scholarly journals fMRI Informed Montage Selection for Transcranial Electrical Stimulation: Frontoparietal Synchronization for Drug Cue Reactivity

2021 ◽  
Author(s):  
Ghazaleh Soleimani ◽  
Rayus Kupliki ◽  
Jerzy Bodurka ◽  
Martin Paulus ◽  
Hamed Ekhtiari

AbstractBackgroundFrontoparietal network (FPN) with multiple cortical nodes is involved in executive functions. Transcranial electrical stimulation (tES) can potentially modulate interactions between these nodes using frontoparietal synchronization (FPS). Here we used fMRI and computational head models (CHMs) to inform electrode montage and dosage selection in FPS.MethodsSixty methamphetamine users completed an fMRI drug cue-reactivity task. Two sets of 4×1 HD electrodes with anode over F3 and F4 were simulated and spheres around maximum electric field in each hemisphere were defined as frontal seeds. Using frontal seeds, a task-based functional connectivity analysis was conducted based on a seed-to-whole brain generalized psychophysiological interaction (gPPI). Electrode placement for parietal sites was selected based on gPPI results. Task-based and resting-state connectivity were compared between fMRI-informed and classic F3-P3/F4-P4 montages.ResultsWhole-brain gPPI showed two significant clusters (left: 506 voxels P=0.006, right: 455 voxels P=0.016), located in the inferior parietal lobule under the CP5 and CP6 electrode location. Pair-wise ROI-based gPPI comparing informed (F3-CP5/F4-CP6) and classic (F3-P3/F4-P4) montages showed significant increased PPI and resting-state connectivity only in the informed montage. Cue-induced craving score was also correlated with left (F3-CP5) frontoparietal connectivity in the fMRI-informed montage.ConclusionThis study proposes an analytic pipeline to select electrode montage and dosage in dual site tES using CHMs and task-based connectivity. Stimulating F3-F4 can tap into both FPN and saliency network (SN) based on the montage selection. Using CHM and fMRI will be essential to navigating ample parameter space in the stimulation protocols for future tES studies.HighlightsWe demonstrated a methodology for montage selection in network-based tESTask-based functional connectivity can inform dual-site tES montage selectionHead models can help to induce balance tES dose in targeted brain regionsTargeting DLPFC with tES can tap into both saliency and frontoparietal networksLower resting-state frontoparietal connectivity before cue exposure followed by a greater craving

Author(s):  
Diego Lombardo ◽  
Catherine Cassé-Perrot ◽  
Jean-Philippe Ranjeva ◽  
Arnaud Le Troter ◽  
Maxime Guye ◽  
...  

AbstractDynamic Functional Connectivity (dFC) in the resting state (rs) is considered as a correlate of cognitive processing. Describing dFC as a flow across morphing connectivity configurations, our notion of dFC speed quantifies the rate at which FC networks evolve in time. Here we probe the hypothesis that variations of rs dFC speed and cognitive performance are selectively interrelated within specific functional subnetworks.In particular, we focus on Sleep Deprivation (SD) as a reversible model of cognitive dysfunction. We found that whole-brain level (global) dFC speed significantly slows down after 24h of SD. However, the reduction in global dFC speed does not correlate with variations of cognitive performance in individual tasks, which are subtle and highly heterogeneous. On the contrary, we found strong correlations between performance variations in individual tasks –including Rapid Visual Processing (RVP, assessing sustained visual attention)– and dFC speed quantified at the level of functional subnetworks of interest. Providing a compromise between classic static FC (no time) and global dFC (no space), modular dFC speed analyses allow quantifying a different speed of dFC reconfiguration independently for sub-networks overseeing different tasks. Importantly, we found that RVP performance robustly correlates with the modular dFC speed of a characteristic frontoparietal module.HighlightsSleep Deprivation (SD) slows down the random walk in FC space implemented by Dynamic Functional Connectivity (dFC) at rest.Whole-brain level slowing of dFC speed does not selectively correlate with fine and taskspecific changes in performanceWe quantify dFC speed separately for different link-based modules coordinated by distinct regional “meta-hubs”Modular dFC speed variations capture subtle and task-specific variations of cognitive performance induced by SD.Author summaryWe interpreted dynamic Functional Connectivity (dFC) as a random walk in the space of possible FC networks performed with a quantifiable “speed”.Here, we analyze a fMRI dataset in which subjects are scanned and cognitively tested both before and after Sleep Deprivation (SD), used as a reversible model of cognitive dysfunction. While global dFC speed slows down after a sleepless night, it is not a sufficiently sensitive metric to correlate with fine and specific cognitive performance changes. To boost the capacity of dFC speed analyses to account for fine and specific cognitive decline, we introduce the notion of modular dFC speed. Capitalizing on an edge-centric measure of functional connectivity, which we call Meta-Connectivity, we isolate subgraphs of FC describing relatively independent random walks (dFC modules) and controlled by distinct “puppet masters” (meta-hubs). We then find that variations of the random walk speed of distinct dFC modules now selectively correlate with SD-induced variations of performance in the different tasks. This is in agreement with the fact that different subsystems – distributed but functionally distinct– oversee different tasks.The high sensitivity of modular dFC analyses bear promise of future applications to the early detection and longitudinal characterization of pathologies such as Alzheimer’s disease.


Author(s):  
Norio Takata ◽  
Nobuhiko Sato ◽  
Yuji Komaki ◽  
Hideyuki Okano ◽  
Kenji F. Tanaka

AbstractA brain atlas is necessary for analyzing structure and function in neuroimaging research. Although various annotation volumes (AVs) for the mouse brain have been proposed, it is common in magnetic resonance imaging (MRI) of the mouse brain that regions-of-interest (ROIs) for brain structures (nodes) are created arbitrarily according to each researcher’s necessity, leading to inconsistent ROIs among studies. One reason for such a situation is the fact that earlier AVs were fixed, i.e. combination and division of nodes were not implemented. This report presents a pipeline for constructing a flexible annotation atlas (FAA) of the mouse brain by leveraging public resources of the Allen Institute for Brain Science on brain structure, gene expression, and axonal projection. A mere two-step procedure with user-specified, text-based information and Python codes constructs FAA with nodes which can be combined or divided objectively while maintaining anatomical hierarchy of brain structures. Four FAAs with total node count of 4, 101, 866, and 1,381 were demonstrated. Unique characteristics of FAA realized analysis of resting-state functional connectivity (FC) across the anatomical hierarchy and among cortical layers, which were thin but large brain structures. FAA can improve the consistency of whole brain ROI definition among laboratories by fulfilling various requests from researchers with its flexibility and reproducibility.Highlights–A flexible annotation atlas (FAA) for the mouse brain is proposed.–FAA is expected to improve whole brain ROI-definition consistency among laboratories.–The ROI can be combined or divided objectively while maintaining anatomical hierarchy.–FAA realizes functional connectivity analysis across the anatomical hierarchy.–Codes for FAA reconstruction is available at https://github.com/ntakata/flexible-annotation-atlas–Datasets for resting-state fMRI in awake mice are available at https://openneuro.org/datasets/ds002551


2019 ◽  
Author(s):  
Chaitanya Ganne ◽  
Walter Hinds ◽  
James Kragel ◽  
Xiaosong He ◽  
Noah Sideman ◽  
...  

AbstractHigh-frequency gamma activity of verbal-memory encoding using invasive-electroencephalogram coupled has laid the foundation for numerous studies testing the integrity of memory in diseased populations. Yet, the functional connectivity characteristics of networks subserving these HFA-memory linkages remains uncertain. By integrating this electrophysiological biomarker of memory encoding from IEEG with resting-state BOLD fluctuations, we estimated the segregation and hubness of HFA-memory regions in drug-resistant epilepsy patients and matched healthy controls. HFA-memory regions express distinctly different hubness compared to neighboring regions in health and in epilepsy, and this hubness was more relevant than segregation in predicting verbal memory encoding. The HFA-memory network comprised regions from both the cognitive control and primary processing networks, validating that effective verbal-memory encoding requires multiple functions, and is not dominated by a central cognitive core. Our results demonstrate a tonic intrinsic set of functional connectivity, which provides the necessary conditions for effective, phasic, task-dependent memory encoding.HighlightsHigh frequency memory activity in IEEG corresponds to specific BOLD changes in resting-state data.HFA-memory regions had lower hubness relative to control brain nodes in both epilepsy patients and healthy controls.HFA-memory network displayed hubness and participation (interaction) values distinct from other cognitive networks.HFA-memory network shared regional membership and interacted with other cognitive networks for successful memory encoding.HFA-memory network hubness predicted both concurrent task (phasic) and baseline (tonic) verbal-memory encoding success.


2020 ◽  
Author(s):  
Giovanni Rabuffo ◽  
Jan Fousek ◽  
Christophe Bernard ◽  
Viktor Jirsa

AbstractAt rest, mammalian brains display a rich complex spatiotemporal behavior, which is reminiscent of healthy brain function and has provided nuanced understandings of several major neurological conditions. Despite the increasingly detailed phenomenological documentation of the brain’s resting state, its principle underlying causes remain unknown. To establish causality, we link structurally defined features of a brain network model to neural activation patterns and their variability. For the mouse, we use a detailed connectome-based model and simulate the resting state dynamics for neural sources and whole brain imaging signals (Blood-Oxygen-Level-Dependent (BOLD), Electroencephalography (EEG)). Under conditions of near-criticality, characteristic neuronal cascades form spontaneously and propagate through the network. The largest neuronal cascades produce short-lived but robust co-fluctuations at pairs of regions across the brain. During these co-activation episodes, long-lasting functional networks emerge giving rise to epochs of stable resting state networks correlated in time. Sets of neural cascades are typical for a resting state network, but different across. We experimentally confirm the existence and stability of functional connectivity epochs comprising BOLD co-activation bursts in mice (N=19). We further demonstrate the leading role of the neuronal cascades in a simultaneous EEG/fMRI data set in humans (N=15), explaining a large part of the variability of functional connectivity dynamics. We conclude that short-lived neuronal cascades are a major robust dynamic component contributing to the organization of the slowly evolving spontaneous fluctuations in brain dynamics at rest.


Author(s):  
Lisa Parikh ◽  
Dongju Seo ◽  
Cheryl Lacadie ◽  
Renata Belfort-DeAguiar ◽  
Derek Groskreutz ◽  
...  

Abstract Context Individuals with type 1 diabetes (T1DM) have alterations in brain activity which have been postulated to contribute to the adverse neurocognitive consequences of T1DM; however, the impact of T1DM and hypoglycemic unawareness on the brain’s resting state activity remains unclear. Objective To determine whether individuals with T1DM and hypoglycemia unawareness (T1DM-Unaware) had changes in the brain resting state functional connectivity compared to healthy controls (HC) and those with T1DM and hypoglycemia awareness (T1DM-Aware). Design Observational study Setting Academic medical center Participants 27 individuals with T1DM and 12 healthy control volunteers participated in the study. Intervention All participants underwent BOLD resting state fMRI brain imaging during a 2-step hyperinsulinemic euglycemic (90 mg/dl)-hypoglycemic (60mg/dl) clamp. Outcome Changes in resting state functional connectivity Results Using two separate methods of functional connectivity analysis, we identified distinct differences in the resting state brain responses to mild hypoglycemia amongst HC, T1DM-Aware and T1DM-Unaware participants, particularly in the angular gyrus, an integral component of the default mode network (DMN). Furthermore, changes in angular gyrus connectivity also correlated with greater symptoms of hypoglycemia (r = 0.461, P = 0.003) as well as higher scores of perceived stress (r = 0.531, P = 0.016). Conclusion These findings provide evidence that individuals with T1DM have changes in the brain’s resting state connectivity patterns, which may be further associated with differences in awareness to hypoglycemia. These changes in connectivity may be associated with alterations in functional outcomes amongst individuals with T1DM.


2019 ◽  
Vol 15 ◽  
pp. P282-P283
Author(s):  
Arman P. Kulkarni ◽  
Cole John Cook ◽  
Gyujoon Hwang ◽  
Veena A. Nair ◽  
Elizabeth M. Meyerand ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document