1,104 research outputs found

    Temporal Multivariate Pattern Analysis (tMVPA): a single trial approach exploring the temporal dynamics of the BOLD signal

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    fMRI provides spatial resolution that is unmatched by non-invasive neuroimaging techniques. Its temporal dynamics however are typically neglected due to the sluggishness of the hemodynamic signal. We present temporal multivariate pattern analysis (tMVPA), a method for investigating the temporal evolution of neural representations in fMRI data, computed on single-trial BOLD time-courses, leveraging both spatial and temporal components of the fMRI signal. We implemented an expanding sliding window approach that allows identifying the time-window of an effect. We demonstrate that tMVPA can successfully detect condition-specific multivariate modulations over time, in the absence of mean BOLD amplitude differences. Using Monte-Carlo simulations and synthetic data, we quantified family-wise error rate (FWER) and statistical power. Both at the group and single-subject levels, FWER was either at or significantly below 5%. We reached the desired power with 18 subjects and 12 trials for the group level, and with 14 trials in the single-subject scenario. We compare the tMVPA statistical evaluation to that of a linear support vector machine (SVM). SVM outperformed tMVPA with large N and trial numbers. Conversely, tMVPA, leveraging on single trials analyses, outperformed SVM in low N and trials and in a single-subject scenario. Recent evidence suggesting that the BOLD signal carries finer-grained temporal information than previously thought, advocates the need for analytical tools, such as tMVPA, tailored to investigate BOLD temporal dynamics. The comparable performance between tMVPA and SVM, a powerful and reliable tool for fMRI, supports the validity of our technique

    Robust Detection of Ocular Dominance Columns in Humans using High Field HSE BOLD fMRI

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    The ability to reliably and reproducibility map high resolution functional architecture using fMRI techniques has been a point of debate in animal as well as human studies. Several animal and human studies have successfully mapped high resolution functional organizations, however, the robustness of the phenomenon (i.e. reproducibility and demonstration in multiple subjects), which would certainly improve the credibility of the data, has been a subject of debate. Here we demonstrate the spatial specificity of Hahn spin echo BOLD by robust mapping of ocular dominance columns in humans at the high magnetic field of 7 T

    Investigation of BOLD using CARR-PURCELL T2 Weighting with SPIRAL Readout

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    It is demonstrated that a Carr-Purcell (CP) technique based on the fully adiabatic pulse sequence (CP-LASER) with SPIRAL readout can be used to generate zoomed images with relatively short acquisition window (at) for the investigation of the mechanisms of the BOLD effect. Based on the capability of the developed technique to refocus the dynamic dephasing, it is demonstrated that the BOLD effect is suppressed as the pulse interval cp of CP-LASER sequence decreased

    Sub Millimeter Analysis of Specificity of SE, GE, and ASE BOLD Responses in the Human Visual Cortex

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    Sub-millimeter spatial resolution applications are becoming of increasing interest in fMRI. Several animal and human studies have successfully mapped high resolution functional organizations. However, it is not known which fMRI technique (which depends on field strength), maximizes contrast to noise as well as specificity to capillaries for sub-millimeter functional mapping. In this work we examine this problem by comparing functional maps, at 0.5mm in plane resolution, of gradient echo BOLD, spin echo BOLD, and asymmetric echo BOLD in human visual cortex at 7 Tesla

    Parallel Imaging with RASER using Multiband Frequency-modulated Excitation Pulses

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    The many advantages of the recently proposed RASER sequence have been demonstrated. Hence, RASER holds great promises for functional MRI (fMRI), particularly for studies of the orbital-frontal cortex and other brain regions near air cavities, which cause distortion and signal loss in conventional EPI methods. However, the single-shot RASER sequence implemented so far inherently presents a set of temporal and spatial limitations that hinders it feasibility and full potential for fMRI applications. It is believed that parallel imaging will help overcome such restrictions. In this work, the RASER acquisition and reconstruction scheme is extended for parallel imaging using tailored pulses for simultaneous multi-band excitation

    The Dynamics of ERP and Hemodynamic Responses at Very Short Stimulus Durations

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    Complementary non-invasive imaging methods on human subjects such as EEG and fMRI can provide new insights into the functioning of the brain and into neurovascular coupling. Particularly, short stimulus durations rather than commonly used standard durations in fMRI experiments are suitable to study the relationship between electrophysiological and vascular measures because of reduction of non-linearities of the hemodynamic response [1]. In this study, using very short stimulus durations (0.1 ms to 5 ms) and measurements with fMRI and EEG we have found that both N75 of the visual evoked potentials and BOLD signal increase and P100 decrease with stimulus duration. In addition, the BOLD signal poststimulus undershoot also tends to deviate more with stimulus duration. These results allow to shed light on whether and which ERP components correlate well with the BOLD signal

    A Comparison of Hemodynamic and Neural Responses in Cat Visual Cortex Using Complex Stimuli

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    We compare fMRI-BOLD responses in anesthetized cats with local field potentials (LFPs), aggregate high-frequency responses (analog-Mua) and spiking activity recorded in primary and higher visual cortex of alert animals. The similarity of the activations in these electrophysiological signals to those in the BOLD is quantified by counting recording sites where different stimuli elicit the same relative activation as in the imaging experiments. Using artificial stimuli, a comparison of BOLD and LFP strongly depends on the frequency range used. Stimulating with complex or natural stimuli reduces this frequency dependence and yields a good match of LFP and BOLD. In general, this match is best between 20 and 50 Hz. The measures of high-frequency activity behave qualitatively different: the responses of the analog-Mua match those of the LFP; the spiking activity shows a low concordance with the BOLD signal. This dissociation of BOLD and spiking activity is most prominent upon stimulation with natural stimul

    Recent Advances in High-Resolution MR Application and Its Implications for Neurovascular Coupling Research

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    The current understanding of fMRI, regarding its vascular origins, is based on numerous assumptions and theoretical modeling, but little experimental validation exists to support or challenge these models. The known functional properties of cerebral vasculature are limited mainly to the large pial surface and the small capillary level vessels. However, a significant lack of knowledge exists regarding the cluster of intermediate-sized vessels, mainly the intracortical, connecting these two groups of vessels and where, arguably, key blood flow regulation takes place. In recent years, advances in MR technology and methodology have enabled the probing of the brain, both structurally and functionally, at resolutions and coverage not previously attainable. Functional MRI has been utilized to map functional units down to the levels of cortical columns and lamina. These capabilities open new possibilities for investigating neurovascular coupling and testing hypotheses regarding fundamental cerebral organization. Here, we summarize recent cutting-edge MR applications for studying neurovascular and functional imaging, both in humans as well as in animal models. In light of the described imaging capabilities, we put forward a theory in which a cortical column, an ensemble of neurons involved in a particular neuronal computation is spatially correlated with a specific vascular unit, i.e., a cluster of an emerging principle vein surrounded by a set of diving arteries. If indeed such a correlation between functional (neuronal) and structural (vascular) units exist as a fundamental intrinsic cortical feature, one could conceivably delineate functional domains in cortical areas that are not known or have not been identified
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