Department of Molecular and Clinical Medicine, Institute of Medicine, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.
Region Vaestra Goetaland, Department of Cardiology, Sahlgrenska University Hospital, Gothenburg, Sweden.
Am J Physiol Heart Circ Physiol. 2023 Dec 1;325(6):H1279-H1289. doi: 10.1152/ajpheart.00335.2023. Epub 2023 Sep 29.
Congenital long QT syndrome (LQTS) carries an increased risk for syncope and sudden death. QT prolongation promotes ventricular extrasystoles, which, in the presence of an arrhythmia substrate, might trigger ventricular tachycardia degenerating into fibrillation. Increased electrical heterogeneity (dispersion) is the suggested arrhythmia substrate in LQTS. In the most common subtype LQT1, physical exercise predisposes for arrhythmia and spatiotemporal dispersion was therefore studied in this context. Thirty-seven patients (57% on β-blockers) and 37 healthy controls (mean age, 31 vs. 35; range, 6-68 vs. 6-72 yr) performed an exercise test. Frank vectorcardiography was used to assess spatiotemporal dispersion as T, T, the ventricular gradient (VG), and the T interval from 10-s signal averages before and 7 ± 2 min after exercise; during exercise too much signal disturbance excluded analysis. Baseline and maximum heart rates as well as estimated exercise intensity were similar, but heart rate recovery was slower in patients. At baseline, QT and heart rate-corrected QT (QT) were significantly longer in patients (as expected), whereas dispersion parameters were numerically larger in controls. After exercise, QT and T increased significantly more in patients (18 ± 23 vs. 7 ± 10 ms and 12 ± 17 vs. 2 ± 6 ms; < 0.001 and < 0.01). There was, however, no difference in the change in T, T, and VG between groups. In conclusion, although temporal dispersion of repolarization increased significantly more after exercise in patients with LQT1, there were no signs of exercise-induced increase in global dispersion of action potential duration and morphology. The arrhythmia substrate/mechanism in LQT1 warrants further study. Physical activity increases the risk for life-threatening arrhythmias in LQTS type 1 (LQT1). The arrhythmia substrate is presumably altered electrical heterogeneity (a.k.a. dispersion). Spatiotemporal dispersion parameters were therefore compared before and after exercise in patients versus healthy controls using Frank vectorcardiography, a novelty. Physical exercise prolonged the time between the earliest and latest complete repolarization in patients versus controls, but did not increase parameters reflecting global dispersion of action potential duration and morphology, another novelty.
先天性长 QT 综合征(LQTS)增加了晕厥和猝死的风险。QT 延长促进室性期前收缩,在心律失常基质存在的情况下,可能引发室性心动过速演变为纤维性颤动。增加的电异质性(弥散)是 LQTS 中的心律失常基质。在最常见的 LQT1 亚型中,体力活动易引发心律失常,因此在这种情况下研究了时空弥散。37 名患者(57%服用β受体阻滞剂)和 37 名健康对照者(平均年龄 31 岁比 35 岁;范围 6-68 岁比 6-72 岁)进行了运动试验。应用 Frank 向量心电图评估 T 间期、T 间期、心室梯度(VG)和运动前 10 秒信号平均与运动后 7±2 分钟的 T 间期的时空弥散;运动中由于信号干扰过多而排除分析。基础心率和最大心率以及估计的运动强度相似,但患者的心率恢复较慢。基础状态下,患者的 QT 和心率校正 QT(QTc)明显延长(预期如此),而对照组的弥散参数数值较大。运动后,患者的 QT 和 T 显著增加(18±23 毫秒比 7±10 毫秒和 12±17 毫秒比 2±6 毫秒;均<0.001 和<0.01)。然而,两组间 T 间期、T 间期和 VG 的变化无差异。总之,尽管 LQT1 患者运动后复极的时间弥散显著增加,但动作电位时程和形态的整体弥散无运动诱导增加的迹象。LQT1 的心律失常基质/机制有待进一步研究。体力活动增加了 1 型长 QT 综合征(LQT1)患者发生危及生命的心律失常的风险。心律失常基质推测为电异质性改变(亦称弥散)。因此,应用 Frank 向量心电图(一项创新)比较了患者与健康对照者运动前后的时空弥散参数。与对照组相比,患者的运动延长了最早与最晚完全复极之间的时间,但未增加反映动作电位时程和形态整体弥散的参数,这是另一项创新。