Clinic for Cardiology, University Hospital of Zurich, Zurich, Switzerland.
Am J Cardiol. 2010 Mar 1;105(5):753-6. doi: 10.1016/j.amjcard.2009.10.056.
Fabry disease (FD) is an X-chromosomal inherited lysosomal storage disease resulting in intracellular storage of globotriaosylceramide. Cardiac involvement is most frequently manifested as left ventricular hypertrophy. However, patients with FD may also have from various conduction abnormalities particularly affecting atrioventricular (AV) conduction. The present study was designed to analyze primarily AV conduction abnormalities on baseline electrocardiograms of patients with FD and to investigate the correlation with echocardiographic findings. Electrocardiograms at rest of 207 patients with FD were compared to echocardiograms. PQ-interval shortening and first-degree AV block could be found in only 29 cases (14%) and 3 cases (1.4%), respectively. No echocardiographic differences could be found in patients with and without PQ-interval shortening, including left ventricular hypertrophy, atrial size, and diastolic parameters. Furthermore, no correlation of the PQ interval with any echocardiographic parameters was detected. There was no difference between men and women in baseline clinical and electrocardiographic parameters. In conclusion, shortening of the PQ interval was not a common electrocardiographic finding in patients newly diagnosed with FD. Furthermore, no correlation with typical echocardiographic findings or disease stage in FD at baseline could be found.
法布里病(FD)是一种 X 连锁遗传性溶酶体贮积病,导致糖鞘脂在细胞内贮积。心脏受累最常表现为左心室肥厚。然而,FD 患者也可能存在各种传导异常,特别是影响房室(AV)传导。本研究旨在分析 FD 患者基线心电图上的 AV 传导异常,并探讨与超声心动图发现的相关性。将 207 例 FD 患者的静息心电图与超声心动图进行比较。仅在 29 例(14%)和 3 例(1.4%)中发现 PQ 间期缩短和一度房室传导阻滞。PQ 间期缩短组和无 PQ 间期缩短组的患者在左心室肥厚、心房大小和舒张参数等方面无超声心动图差异。此外,PQ 间期与任何超声心动图参数均无相关性。男性和女性在基线临床和心电图参数方面无差异。总之,在新诊断的 FD 患者中,PQ 间期缩短不是常见的心电图表现。此外,在 FD 的基线时也未发现与典型超声心动图发现或疾病阶段相关。