Abstract
Magnetic resonance imaging (MRI) is based on the magnetic excitation of body tissue and the reception of returned electromagnetic signals from the body. Excitation induces phase-locked precession of protons with a frequency proportional to the strength of the surrounding magnetic field as described by the Larmor equation. This fact can be exploited for spatial encoding by applying magnetic field gradients along spatial dimensions on top of the strong static magnetic field of the scanner. The obtained frequency-encoded information for each slice is accumulated in two-dimensional k space. The k space data can be transformed into image space by Fourier analysis. Functional MRI (fMRI) allows localizing brain function since increased local neuronal activity leads to a surprisingly strong increase in local blood flow, which itself results in measurable increases in local magnetic field homogeneity. Increased local blood flow delivers chemical energy (glucose and oxygen) to the neurons. The temporary increase and decrease of local blood flow, triggered by increased neu-ronal activity, is called the hemodynamic response starting 2–4 s after stimulus onset. Increased local blood flow results in an oversupply of oxygenated hemoglobin in the vicinity of increased neuronal activity. The oversupply flushes deox-ygenated hemoglobin from the capillaries and the downstream venules. Deoxygenated hemoglobin is paramagnetic reducing the homogeneity of the local magnetic field resulting in a weaker MRI signal than would be measurable without it. Oxygenated hemoglobin is diamagnetic and does not strongly reduce field homogeneity. Since the increased local blood flow replaces deoxygenated hemoglobin with oxygenated hemoglobin, local field homogeneity increases, leading to a stronger MRI signal as compared to a nonacti-vated state. Measured functional brain images thus reflect neuronal activity changes as blood oxygenation level-dependent (BOLD) contrast. Functional images are acquired using the fast echo-planar imaging (EPI) pulse sequence allowing acquisition of a 64 × 64 image matrix in less than 100 ms. To sample signal changes over time, a set of slices typically covering the whole brain is measured repeatedly. Activation of neurons results in a BOLD signal increase of only about 1–5% and lie buried within strong physical and physiological noise fluctuations of similar size. Proper preprocessing steps, including 3D motion correction and removal of drifts, reduce the effect of artifacts increasing the signal-to-noise ratio (SNR). In order to reliably detect stimulus-related effects, proper statistical data analysis is performed. In order to estimate response profiles, condition-related time course episodes may be averaged in various regions-of-interest (ROIs). The core statistical tool in fMRI data analysis is the general linear model (GLM) that allows the analysis of blocked and event-related experimental designs. To run a GLM, a design matrix (model) has to be constructed containing reference functions (predictors, model time courses) for all effects of interest (conditions) as well as confounds. The GLM fits the created model to the data independently for each voxel’s data (time course) providing a set of beta values estimating the effects of each condition. These beta values are compared with each other using contrasts resulting in a statistical value at each voxel. The statistical values of all voxels form a three-dimensional statistical map. To protect against wrongly declaring voxels as significant, statistical maps are thresholded properly by taking into account the multiple comparison problem. This problem is caused by the large number of independently performed statistical tests (one for each voxel). In recent years, parallel imaging techniques have been developed, which allow acquiring MRI data simultaneously with two or more receiver coils. Parallel imaging can be used to increase temporal or spatial resolution. It also helps to reduce EPI imaging artifacts, such as geometrical distortions and signal dropouts in regions of different neighboring tissue types. MRI has not only revolutionized functional brain imaging targeting gray matter neuronal activity but also enabled insights into the human white matter structure using diffusion-weighted magnetic resonance imaging. With proper measurement and modeling schemes including diffusion tensor imaging (DTI), major long-range fiber tracts can be reconstructed using computational trac-tography providing important information to guide neuro-surgical procedures potentially reducing the risk of lesioning important fiber tracts.
Original language | English |
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Title of host publication | Clinical Functional MRI |
Subtitle of host publication | Presurgical Functional Neuroimaging |
Editors | Christoph Stippich |
Publisher | Springer |
Pages | 13-60 |
ISBN (Electronic) | 978-3-662-45123-6 |
ISBN (Print) | 978-3-662-45122-9, 978-3-662-50028-6 |
DOIs | |
Publication status | Published - 2015 |