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心律失常与已确诊的心肌营养不良症患者心脏 MRI 的相关性。

Arrhythmias and cardiac MRI associations in patients with established cardiac dystrophinopathy.

机构信息

Department of Cardiology, NUTH NHS Hospitals Foundation Trust, Newcastle upon Tyne, UK

John Walton Muscular Dystrophy Research Centre, Newcastle University, Newcastle upon Tyne, UK.

出版信息

Open Heart. 2024 Apr 2;11(1):e002590. doi: 10.1136/openhrt-2023-002590.

Abstract

AIMS

Some patients with cardiac dystrophinopathy die suddenly. Whether such deaths are preventable by specific antiarrhythmic management or simply indicate heart failure overwhelming medical therapies is uncertain. The aim of this prospective, cohort study was to describe the occurrence and nature of cardiac arrhythmias recorded during prolonged continuous ECG rhythm surveillance in patients with established cardiac dystrophinopathy and relate them to abnormalities on cardiac MRI.

METHODS AND RESULTS

A cohort of 10 patients (36.3 years; 3 female) with LVEF<40% due to Duchenne (3) or Becker muscular (4) dystrophy or Duchenne muscular dystrophy-gene carrying effects in females (3) were recruited, had cardiac MRI, ECG signal-averaging and ECG loop-recorder implants. All were on standard of care heart medications and none had prior history of arrhythmias.No deaths or brady arrhythmias occurred during median follow-up 30 months (range 13-35). Self-limiting episodes of asymptomatic tachyarrhythmia (range 1-29) were confirmed in 8 (80%) patients (ventricular only 2; ventricular and atrial 6). Higher ventricular arrhythmia burden correlated with extent of myocardial fibrosis (extracellular volume%, p=0.029; native T1, p=0.49; late gadolinium enhancement, p=0.49), but not with LVEF% (p=1.0) on MRI and atrial arrhythmias with left atrial dilatation. Features of VT episodes suggested various underlying arrhythmia mechanisms.

CONCLUSIONS

The overall prevalence of arrhythmias was low. Even in such a small sample size, higher arrhythmia counts occurred in those with larger scar burden and greater ventricular volume, suggesting key roles for myocardial stretch as well as disease progression in arrhythmogenesis. These features overlap with the stage of left ventricular dysfunction when heart failure also becomes overt. The findings of this pilot study should help inform the design of a definitive study of specific antiarrhythmic management in dystrophinopathy.

TRIAL REGISTRATION NUMBER

ISRCTN15622536.

摘要

目的

一些患有心脏肌营养不良症的患者会突然死亡。这些死亡是否可以通过特定的抗心律失常治疗来预防,或者仅仅表明心力衰竭压倒了医疗治疗,目前还不确定。本前瞻性队列研究的目的是描述在经过证实的心脏肌营养不良症患者中进行长时间连续心电图节律监测时记录到的心律失常的发生和性质,并将其与心脏磁共振成像(cardiac MRI)的异常相关联。

方法和结果

本研究纳入了 10 名患者(36.3 岁;3 名女性),这些患者因杜兴氏肌营养不良症(3 名)或贝克肌营养不良症(4 名)或女性中的杜兴氏肌营养不良症基因携带效应(3 名)导致左心室射血分数(LVEF)<40%,并进行了心脏 MRI、心电图信号平均和心电图环记录器植入。所有患者均接受了标准的心脏药物治疗,且均无心律失常病史。在中位随访 30 个月(范围 13-35 个月)期间,没有死亡或心动过缓性心律失常发生。8 名(80%)患者(仅室性心律失常 2 例;室性和房性心律失常 6 例)中确认存在无症状性心动过速(范围 1-29 次)的自限性发作。较高的室性心律失常负担与心肌纤维化程度相关(细胞外容积百分比,p=0.029;固有 T1 值,p=0.49;晚期钆增强,p=0.49),但与 MRI 上的 LVEF%(p=1.0)和左心房扩大的房性心律失常无关。VT 发作的特征提示存在各种潜在的心律失常机制。

结论

心律失常的总体发生率较低。即使在这么小的样本量中,较大的瘢痕负担和更大的心室容积患者的心律失常计数也较高,这表明心肌拉伸以及疾病进展在心律失常发生中起着关键作用。这些特征与心力衰竭也变得明显时左心室功能障碍的阶段重叠。本研究的初步结果应有助于为肌营养不良症的特定抗心律失常治疗的确定性研究提供设计依据。

临床试验注册号

ISRCTN81245577。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c86/10989184/6b30bb93c955/openhrt-2023-002590f01.jpg

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