In this study, 9 obese male participants underwent 6 weeks of sprint interval training (SIT) and changes in visceral, subcutaneous and intra-hepatocellular fat were measured using MRI and MRS at baseline, control (>4 weeks later) and post exercise. Change in liver lipid composition was also assessed.
Study Design After obtaining ethical approval, 9 obese male participants were recruited following informed consent. Participants attended three MR test visits (>4 weeks between visits). On the first visit (baseline) subjects arrived at the SPMIC after overnight fast and were scanned for SAT, VAT and PDFF. This was repeated on a second (control) and third (post-exercise) visit. Between baseline and control visits participants were encouraged to make no changes to their normal habits. Following control visit subjects underwent 3 SIT sessions per week for 6 weeks. During training session participants underwent 5 mins warm-up (50 W), followed by four to six 30 second sprint intervals [4, 6] interspersed with 4.5 mins of active recovery (50 W).
MR Protocol MR measurements were performed on Philip Achieva 3T system and 32 channel XL-Torso coil. SAT and VAT was measured using 2-point mDixon MRI acquired in transverse plane over 3 breath-holds (L4/L5 of spine). A fat mask was generated from fat images using minimum threshold cut-off in intensity histogram [7]. An algorithm was written to generate fat boundaries and volumes within SAT and VAT regions calculated. PDFF was measured using STEAM localized 1H MRS at four echo times (20x20x20mm voxel, bandwidth=2kHz, 1024 data-points, 18 averages at TE=20ms, 9 averages at TE=30,40,60ms, with and without water suppression, figure 1). Spectra were phase corrected, frequency aligned and averaged in jMRUI and AMARES was used to fit 7 Gaussian peaks as described previously [5] before was determined. PDFF was calculated as F/(F+W) where F and W are total corrected fat and water signals respectively.
A saturated fat index was determined as SI = 1 - (Allylic/F) as described previously [8] and extended to determine a short-chain fatty acid index SCI = Methyl/Methylene (figure 2).
Statistics Values are presented as mean ± standard error. Values across visits were analysed using a one-way repeated measures ANOVA, followed up by pairwise comparison using two-tailed Student’s t-tests, corrected for multiple comparisons using Bonferroni adjustment.
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