T2* weighted imaging can be used to study both normal and pathological tissue. These images are commonly obtained using traditional gradient echo sequences which can lead to long scan times that are problematic particularly in a clinical setting. 3D EPI offers a faster alternative with scan times on the order of few minutes. Here, the scan time of T2* weighted 3D EPI scans is further reduced with a shot selective 2D CAIPI acquisition pattern. Whole brain T2* weighted anatomical scans with a resolution of 0.5 mm isotropic were acquired in 1:27 minutes. This holds promising perspectives for future applications in routine examinations.
T2* weighted imaging is a powerful tool to study both normal and pathological tissue, especially at high field strengths. The anatomy and substructures of the brain can be visualized with exceptional detail, including structures within the basal ganglia, and the line of Gennari in the visual cortex. T2* weighted imaging is traditionally performed using a spoiled gradient echo (GRE) sequence [1]. However, to image structural detail of the brain at sub-millimeter resolutions requires a long scan time, even for a limited number of slices [2]. As result, the imaging volume is typically limited, since full brain coverage coincides with excessively long scan times of 1 hour or more for a single acquisition. In the clinical setting however, long scan times are problematic because both patient motion [3] and the cost of examination are increased. More recently, Zwanenburg et al. [4] showed that volumetric 3D EPI protocols can drastically reduce scan time or increase imaging coverage, while maintaining image quality and T2* weighting.
Recent advances in parallel imaging approaches, such as CAIPIRINHA (CAIPI) and compressed sensing, may be used to reduce scan time even further [5-7]. Here we show that the scan time of T2* weighted 3D EPI scans can be reduced considerably, while maintaining high image quality, by using a shot selective 2D CAIPIRINHA acquisition pattern. A shot selective 2D CAIPIRINHA sequence was implemented for multi-shot 3D EPI scans, which, instead of adding extra gradients, leaves them out (Figure 1). The sequence was applied to sub-millimeter T2* weighted 3D EPI anatomical imaging at 7T.
Two healthy participants were scanned in a 7 Tesla Achieva system (Philips, Best, the Netherlands). Whole brain T2* weighted multi-shot 3D EPI anatomical scans were acquired with a 32 channel headcoil [8] (Nova Medical, USA). The following scan parameters were used:
The scans were reconstructed offline in a modified Philips Recon2.0 environment.
First the sequence implementation was evaluated by comparing prospectively and retrospectively undersampled datasets, as displayed in Figure 2. Note that both the aliasing patterns and reconstructions are close to identical, which demonstrates good performance of the implemented sequence.
The sub-millimeter T2* weighted anatomical scans are displayed in Figure 3, both fully sampled (Figure 3a) and undersampled with: SENSE 4 (Figure 3b), CAIPIRINHA 7 (Figure 3c) and SENSE 7 (Figure 3d). These scans have an isotropic resolution of 0.5 mm. Note that the CAIPIRINHA implementation can be used to shorten the total scan time substantially, while preserving the anatomy and structures of the brain.
The results show that the implementation of shot selective 2D CAIPIRINHA patterns for 3D EPI sequences can be used to significantly shorten scan time of sub-millimeter anatomy scans. For whole-brain anatomical imaging with 0.5 mm isotropic resolution the achieved scan time is about 1.5 minute, a reduction by a factor of 4, as compared to the existing implementation of 6 min [4].
The current results are acquired at a field strength of 7T, however, the applied method can be easily translated to more clinically available 3T scanners. This holds promising perspectives for future application in routine examinations among patients.
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