Evidence map›Paper›PMID 26120586›Full record

ArticleBioMed research international2015

Altered Expression Levels of MMP1, MMP9, MMP12, TIMP1, and IL-1β as a Risk Factor for the Elevated IOP and Optic Nerve Head Damage in the Primary Open-Angle Glaucoma Patients.

Lukasz Markiewicz, Dariusz Pytel, Bartosz Mucha, Katarzyna Szymanek, Jerzy Szaflik, Jacek P Szaflik, Ireneusz Majsterek

Open access · hybridAbstract read
In one paragraph

Article in BioMed research international, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
1.7field-weighted citation impact, top 17% 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

33 citing papers in PubMed, 56 citations in OpenAlex.

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  20. Cerium Oxide Nanoparticles Alleviate Hepatic Fibrosis Phenotypes In Vitro.International journal of molecular sciences · 2021
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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

7 authors at 3 institutions in 2 countries.

Lukasz MarkiewiczDepartment of Clinical Chemistry and Biochemistry, Medical University of Lodz, 90-647 Lodz, Poland.
Dariusz PytelDepartment of Cancer Biology, AFCRI, Perelman School of Medicine, University of Pennsylvania, PA 19104, USA ; Department of Biochemistry and Molecular Biology, Hollings Cancer Center, Medical University of South Carolina, Charleston, SC 29425, USA.
Bartosz MuchaDepartment of Clinical Chemistry and Biochemistry, Medical University of Lodz, 90-647 Lodz, Poland.
Katarzyna SzymanekDepartment of Ophthalmology, Medical University of Warsaw, 03-709 Warsaw, Poland.
Jerzy SzaflikDepartment of Ophthalmology, Medical University of Warsaw, 03-709 Warsaw, Poland.
Jacek P SzaflikDepartment of Ophthalmology, Medical University of Warsaw, 03-709 Warsaw, Poland.
Ireneusz MajsterekDepartment of Clinical Chemistry and Biochemistry, Medical University of Lodz, 90-647 Lodz, Poland.
Medical University of Warsaw · PLMedical University of Lodz · PLMedical University of South Carolina · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The aim of presented work was to analyze the impact of particular polymorphic changes in the promoter regions of the -1607 1G/2G MMP1, -1562 C/T MMP9, -82 A/G MMP12, -511 C/T IL-1β, and 372 T/C TIMP1 genes on their expression level in POAG patients. Blood and aqueous humor samples acquired from 50 patients with POAG and 50 control subjects were used for QPCR and protein levels analysis by ELISA. In vivo promoter activity assays were carried on HTM cells using dual luciferase assay. All studied subjects underwent ophthalmic examination, including BCVA, intraocular pressure, slit-lamp examination, gonioscopy, HRT, and OCT scans. Patients with POAG are characterized by an increased mRNA expression of MMP1, MMP9, MMP12, and IL-1β genes as compared to the control group (P < 0.001). Aqueous humor acquired from patients with POAG displayed increased protein expression of MMP1, MMP9, MMP12, and IL-1β compared to the control group (P < 0.001). Allele -1607 1G of MMP1 gene possesses only 42,91% of the -1607 2G allele transcriptional activity and allele -1562 C of MMP9 gene possesses only 21,86% of the -1562 T allele. Increased expression levels of metalloproteinases can be considered as a risk factor for the development of POAG.

Indexed as

AgedAged, 80 and overFemaleGene Expression RegulationGlaucoma, Open-AngleHumansInterleukin-1betaMaleMatrix Metalloproteinase 1Matrix Metalloproteinase 12Matrix Metalloproteinase 9Optic DiskRisk FactorsTissue Inhibitor of Metalloproteinase-1Interleukin-1betaMatrix Metalloproteinase 1Matrix Metalloproteinase 12Matrix Metalloproteinase 9MMP12 protein, humanMMP1 protein, humanMMP9 protein, humanTIMP1 protein, humanTissue Inhibitor of Metalloproteinase-1

Identifiers

PMID26120586
PMCPMC4442285
OpenAlexW1601210246

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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.