Evidence map›Paper›PMID 36319784›Full record

ArticleMolecular biology reports2023

Association of the matrix metalloproteinases (MMPs) family gene polymorphisms and the risk of coronavirus disease 2019 (COVID-19); implications of contribution for development of neurological symptoms in the COVID-19 patients.

Samaneh Ramezani, Fatemeh Ezzatifar, Tahereh Hojjatipour, Maryam Hemmatzadeh, Arezoo Gowhari Shabgah, Jamshid Gholizadeh Navashenaq, Saeed Aslani, Navid Shomali, Mohsen Arabi, Farhad Babaie and 6 more

Erratum issuedOpen access · bronzeAbstract read
In one paragraph

Article in Molecular biology reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
1.1field-weighted citation impact, top 21% 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

8 citing papers in PubMed, 1 synthesis or guideline pooled it, 12 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. Review
  5. Article
  6. Review
  7. Article
  8. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

16 authors at 8 institutions in 2 countries.

Samaneh RamezaniImmunology Research Center, Inflammation and Inflammatory Diseases Division, Medical School, Mashhad University of Medical Sciences, Mashhad, Iran.
Fatemeh EzzatifarMolecular and Cell Biology Research Center, Faculty of Medicine, Mazandaran University of Medical Sciences, Sari, Iran.
Tahereh HojjatipourDepartment of Hematology and Blood Transfusion, Students Research Centre, School of Allied Medicine, Tehran University of Medical Sciences, Tehran, Iran.
Maryam HemmatzadehStudent Research Committee, Tabriz University of Medical Sciences, Tabriz, Iran.
Arezoo Gowhari ShabgahSchool of Medicine, Bam University of Medical Sciences, Bam, Iran.
Jamshid Gholizadeh NavashenaqNoncommunicable Diseases Research Center, Bam University of Medical Sciences, Bam, Iran.
Saeed AslaniDepartment of Immunology, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran.
Navid ShomaliStudent Research Committee, Tabriz University of Medical Sciences, Tabriz, Iran.
Mohsen ArabiDepartment of Physiology, Pharmacology and Medical Physics, School of Medicine, Alborz University of Medical Sciences, Karaj, Iran.
Farhad BabaieCellular and Molecular Research Center, Urmia University of Medical Sciences, Urmia, Iran.
Farhad Jadidi-NiaraghImmunology Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.
Ramin HosseinzadehDepartment of Immunology, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran.
Fahimeh FeizisaniStudent Research Committee, Sarab Faculty of Medical Sciences, Sarab, Iran.
Sara KhodayarNon-Communicable Diseases Research Center, Alborz University of Medical Sciences, Karaj, Iran.
Roghaiyeh SafariMolecular and Cellular Epigenetics (GIGA), Belgium. Molecular and Cellular Biology (TERRA), Gembloux Agro-Bio Tech, University of Liege, Sart-Tilman Liège, University of Liege, Gembloux, Belgium. roghaiyeh.safari@gmail.com.
Hamed MohammadiNon-Communicable Diseases Research Center, Alborz University of Medical Sciences, Karaj, Iran. mohamadi.h86@gmail.com.ORCID http://orcid.org/0000-0001-8963-5990
Jahrom University of Medical Sciences · IRTabriz University of Medical Sciences · IRTehran University of Medical Sciences · IRBam University of Medical Sciences · IRMashhad University of Medical Sciences · IRMazandaran University of Medical Sciences · IRUniversity of Liège · BEUrmia University · IR

Funding

Alborz University of Medical Sciences 99-4209
6 · The paper itself

Abstract

backgroundSeemingly, the Matrix metalloproteinases (MMPs) play a role in the etiopathogenesis of coronavirus disease 2019 (COVID-19). Here in this study, we determined the association of MMP9 rs3918242, MMP3 rs3025058, and MMP2 rs243865 polymorphisms with the risk of COVID-19, especially in those with neurological syndrome (NS).

methodsWe enrolled 500 patients with COVID-19 and 500 healthy individuals. To genotype the target SNPs, the Real-time allelic discrimination technique was used. To determine serum levels of MMPs, Enzyme-linked immunosorbent assay (ELISA) was exerted.

resultsThe MMP9 gene rs3918242 and MMP3 gene rs3025058 SNP were significantly associated with increased COVID-19 risk and susceptibility to COVID-19 with NS. The serum level of MMP-9 and MMP-3 was significantly higher in COVID-19 cases compared with the healthy controls. Serum MMP-9 and MMP-3 levels were also higher in COVID-19 subjects with NS in comparison to the healthy controls. The polymorphisms in MMP genes were not associated with serum level of MMPs.

conclusionMMP9 and MMP3 gene polymorphisms increases the susceptibility to COVID-19 as well as COVID-19 with neurologic syndrome, but they probably have no role in the regulation of serum MMP-9 and MMP-3 levels.

Indexed as

COVID-19Matrix Metalloproteinase 9Genetic Predisposition to DiseaseGenotypeHumansMatrix Metalloproteinase 3Polymorphism, Single NucleotideMatrix Metalloproteinase 3Matrix Metalloproteinase 9Central nervous systemCoronavirus disease 2019Genetic polymorphismMatrix metalloproteinasesNeurological symptoms

Identifiers

PMID36319784
PMCPMC9628292
OpenAlexW4308159903

What OpenQuestion holds

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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.