Cited by 79Genetic Neurodegenerative DiseasesNeuroinflammation and Neurodegeneration MechanismsLysosomal Storage Disorders Research

Cerebrospinal fluid inflammatory biomarkers reflect clinical severity in Huntington's disease

Open access
Rodrigues, Filipe Brogueira, Byrne, Lauren M., McColgan, Peter, Robertson, Nicola, Tabrizi, Sarah J., Zetterberg, Henrik, Wild, Edward J.·2016·PLOS ONE

Abstract

INTRODUCTION: 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. METHODS: 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. RESULTS: 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 = -0.46, p = 0.016), and UHDRS total motor score (r = 0.59, p = 4.5*10-4) after adjustment for age. CONCLUSION: YKL-40 levels in CSF may, after further study, come to have a role as biomarkers for some aspects of HD. Further investigation is needed to support our exploratory findings.

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Integrity signals

Registry

Crossref · 10.1371/journal.pone.0163479

Cites

33 of 33 references verified0 citation errors · 0 not checkable

Statistics

Claims the paper makes

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

Cites

Flagged first, then by citations

Research works printed but not linked: 1

  1. [32]Wild EJ, Borowsky B, HDClarity investigators, editors. HDClarity: A new multi-site cerebrospinal fluid collection initiative to facilitate therapeutic development for Huntington’s disease. 11th Annual CHDI HD Therapeutics Conference 2016; 2016; Palm Springs, CA.

Cited by

Sorted by citations

Authors
Rodrigues, F. B., Byrne, L. M., McColgan, P., Robertson, N., Tabrizi, S. J., Zetterberg, H., & Wild, E. J.
Affiliations
UCL Queen Square Institute of Neurology (GB)
Corresponding author
Wild, Edward J.
Venue
PLOS ONE
Published
2016-09-22
Volume
11
Issue
9
Pages
e0163479
ISSN
1932-6203 (ISSN-L)
OpenAlex
W2521599174
Cited by
79
References
33
Citations by year
2026: 6 · 2025: 8 · 2024: 9 · 2023: 11 · 2022: 9 · 2021: 7 · 2020: 11 · 2019: 5 · 2018: 8 · 2017: 5
FWCI
3.38
Type
journal article
Language
en
Open access
Locations
  • PLoS ONE (publishedVersion, cc-by)
  • PubMed Central (publishedVersion, cc-by)
  • PubMed (publishedVersion)
  • DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
  • UCL Discovery (University College London) (submittedVersion)
Funders
  • CHDI Foundation
  • GlaxoSmithKline foundation
  • Swedish Research Council
  • European Research Council
  • Medical Research Council
  • Knut och Alice Wallenbergs Stiftelse
  • Wolfson Foundation
Topics
  • Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Genetic Neurodegenerative Diseases
  • Life Sciences › Neuroscience › Neurology › Neuroinflammation and Neurodegeneration Mechanisms
  • Health Sciences › Medicine › Physiology › Lysosomal Storage Disorders Research
Keywords
Huntington's disease, cerebrospinal fluid biomarkers, neuroinflammation, YKL-40, chitotriosidase, interleukin-6, TNF-α, IL-1β, neurofilament light chain, tau protein, microglial activation, disease severity, mutation carriers

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review