Deficits in the mimicry of facial expressions in Parkinson’s disease

Background: Humans spontaneously mimic the facial expressions of others, facilitating social interaction. This mimicking behaviour may be impaired in individuals with Parkinson’s disease, for whom the loss of facial movements is a clinical feature. Objective: To assess the presence of facial mimic...

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Main Authors: Steven R. Livingstone, Esztella eVezer, Lucy M. McGarry, Anthony E Lang, Frank A. Russo
Format: Article
Language:English
Published: Frontiers Media S.A. 2016-06-01
Series:Frontiers in Psychology
Subjects:
Online Access:http://journal.frontiersin.org/Journal/10.3389/fpsyg.2016.00780/full
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author Steven R. Livingstone
Steven R. Livingstone
Steven R. Livingstone
Esztella eVezer
Lucy M. McGarry
Anthony E Lang
Anthony E Lang
Frank A. Russo
Frank A. Russo
author_facet Steven R. Livingstone
Steven R. Livingstone
Steven R. Livingstone
Esztella eVezer
Lucy M. McGarry
Anthony E Lang
Anthony E Lang
Frank A. Russo
Frank A. Russo
author_sort Steven R. Livingstone
collection DOAJ
description Background: Humans spontaneously mimic the facial expressions of others, facilitating social interaction. This mimicking behaviour may be impaired in individuals with Parkinson’s disease, for whom the loss of facial movements is a clinical feature. Objective: To assess the presence of facial mimicry in patients with Parkinson’s disease.Method: Twenty-seven non-depressed patients with idiopathic Parkinson’s disease and twenty-eight age-matched controls had their facial muscles recorded with electromyography while they observed presentations of calm, happy, sad, angry, and fearful emotions. Results: Patients exhibited reduced amplitude and delayed onset in the zygomaticus major muscle region (smiling response) following happy presentations (p < 0.001, ANOVA, patients M = 0.02, 95% confidence interval [-0.15–0.18], controls M = 0.26, [0.14–0.37]). Although patients exhibited activation of the corrugator supercilii and medial frontalis (frowning) following sad and fearful presentations, the frontalis response to sad presentations was attenuated relative to controls (p = 0.017, ANOVA, patients, M = .05, [-.08–.18], controls M = .21, [.09–.34]). The amplitude of patients’ zygomaticus activity in response to positive emotions was found to be negatively correlated with response times for ratings of emotional identification, suggesting a motor-behavioral link (r = -0.45, p = 0.02, two-tailed). Conclusions: Patients showed decreased mimicry overall, mimicking other peoples’ frowns to some extent, but presenting with profoundly weakened smiles. These findings open a new avenue of inquiry into the masked face syndrome of PD.
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spelling doaj.art-b9b18e8cbda848d08248ca42b765eb012022-12-22T03:35:55ZengFrontiers Media S.A.Frontiers in Psychology1664-10782016-06-01710.3389/fpsyg.2016.00780190717Deficits in the mimicry of facial expressions in Parkinson’s diseaseSteven R. Livingstone0Steven R. Livingstone1Steven R. Livingstone2Esztella eVezer3Lucy M. McGarry4Anthony E Lang5Anthony E Lang6Frank A. Russo7Frank A. Russo8Ryerson UniversityUniversity of Wisconsin-River FallsToronto Rehabilitation InstituteRyerson UniversityRyerson UniversityUniversity of TorontoToronto Western HospitalRyerson UniversityToronto Rehabilitation InstituteBackground: Humans spontaneously mimic the facial expressions of others, facilitating social interaction. This mimicking behaviour may be impaired in individuals with Parkinson’s disease, for whom the loss of facial movements is a clinical feature. Objective: To assess the presence of facial mimicry in patients with Parkinson’s disease.Method: Twenty-seven non-depressed patients with idiopathic Parkinson’s disease and twenty-eight age-matched controls had their facial muscles recorded with electromyography while they observed presentations of calm, happy, sad, angry, and fearful emotions. Results: Patients exhibited reduced amplitude and delayed onset in the zygomaticus major muscle region (smiling response) following happy presentations (p < 0.001, ANOVA, patients M = 0.02, 95% confidence interval [-0.15–0.18], controls M = 0.26, [0.14–0.37]). Although patients exhibited activation of the corrugator supercilii and medial frontalis (frowning) following sad and fearful presentations, the frontalis response to sad presentations was attenuated relative to controls (p = 0.017, ANOVA, patients, M = .05, [-.08–.18], controls M = .21, [.09–.34]). The amplitude of patients’ zygomaticus activity in response to positive emotions was found to be negatively correlated with response times for ratings of emotional identification, suggesting a motor-behavioral link (r = -0.45, p = 0.02, two-tailed). Conclusions: Patients showed decreased mimicry overall, mimicking other peoples’ frowns to some extent, but presenting with profoundly weakened smiles. These findings open a new avenue of inquiry into the masked face syndrome of PD.http://journal.frontiersin.org/Journal/10.3389/fpsyg.2016.00780/fullemotionParkinson’s diseasefacial expressionsmimicryFacial mimicryHypomimia
spellingShingle Steven R. Livingstone
Steven R. Livingstone
Steven R. Livingstone
Esztella eVezer
Lucy M. McGarry
Anthony E Lang
Anthony E Lang
Frank A. Russo
Frank A. Russo
Deficits in the mimicry of facial expressions in Parkinson’s disease
Frontiers in Psychology
emotion
Parkinson’s disease
facial expressions
mimicry
Facial mimicry
Hypomimia
title Deficits in the mimicry of facial expressions in Parkinson’s disease
title_full Deficits in the mimicry of facial expressions in Parkinson’s disease
title_fullStr Deficits in the mimicry of facial expressions in Parkinson’s disease
title_full_unstemmed Deficits in the mimicry of facial expressions in Parkinson’s disease
title_short Deficits in the mimicry of facial expressions in Parkinson’s disease
title_sort deficits in the mimicry of facial expressions in parkinson s disease
topic emotion
Parkinson’s disease
facial expressions
mimicry
Facial mimicry
Hypomimia
url http://journal.frontiersin.org/Journal/10.3389/fpsyg.2016.00780/full
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