心脏综合征X型患者心脏磁共振与显像心肌灌注的相关性研究

I. Vermeltfoort, P. Raijmakers, O. Bondarenko, A. Zwijnenburg, M. Hofman, G. Teule, A. Beek, A. Rossum
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引用次数: 2

摘要

背景:心脏综合征X是一种定义为胸痛、运动应激试验阳性和/或心肌显像和正常冠状动脉造影时可逆性心肌灌注缺陷的综合征,其缺血性起源仍有争议。在心脏综合征X患者中,没有研究比较应激第一遍心脏磁共振(CMR)与应激单光子发射计算机断层扫描(SPECT)对心肌灌注的影响。心肌mr灌注分析,利用心肌信号增强的归一化上斜率,得到心肌灌注指数(MPI)和心肌灌注储备指数(MPRI)。3名观察人员使用节段模型对SPECT图像进行视觉评分。结果:335个节段中有31个(9%)的MPRI值为1.2,提示局部缺血。SPECT显示335节段中39节段(12%)存在可逆性灌注缺损。然而,MPRI1.2和可逆性灌注缺损的组合仅在3节段中被检测到。结论:我们的数据显示CMR和SPECT显示约10%的应激性心肌灌注异常,提示局部缺血。然而,只有1%的节段心肌缺血的存在与两种检查一致。这一结果可能是导致冠状动脉微血管功能障碍的机制随时间变化的证据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Correlation of Myocardial Perfusion on Cardiac Magnetic Resonance Versus Myocardial Perfusion Scintigraphy in Cardiac Syndrome X
Background: In cardiac syndrome X, which is a syndrome defined as chest pain, positive exercise stress testing and/or reversible myocardial perfusion defects during myocardial scintigraphy and normal coronary angiograms, the ischemic origin is still debated. No previous study compared the myocardial perfusion in stress first-pass cardiac magnetic resonance (CMR) versus stress single-photon emission computed tomography (SPECT) in cardiac syndrome X. Methods: We performed stress SPECT and CMR imaging for 20 syndrome X patients. Perfusion analysis of the CMR was done by using the normalized upslope of myocardial signal enhancement to derive the myocardial perfusion index (MPI) and the myocardial perfusion reserve index (MPRI). The SPECT images were visually scored by 3 observers using a seg- mental model. Results: An MPRI of  1.2 was found for 31 (9%) of the 335 segments, indicating local ischemia. SPECT indicated re- versible perfusion defects for 39 (12%) of the 335 segments. However, the combination of both an MPRI  1.2 and a re- versible perfusion defect was detected in only 3 segments. Conclusions: Our data show about 10% stress-induced myocardial perfusion abnormalities on CMR and SPECT, suggest- ing local ischemia. However, only in 1% of the segments there was concordance for the presence of myocardial ischemia with both exams. This result may be evidence for the variability over time of the mechanisms responsible for coronary microvascular dysfunction.
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