Evidence map›Paper›PMID 39558606›Full record

ArticleJournal of Alzheimer's disease : JAD2025

Tear fluid reflects the altered protein expressions of Alzheimer's disease patients in proteins involved in protein repair and clearance system or the regulation of cytoskeleton.

Virve Kärkkäinen, Sanna Hannonen, Minna Rusanen, Juha-Matti Lehtola, Toni Saari, Hannu Uusitalo, Ville Leinonen, Bernd Thiede, Kai Kaarniranta, Anne M Koivisto and 1 more

Abstract read
In one paragraph

Article in Journal of Alzheimer's disease : JAD, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Neuroinflammation Markers in Tear Fluid of Mild Alzheimer's Disease.Journal of molecular neuroscience : MN · 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

11 authors.

Virve KärkkäinenNeuroCenter, Neurology, Kuopio University Hospital, Kuopio, Finland.ORCID 0009-0007-0918-1388
Sanna HannonenNeuroCenter, Neurology, Kuopio University Hospital, Kuopio, Finland.
Minna RusanenNeuroCenter, Neurology, Kuopio University Hospital, Kuopio, Finland.
Juha-Matti LehtolaNeurology, Institute of Clinical Medicine, School of Medicine, University of Eastern Finland, Kuopio, Finland.
Toni SaariInstitute for Molecular Medicine Finland (FIMM), HiLIFE, University of Helsinki, Helsinki, Finland.
Hannu UusitaloFaculty of Medicine and Health Technology, Eye and Vision Research, Tampere University, Tampere, Finland.
Ville LeinonenNeuroCenter, Neurosurgery, Kuopio University Hospital, Kuopio, Finland.
Bernd ThiedeDepartment of Biosciences, University of Oslo, Oslo, Norway.
Kai KaarnirantaDepartment of Ophthalmology, Institute of Clinical Medicine, School of Medicine, University of Eastern Finland and Kuopio University Hospital, Kuopio, Finland.
Anne M KoivistoNeuroCenter, Neurology, Kuopio University Hospital, Kuopio, Finland.
Tor Paaske UtheimFaculty of Dentistry, Institute of Oral Biology, University of Oslo, Oslo, Norway|.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BackgroundNew biomarkers that improve diagnosis of Alzheimer's disease (AD) are warranted. Tear fluid (TF) containing variety of proteins that reflect pathophysiological changes of systemic diseases makes TF proteins potential biomarker candidates for AD.ObjectiveWe investigated the expression levels of TF proteins in persons with mild AD and cognitively healthy controls (CO) to find out if altered proteins may link to the AD pathophysiology.MethodsWe analyzed the data of the 53 study participants (34 COs, mean age 71 and Mini-Mental State Examination (MMSE) 28.9 ± 1.4 and 19 persons with AD, CDR 0.5-1, mean age 71 and MMSE 23.8 ± 2.8). All went through neurological status examination, cognitive tests, and ophthalmological examination. TF was collected using Schirmer strips. The TF protein content was evaluated via mass spectrometry-based proteomics and label-free quantification.ResultsEleven proteins having a role either in protein repair and clearance system, or regulation of cytoskeleton, showed altered expression in AD group compared to CO group. Seven of them were significantly (

Indexed as

Alzheimer DiseaseCytoskeletonEye ProteinsTearsAgedAged, 80 and overBiomarkersFemaleHumansMaleMiddle AgedProteomicsBiomarkersEye ProteinsAlzheimer's diseasechaperonescytoskeletonpathophysiologyproteomicstear fluid

Identifiers

PMID39558606
PMCPMC13066464

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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.