Evidence map›Paper›PMID 36321325›Full record

ArticleAnnals of clinical and translational neurology2022

Clinical utility of cerebrospinal fluid biomarkers measured by LUMIPULSE

Hisashi Nojima, Satoshi Ito, Akira Kushida, Aki Abe, Wataru Motsuchi, David Verbel, Manu Vandijck, Geert Jannes, Ina Vandenbroucke, Katsumi Aoyagi

Abstract read
In one paragraph

Article in Annals of clinical and translational neurology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 1 pooled it
–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

18 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. ATNIVS biomarker heterogeneity in real-world patients receiving lecanemab.The journal of prevention of Alzheimer's disease · 2026
    Article
  4. Observational
  5. Observational
  6. Article
  7. Fully Automated Measurement of GFAP in CSF Using the LUMIPULSEInternational journal of molecular sciences · 2025
    Article
  8. Article
  9. Article
  10. Article
  11. Alzheimer's Disease-Related Analytes Amyloid-β and Tau in Perilymph: Correlation With Patient Age and Cognitive Score.Otolaryngology--head and neck surgery : official journal of American Academy of Otolaryngology-Head and Neck Surgery · 2024
    Article
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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

10 authors.

Hisashi NojimaFUJIREBIO Inc., 2-1-1, Nishishinjuku, Shinjuku-ku, Tokyo, 163-0410, Japan.ORCID https://orcid.org/0000-0002-8907-5767
Satoshi ItoEisai Co., Ltd. 4-6-10 Koishikawa, Bunkyo-ku, Tokyo, 112-8088, Japan.
Akira KushidaFUJIREBIO Inc., 2-1-1, Nishishinjuku, Shinjuku-ku, Tokyo, 163-0410, Japan.
Aki AbeFUJIREBIO Inc., 2-1-1, Nishishinjuku, Shinjuku-ku, Tokyo, 163-0410, Japan.
Wataru MotsuchiFUJIREBIO Inc., 2-1-1, Nishishinjuku, Shinjuku-ku, Tokyo, 163-0410, Japan.
David VerbelEisai Inc., 200 Metro Boulevard, Nutley, New Jersey, 07110, USA.
Manu VandijckFujirebio-Europe N.V., Technologiepark 6, 9052, Ghent, Belgium.
Geert JannesFujirebio-Europe N.V., Technologiepark 6, 9052, Ghent, Belgium.
Ina VandenbrouckeFujirebio-Europe N.V., Technologiepark 6, 9052, Ghent, Belgium.
Katsumi AoyagiFUJIREBIO Inc., 2-1-1, Nishishinjuku, Shinjuku-ku, Tokyo, 163-0410, Japan.

Funding

Fujirebio Inc
6 · The paper itself

Abstract

objectivesCerebrospinal fluid (CSF) biomarkers of Alzheimer's disease (AD) are well-established in research settings, but their use in routine clinical practice remains a largely unexploited potential. Here, we examined the relationship between CSF biomarkers, measured by a fully automated immunoassay platform, and brain β-amyloid (Aβ) deposition status confirmed by amyloid positron emission tomography (PET).

methodsOne hundred ninety-nine CSF samples from clinically diagnosed AD patients enrolled in a clinical study and who underwent amyloid PET were used for the measurement of CSF biomarkers Aβ 1-40 (Aβ40), Aβ 1-42 (Aβ42), total tau (t-Tau), and phosphorylated tau-181 (p-Tau181) using the LUMIPULSE system. These biomarkers and their combinations were compared to amyloid PET classification (negative or positive) using visual read assessments. Several combinations were also analyzed with a multivariable logistic regression model.

resultsAβ42, t-Tau, and p-Tau181, and the ratios of Aβ42 with other biomarkers had a good diagnostic agreement with amyloid PET imaging. The multivariable logistic regression analysis showed that amyloid PET status was associated with Aβ40 and Aβ42, but other factors, such as MMSE, sex, t-Tau, and p-Tau181, did not significantly add information to the model.

conclusionsCSF biomarkers measured with the LUMIPULSE system showed good agreement with amyloid PET imaging. The ratio of Aβ42 with the other analyzed biomarkers showed a higher correlation with amyloid PET than Aβ42 alone, suggesting that the combinations of biomarkers could be useful in the diagnostic assessment in clinical research and potentially in routine clinical practice.

Indexed as

Alzheimer DiseaseAmyloidBiomarkersBrainHumansPositron-Emission TomographyAmyloidBiomarkers

Identifiers

PMID36321325
PMCPMC9735374

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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.