Shi Cindy Q, Young Lawrence H, Daher Edouard, DiBella Edward V R, Liu Yi-Hwa, Heller Eliot N, Zoghbi Sami, Wackers Frans J Th, Soufer Robert, Sinusas Albert J
Experimental Nuclear Cardiology Laboratory, Division of Cardiovascular Medicine, Department of Internal Medicine, Yale University School of Medicine, New Haven, Connecticut 06520-8017, USA.
J Nucl Med. 2002 Mar;43(3):421-31.
Myocardial ischemia is associated with reduced free fatty acid (FFA) beta-oxidation and increased glucose utilization. This study evaluated the potential of dynamic SPECT imaging of a FFA analog, p-(123)I-iodophenylpentadecanoic acid (IPPA), for detection of ischemia and compares retention of IPPA with (18)F-FDG accumulation.
In a canine model of regional low-flow ischemia (n = 9), serial IPPA SPECT images (2 min per image) were acquired over 52--90 min. In a subset of dogs (n = 6), (18)F-FDG was injected after completing SPECT imaging and allowed to accumulate for 40 min before killing the animals. Flow was assessed with radiolabeled microspheres. Myocardial metabolism was evaluated independently by selective coronary arterial and venous sampling.
Serial IPPA SPECT images showed an initial defect in the ischemic region (0.70% plus minus 0.03% ischemic-to-nonischemic ratio), which normalized within 48 min because of the slower IPPA clearance from the ischemic region (t(1/2) = 54.2 plus minus 3.3 min) relative to the nonischemic region (t(1/2) = 36.7 plus minus 5.6 min) (P < 0.05). Delayed myocardial IPPA and (18)F-FDG activities were correlated (r = 0.70; n = 576 segments), and both were maximally increased in segments with a moderate flow reduction (IPPA, 151% of nonischemic; (18)F-FDG, 450% of nonischemic; P < 0.05).
Serial SPECT imaging showed delayed myocardial clearance of IPPA in ischemic regions with moderate flow reduction, which lead to increased late myocardial retention of IPPA. Retention of IPPA correlated with (18)F-FDG accumulation, supporting the potential of IPPA as a noninvasive marker of ischemic myocardium.
心肌缺血与游离脂肪酸(FFA)β氧化减少和葡萄糖利用增加有关。本研究评估了FFA类似物对-(123)I-碘苯基十五烷酸(IPPA)的动态SPECT成像检测缺血的潜力,并比较了IPPA的滞留情况与(18)F-FDG的积聚情况。
在局部低流量缺血犬模型(n = 9)中,在52 - 90分钟内采集连续的IPPA SPECT图像(每张图像2分钟)。在一部分犬(n = 6)中,在完成SPECT成像后注射(18)F-FDG,并在处死动物前使其积聚40分钟。用放射性微球评估血流。通过选择性冠状动脉和静脉采样独立评估心肌代谢。
连续的IPPA SPECT图像显示缺血区域最初有缺损(缺血与非缺血比值为0.70%±0.03%),由于IPPA从缺血区域清除较慢(t(1/2)=54.2±3.3分钟),相对于非缺血区域(t(1/2)=36.7±5.6分钟),该缺损在48分钟内恢复正常(P<0.05)。延迟的心肌IPPA和(18)F-FDG活性相关(r = 0.70;n = 576节段),并且在血流中度减少的节段中两者均最大程度增加(IPPA,为非缺血节段的151%;(18)F-FDG,为非缺血节段的450%;P<0.05)。
连续SPECT成像显示在血流中度减少的缺血区域心肌对IPPA的清除延迟,这导致心肌对IPPA的晚期滞留增加。IPPA的滞留与(18)F-FDG的积聚相关,支持IPPA作为缺血心肌无创标志物的潜力。