- utilization of gradient fields to generate transverse magnetisation
- flip angles of less than 90°
Compared to the spin echo and inversion recovery sequences, GRE sequences are more versatile. Not only is the basic sequence varied by adding dephasing or rephasing gradients at the end of the sequence, but there is a significant extra variable to specify in addition to the usual TR and TE. This variable is the flip or tip angle of the spins.
The flip angle is usually at or close to 90 degrees for a spin echo sequence but commonly varies over a range of about 10 to 80 degrees with GRE sequences. For the basic GRE sequence FLASH (figure 1) the larger tip angles give more T1 weighting to the image and the smaller tip angle give more T2 or actually T2* weighting to the images.
The gradient echo is generated by the frequency-encode gradient, except that it is used twice in succession, and in opposite directions: it is used in reverse at first to enforce transverse dephasing of spinning protons and then right after, it is used as a readout gradient (like in spin echo MRI) to re-align the dephased protons and hence acquire signal.
Because low flip angles are used, there is some retention of the original longitudinal magnetisation as opposed to the 90° pulse used in spin echo, which completely eliminates the longitudinal magnetisation. As a result, the build up time for longitudinal magnetisation is significantly reduced for the subsequent pulses , allowing faster image acquisition in GE.
Another important feature of GE is that the defacement of spinning protons occurs as a result of T2* decay which is more rapid than the T2 decay process underlying Spin Echo sequence (leading to shorter TE) and is susceptible to static field inhomogeneities (leading to compounded influence of degraded blood products, and metal objects on the signal ).
Images from other GRE sequences such as GRASS and FISP have less intuitive tissue contrast characteristics than FLASH. The FLASH and SPGR sequences show better tissue contrast between white matter and grey matter in the brain and spinal cord than GRASS or FISP and are preferred when the time of acquisition does not have to be very short. GRASS and FISP maintain better SNR than FLASH at short TR times and are therefore preferred with breath-holding techniques, for example.
A vector magnetisation diagram of the GRE sequence is shown below. Note that the spins are refocused by reversing the direction of the spins rather than flipping them over to the other side of the x-y plane as occurs with the spin echo sequence. Gradient refocusing of the spins takes considerably less time than 180 degree RF pulse refocusing. One big disadvantage of GRE sequences is the loss of signal from static magnetic field inhomogeneity. This occurs to a lesser degree with spin echo sequences (and for a different reason). Magnetic susceptibility artifacts are therefore more pronounced on GRE sequences that on spin echo sequences.
- MRI (introduction)
- MR physics
- MR hardware
- signal processing
MRI pulse sequences (basics | abbreviations | parameters)
- spin echo sequences
- inversion recovery sequences
- gradient echo sequences
- fat-suppressed imaging sequences
- diffusion weighted sequences (DWI)
- derived values
- CSF flow studies
- susceptibility weighted imaging (SWI)
- saturation recovery sequences
- echo-planar pulse sequences
- metal artifact reduction sequence
- T1 rho
- spiral pulse sequences
- MR angiography (and venography)
MR spectroscopy (MRS)
- Hunter's angle
- lactate peak: resonates at 1.3 ppm
- lipids peak: resonate at 1.3 ppm
- alanine peak: resonates at 1.48 ppm
- N-acetylaspartate (NAA) peak: resonates at 2.0
- glutamine-glutamate peak: resonate at 2.2-2.4 ppm
- gamma-aminobutyric acid (GABA) peak: resonate at 2.2-2.4 ppm
- 2-hydroxyglutarate peak: resonates at 2.25 ppm
- citrate peak: resonates 2.6 ppm
- creatine peak: resonates at 3.0 ppm
- choline peak: resonates at 3.2 ppm
- myo-inositol peak: resonates at 3.5 ppm
- functional MRI
- MR fingerprinting
- MR hardware and room shielding
- MR software
- patient and physiologic motion
- tissue heterogeneity and foreign bodies
- Fourier transform and Nyqvist sampling theorem
MR contrast agents
- gadolinium ion
- extracellular MRI contrast agents
- hepatobiliary MRI contrast agents
- intravascular (blood pool) MRI contrast agents
- gastrointestinal MRI contrast agents
- tumor-specific MRI contrast agents
- reticuloendothelial MRI contrast agents
- contrast agent safety
- MR safety