Purpose:To investigate the effect of chemical exchange and multicomponent relaxation on the rapid T 2 mapping method, DESPOT2 (driven equilibrium single pulse observation of T 2 ) and the steady-state free precession (SSFP) sequence upon which it is based. Although capable of rapid T 2 determination, an assumption implicit of the method is single-component relaxation. In many biological tissues (such as white and gray matter), it is well established that the T 2 decay curve is more accurately described by the summation of more than one relaxation species.
Materials and Methods:The effects of exchange were first incorporated into the general SSFP magnetization expressions and its effect on the measured SSFP signal investigated using Bloch-McConnell simulations. Corresponding imaging experiments were performed to support the presented theory.
Results:Simulations show the measured multicomponent SSFP signal may be expressed as a linear summation of signal from each species under usual imaging conditions where the repetition time is much less than T 2 . Imaging experiments performed using dairy cream demonstrate strong agreement with the presented theory. Finally, using a dairy cream model, we demonstrate quantification of multicomponent relaxation from multiangle SSFP data for the first time, showing good agreement with reference spin-echo values.Conclusion: SSFP and DESPOT2 may provide a new method for investigating multicomponent systems, such as human brain, and disease processes, such as multiple sclerosis. THE COMBINATION of DESPOT1 and DESPOT2 (driven equilibrium single pulse observation of T 1 and T 2 , respectively), offers a rapid and signal-to-noise ratio (SNR) efficient (SNR per unit scan time) means for voxelwise determination, or mapping, of both the longitudinal (T 1 ) and transverse relaxation times (T 2 ) over large image volumes (i.e., full brain) and with high spatial resolution (1-mm 3 isotropic voxels) (1,2). Typical acquisition times for whole-brain T 1 and T 2 maps is approximately 12-15 minutes (2), with the DESPOT2 acquisition requiring four to six minutes. As has been described in detail previously, the DESPOT2 method derives T 2 information from a series of fully-balanced steady-state free precession (SSFP or true fast imaging with steady precession [TrueFISP]) images, acquired with constant repetition time (TR) and incremented flip angle (␣) (1).An implicit assumption of DESPOT2, however, is that of single-component relaxation, with only a single T 2 value calculated at each imaging voxel. Unfortunately, this assumption may not be appropriate in many biological tissues, owing to the heterogeneous biochemical and microstructural nature of the tissue on the voxel scale (3,4). Within human white and gray matter, for instance, the presence of at least two transverse relaxation times has been well established (Refs. 5-7, among many others), with a fast component (short T 2 less than 50 msec) attributed to a myelin-bound water pool, and a slower T 2 component (long T 2 between 80 and 200 msec) ...