Susceptibility-sensitive magnetic resonance imaging detects human myocardium supplied by a stenotic coronary artery without a contrast agent

被引:82
作者
Wacker, CM
Hartlep, AW
Pfleger, S
Schad, LR
Ertl, G
Bauer, WR
机构
[1] Univ Wurzburg, Dept Cardiol, Med Clin, D-97080 Wurzburg, Germany
[2] DKFZ, German Canc Res Ctr, Dept Med Phys & Biophys, Heidelberg, Germany
[3] Univ Heidelberg, Med Clin Mannheim, D-6800 Mannheim, Germany
关键词
D O I
10.1016/S0735-1097(02)02931-5
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
OBJECTIVES Evaluation of the severity of a coronary artery stenosis is of paramount importance for therapy. A relevant stenosis provokes post-stenotic microvascular dilation with capillary recruitment. This autoregulatory response was investigated in the present study by use of susceptibility-sensitive magnetic resonance imaging (MRI) without contrast agents. BACKGROUND Functional alterations of the microvascular system may be studied noninvasively and without a contrast agent by susceptibility-sensitive MRI, which is based on the paramagnetic property of deoxyhemoglobin. This effect, also referred to as the "blood oxygenation level-dependent (BOLD) effect," is investigated by phase relaxation (T-2*) measurements. METHODS In patients (n = 16) with single-vessel coronary artery disease, no history of myocardial infarction, normal left ventricular function at rest, and a positive stress echocardiogram, the susceptibility-sensitive parameter T-2* was assessed in the myocardium. RESULTS In regions associated with the stenotic artery, T-2* was significantly lower than in residual myocardium (p < 0.01). This difference in T-2* increased after application of the vasodilator dipyridamole (p < 0.001). In patients being re-investigated after therapeutic interventions, the microvascular dilation was partly removed. CONCLUSIONS For the first time, we could show that myocardial BOLD MRI detects post-stenotic capillary recruitment dependent on coronary artery stenosis. (C) 2003 by the American College of Cardiology Foundation.
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页码:834 / 840
页数:7
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