Evidence map›Paper›PMID 33337370›Full record

ArticleJournal of Alzheimer's disease : JAD2021

Quantitative Measurement of Cerebrospinal Fluid Amyloid-β Species by Mass Spectrometry.

Yusuke Seino, Takumi Nakamura, Tomoo Harada, Naoko Nakahata, Takeshi Kawarabayashi, Tetsuya Ueda, Masamitsu Takatama, Mikio Shoji

Open access · greenAbstract read
In one paragraph

Article in Journal of Alzheimer's disease : JAD, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

11 citing papers in PubMed, 22 citations in OpenAlex.

  1. Review
  2. Review
  3. New Research on Biomarkers in Alzheimer's Continuum.Reviews on recent clinical trials · 2025
    Review
  4. Thioflavin T in-gel staining forFrontiers in molecular biosciences · 2025
    Article
  5. Article
  6. Article
  7. The ZmbHLH47-ZmSnRK2.9 Module Promotes Drought Tolerance in Maize.International journal of molecular sciences · 2024
    Article
  8. Annual stability of the plasma Aß40/42 ratio and associated factors.Annals of clinical and translational neurology · 2023
    Article
  9. Article
  10. Review
  11. 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

8 authors at 3 institutions in 1 country.

Yusuke SeinoDepartment of Neurology, Hirosaki National Hospital, Hirosaki, Aomori, Japan.
Takumi NakamuraDepartment of Neurology, Gunma University Graduate School of Medicine, Maebashi, Gunma, Japan.
Tomoo HaradaBioanalysis Department, LSI Medience Corporation, Itabashi-ku, Tokyo, Japan.
Naoko NakahataDepartment of Speech-Language-Hearing Therapy, Hirosaki University of Health and Welfare, Hirosaki, Aomori, Japan.
Takeshi KawarabayashiDementia Center, Geriatrics Research Institute and Hospital, Maebashi, Gunma, Japan.
Tetsuya UedaBioanalysis Department, LSI Medience Corporation, Itabashi-ku, Tokyo, Japan.
Masamitsu TakatamaDementia Center, Geriatrics Research Institute and Hospital, Maebashi, Gunma, Japan.
Mikio ShojiDementia Center, Geriatrics Research Institute and Hospital, Maebashi, Gunma, Japan.
Gunma University · JPHirosaki National Hospital · JPHirosaki University of Health and Welfare · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHigh sensitivity liquid chromatography mass spectrometry (LC-MS/MS) was recently introduced to measure amyloid-β (Aβ) species, allowing for a simultaneous assay that is superior to ELISA, which requires more assay steps with multiple antibodies.

objectiveWe validated the Aβ1-38, Aβ1-40, Aβ1-42, and Aβ1-43 assay by LC-MS/MS and compared it with ELISA using cerebrospinal fluid (CSF) samples to investigate its feasibility for clinical application.

methodsCSF samples from 120 subjects [8 Alzheimer's disease (AD) with dementia (ADD), 2 mild cognitive dementia due to Alzheimer's disease (ADMCI), 14 cognitively unimpaired (CU), and 96 neurological disease subjects] were analyzed. Aβ species were separated using the Shimadzu Nexera X2 system and quantitated using a Qtrap 5500 LC-MS/MS system. Aβ1-40 and Aβ1-42 levels were validated using ELISA.

resultsCSF levels in CU were 666±249 pmol/L in Aβ1-38, 2199±725 pmol/L in Aβ1-40, 153.7±79.7 pmol/L in Aβ1-42, and 9.78±4.58 pmol/L in Aβ1-43. The ratio of the amounts of Aβ1-38, Aβ1-40, Aβ1-42, and Aβ1-43 was approximately 68:225:16:1. Linear regression analyses showed correlations among the respective Aβ species. Both Aβ1-40 and Aβ1-42 values were strongly correlated with ELISA measurements. No significant differences were observed in Aβ1-38 or Aβ1-40 levels between AD and CU. Aβ1-42 and Aβ1-43 levels were significantly lower, whereas the Aβ1-38/1-42, Aβ1-38/1-43, and Aβ1-40/Aβ1-43 ratios were significantly higher in AD than in CU. The basic assay profiles of the respective Aβ species were adequate for clinical usage.

conclusionA quantitative LC-MS/MS assay of CSF Aβ species is as reliable as specific ELISA for clinical evaluation of CSF biomarkers for AD.

Indexed as

Chromatography, High Pressure LiquidTandem Mass SpectrometryAmyloid beta-PeptidesBiomarkersHumansAmyloid beta-PeptidesBiomarkersAβ1-38Aβ1-40Aβ1-42 Aβ1-43cerebrospinal fluidELISAliquid chromatography mass spectrometry

Identifiers

PMID33337370
PMCPMC7902963
OpenAlexW3112206052

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.