Department of Medicine, Heart Research Follow-up Program, University of Rochester Medical Center, Rochester, New York; Department of Public Health Sciences, University of Rochester Medical Center, Rochester, New York.
Department of Medicine, Heart Research Follow-up Program, University of Rochester Medical Center, Rochester, New York.
Am J Cardiol. 2018 Jan 15;121(2):182-187. doi: 10.1016/j.amjcard.2017.10.010. Epub 2017 Nov 13.
Patients with long QT syndrome (LQTS) are at a high risk of cardiac events. Many patients with LQTS are treated with antidepressant drugs (ADs). We investigated the LQTS genotype-specific risk of recurrent cardiac arrhythmic events (CAEs) associated with AD therapy. The study included 59 LQT1 and 72 LQT2 patients from the Rochester-based LQTS Registry with corrected QT (QT) prolongation and a history of AD therapy. Using multivariate Anderson-Gill models, we estimated the LQTS genotype-specific risk of recurrent CAEs (ventricular tachyarrhythmias, aborted cardiac arrest, or sudden cardiac death) associated with time-dependent ADs. Specifically, we examined the risk associated with all ADs, selective serotonin reuptake inhibitor (SSRI), and ADs classified on the CredibleMeds list (www.CredibleMeds.org) as "Conditional" or "Known risk of Torsades de pointes (TdP)." After adjusting for baseline QT duration, sex, and time-dependent beta-blocker usage, there was an increased risk of recurrent CAEs associated with ADs in LQT1 patients (hazard ratio = 3.67, 95% confidence interval 1.98-6.82, p < 0.001) but not in LQT2 patients (hazard ratio = 0.89, 95% confidence interval 0.49-1.64, p = 0.716; LQT1 vs LQT2 interaction, p < 0.001). Similarly, LQT1 patients who were on SSRIs or ADs with "Known risk of TdP" had a higher risk of recurrent CAEs than those patients off all ADs, whereas there was no association in LQT2 patients. ADs with "Conditional risk of TdP" were not associated with the risk of recurrent CAEs in any of the groups. In conclusion, the risk of recurrent CAEs associated with time-dependent ADs is higher in LQT1 patients but not in LQT2 patients. Results suggest a LQTS genotype-specific effect of ADs on the risk of arrhythmic events.
患有长 QT 综合征(LQTS)的患者发生心脏事件的风险很高。许多 LQTS 患者接受抗抑郁药(ADs)治疗。我们研究了与 AD 治疗相关的复发性心律失常事件(CAEs)与 AD 治疗相关的 LQTS 基因型特异性风险。该研究纳入了来自罗切斯特 LQTS 注册中心的 59 例 LQT1 和 72 例 LQT2 患者,这些患者的 QT 间期延长且有 AD 治疗史。我们使用多变量 Anderson-Gill 模型估计了与时间依赖性 AD 相关的复发性 CAEs(室性心动过速、心搏骤停未遂或心源性猝死)的 LQTS 基因型特异性风险。具体而言,我们检查了与所有 AD、选择性 5-羟色胺再摄取抑制剂(SSRIs)以及被 CredibleMeds 清单(www.CredibleMeds.org)列为“有条件”或“已知尖端扭转型室性心动过速(TdP)风险”的 AD 相关的风险。在调整了基线 QT 间期、性别和时间依赖性β受体阻滞剂使用后,LQTS1 患者的 AD 治疗与复发性 CAEs 相关(危险比=3.67,95%置信区间 1.98-6.82,p<0.001),但在 LQT2 患者中则没有(危险比=0.89,95%置信区间 0.49-1.64,p=0.716;LQTS1 与 LQT2 交互作用,p<0.001)。同样,服用 SSRIs 或有“已知 TdP 风险”的 AD 的 LQT1 患者比未服用所有 AD 的患者发生复发性 CAEs 的风险更高,而 LQT2 患者则没有关联。具有“TdP 条件风险”的 AD 在任何一组中均与复发性 CAEs 风险无关。总之,与时间依赖性 AD 相关的复发性 CAEs 的风险在 LQT1 患者中更高,但在 LQT2 患者中则没有。结果表明 AD 对心律失常事件的风险具有 LQTS 基因型特异性效应。