The effect of excessive trabeculation on cardiac rotation-A multimodal imaging study.


Journal

PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081

Informations de publication

Date de publication:
2024
Historique:
received: 06 03 2024
accepted: 16 07 2024
medline: 5 9 2024
pubmed: 5 9 2024
entrez: 5 9 2024
Statut: epublish

Résumé

Cardiac rotational parameters in primary symptomatic left ventricular noncompaction (LVNC) with preserved left ventricular ejection fraction (LVEF) are not well understood. We aimed to analyze cardiac rotation measured with cardiac magnetic resonance feature-tracking (CMR-FT) and speckle-tracking echocardiography (Echo-ST) in LVNC morphology subjects with preserved LVEF and different genotypes and healthy controls. Our retrospective study included 54 LVNC subjects with preserved LVEF and 54 control individuals. We evaluated functional and rotational parameters with CMR in the total study population and with echocardiography in 39 LVNC and 40 C individuals. All LVNC subjects were genotyped with a 174-gene next-generation sequencing panel and grouped into the subgroups: benign (B), variant of uncertain significance (VUS), and pathogenic (P). In comparison with controls, LVNC subjects had reduced apical rotational degree (p = 0.004) and one-third had negative apical rotation. While the degree of apical rotation was comparable between the three genetic subgroups, they differed significantly in the direction of apical rotation (p<0.001). In contrast to control and B groups, all four studied cardiac rotational patterns were identified in the P and VUS subgroups, namely normal rotation, positive and negative rigid body rotation, and reverse rotation. When the CMR-FT and Echo-ST methods were compared, the direction and pattern of cardiac rotation had moderate to good association (p<0.001) whereas the rotational degrees showed no reasonable correlation or agreement. While measuring cardiac rotation using both CMR-FT and Echo-ST methods, subclinical mechanical differences were identified in subjects with LVNC phenotype and preserved LVEF, especially in cases with genetic involvement.

Sections du résumé

BACKGROUND BACKGROUND
Cardiac rotational parameters in primary symptomatic left ventricular noncompaction (LVNC) with preserved left ventricular ejection fraction (LVEF) are not well understood. We aimed to analyze cardiac rotation measured with cardiac magnetic resonance feature-tracking (CMR-FT) and speckle-tracking echocardiography (Echo-ST) in LVNC morphology subjects with preserved LVEF and different genotypes and healthy controls.
METHODS METHODS
Our retrospective study included 54 LVNC subjects with preserved LVEF and 54 control individuals. We evaluated functional and rotational parameters with CMR in the total study population and with echocardiography in 39 LVNC and 40 C individuals. All LVNC subjects were genotyped with a 174-gene next-generation sequencing panel and grouped into the subgroups: benign (B), variant of uncertain significance (VUS), and pathogenic (P).
RESULTS RESULTS
In comparison with controls, LVNC subjects had reduced apical rotational degree (p = 0.004) and one-third had negative apical rotation. While the degree of apical rotation was comparable between the three genetic subgroups, they differed significantly in the direction of apical rotation (p<0.001). In contrast to control and B groups, all four studied cardiac rotational patterns were identified in the P and VUS subgroups, namely normal rotation, positive and negative rigid body rotation, and reverse rotation. When the CMR-FT and Echo-ST methods were compared, the direction and pattern of cardiac rotation had moderate to good association (p<0.001) whereas the rotational degrees showed no reasonable correlation or agreement.
CONCLUSION CONCLUSIONS
While measuring cardiac rotation using both CMR-FT and Echo-ST methods, subclinical mechanical differences were identified in subjects with LVNC phenotype and preserved LVEF, especially in cases with genetic involvement.

Identifiants

pubmed: 39236040
doi: 10.1371/journal.pone.0308035
pii: PONE-D-24-01299
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0308035

Informations de copyright

Copyright: © 2024 Grebur et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Déclaration de conflit d'intérêts

The authors have declared that no competing interests exist.

Auteurs

Kinga Grebur (K)

Heart and Vascular Center of Semmelweis University, Budapest, Hungary.

Balázs Mester (B)

Heart and Vascular Center of Semmelweis University, Budapest, Hungary.

Márton Horváth (M)

Heart and Vascular Center of Semmelweis University, Budapest, Hungary.

Kristóf Farkas-Sütő (K)

Heart and Vascular Center of Semmelweis University, Budapest, Hungary.

Zsófia Gregor (Z)

Heart and Vascular Center of Semmelweis University, Budapest, Hungary.

Anna Réka Kiss (AR)

Heart and Vascular Center of Semmelweis University, Budapest, Hungary.

Attila Tóth (A)

Heart and Vascular Center of Semmelweis University, Budapest, Hungary.

Attila Kovács (A)

Heart and Vascular Center of Semmelweis University, Budapest, Hungary.

Alexandra Fábián (A)

Heart and Vascular Center of Semmelweis University, Budapest, Hungary.

Bálint Károly Lakatos (BK)

Heart and Vascular Center of Semmelweis University, Budapest, Hungary.

Bálint András Fekete (BA)

Heart and Vascular Center of Semmelweis University, Budapest, Hungary.
Department of Pathology and Experimental Cancer Research, Semmelweis University, Budapest, Hungary.

Katalin Csonka (K)

Department of Pathology and Experimental Cancer Research, Semmelweis University, Budapest, Hungary.

Csaba Bödör (C)

Department of Pathology and Experimental Cancer Research, Semmelweis University, Budapest, Hungary.

Béla Merkely (B)

Heart and Vascular Center of Semmelweis University, Budapest, Hungary.

Hajnalka Vágó (H)

Heart and Vascular Center of Semmelweis University, Budapest, Hungary.

Andrea Szűcs (A)

Heart and Vascular Center of Semmelweis University, Budapest, Hungary.

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Classifications MeSH