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Synaptic proteins in CSF relate to Parkinson’s disease stage markers
Recent findings of morphological and functional changes in Parkinson’s disease brains have shown altered synapse formation, but their role in cognitive decline is still an area under exploration. Here we measured the concentration of three key synaptic proteins, Rab3A, SNAP25 and neurogranin by enzy...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5445607/ https://www.ncbi.nlm.nih.gov/pubmed/28649607 http://dx.doi.org/10.1038/s41531-017-0008-2 |
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author | Bereczki, Erika Bogstedt, Anna Höglund, Kina Tsitsi, Panagiota Brodin, Lovisa Ballard, Clive Svenningsson, Per Aarsland, Dag |
author_facet | Bereczki, Erika Bogstedt, Anna Höglund, Kina Tsitsi, Panagiota Brodin, Lovisa Ballard, Clive Svenningsson, Per Aarsland, Dag |
author_sort | Bereczki, Erika |
collection | PubMed |
description | Recent findings of morphological and functional changes in Parkinson’s disease brains have shown altered synapse formation, but their role in cognitive decline is still an area under exploration. Here we measured the concentration of three key synaptic proteins, Rab3A, SNAP25 and neurogranin by enzyme-linked immunosorbent assay, in cerebrospinal fluid from a total of 139 participants (87 controls and 52 Parkinson’s disease patients out of which 30 were drug-naïve) and explored their associations with motor and cognitive symptoms. Associations with motor disease stage (assessed by Hoehn and Yahr scale) and cognitive performance (assessed by the Montreal Cognitive Assessment scores) were explored. An overall increase in the concentration of SNAP25 was found in Parkinson’s disease patients (p = 0.032). Increased neurogranin levels were found in the drug naïve patients subgroup (p = 0.023). Significant associations were observed between increased concentration of neurogranin and cognitive impairment in total Parkinson’s disease group (p = 0.017), as well as in the drug naïve (p = 0.021) and with motor disease stage (p = 0.041). There were no significant disease-driven changes observed in the concentration of Rab3a. Concentrations SNAP25 and neurogranin were increased in cerebrospinal fluid of Parkinson’s disease patients in a disease specific manner and related to cognitive and motor symptom severity. Future longitudinal studies should explore whether cerebrospinal fluid synaptic proteins can predict cognitive decline in Parkinson’s disease. |
format | Online Article Text |
id | pubmed-5445607 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-54456072017-06-23 Synaptic proteins in CSF relate to Parkinson’s disease stage markers Bereczki, Erika Bogstedt, Anna Höglund, Kina Tsitsi, Panagiota Brodin, Lovisa Ballard, Clive Svenningsson, Per Aarsland, Dag NPJ Parkinsons Dis Article Recent findings of morphological and functional changes in Parkinson’s disease brains have shown altered synapse formation, but their role in cognitive decline is still an area under exploration. Here we measured the concentration of three key synaptic proteins, Rab3A, SNAP25 and neurogranin by enzyme-linked immunosorbent assay, in cerebrospinal fluid from a total of 139 participants (87 controls and 52 Parkinson’s disease patients out of which 30 were drug-naïve) and explored their associations with motor and cognitive symptoms. Associations with motor disease stage (assessed by Hoehn and Yahr scale) and cognitive performance (assessed by the Montreal Cognitive Assessment scores) were explored. An overall increase in the concentration of SNAP25 was found in Parkinson’s disease patients (p = 0.032). Increased neurogranin levels were found in the drug naïve patients subgroup (p = 0.023). Significant associations were observed between increased concentration of neurogranin and cognitive impairment in total Parkinson’s disease group (p = 0.017), as well as in the drug naïve (p = 0.021) and with motor disease stage (p = 0.041). There were no significant disease-driven changes observed in the concentration of Rab3a. Concentrations SNAP25 and neurogranin were increased in cerebrospinal fluid of Parkinson’s disease patients in a disease specific manner and related to cognitive and motor symptom severity. Future longitudinal studies should explore whether cerebrospinal fluid synaptic proteins can predict cognitive decline in Parkinson’s disease. Nature Publishing Group UK 2017-02-08 /pmc/articles/PMC5445607/ /pubmed/28649607 http://dx.doi.org/10.1038/s41531-017-0008-2 Text en © The Author(s) 2017 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 Bereczki, Erika Bogstedt, Anna Höglund, Kina Tsitsi, Panagiota Brodin, Lovisa Ballard, Clive Svenningsson, Per Aarsland, Dag Synaptic proteins in CSF relate to Parkinson’s disease stage markers |
title | Synaptic proteins in CSF relate to Parkinson’s disease stage markers |
title_full | Synaptic proteins in CSF relate to Parkinson’s disease stage markers |
title_fullStr | Synaptic proteins in CSF relate to Parkinson’s disease stage markers |
title_full_unstemmed | Synaptic proteins in CSF relate to Parkinson’s disease stage markers |
title_short | Synaptic proteins in CSF relate to Parkinson’s disease stage markers |
title_sort | synaptic proteins in csf relate to parkinson’s disease stage markers |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5445607/ https://www.ncbi.nlm.nih.gov/pubmed/28649607 http://dx.doi.org/10.1038/s41531-017-0008-2 |
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