Evidence map›Paper›PMID 30021611›Full record

ArticleAlzheimer's research & therapy2018

Alzheimer disease pathology and the cerebrospinal fluid proteome.

Loïc Dayon, Antonio Núñez Galindo, Jérôme Wojcik, Ornella Cominetti, John Corthésy, Aikaterini Oikonomidi, Hugues Henry, Martin Kussmann, Eugenia Migliavacca, India Severin and 2 more

Open access · goldAbstract read
In one paragraph

Article in Alzheimer's research & therapy, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 56 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
56citing papers in PubMed, 1 pooled it
8.2field-weighted citation impact, top 2% 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

56 citing papers in PubMed, 1 synthesis or guideline pooled it, 122 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Platelets mirror changes in the frontal lobe antioxidant system in Alzheimer's disease.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2025
    Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. 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

12 authors at 5 institutions in 2 countries.

Loïc DayonNestlé Institute of Health Sciences, Lausanne, Switzerland. loic.dayon@rd.nestle.com.ORCID 0000-0002-8499-270X
Antonio Núñez GalindoNestlé Institute of Health Sciences, Lausanne, Switzerland.
Jérôme WojcikPrecision for Medicine, Geneva, Switzerland.
Ornella CominettiNestlé Institute of Health Sciences, Lausanne, Switzerland.
John CorthésyNestlé Institute of Health Sciences, Lausanne, Switzerland.
Aikaterini OikonomidiOld Age Psychiatry, Department of Psychiatry, CHUV, Lausanne, Switzerland.
Hugues HenryDepartment of Laboratories, CHUV, Lausanne, Switzerland.
Martin KussmannNestlé Institute of Health Sciences, Lausanne, Switzerland.
Eugenia MigliavaccaNestlé Institute of Health Sciences, Lausanne, Switzerland.
India SeverinNestlé Institute of Health Sciences, Lausanne, Switzerland.
Gene L BowmanNestlé Institute of Health Sciences, Lausanne, Switzerland.
Julius PoppOld Age Psychiatry, Department of Psychiatry, CHUV, Lausanne, Switzerland.
Nestlé (Switzerland) · CHHôpital Orthopédique de la Suisse Romande · CHUniversity Hospital of Lausanne · CHUniversity of Auckland · NZUniversity of Geneva · CH

Funding

Outreach, Recruitment and Education CoreP30AG008017 · NIA · OREGON HEALTH & SCIENCE UNIVERSITY · PI KAYE, JEFFREY A · 1990 to 2019
$27.7M
NIA NIH HHS P30 AG008017
6 · The paper itself

Abstract

backgroundAltered proteome profiles have been reported in both postmortem brain tissues and body fluids of subjects with Alzheimer disease (AD), but their broad relationships with AD pathology, amyloid pathology, and tau-related neurodegeneration have not yet been fully explored. Using a robust automated MS-based proteomic biomarker discovery workflow, we measured cerebrospinal fluid (CSF) proteomes to explore their association with well-established markers of core AD pathology.

methodsCross-sectional analysis was performed on CSF collected from 120 older community-dwelling adults with normal (n = 48) or impaired cognition (n = 72). LC-MS quantified hundreds of proteins in the CSF. CSF concentrations of β-amyloid 1-42 (Aβ

resultsWe quantified 790 proteins in CSF samples with MS. Four CSF proteins showed an association with CSF Aβ

conclusionsWe used an MS-based proteomic workflow to profile the CSF proteome in relation to cerebral AD pathology. We report strong evidence of previously reported CSF proteins and several novel CSF proteins specifically associated with amyloid pathology or neuronal injury and tau hyperphosphorylation.

Indexed as

AgedAged, 80 and overAge FactorsAlzheimer DiseaseAmyloid beta-PeptidesApolipoproteins EChromatography, LiquidEducational StatusFemaleHumansMaleMiddle AgedNeuropsychological TestsPeptide FragmentsPhosphorylationProteomeAmyloid beta-Peptidesamyloid beta-protein (1-42)Apolipoproteins EPeptide FragmentsProteomeReelin ProteinRELN protein, humantau ProteinsAlzheimer diseaseAmyloidBiomarkerCerebrospinal fluidCSFMass spectrometryProteomicsTandem mass tagTau

Identifiers

PMID30021611
PMCPMC6052524
OpenAlexW2884550682

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.