Evidence map›Paper›PMID 41014244›Full record

ArticleHuman brain mapping2025

Applying Bayesian Multilevel Modeling to Single Trial Dynamics: A Demonstration in Aversive Conditioning.

Andrew H Farkas, Judith Cediel Escobar, Faith E Gilbert, Christian Panitz, Mingzhou Ding, Andreas Keil

Abstract read
In one paragraph

Article in Human brain mapping, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Andrew H FarkasUniversity of Florida, Gainesville, Florida, USA.
Judith Cediel EscobarUniversity of Florida, Gainesville, Florida, USA.
Faith E GilbertUniversity of Florida, Gainesville, Florida, USA.
Christian PanitzUniversity of Bremen, Bremen, Germany.
Mingzhou DingUniversity of Florida, Gainesville, Florida, USA.
Andreas KeilUniversity of Florida, Gainesville, Florida, USA.

Funding

Ding R01 Administrative SupplementR01MH125615 · NIMH · UNIVERSITY OF FLORIDA · PI DING, MINGZHOU, KEIL, ANDREAS · 2021 to 2025
$2.5M
Advanced 3T for Structural and Functional Imaging at University of FloridaS10OD021726 · OD · UNIVERSITY OF FLORIDA · PI LONG, JOANNA R · 2017 to 2017
$2.0M
NIH HHS S10 OD021726NIMH NIH HHS R01 MH125615NIMH NIH HHS R01MH125615-01A1
6 · The paper itself

Abstract

Aversive conditioning changes visuocortical responses to conditioned cues, and the generalization of these changes to perceptually similar cues may provide mechanistic insights into anxiety and fear disorders. Yet, as in many areas of cognitive neuroscience, testing hypotheses about trial-by-trial dynamics in conditioning paradigms is challenged by poor single-trial signal-to-noise ratios (SNR), missing trials, and inter-individual differences. The present technical report demonstrates how a state-of-the-art Bayesian workflow can overcome these issues, using a preliminary sample of simultaneously recorded EEG-fMRI data. A preliminary group of observers (N = 24) viewed circular gratings varying in orientation, with only one orientation paired with an aversive outcome (noxious electric pulse). Gratings were flickered at 15 Hz to evoke steady-state visual evoked potentials (ssVEPs), recorded with 31 channels of EEG in an MRI scanner. First, the benefits of a Bayesian multilevel structure are demonstrated on the fMRI data by improving a standard fMRI first-level multiple regression. Next, the Bayesian modeling approach is demonstrated by applying a theory-driven learning model to the EEG data. The multilevel structure of the Bayesian learning model informs and constrains estimates per participant, providing an interpretable generative model. In the example analysis provided in this report, it showed superior cross-validation accuracy and provided insights into participant-level learning dynamics. It also isolated the generalization effects of conditioning, providing improved statistical certainty. Lastly, missing trials were interpolated and weighted appropriately using the full model's structure. This is a critical aspect for single-trial analyses of simultaneously recorded physiological measures because each added measure will typically increase the number of trials missing a complete set of observations. The present report aims to illustrate the utility of this analytical framework. It shows how models may be iteratively built and compared in a modern Bayesian workflow. Future models may use different conceptualizations of learning, allow integration of clinically relevant factors, and enable the fusion of different simultaneous recordings such as EEG, autonomic, behavioral, and hemodynamic data.

Indexed as

BrainElectroencephalographyEvoked Potentials, VisualAdultBayes TheoremFemaleHumansMagnetic Resonance ImagingMaleYoung AdultBayesiandifferential conditioninggeneralizationmultilevel‐modelssingle‐trialssteady‐state visually evoked potential

Identifiers

PMID41014244
PMCPMC12476001

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LicenceCC BY
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.