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The significance of uric acid in the diagnosis and treatment of Parkinson disease: An updated systemic review

BACKGROUND: Parkinson disease (PD) is a neurodegenerative disease characterized by chronic and progressive loss of dopaminergic neurons in substansia nigra pars compacta. Oxidative stress is proposed to play a critical role in the pathogenesis of PD. Uric acid (UA), as an important physiological ant...

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Autores principales: Yu, Zhange, Zhang, Shuai, Wang, Dongdong, Fan, Meng, Gao, Fuqiang, Sun, Wei, Li, Zirong, Li, Shiliang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5690738/
https://www.ncbi.nlm.nih.gov/pubmed/29137045
http://dx.doi.org/10.1097/MD.0000000000008502
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author Yu, Zhange
Zhang, Shuai
Wang, Dongdong
Fan, Meng
Gao, Fuqiang
Sun, Wei
Li, Zirong
Li, Shiliang
author_facet Yu, Zhange
Zhang, Shuai
Wang, Dongdong
Fan, Meng
Gao, Fuqiang
Sun, Wei
Li, Zirong
Li, Shiliang
author_sort Yu, Zhange
collection PubMed
description BACKGROUND: Parkinson disease (PD) is a neurodegenerative disease characterized by chronic and progressive loss of dopaminergic neurons in substansia nigra pars compacta. Oxidative stress is proposed to play a critical role in the pathogenesis of PD. Uric acid (UA), as an important physiological antioxidant, is identified a molecular predictor associated with a decreased risk and a slower disease progression for PD and potential neuroprotectant of PD by increasing epidemiological and clinical evidences. Within this review, we will present a comprehensive overview of the data linking UA to PD in recent years. METHODS: We searched PubMed, EMBASE, Web of Science databases for relevant studies. Any observational or experimental studies that evaluated UA and PD were our goal of searching the electric databases. RESULTS: Twelve studies that evaluated UA and PD were identified in this review. We reviewed the roles of UA in the pathogenesis of PD, the association of UA with morbidity, severity/progression, nonmotor symptoms, motor complications of PD, with an attempt to provide new ideas for diagnosis and treatment in PD. CONCLUSION: Our findings supported that lots of clinical and epidemiological data observed lower UA levels in PD patients. Manipulation of UA or its precursors’ concentration could be effective to treat or prevent PD. However, it is still suspectable that higher UA levels are better enough to PD patients. Furthermore, for the complex nature of PD and its heterogeneous genetic and environmental influences, it is inadequate for just manipulating UA in treating the disease.
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spelling pubmed-56907382017-11-28 The significance of uric acid in the diagnosis and treatment of Parkinson disease: An updated systemic review Yu, Zhange Zhang, Shuai Wang, Dongdong Fan, Meng Gao, Fuqiang Sun, Wei Li, Zirong Li, Shiliang Medicine (Baltimore) 6900 BACKGROUND: Parkinson disease (PD) is a neurodegenerative disease characterized by chronic and progressive loss of dopaminergic neurons in substansia nigra pars compacta. Oxidative stress is proposed to play a critical role in the pathogenesis of PD. Uric acid (UA), as an important physiological antioxidant, is identified a molecular predictor associated with a decreased risk and a slower disease progression for PD and potential neuroprotectant of PD by increasing epidemiological and clinical evidences. Within this review, we will present a comprehensive overview of the data linking UA to PD in recent years. METHODS: We searched PubMed, EMBASE, Web of Science databases for relevant studies. Any observational or experimental studies that evaluated UA and PD were our goal of searching the electric databases. RESULTS: Twelve studies that evaluated UA and PD were identified in this review. We reviewed the roles of UA in the pathogenesis of PD, the association of UA with morbidity, severity/progression, nonmotor symptoms, motor complications of PD, with an attempt to provide new ideas for diagnosis and treatment in PD. CONCLUSION: Our findings supported that lots of clinical and epidemiological data observed lower UA levels in PD patients. Manipulation of UA or its precursors’ concentration could be effective to treat or prevent PD. However, it is still suspectable that higher UA levels are better enough to PD patients. Furthermore, for the complex nature of PD and its heterogeneous genetic and environmental influences, it is inadequate for just manipulating UA in treating the disease. Wolters Kluwer Health 2017-11-10 /pmc/articles/PMC5690738/ /pubmed/29137045 http://dx.doi.org/10.1097/MD.0000000000008502 Text en Copyright © 2017 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by-nd/4.0 This is an open access article distributed under the Creative Commons Attribution-NoDerivatives License 4.0, which allows for redistribution, commercial and non-commercial, as long as it is passed along unchanged and in whole, with credit to the author. http://creativecommons.org/licenses/by-nd/4.0
spellingShingle 6900
Yu, Zhange
Zhang, Shuai
Wang, Dongdong
Fan, Meng
Gao, Fuqiang
Sun, Wei
Li, Zirong
Li, Shiliang
The significance of uric acid in the diagnosis and treatment of Parkinson disease: An updated systemic review
title The significance of uric acid in the diagnosis and treatment of Parkinson disease: An updated systemic review
title_full The significance of uric acid in the diagnosis and treatment of Parkinson disease: An updated systemic review
title_fullStr The significance of uric acid in the diagnosis and treatment of Parkinson disease: An updated systemic review
title_full_unstemmed The significance of uric acid in the diagnosis and treatment of Parkinson disease: An updated systemic review
title_short The significance of uric acid in the diagnosis and treatment of Parkinson disease: An updated systemic review
title_sort significance of uric acid in the diagnosis and treatment of parkinson disease: an updated systemic review
topic 6900
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5690738/
https://www.ncbi.nlm.nih.gov/pubmed/29137045
http://dx.doi.org/10.1097/MD.0000000000008502
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