LV and LA mechanics in pediatric HCM: A CMR study of phenotype-genotype correlation

E. Panaioli , V. Dangouloff-Ros , N. Boddaert , D. Bonnet , D. Khraiche
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Abstract

Introduction

The relationship between the genotype variation and phenotype expression in paediatric hypertrophic cardiomyopathy (HCM) has not been fully elucidated. In HCM, fibrosis and hypertrophy contribute to left ventricular (LV) mechanics with a decreased global longitudinal and radial strains (GLS, GRS). The epicardial thickening leads to preserved global circumferential strain (GCS) and LV twist. Feature tracking – cardiac magnetic resonance (FT-CMR) has enhanced the non-invasive assessment of myocardial deformation in HCM. The aim of our study was to assess differences of LV and LA mechanics features on CMR between patients harbouring multiple pathogenic or likely pathogenic variants (MGv, n = 16) or single genetic variations (SGv, n = 35).

Method

Our retrospective CMR study included 51 patients (1.7–18.8 years ago). CMR data were: LV and LA's morphological values, late gadolinium enhancement (LGE) of LA and LV walls, LV feature tracking (FT) derived strain and LV twist (LVT). LV twist was calculated as the difference between basal and apical rotation. The LA feature FT derived strain and function's parameters were computed.

Results

In MGv group, the indexed LV mass 108.8–53.0 vs. 74.3 ± 22.2 in SGv (P = 0.03). LGE was present in 51% patients of the whole cohort, with LGE in 64% of MGv group. LV FT derived strain values were not statistically significant different between groups (MGv vs. SGv: GLS −15.8 ± 5.3 vs. −18.7 ± 4.8, GCS −27.8 ± 8 vs. −31.1 ± 8.6, GRS 44.7 ± 24.6 vs. 62.3 ± 32). LVT was reduced in MGv group (0.04 ± 7.6) vs. (7.4 ± 7.4) in SGv (P = 0.003). LA contractile function did not differ between the groups.

Conclusion

Patients with multiple genetic variants have a greater LV mass and altered LV mechanics with reduced LV twist. This study gives insights in phenotype-genotype correlation in paediatric HCM and warrants larger longitudinal studies to assess its clinical significance (Fig. 1).

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儿童HCM的左心室和左心房力学:表型-基因型相关性的CMR研究
儿童肥厚性心肌病(HCM)基因型变异与表型表达之间的关系尚未完全阐明。在HCM中,纤维化和肥厚导致左心室(LV)力学,整体纵向和径向应变降低(GLS, GRS)。心外膜增厚导致整体环向应变(GCS)和左室扭转保留。特征跟踪-心脏磁共振(FT-CMR)增强了HCM心肌变形的无创评估。本研究的目的是评估具有多种致病或可能致病变异(MGv, n = 16)或单一遗传变异(SGv, n = 35)的患者在CMR时左室和左室力学特征的差异。方法回顾性CMR研究纳入51例患者(1.7-18.8年)。CMR数据包括:左室和左室的形态学值、左室和左室壁的晚期钆增强(LGE)、左室特征跟踪(FT)衍生应变和左室扭转(LVT)。LV扭转被计算为基部和根尖旋转的差值。计算了LA特征FT导出的应变和函数参数。结果MGv组左室指数质量为108.8 ~ 53.0,SGv组为74.3±22.2 (P = 0.03)。整个队列中51%的患者存在LGE, MGv组中有64%的患者存在LGE。各组间LV FT衍生应变值差异无统计学意义(MGv vs. SGv: GLS - 15.8±5.3 vs. - 18.7±4.8,GCS - 27.8±8 vs. - 31.1±8.6,GRS - 44.7±24.6 vs. 62.3±32)。MGv组LVT降低(0.04±7.6),SGv组LVT降低(7.4±7.4)(P = 0.003)。两组间LA收缩功能无差异。结论多基因变异患者左室质量增大,左室力学改变,左室扭转减小。该研究对儿童HCM的表型-基因型相关性提供了见解,并保证进行更大规模的纵向研究以评估其临床意义(图1)。
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来源期刊
Archives of Cardiovascular Diseases Supplements
Archives of Cardiovascular Diseases Supplements CARDIAC & CARDIOVASCULAR SYSTEMS-
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期刊介绍: Archives of Cardiovascular Diseases Supplements is the official journal of the French Society of Cardiology. The journal publishes original peer-reviewed clinical and research articles, epidemiological studies, new methodological clinical approaches, review articles, editorials, and Images in cardiovascular medicine. The topics covered include coronary artery and valve diseases, interventional and pediatric cardiology, cardiovascular surgery, cardiomyopathy and heart failure, arrhythmias and stimulation, cardiovascular imaging, vascular medicine and hypertension, epidemiology and risk factors, and large multicenter studies. Additionally, Archives of Cardiovascular Diseases also publishes abstracts of papers presented at the annual sessions of the Journées Européennes de la Société Française de Cardiologie and the guidelines edited by the French Society of Cardiology.
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