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Vestibular Sensory Conflict During Postural Control, Freezing of Gait, and Falls in Parkinson’s Disease

dc.contributor.authorBohnen, Nicolaas I.
dc.contributor.authorKanel, Prabesh
dc.contributor.authorEmde Boas, Miriam
dc.contributor.authorRoytman, Stiven
dc.contributor.authorKerber, Kevin A.
dc.date.accessioned2022-12-05T16:39:46Z
dc.date.available2023-12-05 11:39:45en
dc.date.available2022-12-05T16:39:46Z
dc.date.issued2022-11
dc.identifier.citationBohnen, Nicolaas I.; Kanel, Prabesh; Emde Boas, Miriam; Roytman, Stiven; Kerber, Kevin A. (2022). "Vestibular Sensory Conflict During Postural Control, Freezing of Gait, and Falls in Parkinson’s Disease." Movement Disorders 37(11): 2257-2262.
dc.identifier.issn0885-3185
dc.identifier.issn1531-8257
dc.identifier.urihttps://hdl.handle.net/2027.42/175201
dc.description.abstractBackgroundThe vestibular system has been implicated in the pathophysiology of episodic motor impairments in Parkinson’s disease (PD), but specific evidence remains lacking.ObjectiveWe investigated the relationship between the presence of freezing of gait and falls and postural failure during the performance on Romberg test condition 4 in patients with PD.MethodsModified Romberg sensory conflict test, fall, and freezing-of-gait assessments were performed in 92 patients with PD (70 males/22 females; mean age, 67.6 ± 7.4 years; Hoehn and Yahr stage, 2.4 ± 0.6; mean Montreal Cognitive Assessment, 26.4 ± 2.8).ResultsFailure during Romberg condition 4 was present in 33 patients (35.9%). Patients who failed the Romberg condition 4 were older and had more severe motor and cognitive impairments than those without. About 84.6% of all patients with freezing of gait had failure during Romberg condition 4, whereas 13.4% of patients with freezing of gait had normal performance (χ2 = 15.6; P < 0.0001). Multiple logistic regression analysis showed that the regressor effect of Romberg condition 4 test failure for the presence of freezing of gait (Wald χ2 = 5.0; P = 0.026) remained significant after accounting for the degree of severity of parkinsonian motor ratings (Wald χ2 = 6.2; P = 0.013), age (Wald χ2 = 0.3; P = 0.59), and cognition (Wald χ2 = 0.3; P = 0.75; total model: Wald χ2 = 16.1; P < 0.0001). Patients with PD who failed the Romberg condition 4 (45.5%) did not have a statistically significant difference in frequency of patients with falls compared with patients with PD without abnormal performance (30.5%; χ2 = 2.1; P = 0.15).ConclusionsThe presence of deficient vestibular processing may have specific pathophysiological relevance for freezing of gait, but not falls, in PD. © 2022 The Authors. Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society
dc.publisherJohn Wiley & Sons, Inc.
dc.subject.otherParkinson’s disease
dc.subject.othermodified Romberg test
dc.subject.othervestibular efficacy
dc.subject.otherfreezing of gait
dc.subject.otherfalls
dc.titleVestibular Sensory Conflict During Postural Control, Freezing of Gait, and Falls in Parkinson’s Disease
dc.typeArticle
dc.rights.robotsIndexNoFollow
dc.subject.hlbtoplevelHealth Sciences
dc.description.peerreviewedPeer Reviewed
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/175201/1/mds29189.pdf
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/175201/2/mds29189_am.pdf
dc.identifier.doi10.1002/mds.29189
dc.identifier.sourceMovement Disorders
dc.identifier.citedreferenceVital D, Hegemann SC, Straumann D, et al. A new dynamic visual acuity test to assess peripheral vestibular function. Arch Otolaryngol Head Neck Surg 2010; 136 ( 7 ): 686 – 691.
dc.identifier.citedreferenceAgrawal Y, Davalos-Bichara M, Zuniga MG, Carey JP. Head impulse test abnormalities and influence on gait speed and falls in older individuals. Otol Neurotol 2013; 34 ( 9 ): 1729 – 1735.
dc.identifier.citedreferenceCohen HS, Kimball KT. Usefulness of some current balance tests for identifying individuals with disequilibrium due to vestibular impairments. J Vestib Res 2008; 18 ( 5–6 ): 295 – 303.
dc.identifier.citedreferenceAgrawal Y, Carey JP, Hoffman HJ, Sklare DA, Schubert MC. The modified Romberg balance test: normative data in U.S. adults. Otol Neurotol 2011; 32 ( 8 ): 1309 – 1311.
dc.identifier.citedreferenceCohen H, Blatchly CA, Gombash LL. A study of the clinical test of sensory interaction and balance. Phys Ther 1993; 73 ( 6 ): 346 – 351. discussion 351–344
dc.identifier.citedreferenceBohnen NI, Kanel P, Zhou Z, et al. Cholinergic system changes of falls and freezing of gait in Parkinson’s disease. Ann Neurol 2019; 85 ( 4 ): 538 – 549.
dc.identifier.citedreferenceBohnen NI, Kanel P, Koeppe RA, et al. Regional cerebral cholinergic nerve terminal integrity and cardinal motor features in Parkinson’s disease. Brain Commun 2021; 3 ( 2 ): fcab109
dc.identifier.citedreferenceTakakusaki K. Neurophysiology of gait: from the spinal cord to the frontal lobe. Mov Disord 2013; 28 ( 11 ): 1483 – 1491.
dc.identifier.citedreferenceHuh YE, Hwang S, Kim K, Chung WH, Youn J, Cho JW. Postural sensory correlates of freezing of gait in Parkinson’s disease. Parkinsonism Relat Disord 2016; 25: 72 – 77.
dc.identifier.citedreferenceVervoort G, Nackaerts E, Mohammadi F, et al. Which aspects of postural control differentiate between patients with Parkinson’s disease with and without freezing of gait? Parkinsons Dis 2013; 2013: 971480
dc.identifier.citedreferenceSri-on J, Tirrell GP, Lipsitz LA, Liu SW. Is there such a thing as a mechanical fall? Am J Emerg Med 2016; 34 ( 3 ): 582 – 585.
dc.identifier.citedreferenceVenhovens J, Meulstee J, Bloem BR, Verhagen WIM. Neurovestibular dysfunction and falls in Parkinson’s disease and atypical parkinsonism: a prospective 1 year follow-up study. Front Neurol 2020; 11: 580285
dc.identifier.citedreferenceLee MH, Durnford SJ, Crowley JS, Rupert AH. Visual vestibular interaction in the dynamic visual acuity test during voluntary head rotation. Aviat Space Environ Med 1997; 68 ( 2 ): 111 – 117.
dc.identifier.citedreferencePereira MP, Gobbi LT, Almeida QJ. Freezing of gait in Parkinson’s disease: evidence of sensory rather than attentional mechanisms through muscle vibration. Parkinsonism Relat Disord 2016; 29: 78 – 82.
dc.identifier.citedreferenceBohnen NI, Muller ML, Koeppe RA, et al. History of falls in Parkinson disease is associated with reduced cholinergic activity. Neurology 2009; 73 ( 20 ): 1670 – 1676.
dc.identifier.citedreferenceBlack RD, Rogers LL, Ade KK, Nicoletto HA, Adkins HD, Laskowitz DT. Non-invasive neuromodulation using time-varying caloric vestibular stimulation. IEEE J Transl Eng Health Med 2016; 4: 2000310
dc.identifier.citedreferenceWilkinson D, Podlewska A, Banducci SE, et al. Caloric vestibular stimulation for the management of motor and non-motor symptoms in Parkinson’s disease. Parkinsonism Relat Disord 2019; 65: 261 – 266.
dc.identifier.citedreferenceWilkinson D, Ade KK, Rogers LL, et al. Preventing episodic migraine with caloric vestibular stimulation: a randomized controlled trial. Headache 2017; 57 ( 7 ): 1065 – 1087.
dc.identifier.citedreferenceCai J, Lee S, Ba F, et al. Galvanic vestibular stimulation (GVS) augments deficient pedunculopontine nucleus (PPN) connectivity in mild Parkinson’s disease: fMRI effects of different stimuli. Front Neurosci 2018; 12: 101
dc.identifier.citedreferenceLiu A, Bi H, Li Y, et al. Galvanic vestibular stimulation improves subnetwork interactions in Parkinson’s disease. J Healthc Eng 2021; 2021: 6632394
dc.identifier.citedreferenceMartens KAE, Hall JM, Gilat M, Georgiades MJ, Walton CC, Lewis SJG. Anxiety is associated with freezing of gait and attentional set-shifting in Parkinson’s disease: a new perspective for early intervention. Gait Posture 2016; 49: 431 – 436.
dc.identifier.citedreferenceFactor SA, Scullin MK, Sollinger AB, et al. Freezing of gait subtypes have different cognitive correlates in Parkinson’s disease. Parkinsonism Relat Disord 2014; 20 ( 12 ): 1359 – 1364.
dc.identifier.citedreferenceMorris R, Smulders K, Peterson DS, et al. Cognitive function in people with and without freezing of gait in Parkinson’s disease. NPJ Parkinsons Dis 2020; 6: 9
dc.identifier.citedreferenceSmith PF, Agrawal Y, Darlington CL. Sexual dimorphism in vestibular function and dysfunction. J Neurophysiol 2019; 121 ( 6 ): 2379 – 2391.
dc.identifier.citedreferenceSmith PF. Vestibular functions and Parkinson’s disease. Front Neurol 2018; 9: 1085
dc.identifier.citedreferenceAgrawal Y, Carey JP, Della Santina CC, Schubert MC, Minor LB. Disorders of balance and vestibular function in US adults: data from the National Health and nutrition examination survey, 2001-2004. Arch Intern Med 2009; 169 ( 10 ): 938 – 944.
dc.identifier.citedreferenceVenhovens J, Meulstee J, Bloem BR, Verhagen WI. Neurovestibular analysis and falls in Parkinson’s disease and atypical parkinsonism. Eur J Neurosci 2016; 43 ( 12 ): 1636 – 1646.
dc.identifier.citedreferencevan Wensen E, van Leeuwen RB, van der Zaag-Loonen HJ, Masius-Olthof S, Bloem BR. Benign paroxysmal positional vertigo in Parkinson’s disease. Parkinsonism Relat Disord 2013; 19 ( 12 ): 1110 – 1112.
dc.identifier.citedreferenceBecker-Bense S, Wittmann C, van Wensen E, van Leeuwen RB, Bloem B, Dieterich M. Prevalence of Parkinson symptoms in patients with different peripheral vestibular disorders. J Neurol 2017; 264 ( 6 ): 1287 – 1289.
dc.identifier.citedreferenceNieuwboer A, Giladi N. Characterizing freezing of gait in Parkinson’s disease: models of an episodic phenomenon. Mov Disord 2013; 28 ( 11 ): 1509 – 1519.
dc.identifier.citedreferenceKennedy PM, Cressman EK, Carlsen AN, Chua R. Assessing vestibular contributions during changes in gait trajectory. Neuroreport 2005; 16 ( 10 ): 1097 – 1100.
dc.identifier.citedreferenceHuh YE, Hwang S, Kim K, Chung WH, Youn J, Cho JW. Reply to letter: the association of postural sensory deficit with freezing of gait in Parkinson’s disease. Parkinsonism Relat Disord 2016; 31: 141 – 142.
dc.identifier.citedreferenceHughes AJ, Daniel SE, Kilford L, Lees AJ. Accuracy of clinical diagnosis of idiopathic Parkinson’s disease: a clinico-pathological study of 100 cases. J Neurol Neurosurg Psychiatry 1992; 55 ( 3 ): 181 – 184.
dc.identifier.citedreferenceNasreddine ZS, Phillips NA, Bedirian V, et al. The Montreal cognitive assessment, MoCA: a brief screening tool for mild cognitive impairment. J Am Geriatr Soc 2005; 53 ( 4 ): 695 – 699.
dc.identifier.citedreferenceBekkers EMJ, Dijkstra BW, Dockx K, Heremans E, Verschueren SMP, Nieuwboer A. Clinical balance scales indicate worse postural control in people with Parkinson’s disease who exhibit freezing of gait compared to those who do not: a meta-analysis. Gait Posture 2017; 56: 134 – 140.
dc.identifier.citedreferenceBekkers EMJ, Dijkstra BW, Heremans E, Verschueren SMP, Bloem BR, Nieuwboer A. Balancing between the two: are freezing of gait and postural instability in Parkinson’s disease connected? Neurosci Biobehav Rev 2018; 94: 113 – 125.
dc.identifier.citedreferenceGoetz CG, Fahn S, Martinez-Martin P, et al. Movement disorder society-sponsored revision of the unified Parkinson’s disease rating scale (MDS-UPDRS): process, format, and clinimetric testing plan. Mov Disord 2007; 22: 41 – 47.
dc.identifier.citedreferenceShumway-Cook A, Horak FB. Assessing the influence of sensory interaction of balance. Suggestion from the field. Phys Ther 1986; 66 ( 10 ): 1548 – 1550.
dc.working.doiNOen
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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