» Articles » PMID: 20233583

Targeted Exercise Therapy for Voice and Swallow in Persons with Parkinson's Disease

Overview
Journal Brain Res
Specialty Neurology
Date 2010 Mar 18
PMID 20233583
Citations 20
Authors
Affiliations
Soon will be listed here.
Abstract

Sensorimotor deficits affecting voice and swallowing ability can have a devastating impact on the quality of life of people with Parkinson disease (PD). Recent scientific findings in animal models of PD pinpoint targeted exercise therapy as a potential treatment to reduce neurochemical loss and decrease parkinsonian symptoms. Although there may be beneficial effects, targeted exercise therapy is not a standard component of therapy for the cranial sensiromotor deficits seen in PD. In this paper, we review the scientific evidence for targeted training for voice and swallowing deficits. The literature search revealed 19 publications that included targeted training for voice and only one publication that included targeted training for swallowing. We summarize 3 main findings: (1) targeted training may be associated with lasting changes in voice behavior; (2) targeted training of sensorimotor actions with anatomical or functional overlap with voice and swallowing may improve voice and swallowing to some degree, but it is unknown whether these effects endure over time; and (3) evidence regarding cranial sensorimotor interventions for Parkinson disease is sparse. We concluded that targeted training for voice and swallow is a promising but understudied intervention for cranial sensorimotor deficits associated with PD and posit that animal models can be useful in designing empirically based studies that further the science on targeted training.

Citing Articles

Tongue and laryngeal exercises improve tongue strength and vocal function outcomes in a Pink1-/- rat model of early Parkinson disease.

Broadfoot C, Hoffmeister J, Lechner S, Krasko M, Lambert E, Russell J Behav Brain Res. 2023; 460:114754.

PMID: 37981125 PMC: 10872343. DOI: 10.1016/j.bbr.2023.114754.


A Randomized Controlled Trial Comparing Physical and Mental Lingual Exercise for Healthy Older Adults.

Szynkiewicz S, Kamarunas E, Drulia T, Nobriga C, Griffin L, ODonoghue C Dysphagia. 2020; 36(3):474-482.

PMID: 32770381 DOI: 10.1007/s00455-020-10164-5.


Treatment of Dysphagia in Parkinson's Disease: A Systematic Review.

Lopez-Liria R, Parra-Egeda J, Vega-Ramirez F, Aguilar-Parra J, Trigueros-Ramos R, Morales-Gazquez M Int J Environ Res Public Health. 2020; 17(11).

PMID: 32526840 PMC: 7312221. DOI: 10.3390/ijerph17114104.


Changes to Ventilation, Vocalization, and Thermal Nociception in the Pink1-/- Rat Model of Parkinson's Disease.

Johnson R, Kelm-Nelson C, Ciucci M J Parkinsons Dis. 2020; 10(2):489-504.

PMID: 32065805 PMC: 8142388. DOI: 10.3233/JPD-191853.


Oro-Pharyngeal Dysphagia in Parkinson's Disease and Related Movement Disorders.

Kwon M, Lee J J Mov Disord. 2019; 12(3):152-160.

PMID: 31556260 PMC: 6763715. DOI: 10.14802/jmd.19048.


References
1.
Robertson S, Thomson F . Speech therapy in Parkinson's disease: a study of the efficacy ad long term effects of intensive treatment. Br J Disord Commun. 1984; 19(3):213-24. DOI: 10.3109/13682828409029837. View

2.
Alexander G, DeLong M . Microstimulation of the primate neostriatum. I. Physiological properties of striatal microexcitable zones. J Neurophysiol. 1985; 53(6):1401-16. DOI: 10.1152/jn.1985.53.6.1401. View

3.
Alexander G, DeLong M . Microstimulation of the primate neostriatum. II. Somatotopic organization of striatal microexcitable zones and their relation to neuronal response properties. J Neurophysiol. 1985; 53(6):1417-30. DOI: 10.1152/jn.1985.53.6.1417. View

4.
DeLong M, Alexander G, Mitchell S, Richardson R . The contribution of basal ganglia to limb control. Prog Brain Res. 1986; 64:161-74. DOI: 10.1016/S0079-6123(08)63411-1. View

5.
Martin B, Corlew M . The incidence of communication disorders in dysphagic patients. J Speech Hear Disord. 1990; 55(1):28-32. DOI: 10.1044/jshd.5501.28. View