Abstract
BackgroundThis study exploits the speed benefits of echo-planar spectroscopic imaging (EPSI) to acquire lipid spectra of skeletal muscle. The main purpose was to develop a high-resolution EPSI technique for clinical MR scanner, to visualise the bulk magnetic susceptibility (BMS) shifts of extra-myocellular lipid (EMCL) spectral lines, and to investigate the feasibility of this method for the assessment of intra-myocellular (IMCL) lipids.MethodsThe study group consisted of six healthy volunteers. A two dimensional EPSI sequence with point-resolved spectroscopy (PRESS) spatial localization was implemented on a 3T clinical MR scanner. Measurements were performed by means of 64×64 spatial matrix and nominal voxel size 3×3×15 mm3. The total net measurement time was 3 min 12 sec for non-water-suppressed (1 acquisition) and 12 min 48 sec for water-suppressed scans (4 acquisitions).ResultsSpectra of the human calf had a very good signal-to-noise ratio and linewidths sufficient to differentiate IMCL resonances from EMCL. The use of a large spatial matrix reduces inter-voxel signal contamination of the strong EMCL signals. Small voxels enabled visualisation of the methylene EMCL spectral line splitting and their BMS shifts up to 0.5 ppm relative to the correspondent IMCL line. The mean soleus muscle IMCL content of our six volunteers was 0.30±0.10 vol% (range 0.18–0.46) or 3.6±1.2 mmol/kg wet weight (range: 2.1–5.4).ConclusionThis study demonstrates that high-spatial resolution PRESS EPSI of the muscle lipids is feasible on standard clinical scanners.
Highlights
Proton (1H) magnetic resonance spectra of lipids in skeletal muscle are dominated by two spectral lines originating from the methylene protons (-CH2-)n of extra- (EMCL) and intramyocellular (IMCL) lipids (EMCLCH2, IMCLCH2)
The anisotropic shape and geometrical arrangement of extra-myocellular lipid (EMCL) compartments result in a bulk magnetic susceptibility (BMS) shift of its spectral lines [3]
Spectra of soleus muscle revealed that magnetic field deviations experienced by the EMCL compartments were in the interval from ca 0.6 to 20.2 ppm in respect of IMCLCH2
Summary
Proton (1H) magnetic resonance spectra of lipids in skeletal muscle are dominated by two spectral lines originating from the methylene protons (-CH2-)n of extra- (EMCL) and intramyocellular (IMCL) lipids (EMCLCH2, IMCLCH2). IMCL are stored in the form of small droplets in a magnetic susceptibility homogeneous environment (cytoplasm) of muscle cells In such circumstances, the positions of IMCL spectral lines are independent in orientation of the myocytes relative to the external magnetic field B0 [2,3]. From Steidle et al study [7] it follows that EMCL spectral line shifts somewhat larger than 0.2 ppm or less than 20.1 ppm relative to IMCL can be expected. The main purpose was to develop a high-resolution EPSI technique for clinical MR scanner, to visualise the bulk magnetic susceptibility (BMS) shifts of extra-myocellular lipid (EMCL) spectral lines, and to investigate the feasibility of this method for the assessment of intra-myocellular (IMCL) lipids
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