Evidence map›Paper›PMID 27405842›Full record

ArticleScientific reports2016

Evaluation of physiological risk factors, oxidant-antioxidant imbalance, proteolytic and genetic variations of matrix metalloproteinase-9 in patients with pressure ulcer.

Khlifi Latifa, Sahli Sondess, Graiet Hajer, Ben-Hadj-Mohamed Manel, Khelil Souhir, Bouzidi Nadia, Jaballah Abir, Ferchichi Salima, Miled Abdelhedi

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
9.6field-weighted citation impact, top 3% 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

11 citing papers in PubMed, 25 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

9 authors at 1 institution in 1 country.

Khlifi LatifaBiochemistry Laboratory CHU Farhat HACHED, Sousse, Tunisia.
Sahli SondessBiochemistry Laboratory CHU Farhat HACHED, Sousse, Tunisia.
Graiet HajerBiochemistry Laboratory CHU Farhat HACHED, Sousse, Tunisia.
Ben-Hadj-Mohamed ManelBiochemistry Laboratory CHU Farhat HACHED, Sousse, Tunisia.
Khelil SouhirBiochemistry Laboratory CHU Farhat HACHED, Sousse, Tunisia.
Bouzidi NadiaBiochemistry Laboratory CHU Farhat HACHED, Sousse, Tunisia.
Jaballah AbirBiochemistry Laboratory CHU Farhat HACHED, Sousse, Tunisia.
Ferchichi SalimaBiochemistry Laboratory CHU Farhat HACHED, Sousse, Tunisia.
Miled AbdelhediBiochemistry Laboratory CHU Farhat HACHED, Sousse, Tunisia.
Hôpital Farhat Hached · TN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pressure ulcer (PU) remains a common worldwide problem in all health care settings, it is synonymous with suffering. PU is a complex disease that is dependent on a number of interrelated factors. It involves multiple mechanisms such as physiological risk factors, chronic inflammation, oxidant-antioxidant imbalance and proteolytic attack on extracellular matrix by matrix metalloproteinases (MMP). Therefore, we propose that these wounds lead to molecular variations that can be detected by assessing biomarkers. In this study, we aimed to evaluate the major clinical elements and biological scars in Tunisian patients suffering from PU. Consistently, non-healing wound remains a challenging clinical problem. The complex challenges of the wound environment, involving nutrient deficiencies, bacterial infection, as well as the critical role played by inflammatory cells, should be considered because of their negative impact on wound healing. In addition, an imbalance between pro-oxidants and antioxidant systems seems to be more aggravated in patients with PU compared to healthy subjects. Of interest, this study provides further evidence to support a core role of the biological activity of MMP-9 in the pathogenesis of PU and indicates that the MMP9-1562 C/T (rs 3918242) functional polymorphism is associated with protection against this disease.

Indexed as

Oxidative StressAdultAgedCase-Control StudiesFemaleHumansMaleMatrix Metalloproteinase 9Middle AgedNutritional StatusPolymorphism, Single NucleotidePressure UlcerProteolysisRisk FactorsTunisiaMatrix Metalloproteinase 9MMP9 protein, human

Identifiers

PMID27405842
PMCPMC4942564
OpenAlexW2474831119

What OpenQuestion holds

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LicenceCC BY
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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.