Evidence map›Paper›PMID 36873395›Full record

ReviewFrontiers in cardiovascular medicine2023

Genetics and pathophysiology of mitral valve prolapse.

Constance Delwarde, Romain Capoulade, Jean Mérot, Solena Le Scouarnec, Nabila Bouatia-Naji, Mengyao Yu, Olivier Huttin, Christine Selton-Suty, Jean-Marc Sellal, Nicolas Piriou and 3 more

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in cardiovascular medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed, 1 pooled it
9.2field-weighted citation impact, top 1% 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

25 citing papers in PubMed, 1 synthesis or guideline pooled it, 42 citations in OpenAlex.

  1. Pooled it
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  5. Mitral Annular Disjunction and Coalescing Myths in Cardiology.Arrhythmia & electrophysiology review · 2026
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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

13 authors at 6 institutions in 2 countries.

Constance DelwardeNantes Université, CHU Nantes, CNRS, INSERM, L'institut du Thorax, Nantes, France.
Romain CapouladeNantes Université, CHU Nantes, CNRS, INSERM, L'institut du Thorax, Nantes, France.
Jean MérotNantes Université, CHU Nantes, CNRS, INSERM, L'institut du Thorax, Nantes, France.
Solena Le ScouarnecNantes Université, CHU Nantes, CNRS, INSERM, L'institut du Thorax, Nantes, France.
Nabila Bouatia-NajiINSERM, PARCC, Université Paris Cité, Paris, France.
Mengyao YuHuman Phenome Institute, Fudan University, Shanghai, China.
Olivier HuttinService de Cardiologie, Institut Lorrain du Coeur et des Vaisseaux Louis Mathieu, CHU de Nancy, Nancy, France.
Christine Selton-SutyService de Cardiologie, Institut Lorrain du Coeur et des Vaisseaux Louis Mathieu, CHU de Nancy, Nancy, France.
Jean-Marc SellalService de Cardiologie, Institut Lorrain du Coeur et des Vaisseaux Louis Mathieu, CHU de Nancy, Nancy, France.
Nicolas PiriouNantes Université, CHU Nantes, CNRS, INSERM, L'institut du Thorax, Nantes, France.
Jean-Jacques SchottNantes Université, CHU Nantes, CNRS, INSERM, L'institut du Thorax, Nantes, France.
Christian DinaNantes Université, CHU Nantes, CNRS, INSERM, L'institut du Thorax, Nantes, France.
Thierry Le TourneauNantes Université, CHU Nantes, CNRS, INSERM, L'institut du Thorax, Nantes, France.
Nantes Université · FRInserm · FRCentre National de la Recherche Scientifique · FRFudan University · CNInstitut du Thorax · FRParis Cardiovascular Research Center · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mitral valve prolapse (MVP) is a common condition affecting 2-3% of the general population, and the most complex form of valve pathology, with a complication rate up to 10-15% per year in advanced stages. Complications include mitral regurgitation which can lead to heart failure and atrial fibrillation, but also life-threatening ventricular arrhythmia and cardiovascular death. Sudden death has been recently brought to the forefront of MVP disease, increasing the complexity of management and suggesting that MVP condition is not properly understood. MVP can occur as part of syndromic conditions such as Marfan syndrome, but the most common form is non-syndromic, isolated or familial. Although a specific X-linked form of MVP was initially identified, autosomal dominant inheritance appears to be the primary mode of transmission. MVP can be stratified into myxomatous degeneration (Barlow), fibroelastic deficiency, and Filamin A-related MVP. While FED is still considered a degenerative disease associated with aging, myxomatous MVP and FlnA-MVP are recognized as familial pathologies. Deciphering genetic defects associated to MVP is still a work in progress; although

Indexed as

animal modelsdachsousFilamin Ageneticmitral valve prolapsemyxomatous diseasepathophysiology

Identifiers

PMID36873395
PMCPMC9978496
OpenAlexW4321089146

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.