Right atrial strain in Anderson-Fabry disease.

IF 2.8 3区 医学 Q2 CARDIAC & CARDIOVASCULAR SYSTEMS Frontiers in Cardiovascular Medicine Pub Date : 2025-02-18 eCollection Date: 2025-01-01 DOI:10.3389/fcvm.2025.1496534
Rosa Lillo, Alessio Cianci, Maria Chiara Meucci, Giulia Iannaccone, Claudio Di Brango, Filippo Tusa, Mario Marsilia, Gaetano Antonio Lanza, Antonella Lombardo, Francesco Burzotta, Francesca Graziani
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Abstract

Background: To date, only limited data are available on right atrium (RA) morphofunctional remodeling in Fabry disease (FD).

Purpose: We aimed to investigate RA structural and functional remodeling in patients with FD vs. healthy controls using 2D speckle tracking echocardiography (STE) and to explore whether any differences exist in FD patients with and without left ventricular hypertrophy (LVH).

Methods: We prospectively enrolled patients with FD and controls matched for age, sex, and cardiovascular risk factors. Patients with FD were divided in two groups according to the presence/absence of LVH (LVH+: left ventricular wall thickness >12 mm). All patients underwent standard echocardiography and STE analysis investigating the mechanics of all cardiac chambers, including RA reservoir, contractile and conduit strain.

Results: A total of 64 patients with FD (50% males; mean age 50 ± 17 years; 51.5% LVH+) and 64 control patients were included in the study. Focusing on right chambers, RA and right ventricular (RV) dimensions were similar between FD and controls. No differences were found for tricuspid annular plane systolic excursion (p = 0.073) and RV fractional area change (p = 0.461), while RV systolic Tissue Doppler velocity was reduced in patients with FD (p = 0.041). STE analysis revealed impaired strain values for all cardiac chambers in FD vs controls, specifically: left ventricular global longitudinal strain (LV-GLS, p < 0.001), left atrial (LA) reservoir strain (p = 0.001), conduit strain (p = 0.012), and contractile strain (p < 0.001), RV-GLS and RV free wall strain (p < 0.001). Similarly, all RA strain phases were significantly reduced in patients with FD compared with control patients (RA reservoir 27.4 ± 11.1 vs. 41.9 ± 8.3%, p < 0.001; RA contractile 9.9 ± 5.1 vs. 18.0 ± 4.9%, p < 0.001; RA conduit 19.1 ± 8.1 vs. 24.1 ± 8.1%, p = 0.001). When comparing FD patients without LVH to controls, it was found that RA reservoir and contractile strains were significantly reduced in the former (p < 0.001). In multivariable linear regression analyses, LA reservoir strain (p = 0.010) and LV-GLS (p = 0.044) emerged as independent correlates of RA mechanics after adjustments were made for RA dimensions, RV systolic function parameters and hypertrophy, and LV maximal wall thickness.

Conclusions: In FD impaired RA strain is a common finding. RA reservoir and contractile strains are reduced in FD patients even before LVH ensues, as compared to controls. LA reservoir strain and LV-GLS show an independent correlation with RA reservoir strain.

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安德森-法布里病的右心房劳损。
背景:迄今为止,关于法布里病(FD)右心房(RA)形态功能重构的数据有限。目的:我们旨在利用二维斑点跟踪超声心动图(STE)研究FD患者与健康对照组的RA结构和功能重构,并探讨伴有和不伴有左室肥厚(LVH)的FD患者是否存在差异。方法:我们前瞻性地招募了年龄、性别和心血管危险因素相匹配的FD患者和对照组。FD患者根据LVH有无分为两组(LVH+:左室壁厚度>12 mm)。所有患者都接受了标准超声心动图和STE分析,调查了所有心室的力学,包括RA储层、收缩和导管应变。结果:共有64例FD患者(男性占50%;平均年龄50±17岁;51.5% LVH+)和64例对照患者纳入研究。关注右心室,RA和右心室(RV)尺寸在FD和对照组之间相似。FD患者的三尖瓣环面收缩偏移(p = 0.073)和右心室分数面积变化(p = 0.461)无差异,而右心室收缩组织多普勒速度降低(p = 0.041)。STE分析显示,与对照组相比,FD组所有心室的应变值受损,特别是:左心室整体纵向应变(LV-GLS, p < 0.001)、左心房(LA)储层应变(p = 0.001)、导管应变(p = 0.012)、收缩应变(p < 0.001)、RV- gls和RV游离壁应变(p < 0.001)。同样,与对照组相比,FD患者的所有RA菌株相均显著减少(RA库27.4±11.1比41.9±8.3%,p p p = 0.001)。将无LVH的FD患者与对照组进行比较,发现在调整RA尺寸、右心室收缩功能参数、肥厚和左心室最大壁厚后,前者RA储层和收缩应变显著降低(p p = 0.010), LV- gls (p = 0.044)成为RA力学的独立相关因素。结论:在FD中受损的RA菌株是常见的发现。与对照组相比,即使在LVH发生之前,FD患者的RA库和收缩菌株也减少了。LA储层应变和LV-GLS与RA储层应变独立相关。
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来源期刊
Frontiers in Cardiovascular Medicine
Frontiers in Cardiovascular Medicine Medicine-Cardiology and Cardiovascular Medicine
CiteScore
3.80
自引率
11.10%
发文量
3529
审稿时长
14 weeks
期刊介绍: Frontiers? Which frontiers? Where exactly are the frontiers of cardiovascular medicine? And who should be defining these frontiers? At Frontiers in Cardiovascular Medicine we believe it is worth being curious to foresee and explore beyond the current frontiers. In other words, we would like, through the articles published by our community journal Frontiers in Cardiovascular Medicine, to anticipate the future of cardiovascular medicine, and thus better prevent cardiovascular disorders and improve therapeutic options and outcomes of our patients.
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