Accelerated Cardiac Magnetic Resonance Imaging in the Mouse Using an Eight-Channel Array at 9.4 Tesla

British Heart Foundation Experimental MR Unit (BMRU), Department of Cardiovascular Medicine, University of Oxford, Oxford OX3 7BN, United Kingdom.
Magnetic Resonance in Medicine (Impact Factor: 3.57). 01/2011; 65(1):60-70. DOI: 10.1002/mrm.22605
Source: PubMed


MRI has become an important tool to noninvasively assess global and regional cardiac function, infarct size, or myocardial blood flow in surgically or genetically modified mouse models of human heart disease. Constraints on scan time due to sensitivity to general anesthesia in hemodynamically compromised mice frequently limit the number of parameters available in one imaging session. Parallel imaging techniques to reduce acquisition times require coil arrays, which are technically challenging to design at ultrahigh magnetic field strengths. This work validates the use of an eight-channel volume phased-array coil for cardiac MRI in mice at 9.4 T. Two- and three-dimensional sequences were combined with parallel imaging techniques and used to quantify global cardiac function, T(1)-relaxation times and infarct sizes. Furthermore, the rapid acquisition of functional cine-data allowed for the first time in mice measurement of left-ventricular peak filling and ejection rates under intravenous infusion of dobutamine. The results demonstrate that a threefold accelerated data acquisition is generally feasible without compromising the accuracy of the results. This strategy may eventually pave the way for routine, multiparametric phenotyping of mouse hearts in vivo within one imaging session of tolerable duration.

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    • "Realizing these competing constraints assessment of cardiac morphology, cardiac chamber quantification and cardiac function assessment require imaging protocols and hardware that are tailored for CMR. The hardware used in current experimental CMR of mice affords images with a typical in-plane spatial resolution of 100–200 µm, heart coverage of 6–13 slices of 1.0 mm thickness and measurement of 10–20 cardiac phases [1], [2], [3], [4], [5], [6], [7], [8], [9], [10]. Although these studies provide acceptable image quality for the quantitative assessment of the left ventricle (LV), assessment of the right ventricle (RV) remains challenging due to the limited image quality of the RV. "
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    ABSTRACT: Cardiac morphology and function assessment by magnetic resonance imaging is of increasing interest for a variety of mouse models in pre-clinical cardiac research, such as myocardial infarction models or myocardial injury/remodeling in genetically or pharmacologically induced hypertension. Signal-to-noise ratio (SNR) constraints, however, limit image quality and blood myocardium delineation, which crucially depend on high spatial resolution. Significant gains in SNR with a cryogenically cooled RF probe have been shown for mouse brain MRI, yet the potential of applying cryogenic RF coils for cardiac MR (CMR) in mice is, as of yet, untapped. This study examines the feasibility and potential benefits of CMR in mice employing a 400 MHz cryogenic RF surface coil, compared with a conventional mouse heart coil array operating at room temperature. The cryogenic RF coil affords SNR gains of 3.0 to 5.0 versus the conventional approach and hence enables an enhanced spatial resolution. This markedly improved image quality--by better deliniation of myocardial borders and enhanced depiction of papillary muscles and trabeculae--and facilitated a more accurate cardiac chamber quantification, due to reduced intraobserver variability. In summary the use of a cryogenically cooled RF probe represents a valuable means of enhancing the capabilities of CMR of mice.
    PLoS ONE 08/2012; 7(8):e42383. DOI:10.1371/journal.pone.0042383 · 3.23 Impact Factor
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    • "In recent years, the availability of rodent models of human disease has led to an increase in in vivo imaging studies of mice and rats. Small-animal MRI is at a less mature stage than human MRI, and recent effort has been concerned with the translation of imaging techniques from clinical systems to high-field, small-animal systems [1,2]. "
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    • "The resolution of the first-pass method may be improved through parallel imaging using multi channel phase array coils and accelerated image acquisitions. Schneider et al recently demonstrated the feasibility of using parallel imaging to achieve threefold acceleration of cine image acquisition in mice [37]. By using similar strategies, it may be possible to perform multi slice first-pass imaging with a spatial resolution that permits accurate delineation of underperfused areas of myocardium, or to assess changes in perfusion in peri-infarct areas in response to dobutamine stress or after experimental therapy with angiogenic cytokines or stem cells. "
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    ABSTRACT: In humans, dynamic contrast CMR of the first pass of a bolus infusion of Gadolinium-based contrast agent has become a standard technique to identify under-perfused regions of the heart and can accurately demonstrate the severity of myocardial infarction. Despite the clinical importance of this method, it has rarely been applied in small animal models of cardiac disease. In order to identify perfusion delays in the infarcted rat heart, here we present a method in which a T1 weighted MR image has been acquired during each cardiac cycle. In isolated perfused rat hearts, contrast agent infusion gave uniform signal enhancement throughout the myocardium. Occlusion of the left anterior descending coronary artery significantly reduced the rate of signal enhancement in anterior regions of the heart, demonstrating that the first-pass method was sensitive to perfusion deficits. In vivo measurements of myocardial morphology, function, perfusion and viability were made at 2 and 8 days after infarction. Morphology and function were further assessed using cine-MRI at 42 days. The perfusion delay was larger in rat hearts that went on to develop greater functional impairment, demonstrating that first-pass CMR can be used as an early indicator of infarct severity. First-pass CMR at 2 and 8 days following infarction better predicted outcome than cardiac ejection fraction, end diastolic volume or end systolic volume. First-pass CMR provides a predictive measure of the severity of myocardial impairment caused by infarction in a rodent model of heart failure.
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