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心血管磁共振心肌特征追踪在多巴酚丁胺应激时检测定量壁运动。

Cardiovascular magnetic resonance myocardial feature tracking detects quantitative wall motion during dobutamine stress.

机构信息

King's College London British Heart Foundation Centre of Excellence, London, UK.

出版信息

J Cardiovasc Magn Reson. 2011 Oct 12;13(1):58. doi: 10.1186/1532-429X-13-58.

DOI:10.1186/1532-429X-13-58
PMID:21992220
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3217847/
Abstract

BACKGROUND

Dobutamine stress cardiovascular magnetic resonance (DS-CMR) is an established tool to assess hibernating myocardium and ischemia. Analysis is typically based on visual assessment with considerable operator dependency. CMR myocardial feature tracking (CMR-FT) is a recently introduced technique for tissue voxel motion tracking on standard steady-state free precession (SSFP) images to derive circumferential and radial myocardial mechanics.We sought to determine the feasibility and reproducibility of CMR-FT for quantitative wall motion assessment during intermediate dose DS-CMR.

METHODS

10 healthy subjects were studied at 1.5 Tesla. Myocardial strain parameters were derived from SSFP cine images using dedicated CMR-FT software (Diogenes MRI prototype; Tomtec; Germany). Right ventricular (RV) and left ventricular (LV) longitudinal strain (EllRV and EllLV) and LV long-axis radial strain (ErrLAX) were derived from a 4-chamber view at rest. LV short-axis circumferential strain (EccSAX) and ErrSAX; LV ejection fraction (EF) and volumes were analyzed at rest and during dobutamine stress (10 and 20 μg · kg⁻¹· min⁻¹).

RESULTS

In all volunteers strain parameters could be derived from the SSFP images at rest and stress. EccSAX values showed significantly increased contraction with DSMR (rest: -24.1 ± 6.7; 10 μg: -32.7 ± 11.4; 20 μg: -39.2 ± 15.2; p < 0.05). ErrSAX increased significantly with dobutamine (rest: 19.6 ± 14.6; 10 μg: 31.8 ± 20.9; 20 μg: 42.4 ± 25.5; p < 0.05). In parallel with these changes; EF increased significantly with dobutamine (rest: 56.9 ± 4.4%; 10 μg: 70.7 ± 8.1; 20 μg: 76.8 ± 4.6; p < 0.05). Observer variability was best for LV circumferential strain (EccSAX ) and worst for RV longitudinal strain (EllRV) as determined by 95% confidence intervals of the difference.

CONCLUSIONS

CMR-FT reliably detects quantitative wall motion and strain derived from SSFP cine imaging that corresponds to inotropic stimulation. The current implementation may need improvement to reduce observer-induced variance. Within a given CMR lab; this novel technique holds promise of easy and fast quantification of wall mechanics and strain.

摘要

背景

多巴酚丁胺负荷心脏磁共振(DS-CMR)是评估冬眠心肌和缺血的一种成熟的工具。分析通常基于具有相当大的操作者依赖性的视觉评估。CMR 心肌特征追踪(CMR-FT)是一种最近引入的技术,用于在标准稳态自由进动(SSFP)图像上对组织体素运动进行跟踪,以得出圆周和径向心肌力学。我们旨在确定 CMR-FT 在中等剂量 DS-CMR 期间进行定量壁运动评估的可行性和可重复性。

方法

在 1.5T 下对 10 名健康受试者进行研究。使用专用的 CMR-FT 软件(Diogenes MRI 原型;Tomtec;德国)从 SSFP 电影图像中获得心肌应变参数。从 4 腔视图在休息时获得右心室(RV)和左心室(LV)纵向应变(EllRV 和 EllLV)和 LV 长轴径向应变(ErrLAX)。在休息和多巴酚丁胺应激时(10 和 20μg·kg⁻¹·min⁻¹)分析 LV 短轴圆周应变(EccSAX)和 ErrSAX;LV 射血分数(EF)和容量。

结果

在所有志愿者中,都可以从 SSFP 图像在休息和应激时得出应变参数。EccSAX 值显示收缩与 DSMR 明显增加(休息:-24.1±6.7;10μg:-32.7±11.4;20μg:-39.2±15.2;p<0.05)。ErrSAX 随着多巴酚丁胺的增加而显著增加(休息:19.6±14.6;10μg:31.8±20.9;20μg:42.4±25.5;p<0.05)。与这些变化平行,EF 随着多巴酚丁胺的增加而显著增加(休息:56.9±4.4%;10μg:70.7±8.1;20μg:76.8±4.6;p<0.05)。通过差异的 95%置信区间确定,观察者变异性最好为 LV 圆周应变(EccSAX),最差为 RV 纵向应变(EllRV)。

结论

CMR-FT 可靠地检测出从 SSFP 电影成像得出的定量壁运动和应变,这与变力刺激相对应。当前的实现可能需要改进,以减少观察者引起的方差。在给定的 CMR 实验室中;这项新技术有望实现壁力学和应变的快速、简便的定量。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e8d8/3217847/cc0c5218aa19/1532-429X-13-58-4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e8d8/3217847/6861f4dd0424/1532-429X-13-58-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e8d8/3217847/ea65e7c34e05/1532-429X-13-58-2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e8d8/3217847/085d9045397e/1532-429X-13-58-3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e8d8/3217847/cc0c5218aa19/1532-429X-13-58-4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e8d8/3217847/6861f4dd0424/1532-429X-13-58-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e8d8/3217847/ea65e7c34e05/1532-429X-13-58-2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e8d8/3217847/085d9045397e/1532-429X-13-58-3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e8d8/3217847/cc0c5218aa19/1532-429X-13-58-4.jpg

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