Data Acquisition for fMRI
SoHyun Han1
1Korea Basic Science Institute, Korea, Republic of

Synopsis

Keywords: Contrast mechanisms: fMRI

This lecture will describe the data acquisition for functional MRI focusing on 2D echo planar imaging (EPI) sequence. Sequence parameters (TE, TR, echo spacing, voxel size, acceleration factors, etc.) will be introduced. Parallel imaging (SENSE, GRAPPA, SMS) methods and typical EPI related artifacts (ghosting, geometric distortions, signal loss) will also be discussed.

Introduction

Blood oxygenation level-dependent (BOLD) functional MRI measures signal changes driven by the magnetic susceptibility of blood [1]. To observe these changes effectively, the contrast by magnetic susceptibility should be sensitive enough to be detected, and temporal resolution should be fast enough to measure its changes. The most popular pulse sequence for BOLD fMRI is the 2D gradient-echo (GE) echo planar imaging (EPI) due to its high sensitivity and time efficiency [2]. This lecture will focus on practical considerations in designing protocols for BOLD fMRI acquisition using 2D GE-EPI sequence [3].

Important parameters in functional MRI acqusition

To detect BOLD fMRI, spatial and temporal properties, and signal-to-noise ratio (SNR) are important parameters to consider. Such properties including SNR, temporal SNR (tSNR), and contrast-to-noise ratio (CNR) are closely related with the imaging parameters TE, TR, voxel size, echo spacing, acceleration factor and so on. The BOLD contrast is based on T2*-weighted contrast which is dependent on the echo time (TE). BOLD contrast can be maximized when TE matches the T2* of the tissue of interest [4]. However, we need to consider that long TE leads to signal drop due to magnetic field inhomogeneities and results in increase of TR. The repetition time (TR) corresponds to acquisition temporal resolution in EPI sequence. To increase temporal resolution, spatial resolution or volume coverage should be decreased. In terms of spatial resolution, high spatial resolution is beneficial to resolve finer structures [5], but it can cause severe image artifact and reduce SNR because of the increase in spatial encoding time. On the other side, lowering spatial resolution induces partial volume effect.

Echo Planar Imaging (EPI)

Echo planar imaging (EPI) acquisition enable 2D k-space sampling in one shot by continuously switching readout and phase encoding gradients. To cover multiple slices, this process is repeated for each slice, resulting in TR as a sampling rate within a few seconds.

Parallel Imaging & Simultaneous multislice

EPI acquisition can be accelerated in both in-plane by reducing the number of spatial encoding steps and the slice direction by exciting multiple slices simultaneously. In-plane acceleration [6,7] can reduce image artifacts by reducing the number of spatial encoding steps, but the image SNR decreases by the square root of the acceleration factor. Acceleration in slice direction can increase the volume coverage without increasing TR, but it leads to an increase in power deposition and decrease image SNR by the poor condition of the image reconstruction problem and shortened T1 recovery [8-11].

EPI artifacts

The most common artifacts in 2D GE-EPI images are FOV/2 ghosts [12], geometric distortion [13], and signal dropout. FOV/2 ghosts are caused by phase errors between the odd and even readout lines of the k-space trajectory due to the system imperfections such as eddy currents. Geometric distortion is caused by the prolonged echo train length in field inhomogeneous areas (air/tissue interfaces). Phase errors are accumulated over time in phase encoding direction. Signal dropout is induced by field inhomogeneities within an imaging voxel. The detail of those artifacts will be explained and approaches to relieve them will be also discussed.

Acknowledgements

No acknowledgement found.

References

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Proc. Intl. Soc. Mag. Reson. Med. 32 (2024)