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Updated: Aug 2, 2026

3D Whole-heart Myocardial Tissue Analysis
Published on: April 12, 2017
Dipyridamole TI-201 SPECT imaging in patients with myocardial bridging
1Department of Nuclear Medicine, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea.
Insights
Myocardial bridging, a condition causing narrowed coronary arteries, can lead to perfusion abnormalities detected by dipyridamole TI-201 SPECT. These defects, particularly in the midanteroseptal wall, may indicate septal branch compression.
Area of Science:
- Cardiology
- Nuclear Cardiology
- Diagnostic Imaging
Background:
- Myocardial bridging can cause exercise-induced perfusion abnormalities, potentially due to shortened diastole from tachycardia.
- Dipyridamole TI-201 SPECT is used to evaluate myocardial perfusion under stress.
Purpose of the Study:
- To assess dipyridamole TI-201 SPECT findings in patients with myocardial bridging.
- To investigate perfusion abnormalities during dipyridamole stress in myocardial bridging.
Main Methods:
- Evaluated dipyridamole TI-201 SPECT images in 12 patients with myocardial bridging (≥50% systolic narrowing).
- Peak heart rate during dipyridamole stress was <110 bpm.
- Compared findings with 118 patients with fixed left anterior descending (LAD) artery disease.
Main Results:
- 71% of myocardial bridging sites showed reversible perfusion defects on dipyridamole TI-201 SPECT.
- High-grade narrowing (>80%) was associated with a higher rate of defects (7/8 sites).
- Isolated midanteroseptal perfusion defects were observed in 5 patients with septal branch compression, not seen in controls.
Conclusions:
- Dipyridamole TI-201 SPECT reveals perfusion abnormalities in myocardial bridging, particularly with high-grade narrowing.
- Myocardial bridging may reduce coronary flow reserve, not exclusively through tachycardia.
- Isolated midanteroseptal perfusion defects suggest septal branch compression in myocardial bridging.
Abstract:
PURPOSE: Exercise-induced myocardial perfusion abnormalities have been reported in patients with myocardial bridging, possibly by tachycardia-induced shortening of diastole. Dipyridamole TI-201 SPECT findings were evaluated in patients with myocardial bridging to assess perfusion abnormalities during dipyridamole stress. MATERIALS AND METHODS: Dipyridamole TI-201 SPECT images of 12 patients with myocardial bridging (> or = 50% systolic narrowing) were evaluated. The peak heart rate during dipyridamole stress was less than 110 beats/min in all patients. The control group was 118 patients with fixed left anterior descending artery (LAD) disease. RESULTS: Fourteen sites of systolic arterial narrowing were present in LAD: two in mid-LAD, seven in distal LAD, and five in septal branches. Dipyridamole TI-201 SPECT showed reversible perfusion defects in three of six sites with 50% to 70% systolic narrowing and seven of eight sites with more than 80% systolic narrowing. Overall, 71% (10 of 14) had a reversible perfusion defect. Five patients with septal branch compression had a perfusion defect in the midanteroseptal wall without an apical abnormality. In the control group, no patient had an isolated perfusion defect in the midanteroseptal wall or septal branch disease (5 of 12 compared with 0 of 118; P < 0.001). CONCLUSIONS: Perfusion abnormalities on dipyridamole TI-201 SPECT are observed in LAD or its branches in patients with high-grade myocardial bridging. Myocardial bridging may decrease coronary flow reserve but not necessarily via tachycardia. Isolated perfusion defects in the midanteroseptal wall may be a characteristic finding of septal branch compression, because a fixed lesion involving a septal branch only is rare.
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