<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Rodrigues FB</submitter><funding>Wolfson Foundation</funding><funding>European Research Council</funding><funding>Medical Research Council</funding><funding>GlaxoSmithKline foundation</funding><funding>Knut och Alice Wallenbergs Stiftelse</funding><funding>CHDI Foundation</funding><funding>Swedish Research Council</funding><funding>Wellcome Trust</funding><pagination>e0163479</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5033331</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>11(9)</volume><pubmed_abstract>&lt;h4>Introduction&lt;/h4>Immune system activation is involved in Huntington's disease (HD) pathogenesis and biomarkers for this process could be relevant to study the disease and characterise the therapeutic response to specific interventions. We aimed to study inflammatory cytokines and microglial markers in the CSF of HD patients.&lt;h4>Methods&lt;/h4>CSF TNF-α, IL-1β, IL-6, IL-8, YKL-40, chitotriosidase, total tau and neurofilament light chain (NFL) from 23 mutation carriers and 14 healthy controls were assayed.&lt;h4>Results&lt;/h4>CSF TNF-α and IL-1β were below the limit of detection. Mutation carriers had higher YKL-40 (p = 0.003), chitotriosidase (p = 0.015) and IL-6 (p = 0.041) than controls. YKL-40 significantly correlated with disease stage (p = 0.007), UHDRS total functional capacity score (r =</pubmed_abstract><journal>PloS one</journal><pubmed_title>Cerebrospinal Fluid Inflammatory Biomarkers Reflect Clinical Severity in Huntington's Disease.</pubmed_title><pmcid>PMC5033331</pmcid><funding_grant_id>MR/M008592/1</funding_grant_id><funding_grant_id>200181/Z/15/Z</funding_grant_id><funding_grant_id>MR/L02053X/1</funding_grant_id><pubmed_authors>Rodrigues FB</pubmed_authors><pubmed_authors>Wild EJ</pubmed_authors><pubmed_authors>Tabrizi SJ</pubmed_authors><pubmed_authors>Byrne LM</pubmed_authors><pubmed_authors>Zetterberg H</pubmed_authors><pubmed_authors>Robertson N</pubmed_authors><pubmed_authors>McColgan P</pubmed_authors></additional><is_claimable>false</is_claimable><name>Cerebrospinal Fluid Inflammatory Biomarkers Reflect Clinical Severity in Huntington's Disease.</name><description>&lt;h4>Introduction&lt;/h4>Immune system activation is involved in Huntington's disease (HD) pathogenesis and biomarkers for this process could be relevant to study the disease and characterise the therapeutic response to specific interventions. We aimed to study inflammatory cytokines and microglial markers in the CSF of HD patients.&lt;h4>Methods&lt;/h4>CSF TNF-α, IL-1β, IL-6, IL-8, YKL-40, chitotriosidase, total tau and neurofilament light chain (NFL) from 23 mutation carriers and 14 healthy controls were assayed.&lt;h4>Results&lt;/h4>CSF TNF-α and IL-1β were below the limit of detection. Mutation carriers had higher YKL-40 (p = 0.003), chitotriosidase (p = 0.015) and IL-6 (p = 0.041) than controls. YKL-40 significantly correlated with disease stage (p = 0.007), UHDRS total functional capacity score (r =</description><dates><release>2016-01-01T00:00:00Z</release><publication>2016</publication><modification>2025-04-25T19:24:29.473Z</modification><creation>2019-03-26T22:48:13Z</creation></dates><accession>S-EPMC5033331</accession><cross_references><pubmed>27657730</pubmed><doi>10.1371/journal.pone.0163479</doi></cross_references></HashMap>