TY - JOUR
T1 - Simultaneous T2 and lipid quantitation using IDEAL-CPMG
AU - Janiczek, Robert L.
AU - Gambarota, Giulio
AU - Sinclair, Christopher D.J.
AU - Yousry, Tarek A.
AU - Thornton, John S.
AU - Golay, Xavier
AU - Newbould, Rexford D.
PY - 2011/11
Y1 - 2011/11
N2 - Muscle damage, edema, and fat infiltration are hallmarks of a range of neuromuscular diseases. The T2 of water, T2,w, in muscle lengthens with both myocellular damage and inflammation and is typically measured using multiple spin-echo or Carr-Purcell-Meiboom-Gill acquisitions. However, microscopic fat infiltration in neuromuscular diseases prevents accurate T2,w quantitation as the longer T2 of fat, T 2,f, masks underlying changes in the water component. Fat saturation can be inconsistent across the imaging volume and removes valuable physiological fat information. A new method is presented that combines iterative decomposition of water and fat with echo asymmetry and least squares estimation with a Carr-Purcell-Meiboom-Gill-sequence. The sequence results in water and fat separated images at each echo time for use in T2,w and T 2,f quantification. With knowledge of the T2,w and T 2,f, a T2-corrected fat fraction map can also be calculated. Monte-Carlo simulations and measurements in phantoms, volunteers, and a patient with inclusion body myositis are demonstrated. In healthy volunteers, uniform T2,w and T2-corrected fat fraction maps are present within all muscle groups. However, muscle-specific patterns of fat infiltration and edema are evident in inclusion body myositis, which demonstrates the power of separating and quantifying the fat and water components.
AB - Muscle damage, edema, and fat infiltration are hallmarks of a range of neuromuscular diseases. The T2 of water, T2,w, in muscle lengthens with both myocellular damage and inflammation and is typically measured using multiple spin-echo or Carr-Purcell-Meiboom-Gill acquisitions. However, microscopic fat infiltration in neuromuscular diseases prevents accurate T2,w quantitation as the longer T2 of fat, T 2,f, masks underlying changes in the water component. Fat saturation can be inconsistent across the imaging volume and removes valuable physiological fat information. A new method is presented that combines iterative decomposition of water and fat with echo asymmetry and least squares estimation with a Carr-Purcell-Meiboom-Gill-sequence. The sequence results in water and fat separated images at each echo time for use in T2,w and T 2,f quantification. With knowledge of the T2,w and T 2,f, a T2-corrected fat fraction map can also be calculated. Monte-Carlo simulations and measurements in phantoms, volunteers, and a patient with inclusion body myositis are demonstrated. In healthy volunteers, uniform T2,w and T2-corrected fat fraction maps are present within all muscle groups. However, muscle-specific patterns of fat infiltration and edema are evident in inclusion body myositis, which demonstrates the power of separating and quantifying the fat and water components.
KW - edema
KW - muscular dystrophy
KW - water-fat separation
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U2 - 10.1002/mrm.22916
DO - 10.1002/mrm.22916
M3 - Article
C2 - 21604292
AN - SCOPUS:80054814007
VL - 66
SP - 1293
EP - 1302
JO - Magnetic Resonance in Medicine
JF - Magnetic Resonance in Medicine
SN - 0740-3194
IS - 5
ER -