Evidence map›Paper›PMID 35816043›Full record

ArticleInvestigative ophthalmology & visual science2022

Altered Regulation of mRNA and miRNA Expression in Epithelial and Stromal Tissue of Keratoconus Corneas.

Tanja Stachon, Mahsa Nastaranpour, Berthold Seitz, Eckart Meese, Lorenz Latta, Suphi Taneri, Navid Ardjomand, Nóra Szentmáry, Nicole Ludwig

Open access · goldAbstract read
In one paragraph

Article in Investigative ophthalmology & visual science, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 pooled it
2.2field-weighted citation impact, top 13% 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

14 citing papers in PubMed, 1 synthesis or guideline pooled it, 15 citations in OpenAlex.

  1. Pooled it
  2. Update on the Physiopathology of Keratoconus.Medical sciences (Basel, Switzerland) · 2026
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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

9 authors at 3 institutions in 2 countries.

Tanja StachonDr. Rolf M. Schwiete Center for Limbal Stem Cell and Aniridia Research, Homburg (Saar), Germany.
Mahsa NastaranpourDr. Rolf M. Schwiete Center for Limbal Stem Cell and Aniridia Research, Homburg (Saar), Germany.
Berthold SeitzDepartment of Ophthalmology, Saarland University Medical Center, Homburg (Saar), Germany.
Eckart MeeseDepartment of Human Genetics and Center for Human and Molecular Biology, Saarland University, Homburg (Saar), Germany.
Lorenz LattaDr. Rolf M. Schwiete Center for Limbal Stem Cell and Aniridia Research, Homburg (Saar), Germany.
Suphi TaneriCenter for Refractive Surgery, Eye Department at St. Francis Hospital, Muenster, Germany.
Navid ArdjomandVision Center for Eye Laser and Eye Surgery, Graz, Austria.
Nóra SzentmáryDr. Rolf M. Schwiete Center for Limbal Stem Cell and Aniridia Research, Homburg (Saar), Germany.
Nicole LudwigDepartment of Human Genetics and Center for Human and Molecular Biology, Saarland University, Homburg (Saar), Germany.
Saarland University · DEFrancis Hospital · DESemmelweis University · HU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: Evaluation of mRNA and microRNA (miRNA) expression in epithelium and stroma of patients with keratoconus. Methods: The epithelium and stroma of eight corneas of eight patients with keratoconus and eight corneas of eight non-keratoconus healthy controls were studied separately. RNA was extracted, and mRNA and miRNA analyses were performed using microarrays. Differentially expressed mRNAs and miRNAs in epithelial and stromal keratoconus samples compared to healthy controls were identified. Selected genes and miRNAs were further validated using RT-qPCR. Results: We discovered 170 epithelial and 1498 stromal deregulated protein-coding mRNAs in KC samples. In addition, in epithelial samples 180 miRNAs and in stromal samples 379 miRNAs were significantly deregulated more than twofold compared to controls. Pathway analysis revealed enrichment of metabolic and axon guidance pathways for epithelial cells and enrichment of metabolic, mitogen-activated protein kinase (MAPK), and focal adhesion pathways for stromal cells. Conclusions: This study demonstrates significant differences in the expression and regulation of mRNAs and miRNAs in the epithelium and stroma of Patients with KC. Also, in addition to the well-known target candidates, we were able to identify further genes and miRNAs that may be associated with keratoconus. Signaling pathways influencing metabolic changes and cell contacts are affected in epithelial and stromal cells of patients with keratoconus.

Indexed as

KeratoconusMicroRNAsCorneaHumansMicroarray AnalysisRNA, MessengerMicroRNAsRNA, Messenger

Identifiers

PMID35816043
PMCPMC9284461
OpenAlexW4285043208

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.