(ÚNKP-23-3-II) Támogató: Nemzeti Kutatás, Fejlesztés és Innovációs Iroda
Az orvos-, egészségtudományi- és gyógyszerészképzés tudományos műhelyeinek fejlesztése(EFOP-3.6.3-VEKOP-16-2017-00009)
Támogató: EFOP-VEKOP
(TKP2021-NKTA-46)
MILAB(RRF-2.3.1-21-2022-00004) Támogató: NKFIH
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.