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Pisa Syndrome in Parkinson's Disease: Evidence for Bilateral Vestibulospinal Dysfunction

INTRODUCTION: Pisa syndrome (PS) is a postural complication of Parkinson's disease (PD). Yet, its pathophysiology remains unclear, although a multifactorial component is probable. Cervical vestibular evoked myogenic potentials (cVEMPs) explore vestibulospinal pathway, but they have not been mea...

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Autores principales: Di Lazzaro, Giulia, Schirinzi, Tommaso, Giambrone, Maria Pia, Di Mauro, Roberta, Palmieri, Maria Giuseppina, Rocchi, Camilla, Tinazzi, Michele, Mercuri, Nicola Biagio, Di Girolamo, Stefano, Pisani, Antonio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6205319/
https://www.ncbi.nlm.nih.gov/pubmed/30410718
http://dx.doi.org/10.1155/2018/8673486
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author Di Lazzaro, Giulia
Schirinzi, Tommaso
Giambrone, Maria Pia
Di Mauro, Roberta
Palmieri, Maria Giuseppina
Rocchi, Camilla
Tinazzi, Michele
Mercuri, Nicola Biagio
Di Girolamo, Stefano
Pisani, Antonio
author_facet Di Lazzaro, Giulia
Schirinzi, Tommaso
Giambrone, Maria Pia
Di Mauro, Roberta
Palmieri, Maria Giuseppina
Rocchi, Camilla
Tinazzi, Michele
Mercuri, Nicola Biagio
Di Girolamo, Stefano
Pisani, Antonio
author_sort Di Lazzaro, Giulia
collection PubMed
description INTRODUCTION: Pisa syndrome (PS) is a postural complication of Parkinson's disease (PD). Yet, its pathophysiology remains unclear, although a multifactorial component is probable. Cervical vestibular evoked myogenic potentials (cVEMPs) explore vestibulospinal pathway, but they have not been measured yet in PD patients with PS (PDPS) to assess a potential vestibular impairment. MATERIALS AND METHODS: We enrolled 15 PD patients, 15 PDPS patients, and 30 healthy controls (HCs). They underwent neurological examination and were examined with Unified Parkinson's Disease Rating Scale II-III (UPDRSII-III), audiovestibular workup, and cVEMP recordings. Data were analysed with Chi-square, one-way ANOVA, multinomial regression, nonparametric, and Spearman's tests. RESULTS: cVEMPs were significantly impaired in both PD and PDPS compared with HCs. PDPS exhibited more severe cVEMP abnormalities with prevalent bilateral loss of potentials, compared with the PD group, in which a prevalent unilateral loss was instead observed. No clinical-neurophysiological correlations emerged. CONCLUSIONS: Differently from HC, cVEMPs are altered in PD. Severity of cVEMPs alterations increases from PD without PS to PDPS, suggesting an involvement of vestibulospinal pathway in the pathophysiology of PS. Our results provide evidence for a significant impairment of cVEMPs in PDPS patients and encourage further studies to test validity of cVEMPs as diagnostic and prognostic biomarkers of PD progression.
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spelling pubmed-62053192018-11-08 Pisa Syndrome in Parkinson's Disease: Evidence for Bilateral Vestibulospinal Dysfunction Di Lazzaro, Giulia Schirinzi, Tommaso Giambrone, Maria Pia Di Mauro, Roberta Palmieri, Maria Giuseppina Rocchi, Camilla Tinazzi, Michele Mercuri, Nicola Biagio Di Girolamo, Stefano Pisani, Antonio Parkinsons Dis Research Article INTRODUCTION: Pisa syndrome (PS) is a postural complication of Parkinson's disease (PD). Yet, its pathophysiology remains unclear, although a multifactorial component is probable. Cervical vestibular evoked myogenic potentials (cVEMPs) explore vestibulospinal pathway, but they have not been measured yet in PD patients with PS (PDPS) to assess a potential vestibular impairment. MATERIALS AND METHODS: We enrolled 15 PD patients, 15 PDPS patients, and 30 healthy controls (HCs). They underwent neurological examination and were examined with Unified Parkinson's Disease Rating Scale II-III (UPDRSII-III), audiovestibular workup, and cVEMP recordings. Data were analysed with Chi-square, one-way ANOVA, multinomial regression, nonparametric, and Spearman's tests. RESULTS: cVEMPs were significantly impaired in both PD and PDPS compared with HCs. PDPS exhibited more severe cVEMP abnormalities with prevalent bilateral loss of potentials, compared with the PD group, in which a prevalent unilateral loss was instead observed. No clinical-neurophysiological correlations emerged. CONCLUSIONS: Differently from HC, cVEMPs are altered in PD. Severity of cVEMPs alterations increases from PD without PS to PDPS, suggesting an involvement of vestibulospinal pathway in the pathophysiology of PS. Our results provide evidence for a significant impairment of cVEMPs in PDPS patients and encourage further studies to test validity of cVEMPs as diagnostic and prognostic biomarkers of PD progression. Hindawi 2018-10-15 /pmc/articles/PMC6205319/ /pubmed/30410718 http://dx.doi.org/10.1155/2018/8673486 Text en Copyright © 2018 Giulia Di Lazzaro et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Di Lazzaro, Giulia
Schirinzi, Tommaso
Giambrone, Maria Pia
Di Mauro, Roberta
Palmieri, Maria Giuseppina
Rocchi, Camilla
Tinazzi, Michele
Mercuri, Nicola Biagio
Di Girolamo, Stefano
Pisani, Antonio
Pisa Syndrome in Parkinson's Disease: Evidence for Bilateral Vestibulospinal Dysfunction
title Pisa Syndrome in Parkinson's Disease: Evidence for Bilateral Vestibulospinal Dysfunction
title_full Pisa Syndrome in Parkinson's Disease: Evidence for Bilateral Vestibulospinal Dysfunction
title_fullStr Pisa Syndrome in Parkinson's Disease: Evidence for Bilateral Vestibulospinal Dysfunction
title_full_unstemmed Pisa Syndrome in Parkinson's Disease: Evidence for Bilateral Vestibulospinal Dysfunction
title_short Pisa Syndrome in Parkinson's Disease: Evidence for Bilateral Vestibulospinal Dysfunction
title_sort pisa syndrome in parkinson's disease: evidence for bilateral vestibulospinal dysfunction
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6205319/
https://www.ncbi.nlm.nih.gov/pubmed/30410718
http://dx.doi.org/10.1155/2018/8673486
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