ArticleBrain connectivity2015
Information Flow Between Resting-State Networks.
Article in Brain connectivity, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.
What it found
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Who cites it
7 citing papers in PubMed.
- Brain connectivity and cognitive functioning in individuals six months after multiorgan failure.NeuroImage. Clinical · 2020Article
- Structure-function multi-scale connectomics reveals a major role of the fronto-striato-thalamic circuit in brain aging.Human brain mapping · 2018Article
- Interaction Information Along Lifespan of the Resting Brain Dynamics Reveals a Major Redundant Role of the Default Mode Network.Entropy (Basel, Switzerland) · 2018Article
- Enhanced prefrontal functional-structural networks to support postural control deficits after traumatic brain injury in a pediatric population.Network neuroscience (Cambridge, Mass.) · 2017Article
- Genetic and Environmental Contributions to Functional Connectivity Architecture of the Human Brain.Cerebral cortex (New York, N.Y. : 1991) · 2016Article
- Top-Down Network Effective Connectivity in Abstinent Substance Dependent Individuals.PloS one · 2016Article
- Lagged and instantaneous dynamical influences related to brain structural connectivity.Frontiers in psychology · 2015Article
Corrections and comments
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Authors and funding
10 authors.
Funding
Abstract
unlabelledThe resting brain dynamics self-organize into a finite number of correlated patterns known as resting-state networks (RSNs). It is well known that techniques such as independent component analysis can separate the brain activity at rest to provide such RSNs, but the specific pattern of interaction between RSNs is not yet fully understood. To this aim, we propose here a novel method to compute the information flow (IF) between different RSNs from resting-state magnetic resonance imaging. After hemodynamic response function blind deconvolution of all voxel signals, and under the hypothesis that RSNs define regions of interest, our method first uses principal component analysis to reduce dimensionality in each RSN to next compute IF (estimated here in terms of transfer entropy) between the different RSNs by systematically increasing k (the number of principal components used in the calculation). When k=1, this method is equivalent to computing IF using the average of all voxel activities in each RSN. For k≥1, our method calculates the k multivariate IF between the different RSNs. We find that the average IF among RSNs is dimension dependent, increasing from k=1 (i.e., the average voxel activity) up to a maximum occurring at k=5 and to finally decay to zero for k≥10. This suggests that a small number of components (close to five) is sufficient to describe the IF pattern between RSNs. Our method--addressing differences in IF between RSNs for any generic data--can be used for group comparison in health or disease. To illustrate this, we have calculated the inter-RSN IF in a data set of Alzheimer's disease (AD) to find that the most significant differences between AD and controls occurred for k=2, in addition to AD showing increased IF w.r.t. CONTROLS: The spatial localization of the k=2 component, within RSNs, allows the characterization of IF differences between AD and controls.
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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.