Evidence map›Paper›PMID 39424426›Full record

ArticleJournal of the American Heart Association2024

Mitral Annular Disjunction in Heritable Thoracic Aortic Disease: Insights From the Montalcino Aortic Consortium.

Kishan L Asokan, Jennifer R Landes, Wannes Renders, Laura Muiño Mosquera, Julie De Backer, David W Jantzen, Anji T Yetman, Gisela Teixido-Tura, Arturo Evangelista, Richmond Jeremy and 10 more

Abstract readMulticenter Study
In one paragraph

Article in Journal of the American Heart Association, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
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

3 citing papers in PubMed.

  1. Review
  2. Mitral Annular Disjunction and Coalescing Myths in Cardiology.Arrhythmia & electrophysiology review · 2026
    Article
  3. 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

20 authors.

Kishan L AsokanUniversity of Texas Health Science Center at Houston TX.ORCID 0009-0007-7214-2939
Jennifer R LandesUniversity of Texas Health Science Center at Houston TX.ORCID 0000-0002-4664-8334
Wannes RendersGhent University Hospital Ghent Belgium.
Laura Muiño MosqueraGhent University Hospital Ghent Belgium.ORCID 0000-0002-3094-7807
Julie De BackerGhent University Hospital Ghent Belgium.ORCID 0000-0001-8878-1507
David W JantzenUniversity of Nebraska Medical Center Omaha NE.
Anji T YetmanUniversity of Nebraska Medical Center Omaha NE.ORCID 0000-0001-6853-578X
Gisela Teixido-TuraUniversity Hospital Vall d'Hebron Barcelona Spain.ORCID 0000-0003-4714-2420
Arturo EvangelistaUniversity Hospital Vall d'Hebron Barcelona Spain.
Richmond JeremyUniversity of Sydney Australia.ORCID 0000-0003-1281-0505
Edward G JonesTexas Children's Hospital Houston TX.ORCID 0000-0002-0318-7582
Shaine MorrisTexas Children's Hospital Houston TX.ORCID 0000-0002-8056-0934
Tam DoanTexas Children's Hospital Houston TX.ORCID 0000-0002-8256-1535
Maral OuzonianUniversity of Toronto Canada.
Alan BravermanWashington University School of Medicine St Louis MO.ORCID 0000-0003-1859-310X
Guillaume JondeauHospital Bichat-Claude Bernard Paris France.ORCID 0000-0002-0101-2076
Olivier MilleronHospital Bichat-Claude Bernard Paris France.ORCID 0000-0002-6517-0559
Dianna M MilewiczUniversity of Texas Health Science Center at Houston TX.ORCID 0000-0002-7806-0068
Siddharth K PrakashUniversity of Texas Health Science Center at Houston TX.ORCID 0000-0001-6341-9624
Montalcino Aortic Consortium *

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMitral annular disjunction (MAD), posterior displacement of the mitral valve leaflet hinge point, predisposes to arrhythmias or sudden cardiac death. We evaluated the burden of MAD, mitral valve prolapse (MVP), and mitral regurgitation (MR) by heritable thoracic aortic disease gene in a cross-sectional analysis of 2014-2023 data in the Montalcino Aortic Consortium registry. METHODS AND

resultsMAD was determined by direct measurement of echocardiographic images. MR and MVP were defined according to current clinical guidelines. Associations were evaluated using χ

conclusionsPathological mitral valve phenotypes are more prevalent in individuals with PV in transforming growth factor-β pathway genes, particularly

Indexed as

Mitral ValveMitral Valve InsufficiencyMitral Valve ProlapseSmad3 ProteinAdultAgedAorta, ThoracicAortic Aneurysm, ThoracicCross-Sectional StudiesEchocardiographyFemaleGenetic Predisposition to DiseaseHumansMaleMiddle AgedPhenotypeSmad3 ProteinSMAD3 protein, humanTransforming Growth Factor betacardiovascular geneticscongenital heart diseaseLoeys–Dietz syndromemitral valvethoracic aortic aneurysms and dissections

Identifiers

PMID39424426
PMCPMC11935710

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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.