Echo time optimization for in‐vivo measurement of unsaturated lipid resonances using J‐difference‐edited MRS

Abstract

AbstractPurposeMeasuring lipid composition provides more information than just total lipid content. Hence, the non‐invasive measurement of unsaturated lipid protons with both high efficiency and precision is of pressing need. This study was to optimize echo time (TE) for the best resolving of J‐difference editing of unsaturated lipid resonances.MethodsThe TE dependence of J‐difference‐edited (JDE) MRS was verified in the density‐matrix simulation, soybean oil phantom, in‐vivo experiments of white adipose tissue (WAT), and skeletal muscles using single‐voxel MEGA‐PRESS sequence at 3T. The peak SNRs and Cramér‐Rao lower bounds (CRLBs) acquired at the proposed TE of 45 ms and previously published TE of 70 ms were compared (eight pairs) in WAT, extramyocelluar lipids (EMCLs), and intramyocellular lipids (IMCLs). The lipid composition in skeletal muscles was compared between healthy males (n = 7) and females (n = 7).ResultsThe optimal TE was suggested as 45 ms. Compared to 70 ms, the mean signal gains at TE of 45 ms were 151% in WAT, 168% in EMCL, 204% in IMCL for allylic resonance, and 52% in EMCL for diallylic resonance. CRLBs were significantly reduced at TE of 45 ms in WAT, EMCL, IMCL for allylic resonance and in EMCL for diallylic resonance. With TE of 45 ms, significant gender differences were found in the lipid composition in EMCL pools, while no difference in IMCL pools.ConclusionThe JDE‐MRS protocol with TE of 45 ms allows improved quantification of unsaturated lipid resonances in vivo and future lipid metabolism investigations.