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Salivary total α-synuclein, oligomeric α-synuclein and SNCA variants in Parkinson’s disease patients

The present study was to evaluate the diagnostic value of salivary total and oligomeric α-synuclein levels in PD. Furthermore, we sought to explore the relationship between salivary total α-synuclein and α-synuclein SNP variants levels. 201 PD patients and 67 controls were recruited, of which there...

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Autores principales: Kang, Wenyan, Chen, Wei, Yang, Qiong, Zhang, Lina, Zhang, Linyuan, Wang, Xiaoying, Dong, Fangyi, Zhao, Yang, Chen, Shuai, Quinn, Thomas J., Zhang, Jing, Chen, Shengdi, Liu, Jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4917865/
https://www.ncbi.nlm.nih.gov/pubmed/27335051
http://dx.doi.org/10.1038/srep28143
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author Kang, Wenyan
Chen, Wei
Yang, Qiong
Zhang, Lina
Zhang, Linyuan
Wang, Xiaoying
Dong, Fangyi
Zhao, Yang
Chen, Shuai
Quinn, Thomas J.
Zhang, Jing
Chen, Shengdi
Liu, Jun
author_facet Kang, Wenyan
Chen, Wei
Yang, Qiong
Zhang, Lina
Zhang, Linyuan
Wang, Xiaoying
Dong, Fangyi
Zhao, Yang
Chen, Shuai
Quinn, Thomas J.
Zhang, Jing
Chen, Shengdi
Liu, Jun
author_sort Kang, Wenyan
collection PubMed
description The present study was to evaluate the diagnostic value of salivary total and oligomeric α-synuclein levels in PD. Furthermore, we sought to explore the relationship between salivary total α-synuclein and α-synuclein SNP variants levels. 201 PD patients and 67 controls were recruited, of which there also had the genetic information of two positive α-synuclein (SNCA) loci. Salivary total α-synuclein was assayed using a highly sensitive Luminex assay and oligomeric α-synuclein was quantified by the combination of Gel filtration chromatography and Western blot, respectively. From our analysis,No difference in salivary total α-synuclein levels was found between PD patients and healthy controls, it decreased with age in PD patients, and was closely associated with genotypic distribution of rs11931074 and rs894278 in PD, respectively. After controlled for age and genders, G allele of rs11931074 was correlated with lower salivary total α-synuclein levels, while G allele of rs894278 was also correlated with the higher levels. Simultaneously, the further study was shown that salivary oligomeric α-synuclein in PD patients significantly increased comparing to healthy controls. In conclusions,our study firstly demonstrated that salivary total α-synuclein levels could be manipulated by different α-synuclein SNPs and salivary oligomeric α-synuclein could be a potential diagnostic indicator of PD.
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spelling pubmed-49178652016-06-27 Salivary total α-synuclein, oligomeric α-synuclein and SNCA variants in Parkinson’s disease patients Kang, Wenyan Chen, Wei Yang, Qiong Zhang, Lina Zhang, Linyuan Wang, Xiaoying Dong, Fangyi Zhao, Yang Chen, Shuai Quinn, Thomas J. Zhang, Jing Chen, Shengdi Liu, Jun Sci Rep Article The present study was to evaluate the diagnostic value of salivary total and oligomeric α-synuclein levels in PD. Furthermore, we sought to explore the relationship between salivary total α-synuclein and α-synuclein SNP variants levels. 201 PD patients and 67 controls were recruited, of which there also had the genetic information of two positive α-synuclein (SNCA) loci. Salivary total α-synuclein was assayed using a highly sensitive Luminex assay and oligomeric α-synuclein was quantified by the combination of Gel filtration chromatography and Western blot, respectively. From our analysis,No difference in salivary total α-synuclein levels was found between PD patients and healthy controls, it decreased with age in PD patients, and was closely associated with genotypic distribution of rs11931074 and rs894278 in PD, respectively. After controlled for age and genders, G allele of rs11931074 was correlated with lower salivary total α-synuclein levels, while G allele of rs894278 was also correlated with the higher levels. Simultaneously, the further study was shown that salivary oligomeric α-synuclein in PD patients significantly increased comparing to healthy controls. In conclusions,our study firstly demonstrated that salivary total α-synuclein levels could be manipulated by different α-synuclein SNPs and salivary oligomeric α-synuclein could be a potential diagnostic indicator of PD. Nature Publishing Group 2016-06-23 /pmc/articles/PMC4917865/ /pubmed/27335051 http://dx.doi.org/10.1038/srep28143 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Kang, Wenyan
Chen, Wei
Yang, Qiong
Zhang, Lina
Zhang, Linyuan
Wang, Xiaoying
Dong, Fangyi
Zhao, Yang
Chen, Shuai
Quinn, Thomas J.
Zhang, Jing
Chen, Shengdi
Liu, Jun
Salivary total α-synuclein, oligomeric α-synuclein and SNCA variants in Parkinson’s disease patients
title Salivary total α-synuclein, oligomeric α-synuclein and SNCA variants in Parkinson’s disease patients
title_full Salivary total α-synuclein, oligomeric α-synuclein and SNCA variants in Parkinson’s disease patients
title_fullStr Salivary total α-synuclein, oligomeric α-synuclein and SNCA variants in Parkinson’s disease patients
title_full_unstemmed Salivary total α-synuclein, oligomeric α-synuclein and SNCA variants in Parkinson’s disease patients
title_short Salivary total α-synuclein, oligomeric α-synuclein and SNCA variants in Parkinson’s disease patients
title_sort salivary total α-synuclein, oligomeric α-synuclein and snca variants in parkinson’s disease patients
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4917865/
https://www.ncbi.nlm.nih.gov/pubmed/27335051
http://dx.doi.org/10.1038/srep28143
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