Near-infrared spectroscopy (NIRS) can be employed to investigate brain activities associated with regional changes of the oxy- and deoxyhemoglobin concentration by measuring the absorption of near-infrared light through the intact skull. NIRS is regarded as a promising neuroimaging modality thanks to its excellent temporal resolution and flexibility for routine monitoring. Recently, the general linear model (GLM), which is a standard method for functional MRI (fMRI) analysis, has been employed for quantitative analysis of NIRS data. However, the GLM often fails in NIRS when there exists an unknown global trend due to breathing, cardiac, vasomotion, or other experimental errors. We propose a wavelet minimum description length (Wavelet-MDL) detrending algorithm to overcome this problem. Specifically, the wavelet transform is applied to decompose NIRS measurements into global trends, hemodynamic signals, and uncorrelated noise components at distinct scales. The minimum description length (MDL) principle plays an important role in preventing over- or underfitting and facilitates optimal model order selection for the global trend estimate. Experimental results demonstrate that the new detrending algorithm outperforms the conventional approaches.
Functional magnetic resonance imaging (fMRI) in the resting state, particularly fMRI based on the blood-oxygenation level-dependent (BOLD) signal, has been extensively used to measure functional connectivity in the brain. However, the mechanisms of vascular regulation that underlie the BOLD fluctuations during rest are still poorly understood. In this work, using dual-echo pseudo-continuous arterial spin labeling and MR angiography (MRA), we assess the spatio-temporal contribution of cerebral blood flow (CBF) to the resting-state BOLD signals and explore how the coupling of these signals is associated with regional vasculature. Using a general linear model analysis, we found that statistically significant coupling between resting-state BOLD and CBF fluctuations is highly variable across the brain, but the coupling is strongest within the major nodes of established resting-state networks, including the default-mode, visual, and task-positive networks. Moreover, by exploiting MRA-derived large vessel (macrovascular) volume fraction, we found that the degree of BOLD–CBF coupling significantly decreased as the ratio of large vessels to tissue volume increased. These findings suggest that the portion of resting-state BOLD fluctuations at the sites of medium-to-small vessels (more proximal to local neuronal activity) is more closely regulated by dynamic regulations in CBF, and that this CBF regulation decreases closer to large veins, which are more distal to neuronal activity.
The focal underdetermined system solver (FOCUSS) was originally designed to obtain sparse solutions by successively solving quadratic optimization problems. This article adapts FOCUSS for a projection reconstruction MR imaging problem to obtain high resolution reconstructions from angular undersampled radial k -space data. We show that FOCUSS is effective for projection reconstruction MRI, since medical images are usually sparse in some sense and the center region of the undersampled radial k -space samples still provides a low resolution, yet meaningful, image essential for the convergence of FOCUSS. Projection reconstruction (PR) with radial k-space trajectory was the first MRI k-space trajectory in MR history (1). However, cartesian k-space trajectory has replaced PR, mainly because of artifacts of PR that are related to B 0 inhomogeneity and to gradient nonlinearity (2). However, recent advances in MR hardware technology have overcome problems related to B 0 inhomogeneity and gradient nonlinearity, and interest in PR has thus been revived. PR has many advantages over the conventional cartesian k-space trajectory (3). Since no phase-encoding gradient is used, PR has a shorter minimum TE, which has made PR particularly desirable for imaging very short T 2 nuclei (3-5). Another advantage of PR is its robustness to the motion artifacts from flow or respiration. One important example is the reduction of motion artifacts in a diffusionweighted MRI (6,7). Furthermore, the aliasing artifacts from radial under-sampling usually appear as streaks, which are visually less distracting than the wrap-around artifacts obtained with cartesian under-sampling.One of the disadvantages of PR is the increased scan time involved if the Nyquist sampling criterion needs to be satisfied. More specifically, the number of radial lines N s required to satisfy the Nyquist criterion is given by (3):where L is the field-of-view (FOV), and k max is the maximum k-space radius. Usually, the number of radial lines acquired by PR is about 57% larger than the number of k-space lines acquired on a cartesian grid, which results in the increased scan time (3). If streak aliasing artifacts can be tolerated in an application, the scan time can be reduced by using angular undersampling. One such undersampled PR application is contrast-enhanced vascular imaging (8).Because of the properties of PR, if the contrast enhanced vessels are located at the center of the FOV, the undersampling aliasing artifacts appear as streaks near the periphery of the FOV and usually do not interfere with vessels located at the center of FOV. Hence, this application of PR for angiography has been a success (8).Rather than tolerating the angular aliasing artifacts, however, the main goal of our research is to develop a novel reconstruction algorithm with minimal angular aliasing. The bases of such a novel algorithm are the following two observations: (a) most medical imaging is sparse in some sense, and (b) the under-sampled PR still provides a meaningful low resolution imag...
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.