Evidence map›Paper›PMID 37897306›Full record

ArticleAnnals of neurology2024

Diagnostic Utility of Cerebrospinal Fluid Biomarkers in Patients with Rapidly Progressive Dementia.

Lindsey A Kuchenbecker, Philip W Tipton, Yuka Martens, Matthew R Brier, Nihal Satyadev, S Richard Dunham, Evelyn B Lazar, Maxwell V Dacquel, Rachel L Henson, Guojun Bu and 6 more

Open access · bronzeAbstract read
In one paragraph

Article in Annals of neurology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 2 pooled it
2.3field-weighted citation impact, top 11% of its field
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

10 citing papers in PubMed, 2 syntheses or guidelines pooled it, 13 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Observational
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
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  10. Review
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

16 authors at 4 institutions in 1 country.

Lindsey A KuchenbeckerDepartment of Neuroscience, Mayo Clinic Florida, Jacksonville, FL, USA.ORCID 0000-0002-2987-1040
Philip W TiptonDepartment of Neurology, Mayo Clinic Florida, Jacksonville, FL, USA.ORCID 0000-0003-4084-2248
Yuka MartensDepartment of Neuroscience, Mayo Clinic Florida, Jacksonville, FL, USA.
Matthew R BrierDepartment of Neurology, Washington University School of Medicine, Saint Louis, MO, USA.ORCID 0000-0001-5987-8705
Nihal SatyadevDepartment of Neurology, Mayo Clinic Florida, Jacksonville, FL, USA.ORCID 0000-0001-7302-2348
S Richard DunhamDepartment of Neurology, Washington University School of Medicine, Saint Louis, MO, USA.ORCID 0000-0003-2840-3955
Evelyn B LazarDepartment of Neurology, Mayo Clinic Florida, Jacksonville, FL, USA.
Maxwell V DacquelDepartment of Neuroscience, Mayo Clinic Florida, Jacksonville, FL, USA.
Rachel L HensonDepartment of Neurology, Washington University School of Medicine, Saint Louis, MO, USA.
Guojun BuDepartment of Neuroscience, Mayo Clinic Florida, Jacksonville, FL, USA.
Michael D GeschwindDepartment of Neurology, University of California, San Francisco, San Francisco, CA, USA.
John C MorrisDepartment of Neurology, Washington University School of Medicine, Saint Louis, MO, USA.
Suzanne E SchindlerDepartment of Neurology, Washington University School of Medicine, Saint Louis, MO, USA.
Elizabeth HerriesDepartment of Neurology, Washington University School of Medicine, Saint Louis, MO, USA.
Neill R Graff-RadfordDepartment of Neurology, Mayo Clinic Florida, Jacksonville, FL, USA.
Gregory S DayDepartment of Neurology, Mayo Clinic Florida, Jacksonville, FL, USA.ORCID 0000-0001-5133-5538
Washington University in St. Louis · USMayo Clinic · USJacksonville College · USUniversity of California, San Francisco · US

Funding

Research Education ComponentP30AG062677 · NIA · MAYO CLINIC ROCHESTER · PI RONALD C PETERSEN · 2019 to 2026
$33.5M
Research Education ComponentP30AG066444 · NIA · WASHINGTON UNIVERSITY · PI DAVID M. HOLTZMAN · 2020 to 2026
$28.7M
PET and MRI Evaluation of Cerebral Inflammation and Metabolic Stress in Relapsing Multiple SclerosisK23NS128325 · NINDS · WASHINGTON UNIVERSITY · PI Matthew Ryan Brier · 2023 to 2026
$931k
Rapidly Progressive Dementia: Moving Beyond CJDK23AG064029 · NIA · WASHINGTON UNIVERSITY · PI DAY, GREGORY SCOTT · 2019 to 2023
$811k
NIA NIH HHS K23 AG064029NIA NIH HHS K23AG064029NIA NIH HHS P30 AG062677NIA NIH HHS P30AG062677NIA NIH HHS P30 AG066444NIA NIH HHS P30AG066444NINDS NIH HHS K23 NS128325
6 · The paper itself

Abstract

objectiveThis study was undertaken to apply established and emerging cerebrospinal fluid (CSF) biomarkers to improve diagnostic accuracy in patients with rapidly progressive dementia (RPD). Overlap in clinical presentation and results of diagnostic tests confounds etiologic diagnosis in patients with RPD. Objective measures are needed to improve diagnostic accuracy and to recognize patients with potentially treatment-responsive causes of RPD.

methodsBiomarkers of Alzheimer disease neuropathology (amyloid-β 42/40 ratio, phosphorylated tau [p-tau181, p-tau231]), neuroaxonal/neuronal injury (neurofilament light chain [NfL], visinin-like protein-1 [VILIP-1], total tau), neuroinflammation (chitinase-3-like protein [YKL-40], soluble triggering receptor expressed on myeloid cells 2 [sTREM2], glial fibrillary acidic protein [GFAP], monocyte chemoattractant protein-1 [MCP-1]), and synaptic dysfunction (synaptosomal-associated protein 25kDa, neurogranin) were measured in CSF obtained at presentation from 78 prospectively accrued patients with RPD due to neurodegenerative, vascular, and autoimmune/inflammatory diseases; 35 age- and sex-matched patients with typically progressive neurodegenerative disease; and 72 cognitively normal controls. Biomarker levels were compared across etiologic diagnoses, by potential treatment responsiveness, and between patients with typical and rapidly progressive presentations of neurodegenerative disease.

resultsAlzheimer disease biomarkers were associated with neurodegenerative causes of RPD. High NfL, sTREM2, and YKL-40 and low VILIP-1 identified patients with autoimmune/inflammatory diseases. MCP-1 levels were highest in patients with vascular causes of RPD. A multivariate model including GFAP, MCP-1, p-tau181, and sTREM2 identified the 44 patients with treatment-responsive causes of RPD with 89% accuracy. Minimal differences were observed between typical and rapidly progressive presentations of neurodegenerative disease.

interpretationSelected CSF biomarkers at presentation were associated with etiologic diagnoses and treatment responsiveness in patients with heterogeneous causes of RPD. The ability of cross-sectional biomarkers to inform upon mechanisms that drive rapidly progressive neurodegenerative disease is less clear. ANN NEUROL 2024;95:299-313.

Indexed as

Alzheimer DiseaseDementiaNeurodegenerative DiseasesAmyloid beta-PeptidesBiomarkersChitinase-3-Like Protein 1Cross-Sectional StudiesHumanstau ProteinsAmyloid beta-PeptidesBiomarkersChitinase-3-Like Protein 1tau Proteins

Identifiers

PMID37897306
PMCPMC10842089
OpenAlexW4388001264

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

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.