Evidence map›Paper›PMID 27412345›Full record

ArticleMolecular diagnosis & therapy2016

MMP-2 (-1306 C/T) Polymorphism Affects Serum Matrix Metalloproteinase (MMP)-2 Levels and Correlates with Chronic Obstructive Pulmonary Disease Severity: A Case-Control Study of MMP-1 and -2 in a Tunisian Population.

Sarra Bchir, Hela Ben Nasr, Amel Ben Anes, Mohamed Benzarti, Abdelhamid Garrouch, Zouhair Tabka, Karim Chahed

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Article in Molecular diagnosis & therapy, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.8field-weighted citation impact, top 24% 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

4 citing papers in PubMed, 8 citations in OpenAlex.

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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 1 country.

Sarra BchirUnité de recherche UR12ES06, Physiologie de l'Exercice et Physiopathologie: de l'Intégré au Moléculaire «Biologie, Médecine et Santé», Faculté de Médecine de Sousse, Université de Sousse, Sousse, Tunisia.
Hela Ben NasrUnité de recherche UR12ES06, Physiologie de l'Exercice et Physiopathologie: de l'Intégré au Moléculaire «Biologie, Médecine et Santé», Faculté de Médecine de Sousse, Université de Sousse, Sousse, Tunisia.
Amel Ben AnesUnité de recherche UR12ES06, Physiologie de l'Exercice et Physiopathologie: de l'Intégré au Moléculaire «Biologie, Médecine et Santé», Faculté de Médecine de Sousse, Université de Sousse, Sousse, Tunisia.
Mohamed BenzartiService de Pneumo-Allergologie, CHU Farhat Hached, Sousse, Tunisia.
Abdelhamid GarrouchService de Pneumo-Allergologie, CHU Farhat Hached, Sousse, Tunisia.
Zouhair TabkaUnité de recherche UR12ES06, Physiologie de l'Exercice et Physiopathologie: de l'Intégré au Moléculaire «Biologie, Médecine et Santé», Faculté de Médecine de Sousse, Université de Sousse, Sousse, Tunisia.
Karim ChahedUnité de recherche UR12ES06, Physiologie de l'Exercice et Physiopathologie: de l'Intégré au Moléculaire «Biologie, Médecine et Santé», Faculté de Médecine de Sousse, Université de Sousse, Sousse, Tunisia. k.chahed@yahoo.fr.
University of Sousse · TNHôpital Farhat Hached · TNUniversity of Monastir · TN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThe aim of this study was to determine the role of MMP-1 (-1607 1G/2G; -519 A/G) and MMP-2 (-1306 C/T; -735 C/T) polymorphisms in the development and severity of chronic obstructive pulmonary disease (COPD) in Tunisian patients. We also evaluated the impact of these genetic variants on serum levels of the corresponding proteins.

methodsThe study included 138 patients with COPD and 216 healthy controls. Pulmonary function was evaluated using body plethysmography, and COPD severity was determined based on forced expiratory volume in 1 s (FEV1%). MMP-1 and MMP-2 variants were determined by polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP), while serum matrix metalloproteinase (MMP)-1 and -2 levels were determined by enzyme-linked immunosorbent assay (ELISA) and activity of MMP-2 was determined by gelatin zymography.

resultsNo significant associations were found between genetic variations in MMP-1 and MMP-2 variants and the risk of development of COPD. Additionally, no significant impact of the MMP-1 (-1607 1G/2G; -519 A/G) and MMP-2 (-735 C/T) polymorphisms was observed on the respective protein levels and clinical parameters of the disease. Interestingly, a significant correlation was identified between the MMP-2 (-1306) C/T and disease severity [p = 0.01; Bonferroni corrected p value (p

conclusionOur data suggest that, although MMP-1 (-1607 1G/2G; -519 A/G) and MMP-2 (-735 C/T) may not affect COPD risk and clinical parameters, the MMP-2 (-1306C/T) variant was correlated to COPD severity. These findings could be related to alterations in the level and activity of MMP-2 in serum from patients carrying the (-1306) CC genotype.

Indexed as

Polymorphism, Single NucleotideAdultAgedBody Mass IndexCase-Control StudiesEnzyme-Linked Immunosorbent AssayFemaleGene FrequencyGenetic Predisposition to DiseaseGenotyping TechniquesHumansLinear ModelsLogistic ModelsMaleMatrix Metalloproteinase 1Matrix Metalloproteinase 2Matrix Metalloproteinase 1Matrix Metalloproteinase 2MMP1 protein, humanMMP2 protein, human

Identifiers

PMID27412345
OpenAlexW2460767744

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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.