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Skin disorders in Parkinson’s disease: potential biomarkers and risk factors

Parkinson’s disease (PD) is one of the most common neurodegenerative disorders, characterized by a symptom triad comprising resting tremor, rigidity, and akinesia. In addition, non-motor symptoms of PD are well recognized and often precede the overt motor manifestations. Cutaneous manifestations as...

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Autores principales: Ravn, Astrid-Helene, Thyssen, Jacob P, Egeberg, Alexander
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5352163/
https://www.ncbi.nlm.nih.gov/pubmed/28331352
http://dx.doi.org/10.2147/CCID.S130319
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author Ravn, Astrid-Helene
Thyssen, Jacob P
Egeberg, Alexander
author_facet Ravn, Astrid-Helene
Thyssen, Jacob P
Egeberg, Alexander
author_sort Ravn, Astrid-Helene
collection PubMed
description Parkinson’s disease (PD) is one of the most common neurodegenerative disorders, characterized by a symptom triad comprising resting tremor, rigidity, and akinesia. In addition, non-motor symptoms of PD are well recognized and often precede the overt motor manifestations. Cutaneous manifestations as markers of PD have long been discussed, and cumulative evidence shows an increased prevalence of certain dermatological disorders in PD. Seborrheic dermatitis is considered to occur as a premotor feature of PD referable to dysregulation of the autonomic nervous system. Also, an increased risk of melanoma has been observed in PD. Light hair color is a known risk factor for melanoma, and interestingly the risk of PD is found to be significantly higher in individuals with light hair color and particularly with red hair. Furthermore, several studies have reported a high prevalence of PD in patients with bullous pemphigoid. Moreover, a 2-fold increase in risk of new-onset PD has been observed in patients with rosacea. Besides the association between PD and various dermatological disorders, the skin may be useful in the diagnosis of PD. Early PD pathology is found not only in the brain but also in extra-neuronal tissues. Thus, the protein α-synuclein, which is genetically associated with PD, is present not only in the CNS but also in the skin. Hence, higher values of α-synuclein have been observed in the skin of patients with PD. Furthermore, an increased risk of PD has been found in the Cys/Cys genotype, which is associated with red hair color. In this review, we summarize the current evidence of the association between PD and dermatological disorders, the cutaneous adverse effects of neurological medications, and describe the potential of skin protein expression and biomarkers in identification of risk and diagnosis of PD.
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spelling pubmed-53521632017-03-22 Skin disorders in Parkinson’s disease: potential biomarkers and risk factors Ravn, Astrid-Helene Thyssen, Jacob P Egeberg, Alexander Clin Cosmet Investig Dermatol Review Parkinson’s disease (PD) is one of the most common neurodegenerative disorders, characterized by a symptom triad comprising resting tremor, rigidity, and akinesia. In addition, non-motor symptoms of PD are well recognized and often precede the overt motor manifestations. Cutaneous manifestations as markers of PD have long been discussed, and cumulative evidence shows an increased prevalence of certain dermatological disorders in PD. Seborrheic dermatitis is considered to occur as a premotor feature of PD referable to dysregulation of the autonomic nervous system. Also, an increased risk of melanoma has been observed in PD. Light hair color is a known risk factor for melanoma, and interestingly the risk of PD is found to be significantly higher in individuals with light hair color and particularly with red hair. Furthermore, several studies have reported a high prevalence of PD in patients with bullous pemphigoid. Moreover, a 2-fold increase in risk of new-onset PD has been observed in patients with rosacea. Besides the association between PD and various dermatological disorders, the skin may be useful in the diagnosis of PD. Early PD pathology is found not only in the brain but also in extra-neuronal tissues. Thus, the protein α-synuclein, which is genetically associated with PD, is present not only in the CNS but also in the skin. Hence, higher values of α-synuclein have been observed in the skin of patients with PD. Furthermore, an increased risk of PD has been found in the Cys/Cys genotype, which is associated with red hair color. In this review, we summarize the current evidence of the association between PD and dermatological disorders, the cutaneous adverse effects of neurological medications, and describe the potential of skin protein expression and biomarkers in identification of risk and diagnosis of PD. Dove Medical Press 2017-03-09 /pmc/articles/PMC5352163/ /pubmed/28331352 http://dx.doi.org/10.2147/CCID.S130319 Text en © 2017 Ravn et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Review
Ravn, Astrid-Helene
Thyssen, Jacob P
Egeberg, Alexander
Skin disorders in Parkinson’s disease: potential biomarkers and risk factors
title Skin disorders in Parkinson’s disease: potential biomarkers and risk factors
title_full Skin disorders in Parkinson’s disease: potential biomarkers and risk factors
title_fullStr Skin disorders in Parkinson’s disease: potential biomarkers and risk factors
title_full_unstemmed Skin disorders in Parkinson’s disease: potential biomarkers and risk factors
title_short Skin disorders in Parkinson’s disease: potential biomarkers and risk factors
title_sort skin disorders in parkinson’s disease: potential biomarkers and risk factors
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5352163/
https://www.ncbi.nlm.nih.gov/pubmed/28331352
http://dx.doi.org/10.2147/CCID.S130319
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