Prognostic value of mid-term cardiovascular magnetic resonance follow-up in patients with non-ischemic dilated cardiomyopathy: a prospective cohort study

医学 射血分数 狼牙棒 四分位间距 心脏病学 内科学 危险系数 比例危险模型 心力衰竭 心脏磁共振成像 经皮冠状动脉介入治疗 扩张型心肌病 置信区间 磁共振成像 心肌梗塞 放射科
作者
Yuanwei Xu,Yangjie Li,Shiqian Wang,Ke Wan,Yinxi Tan,Weihao Li,Jie Wang,Jiajun Guo,Saeed Ghaithan,Wei Cheng,Jiayu Sun,Qing Zhang,Yuchi Han,Yucheng Chen
出处
期刊:Journal of Cardiovascular Magnetic Resonance [BioMed Central]
卷期号:26 (1): 101002-101002 被引量:1
标识
DOI:10.1016/j.jocmr.2024.101002
摘要

The prognostic value of follow-up cardiovascular magnetic resonance (CMR) in dilated cardiomyopathy (DCM) patients is unclear. We aimed to investigate the prognostic value of cardiac function, structure, and tissue characteristics at mid-term CMR follow-up. The study population was a prospectively enrolled cohort of DCM patients who underwent guideline-directed medical therapy with baseline and follow-up CMR, which included measurement of biventricular volume and ejection fraction, late gadolinium enhancement, native T1, native T2, and extracellular volume. During follow-up, major adverse cardiac events (MACE) were defined as a composite endpoint of cardiovascular death, heart transplantation, and heart-failure readmission. Among 235 DCM patients (median CMR interval: 15.3 months; interquartile range: 12.5–19.2 months), 54 (23.0%) experienced MACE during follow-up (median: 31.2 months; interquartile range: 20.8–50.0 months). In multivariable Cox regression, follow-up CMR models showed significantly superior predictive value than baseline CMR models. Stepwise multivariate Cox regression showed that follow-up left ventricular ejection fraction (LVEF; hazard ratio [HR], 0.93; 95% confidence interval [CI], 0.91–0.96; p < 0.001) and native T1 (HR, 1.01; 95% CI, 1.00–1.01; p = 0.030) were independent predictors of MACE. Follow-up LVEF ≥ 40% or stable LVEF < 40% with T1 ≤ 1273 ms indicated low risk (annual event rate < 4%), while stable LVEF < 40% and T1 > 1273 ms or LVEF < 40% with deterioration indicated high risk (annual event rate > 15%). Follow-up CMR provided better risk stratification than baseline CMR. Improvements in the LVEF and T1 mapping are associated with a lower risk of MACE.
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