Dataset Information

Fast multi-component analysis using a joint sparsity constraint for MR fingerprinting.

ABSTRACT:

Purpose

To develop an efficient algorithm for multi-component analysis of magnetic resonance fingerprinting (MRF) data without making a priori assumptions about the exact number of tissues or their relaxation properties.

Methods

Different tissues or components within a voxel are potentially separable in MRF because of their distinct signal evolutions. The observed signal evolution in each voxel can be described as a linear combination of the signals for each component with a non-negative weight. An assumption that only a small number of components are present in the measured field of view is usually imposed in the interpretation of multi-component data. In this work, a joint sparsity constraint is introduced to utilize this additional prior knowledge in the multi-component analysis of MRF data. A new algorithm combining joint sparsity and non-negativity constraints is proposed and compared to state-of-the-art multi-component MRF approaches in simulations and brain MRF scans of 11 healthy volunteers.

Results

Simulations and in vivo measurements show reduced noise in the estimated tissue fraction maps compared to previously proposed methods. Applying the proposed algorithm to the brain data resulted in 4 or 5 components, which could be attributed to different brain structures, consistent with previous multi-component MRF publications.

Conclusions

The proposed algorithm is faster than previously proposed methods for multi-component MRF and the simulations suggest improved accuracy and precision of the estimated weights. The results are easier to interpret compared to voxel-wise methods, which combined with the improved speed is an important step toward clinical evaluation of multi-component MRF.

SUBMITTER: Nagtegaal M

PROVIDER: S-EPMC6899479 | biostudies-literature | 2020 Feb

REPOSITORIES: biostudies-literature

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Publications

Fast multi-component analysis using a joint sparsity constraint for MR fingerprinting.

Nagtegaal Martijn M Koken Peter P Amthor Thomas T Doneva Mariya M

Magnetic resonance in medicine 20190816 2

<h4>Purpose</h4>To develop an efficient algorithm for multi-component analysis of magnetic resonance fingerprinting (MRF) data without making a priori assumptions about the exact number of tissues or their relaxation properties.<h4>Methods</h4>Different tissues or components within a voxel are potentially separable in MRF because of their distinct signal evolutions. The observed signal evolution in each voxel can be described as a linear combination of the signals for each component with a non-n ...[more]

PMID: 31418918

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Project description:T2-hyperintense lesions are the key imaging marker of multiple sclerosis (MS). Previous studies have shown that the white matter surrounding such lesions is often also affected by MS. Our aim was to develop a new method to visualize and quantify the extent of white matter tissue changes in MS based on relaxometry properties. We applied a fast, multi-parametric quantitative MRI approach and used a multi-component MR Fingerprinting (MC-MRF) analysis. We assessed the differences in the MRF component representing prolongedrelaxation time between patients with MS and controls and studied the relation between this component's volume and structural white matter damage identified on FLAIR MRI scans in patients with MS. A total of 48 MS patients at two different sites and 12 healthy controls were scanned with FLAIR and MRF-EPI MRI scans. MRF scans were analyzed with a joint-sparsity multi-component analysis to obtain magnetization fraction maps of different components, representing tissues such as myelin water, white matter, gray matter and cerebrospinal fluid. In the MS patients, an additional component was identified with increased transverse relaxation times compared to the white matter, likely representing changes in free water content. Patients with MS had a higher volume of the long- component in the white matter of the brain compared to healthy controls (B (95%-CI) = 0.004 (0.0006-0.008), p = 0.02). Furthermore, this MRF component had a moderate correlation (correlation coefficient R 0.47) with visible structural white matter changes on the FLAIR scans. Also, the component was found to be more extensive compared to structural white matter changes in 73% of MS patients. In conclusion, our MRF acquisition and analysis captured white matter tissue changes in MS patients compared to controls. In patients these tissue changes were more extensive compared to visually detectable white matter changes on FLAIR scans. Our method provides a novel way to quantify the extent of white matter changes in MS patients, which is underestimated using only conventional clinical MRI scans.

Dataset Information

Fast multi-component analysis using a joint sparsity constraint for MR fingerprinting.

Purpose

Methods

Results

Conclusions

Publications

Fast multi-component analysis using a joint sparsity constraint for MR fingerprinting.

Similar Datasets

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