Evidence map›Paper›PMID 29371517›Full record

ArticleJournal of cardiovascular development and disease2015

Investigation of the Matrix Metalloproteinase-2 Gene in Patients with Non-Syndromic Mitral Valve Prolapse.

Maëlle Perrocheau, Soto Romuald Kiando, Déwi Vernerey, Christian Dina, Pilar Galan, Albert Hagege, Xavier Jeunemaitre, Nabila Bouatia-Naji

Open access · goldAbstract read
In one paragraph

Article in Journal of cardiovascular development and disease, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact, top 97% 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

1 citing paper in PubMed, 3 citations in OpenAlex.

  1. Article
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 5 institutions in 1 country.

Maëlle PerrocheauParis Cardiovascular Research Center, INSERM UMR970, 56 rue Leblanc, Paris F-75015, France. maelle.perrocheau@gmail.com.
Soto Romuald KiandoParis Cardiovascular Research Center, INSERM UMR970, 56 rue Leblanc, Paris F-75015, France. romuald.kiando@inserm.fr.
Déwi VernereyParis Cardiovascular Research Center, INSERM UMR970, 56 rue Leblanc, Paris F-75015, France. dvernerey@chu-besancon.fr.
Christian DinaINSERM UMR1087, CNRS UMR 6291, Institut du Thorax, 8 Quai Moncousu, Nantes F-44007, France. Christian.Dina@univ-nantes.fr.
Pilar GalanEquipe de Recherche en Epidémiologie Nutritionnelle (EREN), Centre d'Epidémiologie et Statistiques Sorbonne Paris Cité, Inserm (U1153), Inra (U1125), Cnam, Université Paris 13, COMUE Sorbonne Paris Cité, Bobigny F-93017, France. p.galan@uren.smbh.univ-paris13.fr.
Albert HagegeParis Cardiovascular Research Center, INSERM UMR970, 56 rue Leblanc, Paris F-75015, France. albert.hagege@aphp.fr.
Xavier JeunemaitreParis Cardiovascular Research Center, INSERM UMR970, 56 rue Leblanc, Paris F-75015, France. xavier.jeunemaitre@inserm.fr.
Nabila Bouatia-NajiParis Cardiovascular Research Center, INSERM UMR970, 56 rue Leblanc, Paris F-75015, France. nabila.bouatia-naji@inserm.fr.
Paris Cardiovascular Research Center · FRDélégation Paris 5 · FRCentre National de la Recherche Scientifique · FREquipe de Recherche en Epidémiologie Nutritionnelle · FRSorbonne Paris Cité · FR

Funding

Gates Foundation INV-010006
6 · The paper itself

Abstract

Non-syndromic mitral valve prolapse (MVP) is a common degenerative valvulopathy, predisposing to arrhythmia and sudden death. The etiology of MVP is suspected to be under genetic control, as supported by familial cases and its manifestation in genetic syndrome (e.g., Marfan syndrome). One candidate etiological mechanism is a perturbation of the extracellular matrix (ECM) remodeling of the valve. To test this hypothesis, we assessed the role of genetic variants in the matrix metalloproteinase 2 gene (

Indexed as

genetic associationmitral valve prolapseMMP2Single Nucelotide Polymorphism

Identifiers

PMID29371517
PMCPMC5753144
OpenAlexW1549956175

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.