Evidence map›Paper›PMID 31659197›Full record

Trial reportScientific reports2019

Proteins and microRNAs are differentially expressed in tear fluid from patients with Alzheimer's disease.

Aidan Kenny, Eva M Jiménez-Mateos, María Ascensión Zea-Sevilla, Alberto Rábano, Pablo Gili-Manzanaro, Jochen H M Prehn, David C Henshall, Jesús Ávila, Tobias Engel, Félix Hernández

Abstract readClinical Trial
In one paragraph

Trial report in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 67 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
67citing papers in PubMed, 1 pooled it
–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

67 citing papers in PubMed, 1 synthesis or guideline pooled it.

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  16. Neuroinflammation Markers in Tear Fluid of Mild Alzheimer's Disease.Journal of molecular neuroscience : MN · 2025
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7 more citing papers are in PubMed but not listed here.

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.

Aidan KennyDepartment of Physiology & Medical Physics, Royal College of Surgeons in Ireland, D02YN77, Dublin, Ireland.
Eva M Jiménez-MateosDiscipline of Physiology, School of Medicine, Trinity College Dublin, The University of Dublin, Dublin, Ireland.
María Ascensión Zea-SevillaDepartment of Neuropathology and Tissue Bank, Fundación CIEN, Instituto de Salud Carlos III, Madrid, Spain.
Alberto RábanoDepartment of Neuropathology and Tissue Bank, Fundación CIEN, Instituto de Salud Carlos III, Madrid, Spain.
Pablo Gili-ManzanaroServicio de Oftalmología, Fundación Hospital Alcorcón, Madrid, Spain.ORCID http://orcid.org/0000-0002-5013-4459
Jochen H M PrehnDepartment of Physiology & Medical Physics, Royal College of Surgeons in Ireland, D02YN77, Dublin, Ireland.
David C HenshallDepartment of Physiology & Medical Physics, Royal College of Surgeons in Ireland, D02YN77, Dublin, Ireland.
Jesús ÁvilaCentro de Biología Molecular "Severo Ochoa" (CSIC-UAM), c/Nicolás Cabrera 1, Universidad Autónoma de Madrid, Cantoblanco, 28049, Madrid, Spain.ORCID http://orcid.org/0000-0002-6288-0571
Tobias EngelDepartment of Physiology & Medical Physics, Royal College of Surgeons in Ireland, D02YN77, Dublin, Ireland. tengel@rcsi.ie.
Félix HernándezCentro de Biología Molecular "Severo Ochoa" (CSIC-UAM), c/Nicolás Cabrera 1, Universidad Autónoma de Madrid, Cantoblanco, 28049, Madrid, Spain. fhernandez@cbm.csic.es.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Alzheimer's disease (AD) is characterized by a progressive loss of neurons and cognitive functions. Therefore, early diagnosis of AD is critical. The development of practical and non-invasive diagnostic tests for AD remains, however, an unmet need. In the present proof-of-concept study we investigated tear fluid as a novel source of disease-specific protein and microRNA-based biomarkers for AD development using samples from patients with mild cognitive impairment (MCI) and AD. Tear protein content was evaluated via liquid chromatography-mass spectrometry and microRNA content was profiled using a genome-wide high-throughput PCR-based platform. These complementary approaches identified enrichment of specific proteins and microRNAs in tear fluid of AD patients. In particular, we identified elongation initiation factor 4E (eIF4E) as a unique protein present only in AD samples. Total microRNA abundance was found to be higher in tears from AD patients. Among individual microRNAs, microRNA-200b-5p was identified as a potential biomarker for AD with elevated levels present in AD tear fluid samples compared to controls. Our study suggests that tears may be a useful novel source of biomarkers for AD and that the identification and verification of biomarkers within tears may allow for the development of a non-invasive and cost-effective diagnostic test for AD.

Indexed as

AgedAged, 80 and overAlzheimer DiseaseBiomarkersEukaryotic Initiation Factor-4EFemaleHumansMaleMicroRNAsTearsBiomarkersEIF4E protein, humanEukaryotic Initiation Factor-4EMicroRNAsMIRN200 microRNA, human

Identifiers

PMID31659197
PMCPMC6817868

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Registered trials

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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.