Background: Clinical studies in patients with MSA document facial motor abnormalities, but no studies have objectively assessed blinking abnormalities in this condition. Methods: We enrolled patients diagnosed as having clinically probable MSA, 20 patients of the parkinsonian phenotype (MSA-P) and 10 patients of the cerebellar phenotype (MSA-C) and 20 healthy controls (HCs). Blinking was recorded with a three-dimensional optoelectronic motion system equipped with dedicated software for data analysis. Results: During voluntary blinking, the interphase pause duration between the closing and opening phases lasted longer in MSA-P and in MSA-C patients than in HCs; the opening phase had increased duration and reduced peak velocity in MSA-P. During reflex blinking, the opening blink phase also lasted longer in MSA-P patients than in HCs. During spontaneous blinking, the rate and kinematics of the closing and opening blinking phases were lower in MSA-P and in MSA-C patients than in HCs. Blink reflex recovery was higher in patients than in HCs. No difference was found between MSA-P patients receiving or not receiving dopaminergic medication. Conclusions: Our objective assessment of upper facial movement documents abnormalities of voluntary, spontaneous, and reflex blinking in patients with MSA-P and MSA-C, reflecting cortical-basal ganglia and brainstem dysfunction. © 2014 International Parkinson and Movement Disorder Society.

Blinking in patients with clinically probable multiple system atrophy / Bologna, Matteo; Marsili, Luca; Nashaba, Khan; Ahmad Khandker Parvez, ; Paparella, Giulia; Nicola, Modugno; Colosimo, Carlo; Fabbrini, Giovanni; Berardelli, Alfredo. - In: MOVEMENT DISORDERS. - ISSN 1531-8257. - 29:3(2014), pp. 415-420. [10.1002/mds.25830]

Blinking in patients with clinically probable multiple system atrophy

BOLOGNA, Matteo;MARSILI, LUCA;Giulia Paparella;COLOSIMO, Carlo;FABBRINI, Giovanni;BERARDELLI, Alfredo
2014

Abstract

Background: Clinical studies in patients with MSA document facial motor abnormalities, but no studies have objectively assessed blinking abnormalities in this condition. Methods: We enrolled patients diagnosed as having clinically probable MSA, 20 patients of the parkinsonian phenotype (MSA-P) and 10 patients of the cerebellar phenotype (MSA-C) and 20 healthy controls (HCs). Blinking was recorded with a three-dimensional optoelectronic motion system equipped with dedicated software for data analysis. Results: During voluntary blinking, the interphase pause duration between the closing and opening phases lasted longer in MSA-P and in MSA-C patients than in HCs; the opening phase had increased duration and reduced peak velocity in MSA-P. During reflex blinking, the opening blink phase also lasted longer in MSA-P patients than in HCs. During spontaneous blinking, the rate and kinematics of the closing and opening blinking phases were lower in MSA-P and in MSA-C patients than in HCs. Blink reflex recovery was higher in patients than in HCs. No difference was found between MSA-P patients receiving or not receiving dopaminergic medication. Conclusions: Our objective assessment of upper facial movement documents abnormalities of voluntary, spontaneous, and reflex blinking in patients with MSA-P and MSA-C, reflecting cortical-basal ganglia and brainstem dysfunction. © 2014 International Parkinson and Movement Disorder Society.
2014
movement control; brainstem; blinking; multiple system atrophy; basal ganglia
01 Pubblicazione su rivista::01a Articolo in rivista
Blinking in patients with clinically probable multiple system atrophy / Bologna, Matteo; Marsili, Luca; Nashaba, Khan; Ahmad Khandker Parvez, ; Paparella, Giulia; Nicola, Modugno; Colosimo, Carlo; Fabbrini, Giovanni; Berardelli, Alfredo. - In: MOVEMENT DISORDERS. - ISSN 1531-8257. - 29:3(2014), pp. 415-420. [10.1002/mds.25830]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/549103
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