PhD Scientific Days 2025

Budapest, 7-9 July 2025

Poster Session II. - U: Cardiovascular Medicine and Research

Quantitative Assessment of Compact and Noncompact Myocardial Layer Thickness in Excessive Trabeculation with Preserved Left Ventricular Function: Genotype-Phenotype Associations

Előadó neve

Dr. Grebur Kinga

Neptun code

GT9FR1

Előadó munkahelye

Semmelweis University, Heart and Vascular Center

Előadó telefonszáma

06300164371

Előadó e-mail címe

gkinga9611@gmail.com

Az előadás címe

Quantitative Assessment of Compact and Noncompact Myocardial Layer Thickness in Excessive Trabeculation with Preserved Left Ventricular Function: Genotype-Phenotype Associations

Szerző(k) neve és munkahelye

Kinga Grebur1, Balázs Mester1, Kristóf Farkas-Sütő1, Flóra Gyulánczi1, Zsófia Gregor1, Anna Réka Kiss1, Márton Horváth1, Bálint András Fekete2, Csaba Bödör2, Hajnalka Vágó1, Béla Merkely1, Andrea Szűcs1

1: Semmelweis University, Heart and Vascular Center
2: Semmelweis University, Department of Pathology and Experimental Cancer Research

Bemutatás módja

Poszter

Szekció

Poster Session II. - U: Cardiovascular Medicine and Research

Language of the presentation

Hungarian

Preferred session

Cardiovascular Medicine and Research

Összefoglaló szövege

Introduction
Compact layer thickness (CLT) below 5 mm has been identified as a prognostic parameter in noncompaction with heart failure, but the significance of CLT in genetically affected excessive trabeculated (LVET) individuals with preserved left ventricular function (LVEF) is unknown.
Aims
We aimed to investigate CLT and noncompact layer thickness (NCLT) in symptomatic LVET individuals with preserved LVEF; to compare these parameters to a control population (C); and to analyse their associations with genetic mutations and clinical manifestation.
Methods
Cardiac MRI images of the 54 LVET (40±14 years, 21 female, EF 65%) and 54 C (39±15 years, 21 female, EF 69%) subjects were used to determine left ventricular volumetric and EF, total, compact and trabeculated muscle mass, basal (bas), mid-ventricular (mid) and apical (apic) CLT and NCLT parameters. Based on the results of the genetic analysis with the 174-gene TruSight Cardio panel, three LVET subgroups were formed: benign (B, n=12), unknown significance (VUS, n=27) and pathogenic (P, n=15).
Results
The LVET population showed significantly higher volumetric, total and trabeculated myocardial mass, bas, mid and apic NCLT and lower EF and apic CLT (LVET: 4.8 mm; C: 5.4 mm; p<0.001) parameters compared to the C group. When comparing the genetic subgroups, significant differences were only found in the values of mid and apic CLT, being lower in P subjects compared to the VUS and B subgroups. CLT and NCLT values did not show any significant correlation with functional parameters. In contrast to NCLT, mid and apic CLT showed a significant correlation with genotype. Furthermore, apic CLT below 5 mm gave a significant association with positive family history and genetic involvement.
Conclusion
Our results suggest that CLT is significantly lower in LVET subjects carrying pathogenic genetic mutations than in sporadic cases, and thus may be useful as part of risk stratification in the follow-up of LVET subjects with preserved LVEF.
Funding
„SUPPORTED BY THE 2024-2.1.1-EKÖP-2024-00004 NEW NATIONAL EXCELLENCE PROGRAM OF THE MINISTRY FOR CULTURE AND INNOVATION FROM THE SOURCE OF THE NATIONAL RESEARCH, DEVELOPMENT AND INNOVATION FUND.”

University

Semmelweis University

Supervisor

Andrea Szűcs

Publication of my abstract

I give consent to the publication of my abstract on the website of the congress.

phd.section.field

in doctoral studies after complex exam (PhD)

Kind

Szabad

Status

elfogadva

Accepted presentation method

poszter

Előadás fájl jóváhagyás

nem rendelkezett róla

Előadó

6844

Start

18:24

End

18:30