Veronica Diveica

Bio: Veronica Diveica is an academic researcher from Bangor University. The author has contributed to research in topics: Theory of mind & Social cognition. The author has an hindex of 1, co-authored 4 publications receiving 4 citations.

The Ventrolateral Anterior Temporal Lobe is Commonly Engaged by Both Mental State Inference and Semantic Association Tasks

Abstract: A key challenge for neurobiological models of social cognition is to elucidate whether brain regions are specialised for that domain. In recent years, discussion surrounding the role of the anterior temporal lobe (ATL) epitomises such debates; some argue it is part of a domain-specific network for social processing, while others claim it is a domain-general hub for semantic representation. In the present study, we used ATL-optimised fMRI to map the contribution of different ATL structures to a variety of paradigms frequently used to probe a crucial social ability, namely theory of mind (ToM). Using multiple tasks enables a clearer attribution of activation to ToM as opposed to idiosyncratic features of stimuli. Further, we directly explored whether these same structures are also activated by a non-social task probing semantic representations. We revealed that common to all of the tasks was activation of a key ventrolateral ATL region that is typically invisible to standard fMRI. This constitutes novel evidence in support of the view that the ventrolateral ATL contributes to social cognition via a domain-general role in the retrieval of conceptual knowledge, and against claims of a specialised social function.

Establishing a Role of the Semantic Control Network in Social Cognitive Processing: A Meta-analysis of Functional Neuroimaging Studies

Abstract: Most leading models of socio-cognitive processing devote little discussion to the nature and neuroanatomical correlates of cognitive control mechanisms. Recently, it has been proposed that the regulation of social behaviours could rely on brain regions specialised in the controlled retrieval of semantic information, namely the anterior inferior frontal gyrus (IFG) and posterior middle temporal gyrus. Accordingly, we set out to investigate whether the neural activation commonly found in social functional neuroimaging studies extends to these ‘semantic control’ regions. We conducted five coordinate-based meta-analyses to combine results of over 500 fMRI/PET experiments and identified the brain regions consistently involved in semantic control, as well as four social abilities: theory of mind, trait inference, empathy and moral reasoning. This allowed an unprecedented parallel review of the neural networks associated with each of these cognitive domains. The results confirmed that the anterior left IFG region involved in semantic control is reliably engaged in all four social domains. This suggests that social cognition could be partly regulated by the neurocognitive system underpinning semantic control.

The Role of the Ventrolateral Anterior Temporal Lobes in Social Cognition

Abstract: A key challenge for neurobiological models of social cognition is to elucidate whether brain regions are specialised for that domain. In recent years, discussion surrounding the role of anterior temporal regions epitomises such debates; some argue the anterior temporal lobe (ATL) is part of a domain-specific network for social processing, while others claim it comprises a domain-general hub for semantic representation. In the present study, we used ATL-optimised fMRI to map the contribution of different ATL structures to a variety of paradigms frequently used to probe a crucial social ability, namely theory of mind (ToM). Using multiple tasks enables a clearer attribution of activation to ToM as opposed to idiosyncratic features of stimuli. Further, we directly explored whether these same structures are also activated by a non-social task probing semantic representations. We revealed that common to all of the tasks was activation of a key ventrolateral ATL region that is often invisible to standard fMRI. This constitutes novel evidence in support of the view that the ventrolateral ATL contributes to social cognition via a domain-general role in semantic processing, and against claims of a specialised social function.

Graded functional organisation in the left inferior frontal gyrus: evidence from task-free and task-based functional connectivity

Abstract: The left inferior frontal gyrus (LIFG) has been ascribed key roles in numerous cognitive domains, including language, executive function and social cognition. However, its functional organisation, and how the specific areas implicated in these cognitive domains relate to each other, is unclear. Possibilities include that the LIFG underpins a domain-general function or, alternatively, that it is characterized by functional differentiation, which might occur in either a discrete or a graded pattern. The aim of the present study was to explore the topographical organisation of the LIFG using a bimodal data-driven approach. To this end, we extracted functional connectivity (FC) gradients from 1) the resting-state fMRI time-series of 150 participants (77 female), and 2) patterns of co-activation derived meta-analytically from task data across a diverse set of cognitive domains. We then sought to characterize the FC differences driving these gradients with seed-based resting-state FC and meta-analytic co-activation modelling analyses. Both analytic approaches converged on an FC profile that shifted in a graded fashion along two main organisational axes. An anterior-posterior gradient shifted from being preferentially associated with high-level control networks (anterior LIFG) to being more tightly coupled with perceptually-driven networks (posterior). A second dorsal-ventral axis was characterized by higher connectivity with domain-general control networks on one hand (dorsal LIFG), and with the semantic network, on the other (ventral). These results provide novel insights into a graded functional organisation of the LIFG underpinning both task-free and task-constrained mental states, and suggest that the LIFG is an interface between distinct large-scale functional networks. Significance statement To understand how function varies across the LIFG, we conducted a detailed, bimodal exploration of the spatial transitions in its voxel-wise FC patterns. We provide novel evidence of graded changes along two main organisational axes. Specifically, the LIFG was characterized by an anterior-posterior gradient, which could reflect a shift in function from perceptually-driven processing to task-oriented control processes. Moreover, we revealed a dorsal-ventral shift in FC that is consistent with the idea that domain-specificity is a core principle underpinning functional organisation of the LIFG. These gradients were replicated across task-free and task-constrained FC measures, suggesting that a similar fundamental organisation underpins both mental states.

The role of the ventrolateral anterior temporal lobes in social cognition

Abstract: A key challenge for neurobiological models of social cognition is to elucidate whether brain regions are specialised for that domain. In recent years, discussion surrounding the role of anterior temporal regions epitomises such debates; some argue the anterior temporal lobe (ATL) is part of a domain-specific network for social processing, while others claim it comprises a domain-general hub for semantic representation. In the present study, we used ATL-optimised fMRI to map the contribution of different ATL structures to a variety of paradigms frequently used to probe a crucial social ability, namely 'theory of mind' (ToM). Using multiple tasks enables a clearer attribution of activation to ToM as opposed to idiosyncratic features of stimuli. Further, we directly explored whether these same structures are also activated by a non-social task probing semantic representations. We revealed that common to all of the tasks was activation of a key ventrolateral ATL region that is often invisible to standard fMRI. This constitutes novel evidence in support of the view that the ventrolateral ATL contributes to social cognition via a domain-general role in semantic processing and against claims of a specialised social function.

Sex and age differences in “theory of mind” across 57 countries using the English version of the “Reading the Mind in the Eyes” Test

Abstract: Significance In the largest study to date (as far as we know) on the “Reading the Mind in the Eyes” Test (Eyes Test)—a performance task of “theory of mind”—we leveraged four unique datasets (total N = 312,739), using the English version of the Eyes Test. We found an on-average female advantage across 57 countries. In line with this is a systematic review of translated (non-English) versions of the Eyes Test identifying an on-average female advantage in eight out of eight different languages. Cross-sectional analyses also showed subtle age differences in Eyes Test scores across the lifespan. We conclude that there is an on-average female advantage across the majority of countries tested. Future research should investigate this in non-English speakers.

Fingerprinting of brain disease: Connectome identifiability in cognitive decline and neurodegeneration

Abstract: In analogy to the friction ridges of a human finger, the functional connectivity patterns of the human brain can be used to identify a given individual from a population. In other words, functional connectivity patterns constitute a marker of human identity, or a ‘brain fingerprint’. Notably, very little is known about whether brain fingerprints are preserved in brain ageing and in the presence of cognitive decline. Using fMRI data of 96 memory clinic subjects, here we show that individuals functional connectivity profiles remain unique even when cognitive impairment occurs. Yet, the patterns of functional connectivity that make the healthy subjects more identifiable change during cognitive decline, suggesting that the brain undergoes functional reconfiguration. Notably, the functional connections that were the most reliable in healthy cohorts disappeared during cognitive decline, leaving room for other stable connections, adapting to the process of neurodegeneration. We believe that these findings could help in moving towards a more personalised medicine and treatment during cognitive decline, and we hope they will set the ground for clinical fingerprinting of brain disease.