Evidence map›Paper›PMID 39835602›Full record

ArticleHuman brain mapping2025

Investigating the Spatio-Temporal Signatures of Language Control-Related Brain Synchronization Processes.

Alexandru Mihai Dumitrescu, Tim Coolen, Vincent Wens, Antonin Rovai, Nicola Trotta, Serge Goldman, Xavier De Tiège, Charline Urbain

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 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. The MINT Sprint 2.0: a Picture Naming Test for Detection of Naming Impairments in ΜCI Due or Not to AD, Greek Version.Archives of clinical neuropsychology : the official journal of the National Academy of Neuropsychologists · 2026
    Article
  2. 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

8 authors.

Alexandru Mihai Dumitrescu *Université libre de Bruxelles (ULB), UNI - ULB Neuroscience Institute, Laboratoire de Neuroanatomie et Neuroimagerie translationnelles (LN2T), Brussels, Belgium.ORCID 0009-0005-0920-8689
Tim Coolen *Université libre de Bruxelles (ULB), UNI - ULB Neuroscience Institute, Laboratoire de Neuroanatomie et Neuroimagerie translationnelles (LN2T), Brussels, Belgium.
Vincent WensUniversité libre de Bruxelles (ULB), UNI - ULB Neuroscience Institute, Laboratoire de Neuroanatomie et Neuroimagerie translationnelles (LN2T), Brussels, Belgium.
Antonin RovaiUniversité libre de Bruxelles (ULB), UNI - ULB Neuroscience Institute, Laboratoire de Neuroanatomie et Neuroimagerie translationnelles (LN2T), Brussels, Belgium.
Nicola TrottaUniversité libre de Bruxelles (ULB), UNI - ULB Neuroscience Institute, Laboratoire de Neuroanatomie et Neuroimagerie translationnelles (LN2T), Brussels, Belgium.
Serge GoldmanUniversité libre de Bruxelles (ULB), UNI - ULB Neuroscience Institute, Laboratoire de Neuroanatomie et Neuroimagerie translationnelles (LN2T), Brussels, Belgium.
Xavier De TiègeUniversité libre de Bruxelles (ULB), UNI - ULB Neuroscience Institute, Laboratoire de Neuroanatomie et Neuroimagerie translationnelles (LN2T), Brussels, Belgium.
Charline UrbainUniversité libre de Bruxelles (ULB), UNI - ULB Neuroscience Institute, Laboratoire de Neuroanatomie et Neuroimagerie translationnelles (LN2T), Brussels, Belgium.

Funding

Fonds Erasme
6 · The paper itself

Abstract

Language control processes allow for the flexible manipulation and access to context-appropriate verbal representations. Functional magnetic resonance imaging (fMRI) studies have localized the brain regions involved in language control processes usually by comparing high vs. low lexical-semantic control conditions during verbal tasks. Yet, the spectro-temporal dynamics of associated brain processes remain unexplored, preventing a proper understanding of the neural bases of language control mechanisms. To do so, we recorded functional brain activity using magnetoencephalography (MEG) and fMRI, while 30 healthy participants performed a silent verb generation (VGEN) and a picture naming (PN) task upon confrontation with pictures requiring low or high lexical-semantic control processes. fMRI confirmed the association between stronger language control processes and increased left inferior frontal gyrus (IFG) perfusion, while MEG revealed these controlled mechanisms to be associated with a specific sequence of early (< 500 ms) and late (> 500 ms) beta-band (de)synchronization processes within fronto-temporo-parietal areas. Particularly, beta-band modulations of event-related (de)synchronization mechanisms were first observed in the right IFG, followed by bilateral IFG and temporo-parietal brain regions. Altogether, these results suggest that beyond a specific recruitment of inferior frontal brain regions, language control mechanisms rely on a complex temporal sequence of beta-band oscillatory mechanisms over antero-posterior areas.

Indexed as

BrainBrain MappingCortical SynchronizationLanguageAdultBeta RhythmFemaleHumansMagnetic Resonance ImagingMagnetoencephalographyMaleYoung Adultbrain synchronization mechanismsfunctional magnetic resonance imaginglanguage control processesmagnetoencephalographyspatio‐temporal brain dynamics

Identifiers

PMID39835602
PMCPMC11747998

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.