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Poster Sessions<br />

1315. Myocardial BOLD Imaging at 3T Using Quantitative T2: Application in a Myocardial Infarct Model<br />

Nilesh R. Ghugre 1 , Venkat Ramanan 1 , Mihaela Pop 2 , Yuesong Yang 1 , Jennifer Barry 1 , Beiping Qiang 1 , Kim<br />

Connelly 3 , Alexander J. Dick 1 , Graham A. Wright 1,2<br />

1 Imaging Research, Sunnybrook Health Sciences Centre, Toronto, ON, Canada; 2 Department of Medical Biophysics, University of<br />

Toronto, Toronto, ON, Canada; 3 Division of Cardiology, St. Michael's Hospital, Toronto, ON, Canada<br />

Coronary vasodilatory dysfunction has been shown in infarcted as well as remote myocardium in patients with acute coronary syndrome. Our study<br />

demonstrates the utility of T2-based BOLD effect in probing regional and longitudinal fluctuations in vasodilatory function in a porcine model of myocardial<br />

infarction at 3T. T2 measurements were performed in remote and infarcted myocardium at rest and after Dipyridamole-induced vasodilation (stress).<br />

Experimental observations indicated that T2 at 3T offers greater sensitivity towards detecting changes in myocardial oxygenation compared to 1.5T,<br />

consistent with a two-compartment theoretical model. Stress-induced vasodilatory response using quantitative T2 can help evaluate remote-zone vascular<br />

function and potentially identity salvageable myocardium in the infarct zone.<br />

MRS of the Heart<br />

Hall B Tuesday 13:30-15:30<br />

1316. MRI/MRS Biomarkers for Response Evaluation in Patients with CABG<br />

Zhuoli Zhang 1 , Shengyong Wu 2 , Ying Liu 3 , Savita Puri 4 , Shara Ramaswamy 5 , Yi Huan 3 , Debiao Li 1<br />

1 Northwestern University, Chicago, IL, United States; 2 Tianjin Medical University; 3 Fourth Military Medical University; 4 University<br />

of Rochester Medical Center; 5 Florida International University<br />

Phosphorus-31 magnetic resonance spectroscopy (31P-MRS) represents a unique instrument to noninvasively monitor myocardial metabolism in humans.<br />

The technique has been used to study the metabolism in myocardium in patients with coronary artery disease (CAD). The measurements permit quantitative<br />

estimation of the phosphocreatine (PCr)/adenosine triphosphate (â-ATP) ratio which reflects the energetic state of the myocardium. Previous studies<br />

investigated the effect of successful coronary artery bypass grafting surgery (CABG) upon left ventricular function. Although residual myocardial viability<br />

in patients with CAD and extensive regional asynergy is associated with improved ventricular function after CABG, the relationship between myocardial<br />

metabolism and heart function after CABG remains unclear. We hypothesized that cardiac function benefits from high-energy phosphate (HEP) and sought<br />

to investigate the relationship between HEP and cardiac function in CAD patients using cine magnetic resonance imaging (cine-MRI) and 31P-MRS.<br />

1317. Cardiac Lipid Content as Determined by Magnetic Resonance Spectroscopy Increases After Exercise<br />

Protocol in the Fasted State<br />

Vera Schrauwen-Hinderling 1 , Lena Bilet 1 , Tineke van de Weijer 1 , Matthijs Hesselink 1 , Jan Glatz 1 , Joachim<br />

Wildberger 1 , Michael Schär 2,3 , Eline Kooi 1 , Patrick Schrauwen 1<br />

1 Maastricht University Medical Center, Maastricht, Netherlands; 2 Johns Hopkins University, Baltimore, United States; 3 Philips Health<br />

Care, Cleveland, United States<br />

Excessive lipid accumulation in the myocardium may predispose to cardiomyopathy. Elevated plasma (free) fatty acids (FA) might be a risk factor herein.<br />

Cardiac lipid content was determined by 1H-MRS in healthy men (fasted state). Subsequently, subjects cycled for two hours and rested for three hours, after<br />

which cardiac lipid content was measured again. All subjects performed this protocol twice: once fasted and once while ingesting glucose to keep FA low.<br />

Cardiac lipid content was elevated after the fasted test day but unchanged when glucose ingestion kept FA low. This suggests that FA are important in<br />

determining cardiac lipid content.<br />

1318. The Role of Cardiac Carbonic Anhydrases in Vivo: A Hyperpolarised 13 C MR Study<br />

Marie Allen Schroeder 1 , Pawel Swietach 1 , Philip Lee 2 , Ferdia A. Gallagher 3,4 , Ben Rowlands 1 , Claudiu T.<br />

Supuran 5 , Kevin M. Brindle, 4,6 , Richard D. Vaughan-Jones 1 , George K. Radda 1,2 , Kieran Clarke 1 , Damian<br />

J. Tyler 1<br />

1 Physiology, Anatomy and Genetics, University of Oxford, Oxford, Oxfordshire, United Kingdom; 2 Biomedical Sciences Institute,<br />

Singapore Bioimaging Consortium, Singapore, Singapore; 3 Radiology, Addenbrooke's Hospital, University of Cambridge, Cambridge,<br />

United Kingdom; 4 Li Ka Shing Centre, CRUK Cambridge Research Institute, Cambridge, United Kingdom; 5 Dipartimento di<br />

Chimica, University of Florence, Florence, Italy; 6 Biochemistry, University of Cambridge, Cambridge, United Kingdom<br />

Carbonic anhydrase (CA) catalyses the hydration of CO 2 to form HCO 3 - and H+, an inter-conversion which serves as a major pH buffer in blood plasma and<br />

inside cells. To date, cardiac isoforms of CA have only been studied in vitro, where their function could be drastically different than in vivo. The aim of this<br />

study was to determine the effects of intra- and extracellular isoforms of CA on CO 2 efflux from the heart, in vivo, based on MRS detection of 13 CO 2<br />

generated from the metabolism of hyperpolarised [1- 13 C]pyruvate. Our results indicated that extracellular CAs do not affect cardiac CO 3 removal under<br />

control perfusion conditions, though may have a role in ischemia. Further, we observed that intracellular CA activity trapped HCO 3 - and H+ within the<br />

myocyte, which could potentially acidify the intracellular space. Physiological levels of cardiac intracellular CA must balance retention of myocardial<br />

bicarbonate to buffer potential acid/base disturbances, without causing excessive intracellular acidification.<br />

1319. Evaluation for Optimal Stress System for Cardiac MR Study<br />

Hee-Won Kim 1,2 , Karam Souibri 3 , Gerald M. Pohost 1,4<br />

1 Radiology, University of Southern California, Los Angeles, CA, United States; 2 Cardiology, Heart and Vascular Institute, Hollywood<br />

Presbyterian Hospital, Los Angeles, CA, United States; 3 Cardiology, University of Southern California, Los Angeles, CA, United<br />

States; 4 Electrical Engineering, University of Southern California, Los Angeles, CA, United States<br />

A stress control system was developed and evaluated to obtain improved precision of the stress MR studies. The stability in stress was achieved by the feedforward<br />

or feedback control and audio-visual stimulation actuated by the error signal. The system performance was evaluated by cardiac P-31 MRS at 3T.

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