Parameter Optimization for Quantitative Signal-Concentration Mapping Using Spoiled Gradient Echo MRI
نویسندگان
چکیده
Rationale and Objectives. Accurate signal to tracer concentration maps are critical to quantitative MRI. The purpose of this study was to evaluate and optimize spoiled gradient echo (SPGR) MR sequences for the use of gadolinium (Gd-DTPA) as a kinetic tracer. Methods. Water-gadolinium phantoms were constructed for a physiologic range of gadolinium concentrations. Observed and calculated SPGR signal to concentration curves were generated. Using a percentage error determination, optimal pulse parameters for signal to concentration mapping were obtained. Results. The accuracy of the SPGR equation is a function of the chosen MR pulse parameters, particularly the time to repetition (TR) and the flip angle (FA). At all experimental values of TR, increasing FA decreases the ratio between observed and calculated signals. Conversely, for a constant FA, increasing TR increases this ratio. Using optimized pulse parameter sets, it is possible to achieve excellent accuracy (approximately 5%) over a physiologic range of concentration tracer concentrations. Conclusion. Optimal pulse parameter sets exist and their use is essential for deriving accurate signal to concentration curves in quantitative MRI.
منابع مشابه
Quantitative contrast-enhanced MRI with superparamagnetic nanoparticles using ultrashort time-to-echo pulse sequences.
PURPOSE Conventional MRI using contrast agents is semiquantitative because it is inherently sensitive to extravoxular susceptibility artifacts, field inhomogeneity, partial voluming, perivascular effects, and motion/flow artifacts. Herein we demonstrate a quantitative contrast-enhanced MRI technique using ultrashort time-to-echo pulse sequences for measuring clinically relevant concentrations o...
متن کاملEffect of Echo Time on the Maximum Relationship between Contrast Agent Concentration and Signal Intensity Using FLAIR Sequence
Introduction Contrast-enhanced fluid-attenuated inversion recovery (FLAIR) is one of the MRI sequences that can be used for detection and evaluation of pathological changes in the brain. In this work, we have studied the effect of different echo times (TE) on the maximum relationship between signal intensity and concentration of the contrast agent using the FLAIR sequence. Materials and Methods...
متن کاملPrecision and accuracy of K estimated by fitting the extended Kety model parameters to DCE-MRI time course data is unaffected by the choice of optimisation algorithm or estimation of T1 using linearisation
Introduction Microvascular characteristics of tumours can be assessed by fitting a tracer kinetic model to contrast agent concentration time course data derived from dynamic contrast-enhanced (DCE-) MRI time series. The estimated model parameters, such as K, can be used to monitor the efficacy of anti-angiogenic drugs. Many optimisation algorithms are available for model fitting and it is impor...
متن کاملSodium Mri of Articular Cartilage with Improved Snr Using Coherent Ssfp Imaging at 7t
PURPOSE: Sodium (Na) MRI offers direct information on the glycosaminoglycan concentration in cartilage. In vivo Na-MRI, however, is very challenging because of low Na sensitivity, low tissue concentration, and short biexponential transverse relaxation times (T2). Sequences capable of maximizing signal-to-noise ratio (SNR) are therefore highly desirable. Many groups addressed this issue by devel...
متن کاملOptimal Flip Angle Set in Spoiled Gradient-Echo MR Imaging Technique
Introduction: In dynmiac contrast enchanted-MRI (DCE-MRI), T1-Weghited spoiled Gradient-Echo (SPGR) sequences are utilized to monitor the distribution of the paramagnetically labeled CAs (contrast agent) in cerebral tumors due to high temporal and spatial resolution [1]. The tissue concentration of CAs measured by CAs effects on the longitudinal relaxation rate of water protons R1 is used by tr...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
عنوان ژورنال:
دوره 2012 شماره
صفحات -
تاریخ انتشار 2012