Wieczorek D et al.: Self-awareness of motor dysfunction in patients with Huntington’s disease in comparison to Parkinson’s disease and cervical dystonia. J Int Neuropsychol Soc 2011; 17: 788–795.
  • Sitek EJ, Thompson JC, Craufurd D et al.: Unawareness of deficits in Huntington’s disease. J Huntingtons Dis 2014; 3: 125–135.
  • Sławek J, Sołtan W, Sitek EJ: Choroba Huntingtona – w 20. rocznicę odkrycia genu IT15; patogeneza, diagnostyka i leczenie. Pol Przegl Neurol 2013; 9: 85–95.
  • Smith MA, Brandt J, Shadmehr R: Motor disorder in Huntington’s disease begins as a dysfunction in error feedback control. Nature 2000; 403: 544–549.
  • Wittwer JE, Webster KE, Hill K: Rhythmic auditory cueing to improve walking in patients with neurological conditions other than Parkinson’s disease – what is the evidence? Disabil Rehabil 2013; 35: 164–176.
  • Yágüez L, Canavan AG, Lange HW et al.: Motor learning by imagery is differentially affected in Parkinson’s and Huntington’s diseases. Behav Brain Res 1999; 102: 115–127.
  • Zielonka D, Mielcarek M, Landwehrmeyer GB: Update on Huntington’s disease: advances in care and emerging therapeutic options. Parkinsonism Relat Disord 2015; 21: 169–178.

Document Type

article

Publication order reference

Identifiers

YADDA identifier

bwmeta1.element.psjd-9ddfbff8-5393-4fd8-bbc0-d900956928ef
JavaScript is turned off in your web browser. Turn it on to take full advantage of this site, then refresh the page.