Evidence map›Paper›PMID 29600353›Full record

ArticleLung2018

The Variants in the 3' Untranslated Region of the Matrix Metalloproteinase 9 Gene as Modulators of Treatment Outcome in Children with Asthma.

Sandra Dragicevic, Mitja Kosnik, Aleksandra Divac Rankov, Matija Rijavec, Katarina Milosevic, Peter Korosec, Maja Skerbinjek Kavalar, Aleksandra Nikolic

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Article in Lung, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.5field-weighted citation impact, top 34% 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

2 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Pharmacogenetics of Pediatric Asthma: Current Perspectives.Pharmacogenomics and personalized medicine · 2020
    Review
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

8 authors at 4 institutions in 3 countries.

Sandra DragicevicInstitute of Molecular Genetics and Genetic Engineering, University of Belgrade, Vojvode Stepe 444a, 11010, Belgrade, Serbia. sandra.d@imgge.bg.ac.rs.ORCID http://orcid.org/0000-0002-1602-1880
Mitja KosnikUniversity Clinic of Respiratory and Allergic Diseases Golnik, Golnik 36, 4204, Golnik, Slovenia.
Aleksandra Divac RankovInstitute of Molecular Genetics and Genetic Engineering, University of Belgrade, Vojvode Stepe 444a, 11010, Belgrade, Serbia.
Matija RijavecUniversity Clinic of Respiratory and Allergic Diseases Golnik, Golnik 36, 4204, Golnik, Slovenia.
Katarina MilosevicDepartment of Pulmonology and Allergology, University Children's Hospital, Tirsova 10, 11000, Belgrade, Serbia.
Peter KorosecUniversity Clinic of Respiratory and Allergic Diseases Golnik, Golnik 36, 4204, Golnik, Slovenia.
Maja Skerbinjek KavalarUniversity Clinical Centre Maribor, Ljubljanska Ulica 5, 2000, Maribor, Slovenia.
Aleksandra NikolicInstitute of Molecular Genetics and Genetic Engineering, University of Belgrade, Vojvode Stepe 444a, 11010, Belgrade, Serbia.
University Clinic of Pulmonary and Allergic Diseases Golnik · SIUniversity of Belgrade · RSUniversity Children's Hospital, Belgrade · RSUniversity of Maribor · SI

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThe maintaining of asthma control is difficult due to high variability in response to therapy among patients. Since matrix metalloproteinase 9 (MMP9) is implicated in inflammation and remodeling of asthmatic airways, it could be associated with adequate response to asthma therapy. The aim of this study was to investigate whether variants in 3' end of the MMP9 gene are associated with clinical phenotype and responsiveness to treatment in children with asthma.

methodsThe study included 127 asthmatic children from Slovenia. Variants in the 3' end of the MMP9 gene were analyzed by direct DNA sequencing and the obtained results were correlated with clinical parameters.

resultsTwo variants were detected, rs13925 and rs20544. For the variant rs20544, statistically significant difference in airway hyperresponsiveness (p = 0.011) and asthma control (p = 0.049) between genotypes was found. Patients with TT genotype had lower airway sensitivity, and after 12 months of treatment showed significant improvement in Asthma Control Test (ACT) scores compared to CC and CT genotype. For the variant rs13925, the association with lung function was observed. The carriers of A allele showed noticeable improvement of lung function after the first 6 months of treatment in comparison to the carriers of G allele (p = 0.046).

conclusionThe main finding of our study is the association of MMP9 genotypes rs20544 TT and rs13925 AA and AG with better asthma control, and indirectly better response to treatment. Based on these results, MMP9 deserves further research as a potential predictive biomarker for asthma.

Indexed as

3' Untranslated RegionsAcetatesAdolescentAnti-Asthmatic AgentsAsthmaBronchodilator AgentsChildCyclopropanesFemaleFluticasoneForced Expiratory VolumeGenetic VariationHumansMaleMatrix Metalloproteinase 9Nitric Oxide3' Untranslated RegionsAcetatesAnti-Asthmatic AgentsBronchodilator AgentsCyclopropanesFluticasoneMatrix Metalloproteinase 9MMP9 protein, humanmontelukastNitric OxideQuinolinesSulfides3′ UTRGenotypeMatrix metalloproteinaseVariant

Identifiers

PMID29600353
OpenAlexW2795784967

What OpenQuestion holds

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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.