Blich Miry, Darawsha Wisam, Eyal Allon, Shehadeh Faheem, Boulous Monther, Gepstein Lior, Suleiman Mahmoud
Inherited Arrhythmia Clinic, Rambam Health Care Campus Haifa, Israel.
Division of Pacing and Electrophysiology, Rambam Health Care Campus Haifa, Israel.
Am J Cardiovasc Dis. 2024 Feb 20;14(1):47-53. doi: 10.62347/CSVQ9929. eCollection 2024.
Dilated cardiomyopathy (DCM) caused by Lamin A/C gene (LMNA) mutation is complicated with atrioventricular conduction disturbances, malignant ventricular arrhythmias and progressive severe heart failure.
We hypothesized that early cardiac resynchronization therapy (CRT) implantation in LMNA mutation carriers with an established indication for pacemaker or implantable cardioverter defibrillator (ICD), may preserve ejection fraction, and delay disease progression to end stage heart failure.
We compared the primary outcomes: time to heart transplantation, death due to end stage heart failure or ventricular tachycardia (VT) ablation and secondary outcomes: change in left ventricular ejection fraction (EF) and ventricular arrhythmia burden between LMNA DCM patients in the early CRT and non-CRT groups.
Of ten LMNA DCM patients (age 51±10 years, QRS 96±14 msec, EF 55±7%) with indication for pacemaker or ICD implantation, five underwent early CRT-D implantation. After 7.2±4 years, three patients (60%) in the non-CRT group reached the primary outcome, compared to no patients in the CRT group (P=0.046). Four patients in non-CRT group (80%) experienced sustained ventricular tachycardia or received appropriate ICD shock compared to 1 patient (20%) in the CRT group (P=0.058). LMNA patients without early CRT had a higher burden of VPC/24 h in 12-lead holter (median 2352 vs 185, P=0.09). Echocardiography showed statistically lower LVEF in the non-CRT group compared to CRT group [(32±15)% vs (61±4)%, 95% CI: 32.97-61.03, P=0.016].
Early CRT implantation in LMNA cardiomyopathy patients, with an indication for pacemaker or ICD, may reduce heart failure deterioration and life-threatening heart failure complications.
由核纤层蛋白A/C基因(LMNA)突变引起的扩张型心肌病(DCM)常伴有房室传导障碍、恶性室性心律失常和进行性严重心力衰竭。
我们假设,对于有起搏器或植入式心脏复律除颤器(ICD)植入适应证的LMNA突变携带者,早期植入心脏再同步治疗(CRT)可能会保留射血分数,并延缓疾病进展至终末期心力衰竭。
我们比较了主要结局:心脏移植时间、因终末期心力衰竭或室性心动过速(VT)消融导致的死亡,以及次要结局:早期CRT组和非CRT组中LMNA DCM患者左心室射血分数(EF)的变化和室性心律失常负担。
在10例有起搏器或ICD植入适应证的LMNA DCM患者(年龄51±10岁,QRS 96±14毫秒,EF 55±7%)中,5例接受了早期CRT-D植入。7.2±4年后,非CRT组有3例患者(60%)达到主要结局,而CRT组无患者达到(P=0.046)。非CRT组有4例患者(80%)发生持续性室性心动过速或接受了适当的ICD电击,而CRT组为1例患者(20%)(P=0.058)。未接受早期CRT的LMNA患者在12导联动态心电图中每24小时室性早搏(VPC)负担更高(中位数2352对185,P=0.09)。超声心动图显示,非CRT组的左心室射血分数(LVEF)在统计学上低于CRT组[(32±15)%对(61±4)%,95%可信区间:32.97-61.03,P=0.016]。
对于有起搏器或ICD适应证的LMNA心肌病患者,早期植入CRT可能会减少心力衰竭恶化和危及生命的心力衰竭并发症。