Search bioRxivSearch

Biology subjects

Geuter, S.

Publications and source records attributed to Geuter, S..

3 recordsLinked to original sources

Modular preprocessing pipelines can reintroduce artifacts into fMRI data

The preprocessing pipelines typically used in both task and restingstate fMRI (rs-fMRI) analysis are modular in nature: They are composed of a number of separate filtering/regression steps, including removal of head motion covariates and band-pass filtering, performed sequentially and in a flexible order. In this paper we illustrate the shortcomings of this approach, as we show how later preprocessing steps can reintroduce artifacts previously removed from the data in prior preprocessing steps. We show that each regression step is a geometric projection of data onto a subspace, and that performing a sequence of projections can move the data into subspaces no longer orthogonal to those previously removed, reintroducing signal related to nuisance covariates. Thus, linear filtering operations are not commutative, and the order in which the preprocessing steps are performed is critical. These issues can arise in practice when any combination of standard preprocessing steps--including motion regression, scrubbing, component-based correction, global signal regression, and temporal filtering--are performed sequentially. In this work we focus primarily on rs-fMRI. We illustrate the problem both theoretically and empirically through application to a test-retest rs-fMRI data set, and suggest remedies. These include (a) combining all steps into a single linear filter, or (b) sequential orthogonalization of covariates/linear filters performed in series.

neuroscience

Multiple brain networks mediating stimulus-pain relationships in humans

The brain transforms nociceptive input into a complex pain experience comprised of sensory, affective, motivational, and cognitive components. However, it is still unclear how pain arises from nociceptive input, and which brain networks coordinate to generate pain experiences. We introduce a new high-dimensional mediation analysis technique to estimate distributed, network-level patterns mediating the relationship between stimulus intensity and pain. In a large-scale analysis of functional magnetic resonance imaging data (N=284), we identify both traditional mediators in somatosensory brain regions and additional mediators located in prefrontal, midbrain, striatal, and default-mode regions unrelated to nociception in standard analyses. The whole brain mediators are specific for pain vs. aversive sounds and are organized in five functional networks. Brain mediators explain 32% more within-subject variance of single-trial pain ratings than previous brain-based models. Our results provide a new, broader view of the networks underlying pain experience, as well as distinct targets for interventions.

neuroscience

Effect Size and Power in fMRI Group Analysis

Multi-subject functional magnetic resonance imaging (fMRI) analysis is often concerned with determining whether there exists a significant population-wide activation in a comparison between two or more conditions. Typically this is assessed by testing the average value of a contrast of parameter estimates (COPE) against zero in a general linear model (GLM) analysis. In this work we investigate several aspects of this type of analysis. First, we study the effects of sample size on the sensitivity and reliability of the group analysis, allowing us to evaluate the ability of small sampled studies to effectively capture population-level effects of interest. Second, we assess the difference in sensitivity and reliability when using volumetric or surface based data. Third, we investigate potential biases in estimating effect sizes as a function of sample size. To perform this analysis we utilize the task-based fMRI data from the 500-subject release from the Human Connectome Project (HCP). We treat the complete collection of subjects (N = 491) as our population of interest, and perform a single-subject analysis on each subject in the population. We investigate the ability to recover population level effects using a subset of the population and standard analytical techniques. Our study shows that sample sizes of 40 are generally able to detect regions with high effect sizes (Cohens d > 0.8), while sample sizes closer to 80 are required to reliably recover regions with medium effect sizes (0.5 < d < 0.8). We find little difference in results when using volumetric or surface based data with respect to standard mass-univariate group analysis. Finally, we conclude that special care is needed when estimating effect sizes, particularly for small sample sizes.

neuroscience