Vizioli, L. | Search bioRxiv

bioRxiv2018

A critical assessment of data quality and venous effects in ultra-high-resolution fMRI

Advances in hardware, pulse sequences, and reconstruction techniques have made it possible to perform functional magnetic resonance imaging (fMRI) at sub-millimeter resolution while maintaining high spatial coverage and acceptable signal-to-noise ratio. Here, we examine whether ultra-high-resolution fMRI can be exploited for routine use in neuroscience research. We conducted fMRI in human visual cortex during a simple event-related visual experiment (7T, gradient-echo EPI, 0.8-mm isotropic voxels, 2.2-s sampling rate, 84 slices), and developed analysis and visualization tools to assess the quality of the data. We make three main observations. First, we find that the acquired fMRI images, combined with appropriate surface-based processing, provide reliable and accurate measurements of fine-scale blood oxygenation level dependent (BOLD) activity patterns. Second, we show that the highly folded structure of cortex causes substantial biases on spatial resolution and data visualization. Third, we examine the well-recognized issue of venous contributions to fMRI signals. In a systematic assessment of large sections of cortex measured at a fine scale, we show that time-averaged T2*-weighted EPI intensity is a simple, robust marker of venous effects. These venous effects are unevenly distributed across cortex, are more pronounced in gyri and outer cortical depths, and are, to a certain degree, in consistent locations across subjects relative to cortical folding. Furthermore, we show that these venous effects are strongly correlated with BOLD responses evoked by the experiment. We conclude that ultra-high-resolution fMRI can provide robust information about fine-scale BOLD activity patterns, but special care must be exercised in visualizing and interpreting these patterns, especially with regards to the confounding influence of the brains vasculature. To help translate these methodological findings to neuroscience research, we provide practical suggestions for both high-resolution and standard-resolution fMRI studies.

neuroscience↗

bioRxiv2018

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

BackgroundfMRI provides spatial resolution that is unmatched by any non-invasive neuroimaging technique. Its temporal dynamics however are typically neglected due to the sluggishness of the hemodynamic based fMRI signal.\n\nNew MethodsWe present temporal multivariate pattern analysis (tMVPA), a method for investigating the temporal evolution of neural representations in fMRI data, computed using pairs of 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.\n\nResultsWe demonstrate that tMVPA can successfully detect condition-specific multivariate modulations over time, in the absence of univariate differences. Using Monte Carlo simulations and synthetic data, we quantified family-wise error rate (FWER) and statistical power. Both at the group and at the single subject level, FWER was either at or significantly below 5%. For the group level, we reached the desired power with 18 subjects and 12 trials; for the single subject scenario, 14 trials were required to achieve comparable power.\n\nComparison with existing methodstMVPA adds a temporal multivariate dimension to the tools available for fMRI analysis, enabling investigations of the evolution of neural representations over time. Moreover, tMVPA permits performing single subject inferential statistics by considering single-trial distribution.\n\nConclusionThe growing interest in fMRI temporal dynamics, motivated by recent evidence suggesting that the BOLD signal carries temporal information at a finer scale than previously thought, advocates the need for analytical tools, such as the tMVPA approach proposed here, tailored to investigating BOLD temporal information.

neuroscience↗