Evidence map›Paper›PMID 39543128›Full record

ArticleNature communications2024

Lateral prefrontal theta oscillations causally drive a computational mechanism underlying conflict expectation and adaptation.

María Paz Martínez-Molina, Gabriela Valdebenito-Oyarzo, Patricia Soto-Icaza, Francisco Zamorano, Alejandra Figueroa-Vargas, Patricio Carvajal-Paredes, Ximena Stecher, César Salinas, Antoni Valero-Cabré, Rafael Polania and 1 more

Abstract read
In one paragraph

Article in Nature communications, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing 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

15 citing papers in PubMed.

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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

11 authors.

María Paz Martínez-MolinaLaboratorio de Neurociencia Social y Neuromodulación, Centro de Investigación en Complejidad Social, (neuroCICS), Facultad de Gobierno, Universidad del Desarrollo, Santiago, Chile.
Gabriela Valdebenito-OyarzoLaboratorio de Neurociencia Social y Neuromodulación, Centro de Investigación en Complejidad Social, (neuroCICS), Facultad de Gobierno, Universidad del Desarrollo, Santiago, Chile.
Patricia Soto-IcazaLaboratorio de Neurociencia Social y Neuromodulación, Centro de Investigación en Complejidad Social, (neuroCICS), Facultad de Gobierno, Universidad del Desarrollo, Santiago, Chile.ORCID 0000-0002-3092-7195
Francisco ZamoranoUnidad de Neuroimágenes Cuantitativas avanzadas (UNICA), Departamento de Imágenes, Clínica Alemana, Santiago, Chile.
Alejandra Figueroa-VargasLaboratorio de Neurociencia Social y Neuromodulación, Centro de Investigación en Complejidad Social, (neuroCICS), Facultad de Gobierno, Universidad del Desarrollo, Santiago, Chile.ORCID 0000-0001-9778-2851
Patricio Carvajal-ParedesLaboratorio de Neurociencia Social y Neuromodulación, Centro de Investigación en Complejidad Social, (neuroCICS), Facultad de Gobierno, Universidad del Desarrollo, Santiago, Chile.
Ximena StecherDepartamento de Imágenes, Facultad de Medicina Clínica Alemana-Universidad del Desarrollo, Santiago, Chile.
César SalinasDepartamento de Imágenes, Facultad de Medicina Clínica Alemana-Universidad del Desarrollo, Santiago, Chile.
Antoni Valero-CabréCausal Dynamics, Plasticity and Rehabilitation Group, FRONTLAB team, Institut du Cerveau et de la Moelle Epinière (ICM), CNRS UMR 7225, INSERM U 1127 and Sorbonne Université, Paris, France.ORCID 0000-0002-5033-2279
Rafael PolaniaDecision Neuroscience Lab, Department of Health Sciences and Technology, ETH Zurich, Zurich, Switzerland.ORCID 0000-0002-6176-6806
Pablo BillekeLaboratorio de Neurociencia Social y Neuromodulación, Centro de Investigación en Complejidad Social, (neuroCICS), Facultad de Gobierno, Universidad del Desarrollo, Santiago, Chile. pbilleke@udd.cl.ORCID 0000-0003-4261-0678

Funding

Fondo Nacional de Desarrollo Científico y Tecnológico (National Fund for Scientific and Technological Development) 1181295
6 · The paper itself

Abstract

Adapting our behavior to environmental demands relies on our capacity to perceive and manage potential conflicts within our surroundings. While evidence implicates the involvement of the lateral prefrontal cortex and theta oscillations in detecting conflict stimuli, their causal role in conflict expectation remains elusive. Consequently, the exact computations and neural mechanisms underlying these cognitive processes still need to be determined. We employed an integrative approach involving cognitive computational modeling, fMRI, TMS, and EEG to establish a causal link between oscillatory brain function, its neurocomputational role, and the resulting conflict processing and adaptation behavior. Our results reveal a computational process underlying conflict expectation, which correlates with BOLD-fMRI and theta activity in the superior frontal gyrus (SFG). Modulation of theta activity via rhythmic TMS applied over the SFG induces endogenous theta activity, which in turn enhances computations associated with conflict expectation. These findings provide evidence for the causal involvement of SFG theta activity in learning and allocating cognitive resources to address forthcoming conflict stimuli.

Indexed as

Conflict, PsychologicalMagnetic Resonance ImagingPrefrontal CortexTheta RhythmAdaptation, PsychologicalAdultBrain MappingCognitionComputer SimulationElectroencephalographyFemaleHumansMaleTranscranial Magnetic StimulationYoung Adult

Identifiers

PMID39543128
PMCPMC11564697

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.