T2* measurement during first-pass contrast-enhanced cardiac perfusion imaging

Laboratory of Cardiac Energetics, National Heart, Lung and Blood Institute, National Institutes of Health, DHHS, Bethesda, Maryland 20892-1061, USA.
Magnetic Resonance in Medicine (Impact Factor: 3.57). 11/2006; 56(5):1132-4. DOI: 10.1002/mrm.21061
Source: PubMed


First-pass contrast-enhanced (CE) myocardial perfusion imaging will experience T(2) (*) effects at peak concentrations of contrast agent. A reduction in the signal intensity of left ventricular (LV) blood due to T(2) (*) losses may effect estimates of the arterial input function (AIF) used for quantitative perfusion measurement. Imaging artifacts may also result from T(2) (*) losses as well as off-resonance due to the bolus susceptibility. We hypothesized that T(2) (*) losses would not be significant for measurement of the AIF in full-dose studies using a short echo time (TE = 0.6 ms). The purpose of this study was to directly measure T(2) (*) in the LV cavity during first-pass perfusion. For single-dose Gd-DTPA (0.1 mmol/kg at 5 ml/s), the LV blood pool T(2) (*) had a mean value of 9 ms (N = 10) at peak enhancement. Distortion of the AIF due to T(2) (*) signal intensity loss will be less than 10% using TE = 0.6 ms.

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    • "The effects of non-uniform magnitude modulation during data acquisition were also numerically simulated for three pairs of (T1, T2*) values in milliseconds: (120, 20), (13, 5), and (5, 2). The T2* values were estimated as approximately half of the T2, based on first-pass measurements in the left ventricle [12]. The T1 and T2 relaxation times correspond to CA concentrations in the RV of ≈1.6, 16 and 46 mmol/L, using relaxivities r1=4.5, r2=5.1 L mmol−1 sec−1. "
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    • "For example, measurements of regional myocardial blood flow (in ml/g/min) can be made using time-intensity curve deconvolution with a measured arterial input function (AIF), usually from the left ventricular cavity or ascending aorta[29,30]. Measurement of the true AIF is affected by short T1s and T2* effects[31] that occur with high contrast agent concentrations during bolus contrast agent passage in the blood pool. This has led to two imaging strategies: 1) the "dual-bolus" method[32,33], which involves AIF measurement during a separate low-dose injection (1/10th or 1/20th the dose) prior to the full-dose injection used for the measurement of myocardial enhancement and 2) the "dual-sequence" method [34-36], which replaces one of the imaging slices with an AIF measurement slice that employs an acquisition that avoids the saturation and T2* effects at high concentrations. "
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