Perfusion weighted imaging using combined gradient/spin echo EPIK: Brain tumour applications in hybrid MR-PET

被引:4
作者
Shah, N. Jon [1 ,2 ,3 ,4 ]
da Silva, Nuno Andre [1 ]
Yun, Seong Dae [1 ]
机构
[1] Forschungszentrum Julich, Inst Neurosci & Med 4, Med Imaging Phys, D-52425 Julich, Germany
[2] Forschungszentrum Julich, Inst Neurosci 11, Mol Neurosci & Neuroimaging, Julich, Germany
[3] Rhein Westfal TH Aachen, Fac Med, Dept Neurol, JARA, Aachen, Germany
[4] Monash Univ, Sch Psychol Sci, Monash Biomed Imaging, Melbourne, Vic, Australia
关键词
EPIK; gradient echo; spin echo; image distortion; MR-PET; multi-contrast; ARTERIAL INPUT FUNCTION; CEREBRAL BLOOD-VOLUME; SUSCEPTIBILITY CONTRAST MRI; DSC-MRI; DCE-MRI; SPIN; SIZE; ACQUISITION; QUANTIFICATION; ACCELERATION;
D O I
10.1002/hbm.24537
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Advanced perfusion-weighted imaging (PWI) methods that combine gradient echo (GE) and spin echo (SE) data are important tools for the study of brain tumours. In PWI, single-shot, EPI-based methods have been widely used due to their relatively high imaging speed. However, when used with increasing spatial resolution, single-shot EPI methods often show limitations in whole-brain coverage for multi-contrast applications. To overcome this limitation, this work employs a new version of EPI with keyhole (EPIK) to provide five echoes: two with GEs, two with mixed GESE and one with SE; the sequence is termed "GESE-EPIK." The performance of GESE-EPIK is evaluated against its nearest relative, EPI, in terms of the temporal signal-to-noise ratio (tSNR). Here, data from brain tumour patients were acquired using a hybrid 3T MR-BrainPET scanner. GESE-EPIK resulted in reduced susceptibility artefacts, shorter TEs for the five echoes and increased brain coverage when compared to EPI. Moreover, compared to EPI, EPIK achieved a comparable tSNR for the first and second echoes and significantly higher tSNR for other echoes. A new method to obtain multi-echo GE and SE data with shorter TEs and increased brain coverage is demonstrated. As proposed here, the workflow can be shortened and the integration of multimodal clinical MR-PET studies can be facilitated.
引用
收藏
页码:4144 / 4154
页数:11
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