A relaxometry-based tissue fraction segmentation using MR fingerprinting method was applied for identifying hippocampal sclerosis. The results demonstrated that tissue-fraction MR fingerprinting method could effectively segment multiple tissue components and mark the possible sclerosis regions, which is critical for clinical application including lesions diagnosis and multicomponent analysis.
20 MTLE patients (10 females and 10 males) diagnosed with HS based on EEG and clinical presentation participated in this study. All the patients were scanned with a series conventional sequences with routine protocols including T1-MPRAGE and T2-TSE prior to MRF scans. The MRF scans were based on an inversion-prepared FISP sequence (FISP-MRF) [5] with 20 slices of both transverse and coronal orientations covering the temporary lobe for patients. The final T1, T2 and Proton density (PD) maps with in-plane spatial resolution of 1.3 × 1.3 mm2 were recognized simultaneously by the sliding-window matching algorithm [6]. All the measurements were performed on a 3T scanner (MAGNETOM Prisma, Siemens Healthcare, Erlangen, Germany) with 20-channel head coil.
The same acquired MRF data were used for post-processing of tissue segmentation as well as MRF parametric recognition while potential fractions of interested multiple components were applied instead of using the dictionary based on T1 and T2 evaluation. The signal equation of rTF-MRF is $$ \widehat{\bf w}=argmin||{\bf S}_{\it voxel}-{\bf Dw}||_{2}\quad{\it s.t.} \left\{{\sum_{n=1}^N}{\bf w}(n)=1,{\bf w}(n)\in[0,1]\right\}\quad\quad\quad\quad\quad(1)$$
where the Svoxel represents the acquired signal curve of each voxel, D is the signal evolutions of interested components that pre-calculated by extended phase graph algorithm [7], and w is potential fractions groups with N interested components. The optimization problem of Eq. (1) can be solved by least square method with additional constraint. Fig.1. shows the brief procedure of rTF-MRF.
Since the prolonged T1 and T2 values in HS lesions, firstly the recognized T1, T2 and PD maps from the same datasets were exploited to decide the possible range of relaxometry of lesions as the prior information for HS patients. Then the each voxel can be segmented into 4 components including CSF (T1/T2=4000/1500ms), gray matter (T1/T2=1300/120ms), white matter (T1/T2=800/80ms) and a suspicious HS component (prior information from MRF results).
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