Morphology of the mural and commissural atrioventricular junction of the mitral valve.

Congenital Abnormalities Heart Valve Diseases Mitral Valve Insufficiency

Journal

Heart (British Cardiac Society)
ISSN: 1468-201X
Titre abrégé: Heart
Pays: England
ID NLM: 9602087

Informations de publication

Date de publication:
07 Nov 2023
Historique:
received: 13 05 2023
accepted: 23 09 2023
medline: 8 11 2023
pubmed: 8 11 2023
entrez: 7 11 2023
Statut: aheadofprint

Résumé

This study investigates mitral annular disjunctions (MAD) in the atrial wall-mitral annulus-ventricular wall junction along the mural mitral leaflet and commissures. We examined 224 adult human hearts (21.9% females, 47.9±17.6 years) devoid of cardiovascular diseases (especially mitral valve disease). These hearts were obtained during forensic medical autopsies conducted between January 2018 and June 2021. MAD was defined as a spatial displacement (≥2 mm) of the leaflet hinge line towards the left atrium. We provided a detailed morphometric analysis (disjunction height) and histological examination of MADs. MADs were observed in 19.6% of all studied hearts. They appeared in 12.1% of mural leaflets. The P1 scallop was the primary site for disjunctions (8.9%), followed by the P2 scallop (5.4%) and P3 scallop (4.5%). MADs were found in 9.8% of all superolateral and 5.8% of all inferoseptal commissures. The average height for leaflet MADs was 3.0±0.6 mm, whereas that for commissural MADs was 2.1±0.5 mm (p<0.0001). The microscopical arrangement of MADs in both the mural leaflet and commissures revealed a disjunction shifted towards left atrial aspect, filled with connective tissue and covered by elongated valve annulus. The size of the MAD remained remarkably uniform and showed no correlation with other anthropometric factors (all p>0.05). In the cohort of the patients with healthy hearts, MAD is present in about 20% of all studied hearts. The MADs identified tend to be localised, confined to a single scallop. Moreover, MADs in the commissures are notably smaller than those in the mural leaflet.

Identifiants

pubmed: 37935571
pii: heartjnl-2023-322965
doi: 10.1136/heartjnl-2023-322965
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© Author(s) (or their employer(s)) 2023. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: None declared.

Auteurs

Agata Krawczyk-Ożóg (A)

Department of Anatomy, Jagiellonian University Medical College, Krakow, Poland krawczyk.ozog@gmail.com.
Clinical Department of Cardiology and Cardiovascular Interventions, University Hospital, Krakow, Poland.

Jakub Batko (J)

Department of Anatomy, Jagiellonian University Medical College, Krakow, Poland.

Barbara Zdzierak (B)

Clinical Department of Cardiology and Cardiovascular Interventions, University Hospital, Krakow, Poland.

Artur Dziewierz (A)

Clinical Department of Cardiology and Cardiovascular Interventions, University Hospital, Krakow, Poland.
2nd Department of Cardiology, Jagiellonian University Medical College, Krakow, Poland.

Kamil Tyrak (K)

Department of Anatomy, Jagiellonian University Medical College, Krakow, Poland.

Filip Bolechała (F)

Department of Forensic Medicine, Jagiellonian University Medical College, Krakow, Poland.

Paweł Kopacz (P)

Department of Forensic Medicine, Jagiellonian University Medical College, Krakow, Poland.

Marcin Strona (M)

Department of Forensic Medicine, Jagiellonian University Medical College, Krakow, Poland.

Krzysztof Gil (K)

Department of Pathophysiology, Jagiellonian University Medical College, Krakow, Poland.

Jakub Hołda (J)

Department of Anatomy, Jagiellonian University Medical College, Krakow, Poland.

Mateusz K Hołda (MK)

Department of Anatomy, Jagiellonian University Medical College, Krakow, Poland.
The University of Manchester, Manchester, UK.

Classifications MeSH