Evidence map›Paper›PMID 31771070›Full record

ArticleJournal of Alzheimer's disease : JAD2020

A New Serum Biomarker Set to Detect Mild Cognitive Impairment and Alzheimer's Disease by Peptidome Technology.

Koji Abe, Jingwei Shang, Xiaowen Shi, Toru Yamashita, Nozomi Hishikawa, Mami Takemoto, Ryuta Morihara, Yumiko Nakano, Yasuyuki Ohta, Kentaro Deguchi and 18 more

Open access · hybridAbstract read
In one paragraph

Article in Journal of Alzheimer's disease : JAD, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
  2. Observational
  3. Review
  4. Peptidomic Approaches and Observations in Neurodegenerative Diseases.International journal of molecular sciences · 2022
    Review
  5. Review
  6. Review
  7. Article
  8. Review
  9. Article
  10. 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

28 authors at 8 institutions in 1 country.

Koji AbeDepartment of Neurology, Okayama University, Okayama, Japan.
Jingwei ShangDepartment of Neurology, Okayama University, Okayama, Japan.
Xiaowen ShiDepartment of Neurology, Okayama University, Okayama, Japan.
Toru YamashitaDepartment of Neurology, Okayama University, Okayama, Japan.
Nozomi HishikawaDepartment of Neurology, Okayama University, Okayama, Japan.
Mami TakemotoDepartment of Neurology, Okayama University, Okayama, Japan.
Ryuta MoriharaDepartment of Neurology, Okayama University, Okayama, Japan.
Yumiko NakanoDepartment of Neurology, Okayama University, Okayama, Japan.
Yasuyuki OhtaDepartment of Neurology, Okayama University, Okayama, Japan.
Kentaro DeguchiDepartment of Neurology, Okayama City Hospital, Okayama, Japan.
Masaki IkedaDepartment of Neurology, Gunma University, Graduate School of Medicine, Maebashi, Japan.
Yoshio IkedaDepartment of Neurology, Gunma University, Graduate School of Medicine, Maebashi, Japan.
Koichi OkamotoDepartment of Neurology, Geriatrics Research Institute and Hospital, Maebashi, Japan.
Mikio ShojiDepartment of Neurology, Geriatrics Research Institute and Hospital, Maebashi, Japan.
Masamitsu TakatamaDepartment of Neurology, Geriatrics Research Institute and Hospital, Maebashi, Japan.
Motohisa KojoDepartment of Neurology, Ako Chuo Hospital, Ako, Japan.
Takeshi KurodaDivision of Neurology, Department of Medicine, Showa University, School of Medicine, Tokyo, Japan.
Kenjiro OnoDivision of Neurology, Department of Medicine, Showa University, School of Medicine, Tokyo, Japan.
Noriyuki KimuraDepartment of Neurology, Faculty of Medicine, Oita University, Oita, Japan.
Etsuro MatsubaraDepartment of Neurology, Faculty of Medicine, Oita University, Oita, Japan.
Yosuke OsakadaDepartment of Neurology, Kurashiki Heisei Hospital, Kurashiki, Japan.
Yosuke WakutaniDepartment of Neurology, Kurashiki Heisei Hospital, Kurashiki, Japan.
Yoshiki TakaoDepartment of Neurology, Kurashiki Heisei Hospital, Kurashiki, Japan.
Yasuto HigashiDepartment of Neurology, Himeji Central Hospital, Himeji, Japan.
Kyoichi AsadaMembrane Protein and Ligand Analysis Center, Protosera Inc., Osaka, Japan.
Takehito SengaMembrane Protein and Ligand Analysis Center, Protosera Inc., Osaka, Japan.
Lyang-Ja LeeMembrane Protein and Ligand Analysis Center, Protosera Inc., Osaka, Japan.
Kenji TanakaMembrane Protein and Ligand Analysis Center, Protosera Inc., Osaka, Japan.
Okayama University · JPProtein Research Foundation · JPKurashiki Central Hospital · JPGunma University · JPOita University · JPShowa University · JPHimeji Medical Center · JPOkayama Prefecture · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundBecause dementia is an emerging problem in the world, biochemical markers of cerebrospinal fluid (CSF) and radio-isotopic analyses are helpful for diagnosing Alzheimer's disease (AD). Although blood sample is more feasible and plausible than CSF or radiological biomarkers for screening potential AD, measurements of serum amyloid- β (Aβ), plasma tau, and serum antibodies for Aβ1 - 42 are not yet well established.

objectiveWe aimed to identify a new serum biomarker to detect mild cognitive impairment (MCI) and AD in comparison to cognitively healthy control by a new peptidome technology.

methodsWith only 1.5μl of serum, we examined a new target plate "BLOTCHIP®" plus a matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF/MS) to discriminate control (n = 100), MCI (n = 60), and AD (n = 99). In some subjects, cognitive Mini-Mental State Examination (MMSE) were compared to positron emission tomography (PET) with Pittsburgh compound B (PiB) and the serum probability of dementia (SPD). The mother proteins of candidate serum peptides were examined in autopsied AD brains.

resultsApart from Aβ or tau, the present study discovered a new diagnostic 4-peptides-set biomarker for discriminating control, MCI, and AD with 87% of sensitivity and 65% of specificity between control and AD (***p < 0.001). MMSE score was well correlated to brain Aβ deposition and to SPD of AD. The mother proteins of the four peptides were upregulated for coagulation, complement, and plasticity (three proteins), and was downregulated for anti-inflammation (one protein) in AD brains.

conclusionThe present serum biomarker set provides a new, rapid, non-invasive, highly quantitative and low-cost clinical application for dementia screening, and also suggests an alternative pathomechanism of AD for neuroinflammation and neurovascular unit damage.

Indexed as

AgedAged, 80 and overAlzheimer DiseaseAmyloid beta-PeptidesAniline CompoundsBiomarkersCognitive DysfunctionFemaleHumansMaleMental Status and Dementia TestsMiddle AgedPeptidesPositron-Emission TomographyPredictive Value of TestsReference Values2-(4'-(methylamino)phenyl)-6-hydroxybenzothiazoleAmyloid beta-PeptidesAniline CompoundsBiomarkersMAPT protein, humanPeptidestau ProteinsThiazolesAlzheimer’s diseasebiomarkercoagulationcomplementMALDI-TOFmild cognitive impairmentneuroinflammationpeptidomeplasticity

Identifiers

PMID31771070
PMCPMC7029318
OpenAlexW2990020330

What OpenQuestion holds

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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.