In ischemic heart disease the presence and extent of collateral circulation can prevent myocardial infarction, or at least limit the damage and reduce the size of infarcts. The objective of this proposal is to characterize the development of coronary collaterals in the heart with methods based on magnetic resonance imaging (MRI). MRI-based measures of collateral growth can define the functional capacity of collaterals to preserve myocardial blood flow and contractile function in regions at risk of infarction. This would be a significant advantage over current angiographic methods used to define the extent of collateral circulation in the heart. The proposed studies will also determine to what degree collateral development in heart translates into an increased capacity of the heart to prevent stress-induced ischemia. The studies will be carried out in an experimental animal model of collateral development with slow progressive occlusion of the left circumflex coronary artery ('ameroid constrictor' model). This animal model of collateral development approximates the progression of coronary artery disease as it occurs in humans. The proposed diagnostic MRI techniques for assessment of collateral blood flow in the heart may in the future allow improved prediction of outcome. Understanding how collateral growth can be followed non-invasively also means that one can assess more effectively new therapies that boost collateral development in the heart and which could markedly change the natural history of coronary artery disease.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
1R01HL065394-01
Application #
6166115
Study Section
Diagnostic Radiology Study Section (RNM)
Project Start
2000-09-20
Project End
2003-07-31
Budget Start
2000-09-20
Budget End
2001-07-31
Support Year
1
Fiscal Year
2000
Total Cost
$293,454
Indirect Cost
Name
University of Minnesota Twin Cities
Department
Radiation-Diagnostic/Oncology
Type
Schools of Medicine
DUNS #
168559177
City
Minneapolis
State
MN
Country
United States
Zip Code
55455
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Muehling, O M; Huber, A; Cyran, C et al. (2007) The delay of contrast arrival in magnetic resonance first-pass perfusion imaging: a novel non-invasive parameter detecting collateral-dependent myocardium. Heart 93:842-7
Selvanayagam, Joseph B; Cheng, Adrian S H; Jerosch-Herold, Michael et al. (2007) Effect of distal embolization on myocardial perfusion reserve after percutaneous coronary intervention: a quantitative magnetic resonance perfusion study. Circulation 116:1458-64
Petersen, Steffen E; Jerosch-Herold, Michael; Hudsmith, Lucy E et al. (2007) Evidence for microvascular dysfunction in hypertrophic cardiomyopathy: new insights from multiparametric magnetic resonance imaging. Circulation 115:2418-25
Muehling, Olaf; Jerosch-Herold, Michael; Cyran, Clemens et al. (2007) Assessment of collateralized myocardium with Cardiac Magnetic Resonance (CMR): transmural extent of infarction but not angiographic collateral vessel filling determines regional function and perfusion in collateral-dependent myocardium. Int J Cardiol 120:38-44
Jerosch-Herold, Michael; Muehling, Olaf; Wilke, Norbert (2006) MRI of myocardial perfusion. Semin Ultrasound CT MR 27:2-10
Selvanayagam, Joseph B; Jerosch-Herold, Michael; Porto, Italo et al. (2005) Resting myocardial blood flow is impaired in hibernating myocardium: a magnetic resonance study of quantitative perfusion assessment. Circulation 112:3289-96
Swingen, Cory; Wang, Xiaoen; Jerosch-Herold, Michael (2004) Evaluation of myocardial volume heterogeneity during end-diastole and end-systole using cine MRI. J Cardiovasc Magn Reson 6:829-35
Jerosch-Herold, Michael; Hu, Xudong; Murthy, Naveen S et al. (2004) Time delay for arrival of MR contrast agent in collateral-dependent myocardium. IEEE Trans Med Imaging 23:881-90
Gallegos, Robert P; Swingen, Cory; Xu, Xunhai James et al. (2004) Infarct extent by MRI correlates with peak serum troponin level in the canine model. J Surg Res 120:266-71

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