Evidence map›Paper›PMID 39283757›Full record

ArticleJournal of clinical laboratory analysis2024

Evaluation of a Chemiluminescent Enzyme Immunoassay for the Detection of Prostaglandin E-Major Urinary Metabolite (PGE-MUM).

Jun Takagi, Kazushige Moriyama, Seiji Arihiro, Tomohiro Kato, Toshiyuki Sakurai, Masayuki Saruta, Mie Wakabayashi, Hidekazu Nasu, Noriko Katagiri, Shintaro Yagi

Abstract read
In one paragraph

Article in Journal of clinical laboratory analysis, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Age-related variations in prostaglandin E-major urinary metabolite values in Japanese children.Pediatrics international : official journal of the Japan Pediatric Society
    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.

Jun TakagiResearch and Development Division, FUJIREBIO Inc., Tokyo, Japan.ORCID https://orcid.org/0009-0000-1547-6915
Kazushige MoriyamaResearch and Development Division, FUJIREBIO Inc., Tokyo, Japan.
Seiji ArihiroDivision of Gastroenterology and Hepatology, Department of Internal Medicine, The Jikei University School of Medicine, Tokyo, Japan.
Tomohiro KatoDivision of Gastroenterology and Hepatology, Department of Internal Medicine, The Jikei University School of Medicine, Tokyo, Japan.
Toshiyuki SakuraiDivision of Gastroenterology and Hepatology, Department of Internal Medicine, The Jikei University School of Medicine, Tokyo, Japan.
Masayuki SarutaDivision of Gastroenterology and Hepatology, Department of Internal Medicine, The Jikei University School of Medicine, Tokyo, Japan.ORCID https://orcid.org/0000-0001-8172-3240
Mie WakabayashiResearch and Development Division, FUJIREBIO Inc., Tokyo, Japan.
Hidekazu NasuResearch and Development Division, FUJIREBIO Inc., Tokyo, Japan.
Noriko KatagiriResearch and Development Division, Advanced Life Science Institute, Inc., Tokyo, Japan.
Shintaro YagiResearch and Development Division, FUJIREBIO Inc., Tokyo, Japan.ORCID https://orcid.org/0000-0002-2671-4058

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundWe developed a fully automated quantitative immunoassay for the detection of prostaglandin E-major urinary metabolite (PGE-MUM). In this study, we evaluated the analytical performance of this assay.

methodsSensitivity, within-run reproducibility, correlation with radioimmunoassay (RIA), cross-reactivity, dilution linearity, spike recovery performance, analyte stability, and effects of coexisting substances were evaluated. The assay was also used to measure PGE-MUM in 211 healthy people.

resultsThe limit of detection and quantification were 1.0 and 1.3 ng/mL, respectively. When the assay was performed six times in a single run, the coefficient of variation ranged from 1.4% to 2.2%. The coefficient of correlation with a preceding RIA method was 0.970 with a correlation slope of 0.88. There was no cross-reactivity with PGE-MUM analogs. Linearity of dilution was confirmed at up to 16-fold dilution with assay results within 100 ± 20% of the theoretical values calculated based on the undiluted sample. Spike recovery was good and ranged from 94% to 101%. Analyte stability was tested by storing samples at 25°C for 6 days, 10°C for 1 month, and by performing up to five freeze-thaw cycles. Assay results were all within 100 ± 10%, the values measured before storage and before the freeze-thaw process. Assay results in healthy people ranged from 3.1 to 162.7 ng/mL (mean: 35.8 ng/mL). After correction for creatinine, the 95% confidence interval was 8.68-42.25 μg/g creatinine.

conclusionThe assay precisely detects PGE-MUM.

Indexed as

Immunoenzyme TechniquesLimit of DetectionLuminescent MeasurementsAdolescentAdultAgedFemaleHumansMaleMiddle AgedProstaglandins ERadioimmunoassayReproducibility of ResultsYoung AdultProstaglandins EimmunoassayPGE‐MUMprostaglandin Eurine

Identifiers

PMID39283757
PMCPMC11520938

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.