A radial IR steady-state free precession technique combined with a principal component based iterative algorithm are demonstrated for rapid high-resolution abdominal T1 mapping. This method yields high quality T1 maps for 10 slices with spatial resolution as high as of 0.83x0.83x3mm from data acquired in a breath-hold or a short free-breathing scan. The method is a significant improvement over existing abdominal T1 mapping techniques.
Quantitative measurements of relaxation parameters is becoming a desired component for clinical diagnosis. T1 maps provide information to characterize neurological disorders [1,2,3], differentiate cirrhotic from healthy liver [4], diagnose declining kidney function [5], tumor malignancy [6], and myocardial infarction [7]. T1 maps are also used for perfusion quantification in dynamic contrast enhancement (DCE) MRI [8].
For abdominal imaging, the acquisition typically needs to fit within a breath-hold, limiting the amount of data acquired for T1 mapping. This affects the spatial and temporal resolution, signal-to-noise ratio (SNR) and/or slice coverage in T1 mapping. In fact, most techniques recently proposed for abdominal T1 mapping yield one slice per breath-hold [9,10,11,12], rendering the method inefficient when anatomical coverage is needed. For better slice coverage, a 3D stack-of-spirals technique with parallel imaging was recently demonstrated for T1 mapping of the abdomen in a breath-hold, but spatial resolution was limited to 2mm in plane [13].
Here we present an inversion-recovery (IR) radial balanced-SSFP (radSSFP) technique for multi-slice high resolution T1 mapping with high SNR. The method is demonstrated for breath-hold and free-breathing abdominal T1 mapping.
In the 2D IR-radSSFP pulse sequence data are continuously acquired following a 180° adiabatic inversion pulse using a train of constant flip angles and a radial k-space trajectory with tiny golden angle view ordering (Figure 1). All data for one slice are collected in a single shot during the recovery time of one inversion pulse (~3s) thus, minimizing the effects of motion. To generate k-space data sets at various inversion time (TI) points, data acquired in a single shot is partitioned into groups (with N=16 radial views per group) and the TI is approximated to the average TI of the views in the group.
Data for multiple slices are acquired by repeating the single shot acquisition. For breath-hold experiments, a slice-selective IR pulse combined with slice interleaving is used to minimize the slice delay and improve scan time efficiency (10 slices in ~20s breath-hold). For free-breathing experiments, a non-selective IR pulse is used to avoid slice cross-talk from out-of-plane motion; a slice delay of 5s allows spin recovery after the inversion pulse. Ten slices are acquired in ~1min free-breathing scan.
The IR-radSSFP sequence was implemented on a Siemens 3T Skyra scanner. Breath-hold and free-breathing experiments were performed at two spatial resolutions on 5 volunteers using a 32-elemenet body coil. The pulse sequence parameters are summarized in Table 1.
Because TI data sets are highly undersampled (4% relative to Nyquist) we use a principal component (PC) based algorithm to reconstruct the data [14]. The algorithm was implemented on 8 Nvidia Tesla P100 GPU using C++ with OpenCL. The algorithm recovers 5 PC images, which are converted into TI images. T1 is then fitted using the model in [15] with the algorithm from [16].
A reproducibility study was conducted by repeating the experiment twice. A Bland-Altman analysis was used to assess reproducibility.
Figure 2 shows representative slices of (a) 1.00×1.00×5.00mm and (b) 0.83×0.83×3.00mm T1 maps obtained from breath-hold IR-radSSFP data, and (c) 1.00×1.00×5.00mm T1 maps obtained from an IR radial FLASH technique. Note the high anatomical detail and overall high quality of the T1 maps generated from IR-radSSFP data. The high spatial resolution and excellent SNR of these T1 maps provides sharp and conspicuous delineation of the kidney cortex and medulla, improved uniform mapping of the liver and spleen parenchyma with fewer ringing artifacts and better SNR than the IR-FLASH technique (both organs should be uniform in normal subjects). Note the smoother mapping of the vertebral bodies and discs with IR-radSSFP due to better SNR.
Figure 3 shows T1 maps from free-breathing IR-radSSFP; blood vessels show bright due to the non-selective IR pulse. Due to the fast imaging time (~3s/slice) the resulting T1 maps retain high quality, showing the potential of the technique for patients that cannot perform breath-holds.
Table 2 shows the T1 values from different organs for 5 subjects. The values match literature reported values [17,18]. The coefficient of variation (CV) derived from a Bland-Altman analysis for the breath-hold experiments were 2.7% (1.00×1.00×5.00mm) and 2.5% (0.83×0.83×3.00mm). The CV for the free-breathing experiments at the 2 resolutions were 2.6% and 2.4%, respectively, showing a high degree of agreement in the mean T1 values from 2 separated experiments.
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