Division of Cardiology, Johns Hopkins Medical Institutions, Baltimore, MD, USA.
Circ Cardiovasc Imaging. 2012 Mar;5(2):178-86. doi: 10.1161/CIRCIMAGING.111.968024. Epub 2012 Jan 20.
Annually, ≈80,000 Americans receive guideline-based primary prevention implantable cardioverter-defibrillators (ICDs), but appropriate firing rates are low. Current selection criteria for ICDs rely on left ventricular ejection fraction, which lacks sensitivity and specificity. Because scar-related myocardial tissue heterogeneity is a substrate for life-threatening arrhythmias, we hypothesized that cardiac magnetic resonance identification of myocardial heterogeneity improves risk stratification through (1) its association with adverse cardiac events independent of clinical factors and biomarker levels and (2) its ability to identify particularly high- and low-risk subgroups.
In 235 patients with chronic ischemic and nonischemic cardiomyopathy with a left ventricular ejection fraction of ≤35% undergoing clinically indicated primary prevention ICD implantation, gadolinium-enhanced cardiac magnetic resonance was prospectively performed to quantify the amount of heterogeneous myocardial tissue (gray zone [GZ]) and dense core scar. Serum high-sensitivity C-reactive protein (hsCRP) and other biomarkers were assayed. The primary end point was appropriate ICD shock for ventricular tachycardia/fibrillation or cardiac death, which occurred in 45 (19%) patients at a 3.6-year median follow-up. On univariable analysis, only diuretics, hsCRP, GZ, and core scar were associated with outcome. After multivariable adjustment, GZ and hsCRP remained independently associated with outcome (P<0.001). Patients in the lowest tertile for both GZ and hsCRP (n=42) were at particularly low risk (0.7% per year event rate), whereas those in the highest tertile for both GZ and hsCRP (n=32) had an event rate of 16.1% per year, P<0.001.
In a cohort of primary prevention ICD candidates, combining a myocardial heterogeneity index with an inflammatory biomarker identified a subgroup with a very low risk for adverse cardiac events, including ventricular arrhythmias. This novel approach warrants further investigation to confirm its value as a clinical risk stratification tool. Clinical Trial Registration- URL: http://www.clinicaltrials.gov. Unique identifier: NCT00181233.
每年,约有 8 万名美国人接受基于指南的植入式心脏复律除颤器(ICD)一级预防,但适当的电击率较低。目前 ICD 的选择标准依赖于左心室射血分数,但其缺乏敏感性和特异性。由于与瘢痕相关的心肌组织异质性是危及生命的心律失常的基础,我们假设心脏磁共振识别心肌异质性通过以下方式改善风险分层:(1)它与临床因素和生物标志物水平无关,与不良心脏事件相关联;(2)它能够识别特别高风险和低风险亚组。
在 235 名患有慢性缺血性和非缺血性心肌病且左心室射血分数≤35%的患者中,进行了临床指示的一级预防 ICD 植入,前瞻性地进行钆增强心脏磁共振检查,以量化不均匀心肌组织(灰色区[GZ])和致密核心瘢痕的量。检测血清高敏 C 反应蛋白(hsCRP)和其他生物标志物。主要终点是适当的 ICD 电击治疗室性心动过速/颤动或心脏性死亡,在中位数 3.6 年的随访中,有 45 例(19%)患者发生该事件。在单变量分析中,只有利尿剂、hsCRP、GZ 和核心瘢痕与结果相关。多变量调整后,GZ 和 hsCRP 仍然与结果独立相关(P<0.001)。GZ 和 hsCRP 均处于最低三分位的患者(n=42)风险特别低(每年 0.7%的事件发生率),而 GZ 和 hsCRP 均处于最高三分位的患者(n=32)的每年事件发生率为 16.1%,P<0.001。
在一级预防 ICD 候选者队列中,将心肌异质性指数与炎症生物标志物相结合,可确定一组发生不良心脏事件(包括室性心律失常)的风险极低的亚组。这种新方法需要进一步研究以确认其作为临床风险分层工具的价值。临床试验注册-网址:http://www.clinicaltrials.gov。唯一标识符:NCT00181233。