Division of Cardiology, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
Division of Neurology, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
Pediatr Neurol. 2021 Apr;117:29-33. doi: 10.1016/j.pediatrneurol.2021.01.004. Epub 2021 Jan 23.
Friedreich ataxia is the most commonly inherited ataxia; nearly 60% of deaths are cardiac in nature, with one in eight deaths due to arrhythmia. Additional or irregular heartbeats, measured as ectopy, can be quantified using portable heart rhythm monitoring. We sought to describe the ectopic burden in Friedreich ataxia.
Using a natural history study of patients with Friedreich ataxia at a single center, we analyzed portable heart rhythm monitors (Holters). Ectopic burden was defined as the proportion of atrial or ventricular ectopic beats over total beats.
Of 456 patients, 131 had Holters. Sixty-eight (52.0%) were male, median age of symptom onset was 8.0 years (5.0 to 13.0, n = 111), median age at time of Holter was 17.3 years (interquartile range [IQR] 12.9 to 22.8, n = 129), and median duration of illness was 8.7 years (IQR 5.3 to 11.6, n = 110). Median GAA length on the shorter FXN allele was 706.0 (IQR 550.0 to 840.0, n = 112). Eight (7.8%, n = 103) had diminished cardiac function, and 74 (74.0%, n = 100) had ventricular hypertrophy. Ninety patients (83.0%) had atrial ectopy (supraventricular ectopy [SVE]): 85 (78.0%) with rare SVE (>0% to 5%) and five (5.0%) with frequent SVE (>10%). Twenty-five (19.0%) had supraventricular runs, and one (0.8%) had atrial fibrillation/flutter. Forty-five (41.0%) had ventricular ectopy (VE): 43 (39.0%) with rare VE (0% to 5%) and two (2.0%) with moderate VE (5% to 10%). Compared with patients with none and rare SVE, patients with frequent SVE had longer disease duration (18.3 versus 4.6 versus 9.0 years, P = 0.0005).
Patients with longer disease duration had higher rates of SVE. Heart rhythm monitoring may be considered for risk stratification; however, longitudinal analysis is needed.
弗里德里希共济失调是最常见的遗传性共济失调;近 60%的死亡是心脏性质的,其中八分之一的死亡是由于心律失常。额外的或不规则的心跳,以异位来衡量,可以使用便携式心律监测仪进行量化。我们旨在描述弗里德里希共济失调中的异位负担。
我们在一个中心的弗里德里希共济失调患者的自然史研究中,分析了便携式心律监测仪(动态心电图)。异位负担定义为心房或室性异位搏动占总搏动的比例。
在 456 名患者中,有 131 名进行了动态心电图检查。68 名(52.0%)为男性,症状发作的中位年龄为 8.0 岁(5.0 至 13.0,n=111),动态心电图检查时的中位年龄为 17.3 岁(四分位距[IQR]12.9 至 22.8,n=129),中位病程为 8.7 年(IQR 5.3 至 11.6,n=110)。较短 FXN 等位基因上 GAA 长度的中位数为 706.0(IQR 550.0 至 840.0,n=112)。8 名(7.8%,n=103)患者存在心功能减退,74 名(74.0%,n=100)患者存在心室肥厚。90 名(83.0%)患者有心房异位(室上性异位[SVT]):85 名(78.0%)为罕见 SVT(>0%至 5%),5 名(5.0%)为频发 SVT(>10%)。25 名(19.0%)患者有心房性心动过速,1 名(0.8%)患者有心房颤动/扑动。45 名(41.0%)患者有心室异位(VE):43 名(39.0%)为罕见 VE(0%至 5%),2 名(2.0%)为中度 VE(5%至 10%)。与无 SVT 和罕见 SVT 的患者相比,频发 SVT 的患者病程较长(18.3 年、4.6 年和 9.0 年,P=0.0005)。
病程较长的患者 SVT 发生率较高。心律监测仪可能用于风险分层;然而,需要进行纵向分析。