Abstract

In magnetic resonance imaging, precise measurements of longitudinal relaxation time (T1) is crucial to acquire useful information that is applicable to numerous clinical and neuroscience applications. In this work, we investigated the precision of T1 relaxation time as measured using the variable flip angle method with emphasis on the noise propagated from radiofrequency transmit field () measurements. The analytical solution for T1 precision was derived by standard error propagation methods incorporating the noise from the three input sources: two spoiled gradient echo (SPGR) images and a map. Repeated in vivo experiments were performed to estimate the total variance in T1 maps and we compared these experimentally obtained values with the theoretical predictions to validate the established theoretical framework. Both the analytical and experimental results showed that variance in the map propagated comparable noise levels into the T1 maps as either of the two SPGR images. Improving precision of the measurements significantly reduced the variance in the estimated T1 map. The variance estimated from the repeatedly measured in vivo T1 maps agreed well with the theoretically-calculated variance in T1 estimates, thus validating the analytical framework for realistic in vivo experiments. We concluded that for T1 mapping experiments, the error propagated from the map must be considered. Optimizing the SPGR signals while neglecting to improve the precision of the map may result in grossly overestimating the precision of the estimated T1 values.

Highlights

  • Measurement of the longitudinal relaxation time (T1) of a sample is of paramount importance as evidenced by the fact that methods for its measurement appeared soon after the invention of NMR (Drain, 1949; Hahn, 1949)

  • Increased spoiling resulted in improved precision of the B+1 maps, which in turn reduced the variance of the T1 estimates both experimentally and theoretically

  • Using the variable flip angles (VFA) method, the precision of T1 relaxation time measurements depends on the signal-to-noise ratio (SNR) of the spoiled gradient echo (SPGR) images but, crucially, on the error propagated from the B+1 map that is used to correct the bias caused by spatial inhomogeneity in the achieved flip angle

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Summary

Introduction

Measurement of the longitudinal relaxation time (T1) of a sample is of paramount importance as evidenced by the fact that methods for its measurement appeared soon after the invention of NMR (Drain, 1949; Hahn, 1949). Typically taken as the gold standard, the inversion recovery approach is very time consuming (Stikov et al, 2015). Precision of VFA T1 Mapping dimensional (3D) spoiled gradient echo (SPGR) (Haase et al., 1986) images with short repetition times, variable flip angles (VFA) (Christensen et al, 1974; Fram et al, 1987) and appropriate spoiling (Zur et al, 1991; Ganter, 2006) offers a means of obtaining whole brain T1 maps in clinically feasible times (Deoni et al, 2005; Helms et al, 2008). Numerous methods exist for obtaining a B+1 map (Insko and Bolinger, 1993; Cunningham et al, 2006; Jiru and Klose, 2006; Dowell and Tofts, 2007; Yarnykh, 2007; Lutti et al, 2010; Sacolick et al, 2010; Nehrke and Börnert, 2012)

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