<HashMap><database>biostudies-literature</database><scores><citationCount>0</citationCount><reanalysisCount>0</reanalysisCount><viewCount>45</viewCount><searchCount>0</searchCount></scores><additional><submitter>Wijeyekoon RS</submitter><funding>Medical Research Council Canada</funding><funding>Wellcome Trust-MRC Cambridge Stem Cell Institute(203151/Z/16/Z)</funding><funding>ACT</funding><funding>Rosetrees Trust</funding><funding>Medical Research Council</funding><funding>National Institute for Health Research (NIHR)</funding><funding>Wellcome Trust Clinical Research Career Development Fellowship</funding><funding>NIHR Cambridge Biomedical Research Centre Dementia and Neurodegeneration Theme</funding><funding>Cambridge Centre for Parkinson's Plus</funding><funding>Wellcome Trust</funding><funding>Addenbrooke's Charitable Trust, Cambridge University Hospitals</funding><pagination>1062-1066</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8629119</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>35(6)</volume><pubmed_abstract>&lt;h4>Introduction&lt;/h4>Immune markers are altered in Parkinson's disease (PD), but relationships between cerebrospinal fluid (CSF) and plasma cytokines and associations with neurodegeneration-associated proteins remain unclear.&lt;h4>Methods&lt;/h4>CSF and plasma samples and demographic/clinical measures were obtained from 35 PD patients. CSF samples were analyzed for cytokines (together with plasma) and for α-synuclein, amyloid β(1-42) peptide, total tau, and phospho(Thr231)-tau.&lt;h4>Results&lt;/h4>There were no CSF-plasma cytokine correlations. Interleukin (IL)-8 was higher and interferon-γ, IL-10, and tumor necrosis factor-α were lower in CSF versus plasma. In CSF, total tau correlated positively with IL-8 and IL-1β, whereas α-synuclein correlated positively with amyloid β(1-42) and negatively with semantic fluency (a known marker of PD dementia risk).&lt;h4>Discussion&lt;/h4>CSF and peripheral cytokine profiles in PD are not closely related. Associations between CSF IL-8 and IL-1β and tau suggest that CSF inflammatory changes may relate to tau pathology within PD. CSF α-synuclein/amyloid β may reflect the risk of developing PD dementia. © 2020 The Authors. Movement Disorders published by Wiley Periodicals, Inc. on behalf of International Parkinson and Movement Disorder Society.</pubmed_abstract><journal>Movement disorders : official journal of the Movement Disorder Society</journal><pubmed_title>Cerebrospinal Fluid Cytokines and Neurodegeneration-Associated Proteins in Parkinson's Disease.</pubmed_title><pmcid>PMC8629119</pmcid><funding_grant_id>M369‐F1</funding_grant_id><funding_grant_id>MR/R007446/1</funding_grant_id><funding_grant_id>NF-SI-0616-10011</funding_grant_id><funding_grant_id>214571/Z/18/Z</funding_grant_id><funding_grant_id>ACF-2015-23-501</funding_grant_id><funding_grant_id>MC_PC_17230</funding_grant_id><funding_grant_id>146281</funding_grant_id><funding_grant_id>PF15/CWG</funding_grant_id><funding_grant_id>(214571/Z/18/Z)</funding_grant_id><funding_grant_id>203151/Z/16/Z</funding_grant_id><funding_grant_id>M369-F1</funding_grant_id><funding_grant_id>MC_PC_12009</funding_grant_id><funding_grant_id>RG77199</funding_grant_id><funding_grant_id>NF‐SI‐0616‐10011</funding_grant_id><pubmed_authors>Breen DP</pubmed_authors><pubmed_authors>Williams-Gray CH</pubmed_authors><pubmed_authors>Wijeyekoon RS</pubmed_authors><pubmed_authors>Farrell K</pubmed_authors><pubmed_authors>Barker RA</pubmed_authors><pubmed_authors>Moore SF</pubmed_authors><view_count>45</view_count></additional><is_claimable>false</is_claimable><name>Cerebrospinal Fluid Cytokines and Neurodegeneration-Associated Proteins in Parkinson's Disease.</name><description>&lt;h4>Introduction&lt;/h4>Immune markers are altered in Parkinson's disease (PD), but relationships between cerebrospinal fluid (CSF) and plasma cytokines and associations with neurodegeneration-associated proteins remain unclear.&lt;h4>Methods&lt;/h4>CSF and plasma samples and demographic/clinical measures were obtained from 35 PD patients. CSF samples were analyzed for cytokines (together with plasma) and for α-synuclein, amyloid β(1-42) peptide, total tau, and phospho(Thr231)-tau.&lt;h4>Results&lt;/h4>There were no CSF-plasma cytokine correlations. Interleukin (IL)-8 was higher and interferon-γ, IL-10, and tumor necrosis factor-α were lower in CSF versus plasma. In CSF, total tau correlated positively with IL-8 and IL-1β, whereas α-synuclein correlated positively with amyloid β(1-42) and negatively with semantic fluency (a known marker of PD dementia risk).&lt;h4>Discussion&lt;/h4>CSF and peripheral cytokine profiles in PD are not closely related. Associations between CSF IL-8 and IL-1β and tau suggest that CSF inflammatory changes may relate to tau pathology within PD. CSF α-synuclein/amyloid β may reflect the risk of developing PD dementia. © 2020 The Authors. Movement Disorders published by Wiley Periodicals, Inc. on behalf of International Parkinson and Movement Disorder Society.</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 Jun</publication><modification>2024-11-10T01:50:11.542Z</modification><creation>2022-02-11T13:43:53.665Z</creation></dates><accession>S-EPMC8629119</accession><cross_references><pubmed>32413185</pubmed><doi>10.1002/mds.28015</doi></cross_references></HashMap>