- Workshop presentation
- Open Access
Characterization of T1 bias from lipids in MOLLI and SASHA pulse sequences
© Thiesson et al; licensee BioMed Central Ltd. 2015
- Published: 3 February 2015
- Lipid Concentration
- Fabry Disease
- Spectral Line Shape
- Frequency Increment
- Siemens Sonata
Increased myocardial T1 values are associated with fibrosis and edema, while decreased values in Fabry disease have been attributed to the short T1 of infiltrative lipids [1, 2]. The relationship between lipid concentration (LC) and best-fit T1 values is unknown. This study aims to determine the dependence of MOLLI and SASHA T1 values on LC.
MOLLI and SASHA T1 mapping sequences are based on the bSSFP acquisition. bSSFP signal yield as a function of off-resonance frequency is well characterized [4, 5], with phase inversion in sequential "bSSFP bands" and a profile shift as a function of resonance frequency, resulting in constructive/destructive interference between water and fat [6, 7]. We hypothesized that lipids may decrease or increase T1 values as a function of off-resonance frequency.
Bloch equation simulations of MOLLI and SASHA for 0:2:10% LC incorporated exact pulse sequence parameters including slice profiles and an accurate fat spectral line shape.
MOLLI and SASHA acquisitions (identical to simulations) were repeated 50 times, spanning 450 Hz of off-resonance (1.25 bSSFP bands) in both phantoms (LC of 0.5-10%), and in-vivo in three calf muscle regions with different LC . Acquisition Parameters: 1.5T Siemens Sonata, single-shot bSSFP, 1.35/2.7ms TE/TR, 192x72 matrix, 360x270 mm FOV, 70° SASHA flip, 35° MOLLI flip . T1 values were calculated using standard Look-Locker correction (MOLLI) or 2 and 3 parameter exponential models (SASHA) at each frequency increment across the bSSFP band.
Relatively low LC results in clinically relevant negative or positive shifts in tissue T1 over a narrow range of off-resonance frequencies with MOLLI and SASHA. Thus, increased or decreased native T1 values can potentially be ascribed to lipids, which can confound underlying increased water T1 values ascribed to fibrosis or edema and complicate the use of T1 mapping for indirect identification of lipids via reduced T1 values [1, 2].
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