Evidence map›Paper›PMID 39594187›Full record

ArticleDiagnostics (Basel, Switzerland)2024

Glial Fibrillary Acidic Protein's Usefulness as an Astrocyte Biomarker Using the Fully Automated LUMIPULSE

Jo Kamada, Tomohiro Hamanaka, Aya Oshimo, Hideo Sato, Tomonori Nishii, Marika Fujita, Yoshiharu Makiguchi, Miki Tanaka, Katsumi Aoyagi, Hisashi Nojima

Abstract read
In one paragraph

Article in Diagnostics (Basel, Switzerland), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Fully Automated Measurement of GFAP in CSF Using the LUMIPULSEInternational journal of molecular sciences · 2025
    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

10 authors.

Jo KamadaFUJIREBIO Inc., 1-8-1 Akasaka, Minato-ku, Tokyo 107-0052, Japan.
Tomohiro HamanakaFUJIREBIO Inc., 1-8-1 Akasaka, Minato-ku, Tokyo 107-0052, Japan.
Aya OshimoFUJIREBIO Inc., 1-8-1 Akasaka, Minato-ku, Tokyo 107-0052, Japan.
Hideo SatoFUJIREBIO Inc., 1-8-1 Akasaka, Minato-ku, Tokyo 107-0052, Japan.
Tomonori NishiiFUJIREBIO Inc., 1-8-1 Akasaka, Minato-ku, Tokyo 107-0052, Japan.
Marika FujitaFUJIREBIO Inc., 1-8-1 Akasaka, Minato-ku, Tokyo 107-0052, Japan.
Yoshiharu MakiguchiFUJIREBIO Inc., 1-8-1 Akasaka, Minato-ku, Tokyo 107-0052, Japan.
Miki TanakaFUJIREBIO Inc., 1-8-1 Akasaka, Minato-ku, Tokyo 107-0052, Japan.
Katsumi AoyagiFUJIREBIO Inc., 1-8-1 Akasaka, Minato-ku, Tokyo 107-0052, Japan.
Hisashi NojimaFUJIREBIO Inc., 1-8-1 Akasaka, Minato-ku, Tokyo 107-0052, Japan.ORCID 0000-0002-8907-5767

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundGlial fibrillary acidic protein (GFAP) is an important biomarker for neuroinflammatory conditions. Recently, advancements in the treatment of neurological diseases have highlighted the increasing importance of biomarkers, creating a demand for accurate and simple measurement systems for GFAP levels, which are essential for both research and clinical applications. This study presents the development and validation of a novel fully automated immunoassay for the quantitative determination of GFAP levels in biological samples.

methodsWe examined the analytical performance of the GFAP assay on the LUMIPULSE platform. The assay's parameters, including antibody concentrations, incubation times, and detection methods, were optimized to enhance sensitivity and specificity. GFAP levels were measured in 396 serum or plasma samples, comprising both healthy controls and patients with neurodegenerative diseases.

resultsIn the analytical performance studies, intra- and inter-assay coefficients of variation (CV) were below 5%, indicating high reproducibility. Additionally, the assay demonstrated good linearity over the measurement range. The limit of quantification (LoQ) for this assay was 6.0 pg/mL, which is sufficient for measuring specimens from healthy controls. In clinical validation studies, GFAP levels were significantly elevated in patients with neurodegenerative diseases compared to healthy controls.

conclusionsThis automated GFAP assay provides a robust and reliable tool for GFAP measurement, facilitating further research into GFAP's role in neurological disorders and potentially aiding in the diagnosis and monitoring of these conditions.

Indexed as

chemiluminescent enzyme immunoassayglial fibrillary acidic proteinneurological biomarker

Identifiers

PMID39594187
PMCPMC11593324

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.