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镰状β地中海贫血患者运动诱发的心肌灌注异常:锝-99m替曲膦门控单光子发射计算机断层显像研究

Exercise-induced myocardial perfusion abnormalities in sickle beta-thalassemia: Tc-99m tetrofosmin gated SPECT imaging study.

作者信息

Aessopos A, Tsironi M, Vassiliadis I, Farmakis D, Fountos A, Voskaridou E, Perakis A, Defteraios S, Loutradi A, Loukopoulos D

机构信息

First Department of Medicine, University of Athens, Medical School, Laiko Hospital, Athens, Greece.

出版信息

Am J Med. 2001 Oct 1;111(5):355-60. doi: 10.1016/s0002-9343(01)00835-x.

Abstract

PURPOSE

To determine the mechanism of myocardial ischemia in patients with sickle beta-thalassemia, we performed a scintigraphic evaluation of myocardial perfusion during exercise.

SUBJECTS AND METHODS

We studied 30 patients with sickle beta-thalassemia, (mean [+/-SD] age, 37 +/- 10 years) who had no electrocardiographic (ECG), radiographic, or echo-Doppler signs of pulmonary hypertension, left ventricular hypertrophy, or impaired contractility. All patients had a hemoglobin level greater than 7 g/dL. Treadmill exercise test was performed according to the Bruce protocol. Myocardial perfusion was assessed by single-photon emission computed tomography, using Tetrofosmin Tc-99 m Myoview as radiotracer, at peak exercise and again 4 hours later.

RESULTS

Eight patients (27%) developed stress-induced scintigraphic perfusion abnormalities that were reversible in all but 1 patient. Subsequent coronary angiograms were normal in all 8 patients. ST segment depression was seen during exercise in 5 of the 7 patients who had reversible perfusion defects. Except for a significantly greater white blood cell count, these 5 patients did not differ from the rest of patients by sex, age, hemoglobin level, percentage hemoglobin F, beta-thalassemia genotype, or risk factors for coronary artery disease. Three of the 5 patients with perfusion and ECG abnormalities (and another with only perfusion defects) developed a stress-induced sickling crisis.

CONCLUSION

Physical stress may induce myocardial ischemia in sickle beta-thalassemia patients with normal coronary arteries and elicit painful crises. The sickling process, activated by exercise, could be the common underlying mechanism.

摘要

目的

为了确定镰状β地中海贫血患者心肌缺血的机制,我们对运动期间的心肌灌注进行了闪烁显像评估。

对象与方法

我们研究了30例镰状β地中海贫血患者(平均年龄[±标准差]为37±10岁),这些患者没有心电图(ECG)、影像学或超声多普勒显示的肺动脉高压、左心室肥厚或收缩功能受损的迹象。所有患者的血红蛋白水平均高于7 g/dL。根据布鲁斯方案进行跑步机运动试验。使用锝-99m替曲膦(Myoview)作为放射性示踪剂,在运动高峰时及4小时后通过单光子发射计算机断层扫描评估心肌灌注。

结果

8例患者(27%)出现了应激诱导的闪烁显像灌注异常,除1例患者外,其余均为可逆性异常。随后对所有8例患者进行的冠状动脉造影均正常。在7例有可逆性灌注缺损的患者中,有5例在运动期间出现ST段压低。除白细胞计数显著更高外,这5例患者在性别、年龄、血红蛋白水平、血红蛋白F百分比、β地中海贫血基因型或冠状动脉疾病危险因素方面与其他患者无差异。5例有灌注和ECG异常的患者中有3例(另1例仅有灌注缺损)发生了应激诱导的镰状细胞危象。

结论

身体应激可能在冠状动脉正常的镰状β地中海贫血患者中诱发心肌缺血并引发疼痛危象。运动激活的镰状化过程可能是共同的潜在机制。

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