1 Department of Cardiac, Thoracic and Vascular Sciences University of Padova Italy.
2 Division of Radiology Department of Medicine University of Padova Italy.
J Am Heart Assoc. 2018 Nov 20;7(22):e009855. doi: 10.1161/JAHA.118.009855.
Background The new designation of arrhythmogenic cardiomyopathy defines a broader spectrum of disease phenotypes, which include right dominant, biventricular, and left dominant variants. We evaluated the relationship between electrocardiographic findings and contrast-enhanced cardiac magnetic resonance phenotypes in arrhythmogenic cardiomyopathy. Methods and Results We studied a consecutive cohort of patients with a definite diagnosis of arrhythmogenic cardiomyopathy, according to 2010 International Task Force criteria, who underwent electrocardiography and contrast-enhanced cardiac magnetic resonance. Both depolarization and repolarization electrocardiographic abnormalities were correlated with the severity of dilatation/dysfunction, either global or regional, of both ventricles and the presence and regional distribution of late gadolinium enhancement. The study population included 79 patients (60% men). There was a statistically significant relationship between the presence and extent of T-wave inversion across a 12-lead ECG and increasing values of median right ventricular ( RV ) end-diastolic volume ( P<0.001) and decreasing values of RV ejection fraction ( P<0.001). The extent of T-wave inversion to lateral leads predicted a more severe RV dilatation rather than a left ventricular involvement because of the leftward displacement of the dilated RV , as evidenced by contrast-enhanced cardiac magnetic resonance. A terminal activation delay of >55 ms in the right precordial leads (V1-V3) was associated with higher RV volume ( P=0.014) and lower RV ejection fraction ( P=0.053). Low QRS voltages in limb leads predicted the presence ( P=0.004) and amount ( P<0.001) of left ventricular late gadolinium enhancement. Conclusions The study results indicated that electrocardiographic abnormalities predict the arrhythmogenic cardiomyopathy phenotype in terms of severity of RV disease and left ventricular involvement, which are among the most important determinants of the disease outcome.
致心律失常性心肌病的新命名定义了更广泛的疾病表型谱,包括右优势型、双心室型和左优势型。我们评估了心电图表现与致心律失常性心肌病对比增强心脏磁共振表型之间的关系。
我们连续研究了一组根据 2010 年国际工作组标准明确诊断为致心律失常性心肌病的患者,这些患者接受了心电图和对比增强心脏磁共振检查。去极化和复极化心电图异常与两个心室的扩张/功能障碍的严重程度相关,包括整体和局部,以及晚期钆增强的存在和局部分布。研究人群包括 79 名患者(60%为男性)。在 12 导联心电图上 T 波倒置的存在和范围与右心室(RV)末期舒张容积(P<0.001)的增加值和 RV 射血分数(P<0.001)的降低值呈统计学显著相关。T 波倒置范围较大的导联预测 RV 扩张更为严重,而不是由于扩张的 RV 向左移位导致左心室受累,这可以通过对比增强心脏磁共振证实。右胸前导联(V1-V3)的终末激活延迟>55 ms 与 RV 容积较高(P=0.014)和 RV 射血分数较低(P=0.053)相关。肢体导联低 QRS 波电压预测左心室晚期钆增强的存在(P=0.004)和程度(P<0.001)。
研究结果表明,心电图异常可预测致心律失常性心肌病表型,包括 RV 疾病的严重程度和左心室受累,这些是疾病结局的最重要决定因素之一。