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Salivary DJ-1 could be an indicator of Parkinson's disease progression

Objective: The goal of the current investigation was to explore whether salivary DJ-1 could be a potential biomarker for monitoring disease progression in Parkinson's disease (PD) by evaluating the association between salivary DJ-1 concentrations and nigrostriatal dopaminergic function. Methods...

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Autores principales: Kang, Wen-Yan, Yang, Qiong, Jiang, Xu-Feng, Chen, Wei, Zhang, Lin-Yuan, Wang, Xiao-Ying, Zhang, Li-Na, Quinn, Thomas J., Liu, Jun, Chen, Sheng-Di
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4047660/
https://www.ncbi.nlm.nih.gov/pubmed/24936184
http://dx.doi.org/10.3389/fnagi.2014.00102
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author Kang, Wen-Yan
Yang, Qiong
Jiang, Xu-Feng
Chen, Wei
Zhang, Lin-Yuan
Wang, Xiao-Ying
Zhang, Li-Na
Quinn, Thomas J.
Liu, Jun
Chen, Sheng-Di
author_facet Kang, Wen-Yan
Yang, Qiong
Jiang, Xu-Feng
Chen, Wei
Zhang, Lin-Yuan
Wang, Xiao-Ying
Zhang, Li-Na
Quinn, Thomas J.
Liu, Jun
Chen, Sheng-Di
author_sort Kang, Wen-Yan
collection PubMed
description Objective: The goal of the current investigation was to explore whether salivary DJ-1 could be a potential biomarker for monitoring disease progression in Parkinson's disease (PD) by evaluating the association between salivary DJ-1 concentrations and nigrostriatal dopaminergic function. Methods: First, in 74 patients with PD and 12 age-matched normal controls, single photon emission computed tomography (SPECT) imaging with labeled dopamine transporters (DAT) ((99m)Tc-TRODAT-1), which has been used for measuring DAT density in PD was prformed. Then, the DJ-1 level in their saliva was analyzed by quantitative and sensitive Luminex assay and compared to caudate or putamen DAT density. Finally, based on the above, our cross-section study was carried out in 376 research volunteers (285 patients with PD and 91 healthy controls) to measure salivary DJ-1 level. Results: From our analysis, we found a correlation between salivary concentration of DJ-1 and putamen nucleus uptake of (99m)Tc-TRODAT-1 in the PD group. Although salivary DJ-1 levels were not affected by UPDRS scores, gender, age, and pharmacotherapy, DJ-1 levels in H&Y 4 stage of PD were higher than those in H&Y 1-3 stage as well as those in healthy controls. Salivary DJ-1 also decreased significantly in mixed type PD patients compared to the tremor-dominant type (TDT) and akinetic-rigid dominant type (ARDT) PD patients. Conclusions: According to the investigation in a large cohort, we reported for the first time the prognostic potential of the salivary DJ-1 as a biomarker for evaluating nigrostriatal dopaminergic function in PD.
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spelling pubmed-40476602014-06-16 Salivary DJ-1 could be an indicator of Parkinson's disease progression Kang, Wen-Yan Yang, Qiong Jiang, Xu-Feng Chen, Wei Zhang, Lin-Yuan Wang, Xiao-Ying Zhang, Li-Na Quinn, Thomas J. Liu, Jun Chen, Sheng-Di Front Aging Neurosci Neuroscience Objective: The goal of the current investigation was to explore whether salivary DJ-1 could be a potential biomarker for monitoring disease progression in Parkinson's disease (PD) by evaluating the association between salivary DJ-1 concentrations and nigrostriatal dopaminergic function. Methods: First, in 74 patients with PD and 12 age-matched normal controls, single photon emission computed tomography (SPECT) imaging with labeled dopamine transporters (DAT) ((99m)Tc-TRODAT-1), which has been used for measuring DAT density in PD was prformed. Then, the DJ-1 level in their saliva was analyzed by quantitative and sensitive Luminex assay and compared to caudate or putamen DAT density. Finally, based on the above, our cross-section study was carried out in 376 research volunteers (285 patients with PD and 91 healthy controls) to measure salivary DJ-1 level. Results: From our analysis, we found a correlation between salivary concentration of DJ-1 and putamen nucleus uptake of (99m)Tc-TRODAT-1 in the PD group. Although salivary DJ-1 levels were not affected by UPDRS scores, gender, age, and pharmacotherapy, DJ-1 levels in H&Y 4 stage of PD were higher than those in H&Y 1-3 stage as well as those in healthy controls. Salivary DJ-1 also decreased significantly in mixed type PD patients compared to the tremor-dominant type (TDT) and akinetic-rigid dominant type (ARDT) PD patients. Conclusions: According to the investigation in a large cohort, we reported for the first time the prognostic potential of the salivary DJ-1 as a biomarker for evaluating nigrostriatal dopaminergic function in PD. Frontiers Media S.A. 2014-06-06 /pmc/articles/PMC4047660/ /pubmed/24936184 http://dx.doi.org/10.3389/fnagi.2014.00102 Text en Copyright © 2014 Kang, Yang, Jiang, Chen, Zhang, Wang, Zhang, Quinn, Liu and Chen. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Kang, Wen-Yan
Yang, Qiong
Jiang, Xu-Feng
Chen, Wei
Zhang, Lin-Yuan
Wang, Xiao-Ying
Zhang, Li-Na
Quinn, Thomas J.
Liu, Jun
Chen, Sheng-Di
Salivary DJ-1 could be an indicator of Parkinson's disease progression
title Salivary DJ-1 could be an indicator of Parkinson's disease progression
title_full Salivary DJ-1 could be an indicator of Parkinson's disease progression
title_fullStr Salivary DJ-1 could be an indicator of Parkinson's disease progression
title_full_unstemmed Salivary DJ-1 could be an indicator of Parkinson's disease progression
title_short Salivary DJ-1 could be an indicator of Parkinson's disease progression
title_sort salivary dj-1 could be an indicator of parkinson's disease progression
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4047660/
https://www.ncbi.nlm.nih.gov/pubmed/24936184
http://dx.doi.org/10.3389/fnagi.2014.00102
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