Evidence map›Paper›PMID 29487167›Full record

ArticleJournal of neurology, neurosurgery, and psychiatry2018

Neurofilament light chain and tau concentrations are markedly increased in the serum of patients with sporadic Creutzfeldt-Jakob disease, and tau correlates with rate of disease progression.

Andrew Geoffrey Bourne Thompson, Connie Luk, Amanda J Heslegrave, Henrik Zetterberg, Simon H Mead, John Collinge, Graham S Jackson

Abstract read
In one paragraph

Article in Journal of neurology, neurosurgery, and psychiatry, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

41 citing papers in PubMed.

  1. Article
  2. Article
  3. Increase of Plasma Biomarkers in Friedreich's Ataxia: Potential Insights into Disease Pathology.Movement disorders : official journal of the Movement Disorder Society · 2025
    Article
  4. Clinical use and reporting of neurofilament quantification in neurological disorders: A global overview.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2025
    Article
  5. Review
  6. Diagnosis of Prion Diseases.Sub-cellular biochemistry · 2025
    Review
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Review
  18. Article
  19. Neurofilaments contribution in clinic: state of the art.Frontiers in aging neuroscience · 2022
    Review
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Andrew Geoffrey Bourne ThompsonMRC Prion Unit at UCL, UCL Institute of Prion Diseases, London, UK.
Connie LukMRC Prion Unit at UCL, UCL Institute of Prion Diseases, London, UK.
Amanda J HeslegraveDepartment of Molecular Neuroscience, UCL Institute of Neurology, London, UK.
Henrik ZetterbergDepartment of Molecular Neuroscience, UCL Institute of Neurology, London, UK.
Simon H MeadMRC Prion Unit at UCL, UCL Institute of Prion Diseases, London, UK.
John CollingeMRC Prion Unit at UCL, UCL Institute of Prion Diseases, London, UK.
Graham S JacksonMRC Prion Unit at UCL, UCL Institute of Prion Diseases, London, UK.

Funding

Department of HealthMedical Research Council G0400713Medical Research Council MC_U123160651Medical Research Council MC_U123170362Medical Research Council MC_UU_00024/1Wellcome Trust
6 · The paper itself

Abstract

objectivesA blood-based biomarker of neuronal damage in sporadic Creutzfeldt-Jakob disease (sCJD) will be extremely valuable for both clinical practice and research aiming to develop effective therapies.

methodsWe used an ultrasensitive immunoassay to measure two candidate biomarkers, tau and neurofilament light (NfL), in serum from patients with sCJD and healthy controls. We tested longitudinal sample sets from six patients to investigate changes over time, and examined correlations with rate of disease progression and associations with known phenotype modifiers.

resultsSerum concentrations of both tau and NfL were increased in patients with sCJD. NfL distinguished patients from controls with 100% sensitivity and 100% specificity. Tau did so with 91% sensitivity and 83% specificity. Both tau and NfL appeared to increase over time in individual patients, particularly in those with several samples tested late in their disease. Tau, but not NfL, was positively correlated with rate of disease progression, and was particularly increased in patients homozygous for methionine at codon 129 of

conclusionsThese findings independently replicate other recent studies using similar methods and offer novel insights. They show clear promise for these blood-based biomarkers in prion disease. Future work should aim to fully establish their potential roles for monitoring disease progression and response to therapies.

Indexed as

AdultAgedAged, 80 and overBiomarkersCase-Control StudiesCreutzfeldt-Jakob SyndromeDisease ProgressionFemaleHumansMaleMiddle AgedNeurofilament ProteinsSensitivity and Specificitytau ProteinsBiomarkersneurofilament protein LNeurofilament Proteinstau ProteinsbiomarkerCreutzfeldt-Jakob Diseaseneurofilament lightprion diseasetau

Identifiers

PMID29487167
PMCPMC6109239

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.