Helmsley Electrophysiology Center, Icahn School of Medicine at Mount Sinai, New York, New York, USA.
The BioMedical Engineering and Imaging Institute (BMEII), Icahn School of Medicine at Mount Sinai, New York, New York, USA.
JACC Clin Electrophysiol. 2023 Aug;9(8 Pt 3):1709-1716. doi: 10.1016/j.jacep.2023.04.011. Epub 2023 May 24.
Sustained ventricular tachycardia and sudden cardiac death due to degenerative mitral valve prolapse (MVP) can occur in the absence of severe mitral regurgitation (MR). A significant percentage of patients with MVP-related sudden death do not have any evidence of replacement fibrosis, suggesting other unrecognized proarrhythmic factors may place these patients at risk.
This study aims to characterize myocardial fibrosis/inflammation and ventricular arrhythmia complexity in patients with MVP and only mild or moderate MR.
Prospective observational study of patients with MVP and only mild or moderate MR underwent ventricular arrhythmia characterization and hybrid positron emission tomography (PET)/magnetic resonance imaging (MRI). Coregistered hybrid Ffluorodeoxyglucose (F-FDG)-PET and MRI late gadolinium enhancement images were assessed and categorized. Recruitment occurred in the cardiac electrophysiology clinic.
In 12 patients with degenerative MVP with only mild or moderate MR, of which a majority had complex ventricular ectopy (n = 10, 83%), focal (or focal-on-diffuse) uptake of F-FDG (PET-positive) was detected in 83% (n = 10) of patients. Three-quarters of the patients (n = 9, 75%) had FDG uptake that coexisted with areas of late gadolinium enhancement (PET/MRI-positive). Abnormal T1, T2 and extracellular volume (ECV) values were observed in 58% (n = 7), 25% (n = 3), and 16% (n = 2), respectively.
Most patients with degenerative MVP, ventricular ectopy, and mild or moderate MR show myocardial inflammation that is concordant with myocardial scar. Further study is needed to determine whether these findings contribute to the observation that most MVP-related sudden deaths occur in patients with less than severe MR.
退行性二尖瓣脱垂(MVP)可导致持续性室性心动过速和心源性猝死,即使不存在严重的二尖瓣反流(MR)也是如此。有相当一部分 MVP 相关性心源性猝死患者没有任何替代纤维化的证据,这表明可能存在其他未被识别的致心律失常因素,使这些患者面临风险。
本研究旨在描述 MVP 且仅有轻度或中度 MR 的患者的心肌纤维化/炎症和室性心律失常复杂性。
前瞻性观察性研究纳入了 MVP 且仅有轻度或中度 MR 的患者,这些患者接受了室性心律失常特征描述和杂交正电子发射断层扫描(PET)/磁共振成像(MRI)检查。评估和分类了融合氟脱氧葡萄糖(F-FDG)-PET 和 MRI 晚期钆增强图像。招募在心脏电生理诊所进行。
在 12 名 MVP 退行性变且仅有轻度或中度 MR 的患者中,大多数患者存在复杂室性心律失常(n = 10,83%),其中 83%(n = 10)的患者检测到 F-FDG(PET 阳性)摄取局灶性(或局灶性-弥漫性)摄取。75%(n = 9)的患者有 FDG 摄取与晚期钆增强区域共存(PET/MRI 阳性)。58%(n = 7)的患者存在异常 T1、T2 和细胞外容积(ECV)值,分别为 25%(n = 3)和 16%(n = 2)。
大多数 MVP、室性心律失常和轻度或中度 MR 的退行性患者表现出与心肌瘢痕一致的心肌炎症。需要进一步研究以确定这些发现是否导致 MVP 相关性心源性猝死大多发生在 MR 不严重的患者中的观察结果。