Abstract
Purpose: To examine and compare properties of high-molarity contrast agent gadobutrol (Gadovlst) and weakly protein-binding agent gadobenate-dimeglumine (MultiHance®) in dynamic susceptibility contrast (DSC) perfusion imaging at 3 T. Materials and Methods: Sixteen healthy volunteers underwent three separate examinations with contrast agent doses of 0.1 and 0.2 mmol/kg body weight (bw) gadobutrol and 0.1 mmol/kg bw gadobenate-dimeglumine. Maps of relative regional cerebral blood volume (rCBV) and blood flow (rCBF) were calculated using deconvolution based on singular value decomposition. Signal and concentration time curves, the concentration-to-noise ratio (SNRc), and gray matter (GM)-to-white matter (WM) rCBV and rCBF contrast and ratios were evaluated in a region of interest (ROI)-based analysis. Image quality of calculated parametric maps was assessed in direct visual comparison and with respect to suitability for diagnostic purposes. Results: The contrast agents displayed very similar results in the 0.1 mmol/kg examinations, both with respect to the quantitative evaluation parameters and in the qualitative assessment of the calculated parametric maps. Maps from 0.2 mmol/kg examinations were rated as being superior in quality, but with respect to diagnostic suitability all contrast agents and doses yielded images of sufficient quality. Conclusion: At 3 T, a gadobutrol or gadobenate-dimeglumine dose of 0.1 mmol/kg is sufficient for DSC magnetic resonance imaging (MRI) perfusion assessment. At the used small injection volumes, the tissue concentration curve was determined only by the gadolinium (Gd) dosage in mmol/kg, and the T2* relaxation effects of the two agents can be considered to be nearly identical in the applied gradient-echo (GRE) sequence. © 2005 Wiley-Liss, Inc.
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Thilmann, O., Larsson, E. M., Björkman-Burtscher, I. M., Ståhlberg, F., & Wirestam, R. (2005). Comparison of contrast agents with high molarity and with weak protein binding in cerebral perfusion imaging at 3 T. Journal of Magnetic Resonance Imaging, 22(5), 597–604. https://doi.org/10.1002/jmri.20420
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