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Heinzle, J.

Publications and source records attributed to Heinzle, J..

At least 19 recordsLinked to original sources

Modelling Metacognition: A Joint Prediction-Confidence Model for Predictive Inference Task Data

Metacognition is the ability to reflect on and evaluate our own cognitive processes. It is often altered in psychopathology. Yet, the computational mechanisms underlying these alterations remain unclear. In this work, we extend Hierarchical Gaussian Filter (HGF) models to jointly fit trial-by-trial predictions and confidence ratings in a predictive inference task, providing an individualised characterisation on metacognitive processing. Applying our cognitive computational model to a large subclinical open dataset (N=430), we are able to achieve, on average, excellent fit of prediction responses [Formula] and a moderate to good fit of confidence ratings [Formula]. Analysis of experimental change-points revealed that our model accurately captures confidence self-reports dynamics around these change-points. Posterior parameter estimates reveal a negative effect of sensory input prediction errors and a positive effect of sensory input prediction precision on confidence ratings, respectively. In addition, we replicate state-of-the-art findings related to compulsivity as measured by a transdiagnostic factor score, such as inflated confidence and a decoupling of action updates (here, prediction errors) and confidence in compulsivity. These results demonstrate the robustness of our methodology and the potential of joint prediction-confidence modelling to uncover latent metacognitive alterations in psychopathology.

neuroscience↗

Perceived Control Over Breathing Perturbations Depends on Interosensory Input and Prediction Error

Interoception and homeostatic/allostatic control are not only fundamental for survival but play a key role for maintaining somatic and mental health. Furthermore, metacognitive evaluations of these processes, such as perceived failure of allostatic regulation, have been proposed to underlie the experience of chronic symptoms, such as chronic fatigue. A central question in this regard is what mechanisms the brain uses to evaluate control over bodily states. A prominent computational proposal posits that this is achieved by monitoring of interoceptive prediction errors (PEs). However, to date, this proposal has not been tested experimentally. Here, we tested this hypothesis by applying computational process models of perceived control to data from a novel behavioural paradigm, the Respiratory Metacognition of Control Task (RMCT). The RMCT manipulates control over breathing by changing inspiratory resistive loads as a function of control achieved in a gamified prediction task. We developed and compared trial-by-trial generative models of perceived explicit control in the RMCT, using data from 50 volunteers in a pre-registered analysis. Bayesian model selection suggested that perceived control over breathing is best explained as a function of both trial-wise interoceptive outcomes (breathing with or without an inspiratory resistive load) and trial-wise PEs about respiratory resistance. These results support a longstanding computational proposal of how the brain detects failures of bodily regulation and provide a mechanistic model for understanding inter-individual differences in perceived control over bodily states.

neuroscience↗

Differences in layer-specific activation of the insula during interoceptive vs. exteroceptive attention

Attention modulates the relative weighting of information and plays a critical role in modern theories of perception. While its role in exteroceptionthe perception of the external environmenthas been extensively studied, attentional processes in interoception, the perception of bodily states, are less well understood. In this study, we exploited high-field (7 Tesla) functional magnetic resonance imaging and concurrent field monitoring to investigate interoceptive attention at the level of cortical layers during a heartbeat attention task. Voxel-wise analyses reveal increased activity in the bilateral dorsal mid-insula during interoceptive attention (attending to ones heartbeat) compared to exteroceptive attention (attending to auditory white noise). Layer-specific analyses further demonstrate that this difference in activity is significantly higher in upper compared to lower cortical layers. This activation pattern persists after accounting for potential vascular artifacts through a deconvolution analysis with a physiological point spread function (PSF). To our knowledge, these findings represent the first empirical demonstration of layer-specific processes during interoceptive attention in human cortex. They may prove useful to inform and constrain theories of computational principles and physiological implementation of interoception.

neuroscience↗

Test-retest reliability of auditory MMN measured with OPM-MEG

In this paper, we report results from an investigation of auditory mismatch responses as measured by magnetoencephalography (MEG) based on optically pumped magnetometers (OPM). Specifically, as part of a quality control study, we examined the reliability and validity of auditory mismatch negativity (MMN) recordings, obtained with a newly installed OPM-MEG system. Based on OPM-MEG data from 30 healthy volunteers, measured twice with an established auditory MMN paradigm with frequency deviants, we examined the following questions: First, we focused on construct validity and examined whether OPM-MEG measurements of MMN responses (in terms of event-related fields, ERFs) were qualitatively comparable to previous MMN findings from studies using EEG or MEG based on superconducting quantum interference devices (SQUIDs). In particular, we examined whether significant MMN responses measured by OPM-MEG occurred in a comparable time window and showed a similar topography as in previous EEG/MEG studies of MMN. Second, we quantified test-retest reliability of MMN amplitude and latency over two separate measurement sessions. The results of our analyses show that MMN responses recorded with OPM-MEG are in good agreement with previously reported MMN results in terms of timing and topography. Furthermore, the comparison of group-level MMN topographies and timeseries shows excellent consistency across the two measurement sessions. Our quantitative test-retest reliability analyses at the sensor level indicate good reliability for MMN amplitude, but poor reliability for MMN latency. Overall, our findings suggest that OPM-MEG measurements of auditory MMN (i) are comparable to results from EEG and SQUID-based MEG and (ii) show good test-retest reliability for amplitude measures at the sensor level. Notably, these results were achieved in an "out of the box" state of the OPM-MEG system, shortly after installation and without further optimisation. The reason for the insufficient reliability for MMN latency we observed is currently under investigation and represents an important target for future improvements.

neuroscience↗

Thermoceptive predictions and prediction errors in the anterior insula

Contemporary theories of interoception propose that the brain constructs a model of the body for predicting the states and allostatic needs of all organs, including the skin, and updates this model using prediction error signals. However, empirical tests of this proposal are scarce in humans. This computational neuroimaging study investigated the presence and location of thermoceptive predictions and prediction errors in the brain using probabilistic manipulations of skin temperature in a novel interoceptive learning paradigm. Using functional MRI in healthy volunteers, we found that a Bayesian model provided a better account of participants skin temperature predictions than a non-Bayesian model. Further, activity in a network including the anterior insula was associated with trial-wise predictions and precision-weighted prediction errors. Our findings provide further evidence that the anterior insula plays a key role in implementing the brains model of the body, and raise important questions about the structure of this model.

neuroscience↗

Bayesian Workflow for Generative Modeling in Computational Psychiatry

Computational (generative) modelling of behaviour has considerable potential for clinical applications. In order to unlock the potential of generative models, reliable statistical inference is crucial. For this, Bayesian workflow has been suggested which, however, has rarely been applied in Translational Neuromodeling and Computational Psychiatry (TN/CP) so far. Here, we present a worked example of Bayesian workflow in the context of a typical application scenario for TN/CP. This application example uses Hierarchical Gaussian Filter (HGF) models, a family of computational models for hierarchical Bayesian belief updating. When equipped with a suitable response model, HGF models can be fit to behavioural data from cognitive tasks; these data frequently consist of binary responses and are typically univariate. This poses challenges for statistical inference due to the limited information contained in such data. We present a novel set of response models that allow for simultaneous inference from multivariate (here: two) behavioural data types. Using both simulations and empirical data from a speed-incentivised associative reward learning (SPIRL) task, we show that harnessing information from two different data streams (binary responses and continuous response times) improves the accuracy of inference (specifically, identifiability of parameters and models). Moreover, we find a linear relationship between log-transformed response times in the SPIRL task and participants uncertainty about the outcome. Our analysis illustrates the benefits of Bayesian workflow for a typical use case in TN/CP. We argue that adopting Bayesian workflow for generative modelling helps increase the transparency and robustness of results, which in turn is of fundamental importance for the long-term success of TN/CP.

neuroscience↗

GABAergic modulation of conflict adaptation and response inhibition

Adaptive behavior is only possible by stopping stereotypical actions to generate new plans according to internal goals. It is response inhibition --the ability to stop actions automatically triggered by exogenous cues-- that allows for the flexible interplay between bottom-up, stimulus driven behaviors, and top-down strategies. In addition to response inhibition, cognitive control draws on conflict adaptation, the facilitation of top-down actions following high conflict situations. It is currently unclear whether and how response inhibition and conflict adaptation depend on GABAergic signaling, the main inhibitory neurotransmitter in the human brain. Here, we applied a recently developed computational model (SERIA) to data from two studies (N=150 & 50) of healthy volunteers performing Simon and antisaccade tasks. One of these datasets was acquired under placebo-controlled pharmacological enhancement of GABAergic transmission (lorazepam, an allosteric modulator of the GABA-A receptor). Our model-based results suggest that enhanced GABA-A signaling boosts conflict adaptation but impairs response inhibition. More generally, our computational approach establishes a unified account of response inhibition and conflict adaptation in the Simon and antisaccade tasks and provides a novel tool for quantifying specific aspects of cognitive control and their modulation by pharmacology or disease. Author SummaryOur capacity to prepare for situations that afford conflicting responses (conflict adaptation) and to stop our immediate impulses in these scenarios (response inhibition) are the hallmark of cognitive control. As these abilities require both the stopping or slowing of response tendencies, a natural question is whether they are mediated by inhibitory neurotransmission in the brain. Here, we combined computational modeling with two experiments to investigate how conflict adaptation and response inhibition interact with each other (experiment 1) and how these are modulated by lorazepam (experiment 2), a positive modulator of the GABA-A receptor, one of the main inhibitory receptors in the human brain. Using our computational model to disentangle conflict adaptation and response inhibition, our results indicate that while lorazepam impaired response inhibition, it improved conflict adaptation. Thus, our results suggests that conflict adaptation is mediated by GABA-A neurotransmission.

neuroscience↗

TAPAS: an open-source software package for Translational Neuromodeling and Computational Psychiatry

Psychiatry faces fundamental challenges with regard to mechanistically guided differential diagnosis, as well as prediction of clinical trajectories and treatment response of individual patients. This has motivated the genesis of two closely intertwined fields: (i) Translational Neuromodeling (TN), which develops "computational assays" for inferring patient-specific disease processes from neuroimaging, electrophysiological, and behavioral data; and (ii) Computational Psychiatry (CP), with the goal of incorporating computational assays into clinical decision making in everyday practice. In order to serve as objective and reliable tools for clinical routine, computational assays require end-to-end pipelines from raw data (input) to clinically useful information (output). While these are yet to be established in clinical practice, individual components of this general end-to-end pipeline are being developed and made openly available for community use. In this paper, we present the Translational Algorithms for Psychiatry-Advancing Science (TAPAS) software package, an open-source collection of building blocks for computational assays in psychiatry. Collectively, the tools in TAPAS presently cover several important aspects of the desired end-to-end pipeline, including: (i) tailored experimental designs and optimization of measurement strategy prior to data acquisition, (ii) quality control during data acquisition, and (iii) artifact correction, statistical inference, and clinical application after data acquisition. Here, we review the different tools within TAPAS and illustrate how these may help provide a deeper understanding of neural and cognitive mechanisms of disease, with the ultimate goal of establishing automatized pipelines for predictions about individual patients. We hope that the openly available tools in TAPAS will contribute to the further development of TN/CP and facilitate the translation of advances in computational neuroscience into clinically relevant computational assays.

neuroscience↗

Technical Note: A fast and robust integrator of delay differential equations in DCM for electrophysiological data

Dynamic causal models (DCMs) of electrophysiological data allow, in principle, for inference on hidden, bulk synaptic function in neural circuits. The directed influences between the neuronal elements of modeled circuits are subject to delays due to the finite transmission speed of axonal connections. Ordinary differential equations are therefore not adequate to capture the ensuing circuit dynamics, and delay differential equations (DDEs) are required instead. Previous work has illustrated that the integration of DDEs in DCMs benefits from sophisticated integration schemes in order to ensure rigorous parameter estimation and correct model identification. However, integration schemes that have been proposed for DCMs either emphasise speed (at the possible expense of accuracy) or robustness (but with computational costs that are problematic in practice). In this technical note, we propose an alternative integration scheme that overcomes these shortcomings and offers high computational efficiency while correctly preserving the nature of delayed effects. This integration scheme is available as open-source code in the Translational Algorithms for Psychiatry-Advancing Science (TAPAS) toolbox and can be easily integrated into existing software (SPM) for the analysis of DCMs for electrophysiological data. While this paper focuses on its application to the convolution-based formalism of DCMs, the new integration scheme can be equally applied to more advanced formulations of DCMs (e.g. conductance based models). Our method provides a new option for electrophysiological DCMs that offers the speed required for scientific projects, but also the accuracy required for rigorous translational applications, e.g. in computational psychiatry.

neuroscience↗

An Introduction to Thermodynamic Integration and Application to Dynamic Causal Models

In generative modeling of neuroimaging data, such as dynamic causal modeling (DCM), one typically considers several alternative models, either to determine the most plausible explanation for observed data (Bayesian model selection) or to account for model uncertainty (Bayesian model averaging). Both procedures rest on estimates of the model evidence, a principled trade-off between model accuracy and complexity. In the context of DCM, the log evidence is usually approximated using variational Bayes. Although this approach is highly efficient, it makes distributional assumptions and is vulnerable to local extrema. This paper introduces the use of thermodynamic integration (TI) for Bayesian model selection and averaging in the context of DCM. TI is based on Markov chain Monte Carlo sampling which is asymptotically exact but orders of magnitude slower than variational Bayes. In this paper, we explain the theoretical foundations of TI, covering key concepts such as the free energy and its origins in statistical physics. Our aim is to convey an in-depth understanding of the method starting from its historical origin in statistical physics. In addition, we demonstrate the practical application of TI via a series of examples which serve to guide the user in applying this method. Furthermore, these examples demonstrate that, given an efficient implementation and hardware capable of parallel processing, the challenge of high computational demand can be overcome successfully. The TI implementation presented in this paper is freely available as part of the open source software TAPAS. Author summaryWhen fitting computational models to data in the setting of Bayesian inference, a user has the choice between two broad classes of algorithms: variational inference and Monte Carlo simulation. While both methods have advantages and drawbacks, variational inference has become standard in the domain of modelling directed brain connectivity due to its computational efficiency, especially when the challenges to select between competing hypotheses that explain the observed data. By contrast, the high computational demand by Monte Carlo methods has so far prevented their widespread use for inference on brain connectivity, despite their capability to overcome some of the shortcomings of variational inference. In this paper, we introduce the user to thermodynamic integration (TI), a Monte Carlo method designed for model fitting and model selection. By covering its foundations and historical origins in statistical physics, we hope to convey an in-depth understanding of TI that goes beyond a purely technical treatment. In addition, we also provide examples for concrete applications, demonstrating that, given an efficient implementation and up-to-date hardware, the challenge of high computational demand can be overcome successfully.

neuroscience↗

A Hilbert-based method for processing respiratory timeseries

In this technical note, we introduce a new method for estimating changes in respiratory volume per unit time (RVT) from respiratory bellows recordings. By using techniques from the electrophysiological literature, in particular the Hilbert transform, we show how we can better characterise breathing rhythms, with the goal of improving physiological noise correction in functional magnetic resonance imaging (fMRI). Specifically, our approach leads to a representation with higher time resolution and better captures atypical breathing events than current peak-based RVT estimators. Finally, we demonstrate that this leads to an increase in the amount of respiration-related variance removed from fMRI data when used as part of a typical preprocessing pipeline. Our implementation will be publicly available as part of the PhysIO package, which is distributed as part of the open-source TAPAS toolbox (translationalneuromodeling.org/tapas). HighlightsO_LIWe introduce a new estimator for respiratory volume per unit time from respiratory recordings. C_LIO_LIWe demonstrate how this is able to accurately characterise atypical breathing events. C_LIO_LIThis removes significantly more variance when used as a confound regressor for fMRI data. C_LIO_LIOur implementation will be included in PhysIO, released as part of TAPAS: translationalneuromodeling.org/tapas. C_LI

neuroscience↗

Regression dynamic causal modeling for resting-state fMRI

AO_SCPLOWBSTRACTC_SCPLOW"Resting-state" functional magnetic resonance imaging (rs-fMRI) is widely used to study brain connectivity. So far, researchers have been restricted to measures of functional connectivity that are computationally efficient but undirected, or to effective connectivity estimates that are directed but limited to small networks. Here, we show that a method recently developed for task-fMRI - regression dynamic causal modeling (rDCM) - extends to rs-fMRI and offers both directional estimates and scalability to whole-brain networks. First, simulations demonstrate that rDCM faithfully recovers parameter values over a wide range of signal-to-noise ratios and repetition times. Second, we test construct validity of rDCM in relation to an established model of effective connectivity, spectral DCM. Using rs-fMRI data from nearly 200 healthy participants, rDCM produces biologically plausible results consistent with estimates by spectral DCM. Importantly, rDCM is computationally highly efficient, reconstructing whole-brain networks (>200 areas) within minutes on standard hardware. This opens promising new avenues for connectomics.

neuroscience↗

Dynamic causal modeling of layered magnetoencephalographic event-related responses

The layered architecture of cortex is thought to play a fundamental role in shaping cortical computations. However, direct electrophysiological measurements of layered activity are not possible non-invasively in humans. Recent advances have shown that a distinction of two layers can be achieved using magnetoencephalography in combination with head casts and advanced spatial modeling. In this technical note, we present a dynamic causal model of a single cortical microcircuit that models event related potentials. The model captures the average dynamics of a detailed two layered circuit. It combines a temporal model of neural dynamics with a spatial model of a layer specific lead field to facilitate layer separation. In simulations we show that the spatial arrangement of the two layers can be successfully recovered using Bayesian inference. The layered model can also be distinguished from a single dipole model. We conclude that precision magnetoencephalography in combination with detailed dynamical system modeling can be used to study non-invasively the fast dynamics of layered computations.

neuroscience↗

Model-based prediction of muscarinic receptor function from auditory mismatch negativity responses

AO_SCPLOWBSTRACTC_SCPLOWDrugs affecting neuromodulation, for example by dopamine or acetylcholine, take centre stage among therapeutic strategies in psychiatry. These neuromodulators can change both neuronal gain and synaptic plasticity and therefore affect electrophysiological measures. An important goal for clinical diagnostics is to exploit this effect in the reverse direction, i.e., to infer the status of specific neuromodulatory systems from electrophysiological measures. In this study, we provide proof-of-concept that the functional status of cholinergic (specifically muscarinic) receptors can be inferred from electrophysiological data using generative (dynamic causal) models. To this end, we used epidural EEG recordings over two auditory cortical regions during a mismatch negativity (MMN) paradigm in rats. All animals were treated, across sessions, with muscarinic receptor agonists and antagonists at different doses. Together with a placebo condition, this resulted in five levels of muscarinic receptor status. Using a dynamic causal model - embodying a small network of coupled cortical microcircuits - we estimated synaptic parameters and their change across pharmacological conditions. The ensuing parameter estimates associated with (the neuromodulation of) synaptic efficacy showed both graded muscarinic effects and predictive validity between agonistic and antagonistic pharmacological conditions. This finding illustrates the potential utility of generative models of electrophysiological data as computational assays of muscarinic function. In application to EEG data of patients from heterogeneous spectrum diseases, e.g. schizophrenia, such models might help identify subgroups of patients that respond differentially to cholinergic treatments. SO_SCPLOWIGNIFICANCEC_SCPLOW SO_SCPLOWTATEMENTC_SCPLOWIn psychiatry, the vast majority of pharmacological treatments affect actions of neuromodulatory transmitters, e.g. dopamine or acetylcholine. As treatment is largely trial-and-error based, one of the goals for computational psychiatry is to construct mathematical models that can serve as "computational assays" and infer the status of specific neuromodulatory systems in individual patients. This neuro-modelling strategy has great promise for electrophysiological data in particular but requires careful validation. The present study demonstrates that the functional status of cholinergic (muscarinic) receptors can be inferred from electrophysiological data using dynamic causal models of neural circuits. While accuracy needs to be enhanced and our results must be replicated in larger samples, our current results provide proof-of-concept for computational assays of muscarinic function using EEG.

neuroscience↗

Advances in Spiral fMRI: A High-resolution Study with Single-shot Acquisition

Spiral fMRI has been put forward as a viable alternative to rectilinear echo-planar imaging, in particular due to its enhanced average k-space speed and thus high acquisition efficiency. This renders spirals attractive for contemporary fMRI applications that require high spatiotemporal resolution, such as laminar or columnar fMRI. However, in practice, spiral fMRI is typically hampered by its reduced robustness and ensuing blurring artifacts, which arise from imperfections in both static and dynamic magnetic fields. Recently, these limitations have been overcome by the concerted application of an expanded signal model that accounts for such field imperfections, and its inversion by iterative image reconstruction. In the challenging ultra-high field environment of 7 Tesla, where field inhomogeneity effects are aggravated, both multi-shot and single-shot 2D spiral imaging at sub-millimeter resolution was demonstrated with high depiction quality and anatomical congruency. In this work, we further these advances towards a time series application of spiral readouts, namely, single-shot spiral BOLD fMRI at 0.8 mm in-plane resolution. We demonstrate that high-resolution spiral fMRI at 7 T is not only feasible, but delivers both excellent image quality, BOLD sensitivity, and spatial specificity of the activation maps, with little artifactual blurring. Furthermore, we show the versatility of the approach with a combined in/out spiral readout at a more typical resolution (1.5 mm), where the high acquisition efficiency allows to acquire two images per shot for improved sensitivity by echo combination. HighlightsO_LIThis work reports the first fMRI study at 7T with high-resolution spiral readout gradient waveforms. C_LIO_LIWe achieve spiral fMRI with sub-millimeter resolution (0.8 mm, FOV 230 mm), acquired in a single shot (36 slices in 3.3 s). C_LIO_LISpiral images exhibit intrinsic geometric congruency to anatomical scans, and spatially specific activation patterns. C_LIO_LIImage reconstruction rests on a signal model expanded by measured trajectories and static field maps, inverted by cg-SENSE. C_LIO_LIWe assess generalizability of the approach for spiral in/out readouts, providing two images per shot (1.5 mm resolution). C_LI

neuroscience↗

Computational dissociation of dopaminergic and cholinergic effects on voluntary behavior and inhibitory control

BackgroundPatients with schizophrenia make more errors than healthy subjects on the antisaccade task. In this paradigm, participants are required to inhibit a reflexive saccade to a target and to select the correct action (a saccade in the opposite direction). While the precise origin of this deficit is not clear, it has been connected to aberrant dopaminergic and cholinergic neuromodulation. MethodsTo study the impact of dopamine and acetylcholine on inhibitory control and action selection, we administered two selective drugs (levodopa 200mg/galantamine 8mg) to healthy volunteers (N=100) performing the antisaccade task. A computational model (SERIA) was employed to separate the contribution of inhibitory control and action selection to empirical reaction times and error rates. ResultsModeling suggested that levodopa improved action selection (at the cost of increased reaction times) but did not have a significant effect on inhibitory control. By contrast, according to our model, galantamine affected inhibitory control in a dose dependent fashion, reducing inhibition failures at low doses and increasing them at higher levels. These effects were sufficiently specific that the computational analysis allowed for identifying the drug administered to an individual with 70% accuracy. ConclusionsOur results do not support the hypothesis that elevated tonic dopamine strongly impairs inhibitory control. Rather levodopa improved the ability to select correct actions. Instead, inhibitory control was modulated by cholinergic drugs. This approach may provide a starting point for future computational assays that differentiate neuromodulatory abnormalities in heterogeneous diseases like schizophrenia.

pharmacology and toxicology↗

Thermodynamic integration for dynamic causal models

In generative modeling of neuroimaging data, such as dynamic causal modeling (DCM), one typically considers several alternative models, either to determine the most plausible explanation for observed data (Bayesian model selection) or to account for model uncertainty (Bayesian model averaging). Both procedures rest on estimates of the model evidence, a principled trade-off between model accuracy and complexity. In DCM, the log evidence is usually approximated using variational Bayes (VB) under the Laplace approximation (VBL). Although this approach is highly efficient, it makes distributional assumptions and can be vulnerable to local extrema. An alternative to VBL is Markov Chain Monte Carlo (MCMC) sampling, which is asymptotically exact but orders of magnitude slower than VB. This has so far prevented its routine use for DCM.\n\nThis paper makes four contributions. First, we introduce a powerful MCMC scheme - thermodynamic integration (TI) - to neuroimaging and present a derivation that establishes a theoretical link to VB. Second, this derivation is based on a tutorial-like introduction to concepts of free energy in physics and statistics. Third, we present an implementation of TI for DCM that rests on population MCMC. Fourth, using simulations and empirical functional magnetic resonance imaging (fMRI) data, we compare log evidence estimates obtained by TI, VBL, and other MCMC-based estimators (prior arithmetic mean and posterior harmonic mean). We find that model comparison based on VBL gives reliable results in most cases, justifying its use in standard DCM for fMRI. Furthermore, we demonstrate that for complex and/or nonlinear models, TI may provide more robust estimates of the log evidence. Importantly, accurate estimates of the model evidence can be obtained with TI in acceptable computation time. This paves the way for using DCM in scenarios where the robustness of single-subject inference and model selection becomes paramount, such as differential diagnosis in clinical applications.

neuroscience↗

Feature-specific prediction errors for visual mismatch support predictive coding accounts of perception

Predictive coding (PC) theory posits that our brain employs a predictive model of the environment to infer the causes of its sensory inputs. A fundamental but untested prediction of this theory is that the same stimulus should elicit distinct precision weighted prediction errors (pwPEs) when different (feature-specific) predictions are violated, even in the absence of attention. Here, we tested this hypothesis using functional magnetic resonance imaging (fMRI) and a multi-feature roving visual mismatch paradigm where rare changes in either color (red, green), or emotional expression (happy, fearful) of faces elicited pwPE responses in human participants. Using a computational model for learning and inference, we simulated pwPE trajectories of a Bayes-optimal observer and used these to analyze changes in blood oxygen level dependent (BOLD) responses to changes in color and emotional expression of faces while participants engaged in a distractor task. Controlling for visual attention by eye-tracking, we found pwPE responses to unexpected color changes in the fusiform gyrus. Conversely, unexpected changes of facial emotions elicited pwPE responses in thalamo-cortico-cerebellar structures associated with emotion processing. Our results support a general role of PC across perception, from low-level to complex and socially relevant object features, and suggest that monitoring of the social environment occurs continuously and automatically, even in the absence of attention.\n\nHighlightsPredictive coding (PC) implies that brain responses should reflect transient precision weighted prediction errors (pwPEs). By using fMRI we show that rare changes in color or emotional expression of human faces elicit pwPE responses in dedicated neuronal circuits with known specialization in processing color and emotion-related information, respectively. Our results demonstrate that physically identical stimuli elicit pwPEs in distinct neuronal circuits when different (feature-specific) predictions are violated, depending on current sensory expectations based on prior stimulus context. The demonstration of pwPEs in visual areas as well as in emotion processing structures lends experimental support to theoretical accounts of PC in color and social perception, respectively.

neuroscience↗