{"title":"Pattern Separation and Pattern Completion Within the Hippocampal Circuit During Naturalistic Stimuli","authors":"Lili Sun, Siyang Li, Peng Ren, Qiuyi Liu, Zhipeng Li, Xia Liang","doi":"10.1002/hbm.70150","DOIUrl":"10.1002/hbm.70150","url":null,"abstract":"<p>Pattern separation and pattern completion in the hippocampus play a critical role in episodic learning and memory. However, there is limited empirical evidence supporting the role of the hippocampal circuit in these processes during complex continuous experiences. In this study, we analyzed high-resolution fMRI data from the “<i>Forrest Gump</i>” open-access dataset (16 participants) using a sliding-window temporal autocorrelation approach to investigate whether the canonical hippocampal circuit (DG-CA3-CA1-SUB) shows evidence consistent with the occurrence of pattern separation or pattern completion during a naturalistic audio movie task. Our results revealed that when processing continuous naturalistic stimuli, the DG-CA3 pair exhibited evidence consistent with the occurrence of the pattern separation process, whereas both the CA3-CA1 and CA1-SUB pairs showed evidence consistent with pattern completion. Moreover, during the latter half of the audio movie, we observed evidence consistent with a reduction in pattern completion in the CA3-CA1 pair and an increase in pattern completion in the CA1-SUB pair. Overall, these findings improve our understanding of the evidence related to the occurrence of pattern separation and pattern completion processes during natural experiences.</p>","PeriodicalId":13019,"journal":{"name":"Human Brain Mapping","volume":"46 2","pages":""},"PeriodicalIF":3.5,"publicationDate":"2025-01-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11775762/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143058981","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Georgia E. Kapetaniou, Marius Moisa, Christian C. Ruff, Philippe N. Tobler, Alexander Soutschek
{"title":"Frontopolar Cortex Interacts With Dorsolateral Prefrontal Cortex to Causally Guide Metacognition","authors":"Georgia E. Kapetaniou, Marius Moisa, Christian C. Ruff, Philippe N. Tobler, Alexander Soutschek","doi":"10.1002/hbm.70146","DOIUrl":"10.1002/hbm.70146","url":null,"abstract":"<p>Accurate metacognitive judgments about an individual's performance in a mental task require the brain to have access to representations of the quality and difficulty of first-order cognitive processes. However, little is known about how accurate metacognitive judgments are implemented in the brain. Here, we combine brain stimulation with functional neuroimaging to determine the neural and psychological mechanisms underlying the frontopolar cortex's (FPC) role in metacognition. Specifically, we evaluate two-layer neural architectures positing that FPC enables metacognitive judgments by communicating with brain regions encoding first-order decision difficulty. In support of two-layer architectures of metacognition, we found that high-intensity transcranial alternating current stimulation (tACS; 4 mA peak-to-peak) over FPC impaired metacognitive accuracy; at the neural level, this impairment was reflected by reduced coupling between FPC and dorsolateral prefrontal cortex (DLPFC), particularly during difficult metacognitive judgments. We also evaluated conceptual accounts assuming that metacognition relies on self-directed mentalizing. However, we observed no influence of FPC tACS on mentalizing performance and only a weak overlap of the networks underlying metacognition and mentalizing. Together, our findings put the FPC at the center of a two-layer architecture that enables accurate evaluations of cognitive processes, mainly via the FPC's connectivity with regions encoding first-level task difficulty, with little contributions from mentalizing-related processes.</p>","PeriodicalId":13019,"journal":{"name":"Human Brain Mapping","volume":"46 2","pages":""},"PeriodicalIF":3.5,"publicationDate":"2025-01-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11775761/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143058967","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Long-Term Post-Stroke Cognition in Patients With Minor Ischemic Stroke is Related to Tract-Based Disconnection Induced by White Matter Hyperintensities","authors":"Renaud Lopes, Grégory Kuchcinski, Thibaut Dondaine, Loïc Duron, Anne-Marie Mendyk, Hilde Hénon, Charlotte Cordonnier, Jean-Pierre Pruvo, Régis Bordet, Xavier Leclerc","doi":"10.1002/hbm.70138","DOIUrl":"10.1002/hbm.70138","url":null,"abstract":"<p>Over a third of minor stroke patients experience post-stroke cognitive impairment (PSCI), but no validated tools exist to identify at-risk patients early. This study investigated whether disconnection features derived from infarcts and white matter hyperintensities (WMH) could serve as markers for short- and long-term cognitive decline in first-ever minor ischemic stroke patients. First-ever minor ischemic stroke patients (NIHSS ≤ 7) were prospectively followed at 72-h, 6 months, and 36 months post-stroke with cognitive tests and brain MRI. Infarct and WMH volumes were semi-automatically assessed on DWI and FLAIR sequences. Bayesian tract-based disconnection models estimated remote pathological effects of infarcts and WMH. Associations between disconnection features and cognitive outcomes were analyzed using canonical correlation analyses, adjusted for age, education, and multiple comparisons. Among 105 patients (31% female, mean age 63 ± 12 years), infarct volume averaged 10.28 ± 17.10 cm<sup>3</sup> and predominantly involved the middle cerebral artery territory (83%). WMH burden was higher in frontal periventricular white matter. Infarct-based features did not significantly relate to PCSI. However, a WMH-derived disconnection factor, involving commissural and frontal tracts, and the right superior longitudinal fasciculus, was significantly associated with PSCI at 6 months (OR = 9.96, <i>p</i> value = 0.02) and 36 months (OR = 12.27, <i>p</i> value = 0.006), particularly in executive/attention, language, and visuospatial domains. This factor, unrelated to WMH volume, outperformed demographic and clinical predictors of PSCI. WMH-induced disconnection may be associated with short- and long-term PSCI in minor stroke. Routine MR-derived features could identify at-risk patients for rehabilitation trials.</p>","PeriodicalId":13019,"journal":{"name":"Human Brain Mapping","volume":"46 2","pages":""},"PeriodicalIF":3.5,"publicationDate":"2025-01-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11770330/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143046658","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Julie K. Wisch, Kalen Petersen, Peter R. Millar, Omar Abdelmoity, Ganesh M. Babulal, Karin L. Meeker, Meredith N. Braskie, Kristine Yaffe, Arthur W. Toga, Sid O'Bryant, Beau M. Ances, the HABS-HD Study Team
{"title":"Cross-Sectional Comparison of Structural MRI Markers of Impairment in a Diverse Cohort of Older Adults","authors":"Julie K. Wisch, Kalen Petersen, Peter R. Millar, Omar Abdelmoity, Ganesh M. Babulal, Karin L. Meeker, Meredith N. Braskie, Kristine Yaffe, Arthur W. Toga, Sid O'Bryant, Beau M. Ances, the HABS-HD Study Team","doi":"10.1002/hbm.70133","DOIUrl":"10.1002/hbm.70133","url":null,"abstract":"<p>Neurodegeneration is presumed to be the pathological process measure most proximal to clinical symptom onset in Alzheimer Disease (AD). Structural MRI is routinely collected in research and clinical trial settings. Several quantitative MRI-based measures of atrophy have been proposed, but their low correspondence with each other has been previously documented. The purpose of this study was to identify which commonly used structural MRI measure (hippocampal volume, cortical thickness in AD signature regions, or brain age gap [BAG]) had the best correspondence with the Clinical Dementia Rating (CDR) in an ethno-racially diverse sample. 2870 individuals recruited by the Healthy and Aging Brain Study—Health Disparities completed both structural MRI and CDR evaluation. Of these, 1887 individuals were matched on ethno-racial identity (Mexican American [MA], non-Hispanic Black [NHB], and non-Hispanic White [NHW]) and CDR (27% CDR > 0). We estimated brain age using two pipelines (DeepBrainNet, BrainAgeR) and then calculated BAG as the difference between the estimated brain age and chronological age. We also quantified their hippocampal volumes using HippoDeep and cortical thicknesses (both an AD-specific signature and average whole brain) using FreeSurfer. We used ordinal regression to evaluate associations between neuroimaging measures and CDR and to test whether these associations differed between ethno-racial groups. Higher BAG (<i>p</i><sub>DeepBrainNet</sub> <i>=</i> 0.0002; <i>p</i><sub>BrainAgeR</sub> <i>=</i> 0.00117) and lower hippocampal volume (<i>p =</i> 0.0015) and cortical thickness (<i>p <</i> 0.0001) were associated with worse clinical status (higher CDR). AD signature cortical thickness had the strongest relationship with CDR (AIC<sub>DeepBrainNet</sub> = 2623, AIC<sub>whole cortex</sub> = 2588, AIC<sub>BrainAgeR</sub> = 2533, AIC<sub>Hippocampus</sub> = 2293, AIC<sub>Signature Cortical Thickness</sub> = 1903). The relationship between CDR and atrophy measures differed between ethno-racial groups for both BAG estimates and hippocampal volume, but not for cortical thickness. We interpret the lack of an interaction between ethno-racial identity and AD signature cortical thickness on CDR as evidence that cortical thickness effectively captures sources of disease-related atrophy that may differ across racial and ethnic groups. Cortical thickness had the strongest association with CDR. These results suggest that cortical thickness may be a more sensitive and generalizable marker of neurodegeneration than hippocampal volume or BAG in ethno-racially diverse cohorts.</p>","PeriodicalId":13019,"journal":{"name":"Human Brain Mapping","volume":"46 2","pages":""},"PeriodicalIF":3.5,"publicationDate":"2025-01-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11770891/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143046634","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Nadia Bounoua, Anna Stumps, Leah Church, Jeffrey M. Spielberg, Naomi Sadeh
{"title":"Deciphering the Neural Effects of Emotional, Motivational, and Cognitive Challenges on Inhibitory Control Processes","authors":"Nadia Bounoua, Anna Stumps, Leah Church, Jeffrey M. Spielberg, Naomi Sadeh","doi":"10.1002/hbm.70137","DOIUrl":"10.1002/hbm.70137","url":null,"abstract":"<p>Converging lines of research indicate that inhibitory control is likely to be compromised in contexts that place competing demands on emotional, motivational, and cognitive systems, potentially leading to damaging impulsive behavior. The objective of this study was to identify the neural impact of three challenging contexts that typically compromise self-regulation and weaken impulse control. Participants included 66 healthy adults (<i>M</i>/<i>SD</i><sub>age</sub> = 29.82/10.21 years old, 63.6% female) who were free of psychiatric disorders and psychotropic medication use. Participants completed a set of novel Go/NoGo (GNG) paradigms in the scanner, which manipulated contextual factors to induce (i) aversive emotions, (ii) appetitive drive, or (iii) concurrent working memory load. Voxelwise analysis of neural activation during each of these tasks was compared to that of a neutral GNG task. Findings revealed differential inhibition-related activation in the aversive emotions and appetitive drive GNG tasks relative to the neutral task in frontal, parietal and temporal cortices, suggesting emotional and motivational contexts may suppress activation of these cortical regions during inhibitory control. In contrast, the GNG task with a concurrent working memory load showed widespread increased activation across the cortex compared to the neutral task, indicative of enhanced recruitment of executive control regions. Results suggest the neural circuitry recruited for inhibitory control varies depending on the concomitant emotional, motivational, and cognitive demands of a given context. This battery of GNG tasks can be used by researchers interested in studying unique patterns of neural activation associated with inhibitory control across three clinically relevant contexts that challenge self-regulation and confer risk for impulsive behavior.</p>","PeriodicalId":13019,"journal":{"name":"Human Brain Mapping","volume":"46 2","pages":""},"PeriodicalIF":3.5,"publicationDate":"2025-01-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11758444/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143033099","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
David Linhardt, Michael Woletz, Pedro M. Paz-Alonso, Christian Windischberger, Garikoitz Lerma-Usabiaga
{"title":"Biases in Volumetric Versus Surface Analyses in Population Receptive Field Mapping","authors":"David Linhardt, Michael Woletz, Pedro M. Paz-Alonso, Christian Windischberger, Garikoitz Lerma-Usabiaga","doi":"10.1002/hbm.70140","DOIUrl":"10.1002/hbm.70140","url":null,"abstract":"<p>Population receptive field (pRF) mapping is a quantitative functional MRI (fMRI) analysis method that links visual field positions with specific locations in the visual cortex. A common preprocessing step in pRF analyses involves projecting volumetric fMRI data onto the cortical surface, typically leading to upsampling of the data. This process may introduce biases in the resulting pRF parameters. Using publicly available analysis containers, we compared pRF maps generated from the original volumetric with those from upsampled surface data. Our results show substantial increases in pRF coverage in the central visual field of upsampled datasets. These effects were consistent across early visual cortex areas V1-3. Further analysis indicates that this bias is primarily driven by the nonlinear relationship between cortical distance and visual field eccentricity, known as cortical magnification. Our results underscore the importance of understanding and addressing biases introduced by processing steps to ensure accurate interpretation of pRF mapping data, particularly in cross-study comparisons.</p>","PeriodicalId":13019,"journal":{"name":"Human Brain Mapping","volume":"46 2","pages":""},"PeriodicalIF":3.5,"publicationDate":"2025-01-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11758450/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143033097","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Emile d'Angremont, Remco Renken, Sygrid van der Zee, Erik F. J. de Vries, Teus van Laar, Iris E. C. Sommer
{"title":"Cholinergic Denervation Patterns in Parkinson's Disease Associated With Cognitive Impairment Across Domains","authors":"Emile d'Angremont, Remco Renken, Sygrid van der Zee, Erik F. J. de Vries, Teus van Laar, Iris E. C. Sommer","doi":"10.1002/hbm.70047","DOIUrl":"10.1002/hbm.70047","url":null,"abstract":"<p>Cognitive impairment is considered to be one of the key features of Parkinson's disease (PD), ultimately resulting in PD-related dementia in approximately 80% of patients over the course of the disease. Several distinct cognitive syndromes of PD have been suggested, driven by different neurotransmitter deficiencies and thus requiring different treatment regimes. In this study, we aimed to identify characteristic brain covariance patterns that reveal how cholinergic denervation is related to PD and to cognitive impairment, focusing on four domains, including attention, executive functioning, memory, and visuospatial cognition. We applied scaled sub-profile model principal component analysis to reveal cholinergic-specific disease-related and cognition-related covariance patterns using [<sup>18</sup>F]fluoroethoxybenzovesamicol PET imaging. Stepwise logistic regression was applied to predict disease state (PD vs. healthy control). Linear regression models were applied to predict cognitive functioning within the PD group, for each cognitive domain separately. We assessed the performance of the identified patterns with leave-one-out cross validation and performed bootstrapping to assess pattern stability. We included 34 PD patients with various levels of cognitive dysfunction and 10 healthy controls, with similar age, sex, and educational level. The disease-related cholinergic pattern was strongly discriminative (AUC 0.91), and was most prominent in posterior brain regions, with lower tracer uptake in patients compared to controls. We found largely overlapping cholinergic-specific patterns across cognitive domains, with positive correlations between tracer uptake in the opercular cortex, left dorsolateral prefrontal cortex and posterior cingulate gyrus, among other regions, and attention, executive, and visuospatial functioning. Cross validation showed significant correlations between predicted and measured cognition scores, with the exception of memory. We identified a robust structural covariance pattern for the assessment of cholinergic dysfunction related to PD, as well as overlapping cholinergic patterns related to attentional, executive- and visuospatial impairment in PD patients.</p>","PeriodicalId":13019,"journal":{"name":"Human Brain Mapping","volume":"46 2","pages":""},"PeriodicalIF":3.5,"publicationDate":"2025-01-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11755113/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143058901","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Athena Taymourtash, Ernst Schwartz, Karl-Heinz Nenning, Roxane Licandro, Patric Kienast, Veronika Hielle, Daniela Prayer, Gregor Kasprian, Georg Langs
{"title":"Measuring the effects of motion corruption in fetal fMRI","authors":"Athena Taymourtash, Ernst Schwartz, Karl-Heinz Nenning, Roxane Licandro, Patric Kienast, Veronika Hielle, Daniela Prayer, Gregor Kasprian, Georg Langs","doi":"10.1002/hbm.26806","DOIUrl":"10.1002/hbm.26806","url":null,"abstract":"<p>Irregular and unpredictable fetal movement is the most common cause of artifacts in in utero functional magnetic resonance imaging (fMRI), affecting analysis and limiting our understanding of early functional brain development. The accurate detection of corrupted functional connectivity (FC) resulting from motion artifacts or preprocessing, instead of neural activity, is a prerequisite for reliable and valid analysis of FC and early brain development. Approaches to address this problem in adult data are of limited utility in fetal fMRI. In this study, we evaluate a novel technique for robust computational assessment of motion artifacts, and the quantitative comparison of regression models for artifact removal in fetal FC analysis. It exploits the association between dynamic FC and non-stationarity of fetal movement, to detect residual noise. To validate our motion artifact detection technique in detail, we used a parametric generative model for neural events and fMRI blood oxygenation level-dependent (BOLD) signal. We conducted a systematic evaluation of 11 commonly used regression models in a sample of 70 fetuses with gestational age of 19–39 weeks. Results demonstrate that the proposed method has better accuracy in identifying corrupted FC compared to methods designed for adults. The technique, suggests that censoring, global signal regression and anatomical component-based regression models are the most effective models for compensating motion. The benchmarking technique, and the generative model for realistic fetal fMRI BOLD enables investigators conducting in utero fMRI analysis to effectively quantify the impact of fetal motion and evaluate alternative regression strategies for mitigating this impact. The code is publicly available at: https://github.com/cirmuw/fetalfMRIproc.</p>","PeriodicalId":13019,"journal":{"name":"Human Brain Mapping","volume":"46 2","pages":""},"PeriodicalIF":3.5,"publicationDate":"2025-01-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11755121/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143023198","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Lanxin Ji, Mark Duffy, Bosi Chen, Amyn Majbri, Christopher J. Trentacosta, Moriah Thomason
{"title":"Whole Brain MRI Assessment of Age and Sex-Related R2* Changes in the Human Fetal Brain","authors":"Lanxin Ji, Mark Duffy, Bosi Chen, Amyn Majbri, Christopher J. Trentacosta, Moriah Thomason","doi":"10.1002/hbm.70073","DOIUrl":"10.1002/hbm.70073","url":null,"abstract":"<p>Iron in the brain is essential to neurodevelopmental processes, as it supports neural functions, including processes of oxygen delivery, electron transport, and enzymatic activity. However, the development of brain iron before birth is scarcely understood. By estimating R2* (1/T2*) relaxometry from a sizable sample of fetal multiecho echo-planar imaging (EPI) scans, which is the standard sequence for functional magnetic resonance imaging (fMRI), across gestation, this study investigates age and sex-related changes in iron, across regions and tissue segments. Our findings reveal that brain R2* levels significantly increase throughout gestation spanning many different regions, except the frontal lobe. Furthermore, females exhibit a faster rate of R2* increase compared to males, in both gray matter and white matter. This sex effect is particularly notable within the left insula. This work represents the first MRI examination of iron accumulation and sex differences in developing fetal brains. This is also the first study to establish R2* estimation methodology in fetal multiecho functional MRI.</p>","PeriodicalId":13019,"journal":{"name":"Human Brain Mapping","volume":"46 2","pages":""},"PeriodicalIF":3.5,"publicationDate":"2025-01-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11754245/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143023201","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Alexandru Mihai Dumitrescu, Tim Coolen, Vincent Wens, Antonin Rovai, Nicola Trotta, Serge Goldman, Xavier De Tiège, Charline Urbain
{"title":"Investigating the Spatio-Temporal Signatures of Language Control–Related Brain Synchronization Processes","authors":"Alexandru Mihai Dumitrescu, Tim Coolen, Vincent Wens, Antonin Rovai, Nicola Trotta, Serge Goldman, Xavier De Tiège, Charline Urbain","doi":"10.1002/hbm.70109","DOIUrl":"10.1002/hbm.70109","url":null,"abstract":"<p>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.</p>","PeriodicalId":13019,"journal":{"name":"Human Brain Mapping","volume":"46 2","pages":""},"PeriodicalIF":3.5,"publicationDate":"2025-01-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11747998/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143004584","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}