Junttila M Juhani, Brugada Pedro, Hong Kui, Lizotte Eric, DE Zutter Marc, Sarkozy Andrea, Brugada Josep, Benito Begona, Perkiomaki Juha S, Mäkikallio Timo H, Huikuri Heikki V, Brugada Ramon
Division of Cardiology, Department of Medicine, University of Oulu, Finland.
J Cardiovasc Electrophysiol. 2008 Apr;19(4):380-3. doi: 10.1111/j.1540-8167.2007.01050.x. Epub 2007 Dec 12.
Brugada syndrome (BrS) is an inherited disorder that predisposes some subjects to sudden cardiac death (SCD). It is not well established which BrS patients are at risk of severe arrhythmias. Our aim was to study whether standard 12-lead electrocardiogram (ECG) would give useful information for this purpose.
This study included 200 BrS probands (142 male, 62%; mean age 42 +/- 16 years). Symptoms related to BrS were defined as syncope, documented ventricular tachyarrhythmia, or SCD. We determined PR, QRS, QTc, T(peak), and T(end) interval from leads II and V(2) and QRS from lead V(5), R'/S ratio from lead aVR (aVR sign), QRS axis, and J-point elevation amplitude from right precordial leads from the baseline ECGs.
Sixty-six subjects (33%) had experienced symptoms related to BrS. The only significant difference between the symptomatic and asymptomatic BrS subjects was the QRS duration measured from lead II or lead V(2), for example, the mean QRS in V(2) was 115 +/- 26 ms in symptomatic versus 104 +/- 19 ms in asymptomatic patients (P < 0.001). The optimized cut-off point of V(2) QRS > or =120 ms gave an odds ratio (OR) of 2.5 (95% CI: 1.4-4.6, P = 0.003) for being symptomatic. In a multivariate analysis adjusted with gender, age, and SCN5A mutation, the OR was 2.6 (95% CI: 1.4-4.8, P = 0.004).
Prolonged QRS duration, measured from standard 12-lead ECG, is associated with symptoms and could serve as a simple noninvasive risk marker of vulnerability to life-threatening ventricular arrhythmias in BrS.
布加综合征(BrS)是一种遗传性疾病,使一些患者易发生心源性猝死(SCD)。目前尚不清楚哪些布加综合征患者有发生严重心律失常的风险。我们的目的是研究标准12导联心电图(ECG)是否能为此提供有用信息。
本研究纳入200例布加综合征先证者(142例男性,占62%;平均年龄42±16岁)。与布加综合征相关的症状定义为晕厥、记录到的室性快速心律失常或心源性猝死。我们从基线心电图的II导联和V₂导联测定PR、QRS、QTc、T(峰)和T(终)间期,从V₅导联测定QRS,从aVR导联测定R′/S比值(aVR征)、QRS电轴以及右胸前导联的J点抬高幅度。
66例患者(33%)曾出现与布加综合征相关的症状。有症状和无症状的布加综合征患者之间唯一显著的差异是从II导联或V₂导联测得的QRS时限,例如,有症状患者V₂导联的平均QRS为115±26毫秒,而无症状患者为104±19毫秒(P<0.001)。V₂导联QRS≥120毫秒的优化切点得出有症状的比值比(OR)为2.5(95%可信区间:1.4 - 4.6,P = 0.003)。在对性别、年龄和SCN5A突变进行校正的多变量分析中,OR为2.6(95%可信区间:1.4 - 4.8,P = 0.004)。
从标准12导联心电图测得的QRS时限延长与症状相关,可作为布加综合征患者发生危及生命的室性心律失常易感性的简单非侵入性风险标志物。