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Potvin, S.

Publications and source records attributed to Potvin, S..

2 recordsLinked to original sources

Towards a Neurobiologically-driven Ontology of Mental Functions:A Data-driven Summary of the Twenty Years of Neuroimaging Meta-Analyses

A persistent effort in neuroscience has been to pinpoint the neurobiological substrates that support mental processes. The Research Domain Criteria (RDoC) aims to develop a new framework based on fundamental neurobiological dimensions. However, results from several meta-analysis of task-based fMRI showed substantial spatial overlap between several mental processes including emotion and anticipatory processes, irrespectively of the valence. Consequently, there is a crucial need to better characterize the core neurobiological processes using a data-driven techniques, given that these analytic approaches can capture the core neurobiological processes across neuroimaging literature that may not be identifiable through expert-driven categories. Therefore, we sought to examine the main data-driven co-activation networks across the past 20 years of published meta-analyses on task-based fMRI studies. We manually extracted 19,822 coordinates from 1,347 identified meta-analytic experiments. A Correlation-Matrix-Based Hierarchical Clustering was conducted on spatial similarity between these meta-analytic experiments, to identify the main co-activation networks. Activation likelihood estimation was then used to identify spatially convergent brain regions across experiments in each network. Across 1,347 meta-analyses, we found 13 co-activation networks which were further characterized by various psychological terms and distinct association with receptor density maps and intrinsic functional connectivity networks. At a fMRI activation resolution, neurobiological processes seem more similar than different across various mental functions. We discussed the potential limitation of linking brain activation to psychological labels and investigated potential avenues to tackle this long-lasting research question.

neuroscience↗

Neuropsychiatric mutations delineate functional brain connectivity dimensions contributing to autism and schizophrenia

16p11.2 and 22q11.2 Copy Number Variants (CNVs) confer high risk for Autism Spectrum Disorder (ASD), schizophrenia (SZ), and Attention-Deficit-Hyperactivity-Disorder (ADHD), but their impact on functional connectivity (FC) remains unclear. We analyzed resting-state functional magnetic resonance imaging data from 101 CNV carriers, 755 individuals with idiopathic ASD, SZ, or ADHD and 1,072 controls. We used CNV FC-signatures to identify dimensions contributing to complex idiopathic conditions. CNVs had large mirror effects on FC at the global and regional level. Thalamus, somatomotor, and posterior insula regions played a critical role in dysconnectivity shared across deletions, duplications, idiopathic ASD, SZ but not ADHD. Individuals with higher similarity to deletion FC-signatures exhibited worse cognitive and behavioral symptoms. Deletion similarities identified at the connectivity level could be related to the redundant associations observed genome-wide between gene expression spatial patterns and FC-signatures. Results may explain why many CNVs affect a similar range of neuropsychiatric symptoms.

neuroscience↗