Evidence map›Paper›PMID 18784838›Full record

ArticlePloS one2008

Matrix metalloproteinase gene polymorphisms and bronchopulmonary dysplasia: identification of MMP16 as a new player in lung development.

Alice Hadchouel, Fabrice Decobert, Marie-Laure Franco-Montoya, Isabelle Halphen, Pierre-Henri Jarreau, Olivier Boucherat, Emmanuel Martin, Alexandra Benachi, Serge Amselem, Jacques Bourbon and 2 more

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in PloS one, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT00904774 (Polymorphisms of Genes Controlling Alveolar Development and Risk of Bronchopulmonary Dysplasia), which is not on this map. Cited by 35 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed, 1 pooled it
2.5field-weighted citation impact, top 11% 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.

NCT00904774 unknown statusnot on this mapstarted 2009, after this paper: background citation

Polymorphisms of Genes Controlling Alveolar Development and Risk of Bronchopulmonary Dysplasia

TypeobservationalSponsorCentre Hospitalier Intercommunal CreteilRan2009Enrolled800ConditionsBronchopulmonary Dysplasia
3 · Its place in the literature

Who cites it

35 citing papers in PubMed, 1 synthesis or guideline pooled it, 71 citations in OpenAlex.

  1. Pooled it
  2. Trial
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  4. Review
  5. Article
  6. Article
  7. Review
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  10. Article
  11. Role of the LRP1-pPyk2-MMP9 pathway in hyperoxia-induced lung injury in neonatal rats.Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics · 2021
    Article
  12. Article
  13. CircRNA has_circ_0001806 promotes hepatocellular carcinoma progression via the miR-193a-5p/MMP16 pathway.Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologica · 2021
    Article
  14. Association of Gene Polymorphism ofOpen access Macedonian journal of medical sciences · 2019
    Article
  15. Article
  16. Article
  17. Biochemical and Biological Attributes of Matrix Metalloproteinases.Progress in molecular biology and translational science · 2017
    Review
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  19. Review
  20. 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

12 authors at 4 institutions in 1 country.

Alice HadchouelINSERM, Unité 841, IMRB, équipe 06, Créteil, France.
Fabrice Decobert
Marie-Laure Franco-Montoya
Isabelle Halphen
Pierre-Henri Jarreau
Olivier Boucherat
Emmanuel Martin
Alexandra Benachi
Serge Amselem
Jacques Bourbon
Claude Danan
Christophe Delacourt
Inserm · FRDélégation Paris 5 · FRHôpital Necker-Enfants Malades · FRIntegraGen (France) · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAlveolarization requires coordinated extracellular matrix remodeling, a process in which matrix metalloproteinases (MMPs) play an important role. We postulated that polymorphisms in MMP genes might affect MMP function in preterm lungs and thus influence the risk of bronchopulmonary dysplasia (BPD). METHODS AND

findingsTwo hundred and eighty-four consecutive neonates with a gestational age of <28 weeks were included in this prospective study. Forty-five neonates developed BPD. Nine single-nucleotide polymorphisms (SNPs) were sought in the MMP2, MMP14 and MMP16 genes. After adjustment for birth weight and ethnic origin, the TT genotype of MMP16 C/T (rs2664352) and the GG genotype of MMP16 A/G (rs2664349) were found to protect from BPD. These genotypes were also associated with a smaller active fraction of MMP2 and with a 3-fold-lower MMP16 protein level in tracheal aspirates collected within 3 days after birth. Further evaluation of MMP16 expression during the course of normal human and rat lung development showed relatively low expression during the canalicular and saccular stages and a clear increase in both mRNA and protein levels during the alveolar stage. In two newborn rat models of arrested alveolarization the lung MMP16 mRNA level was less than 50% of normal.

conclusionsMMP16 may be involved in the development of lung alveoli. MMP16 polymorphisms appear to influence not only the pulmonary expression and function of MMP16 but also the risk of BPD in premature infants.

Indexed as

Gene Expression RegulationPolymorphism, GeneticAnimalsBronchopulmonary DysplasiaFemaleHumansInfant, NewbornInfant, PrematureLungMaleMatrix Metalloproteinase 16Prospective StudiesRatsRats, Sprague-DawleySurface-Active AgentsTracheaMatrix Metalloproteinase 16Surface-Active Agents

Identifiers

PMID18784838
PMCPMC2527515
OpenAlexW2060737085

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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.