One version of a new ultrafast gradient-echo-based 3D imaging technique using spatiotemporal encoding (RASE-I) is proposed which can provide very short TEs in some slices. RASE-I maintains most of appealing features of other spin-echo-based SPEN imaging methods including no Nyquist ghosting and high tolerance to field inhomogeneities. It is barely affected by T2* signal modulation and less sensitive to T2* effects due to local rephasing mechanism along the SPEN direction. Its performance is demonstrated by lemon and in-vivo mouse kidney imaging at 9.4T, including the measurement of dose-dependent arterial-input-function (AIF) of kidney-feeding artery.
Figure 1 illustrates the sequence diagram of RASE-I. A frequency-swept chirp pulse is used for sequential spin excitation which produces a quadratic phase that localizes a signal in both time and space in the presence of gradient. In RASE-I, spin excitation is performed with a much shorter duration than data acquisition by using a shortened chirp pulse (≤ 1ms), which allows very short TEs in some slices defined by early rephasing spins. During the data acquisition, spin isochromats are sequentially and locally rephased but in reverse order of sequential excitation by applying another gradient with opposite polarity to the slab-selective gradient. The slab-selective direction is spatiotemporally encoded3, which makes the spins of the same slice experience the same TE unlike EPI. Images were reconstructed offline with MATLAB (ver.8.2.0; R2013b) using the super-resolution algorithm4. For lemon imaging, 2D-GRE, GE-EPI, and RASE-I sequences were used for comparison. Same scan parameters were: FOV = 65 × 65mm2, matrix = 128 × 128, number of slices = 48, slice thickness (THK) = 0.3125mm. In GRE imaging as a reference, TR/TE = 310/3ms, flip angle (FA) = 33°. In GE-EPI imaging, shot-TR/TE = 3,600/36.6ms, FA = 90°. In RASE-I imaging, shot-TR/TE = 57/(1.9~26.4)ms, FA = 14.3°, R-value (pulse_length × bandwidth) = 256. To validate the feasibility of RASE-I for DCE-MRI applications, dose-dependent AIF of kidney-feeding artery was measured in in-vivo mice at three different injection doses of Gd-DOTA(0.1, 0.2, and 0.3 mmol/kg, n = 2 each). For estimation of absolute Gd-concentration, signal intensity was converted to R1 using the following equations5,6:
$$R_{1}\left(t\right)=\frac{1}{TR}\ln\left(\frac{S_{0}\sin(FA)e^{\frac{TE}{T_2^*}}-S(t)\cos(FA)}{S_{0}\sin(FA)e^{\frac{TE}{T_2^*}}-S(t)}\right)$$ [1]
$$S_{0}=S_{ss}\frac{1-cos(FA)e^{\frac{TR}{T_{1,0}}}}{(1-e^{\frac{TR}{T_{1,0}}})sin(FA)e^{\frac{TE}{c_2^*}}}$$ [2]
where Sss and S(t) are pre- and post-injection signal intensities, respectively. T2* contribution was ignored due to short TE. R1 was then converted to Gd-concentration using5:
$$\frac{1}{T_{1}}=r_{1},Gd-DOTA\times C_{p}\times\left(1-H_{ct}\right)+\frac{1}{T_{1,0}}$$ [3]
where r1,Gd is T1 relaxivity of Gd-DOTA (= 4.156 s-1·mM-1), Cp is Gd-concentration in plasma. Hct is a portion of hematocrits (= 0.45)7. T1,0 and T1 are pre- and post-injection relaxation times, respectively. For RASE-I imaging, scan parameters were: TR/TE = 21/(2~18) ms, pulse duration = 0.7ms, FA = 35°, FOV = 35×35mm2, matrix = 96×96, THK = 0.3125mm, temporal resolution = 2.16s, number of slices = 48, and R-value = 256. In TSE imaging for T1,0 and T1 measurements, TE = 5.07ms, TR = 110 to 5,000ms, turbo factor = 4. T1,0 values at the artery region were averaged in six mice to be 1.5s. Total acquisition time was 10min 4.8s and contrast agent was injected 1 minute before acquisition.