scholarly journals Differential functional brain network connectivity during visceral interoception as revealed by independent component analysis of fMRI time-series

2015 ◽  
Vol 36 (11) ◽  
pp. 4438-4468 ◽  
Author(s):  
Behnaz Jarrahi ◽  
Dante Mantini ◽  
Joshua Henk Balsters ◽  
Lars Michels ◽  
Thomas M. Kessler ◽  
...  
2021 ◽  
Vol 12 ◽  
Author(s):  
Caroline M. Kelsey ◽  
Katrina Farris ◽  
Tobias Grossmann

Variability in functional brain network connectivity has been linked to individual differences in cognitive, affective, and behavioral traits in adults. However, little is known about the developmental origins of such brain-behavior correlations. The current study examined functional brain network connectivity and its link to behavioral temperament in typically developing newborn and 1-month-old infants (M [age] = 25 days; N = 75) using functional near-infrared spectroscopy (fNIRS). Specifically, we measured long-range connectivity between cortical regions approximating fronto-parietal, default mode, and homologous-interhemispheric networks. Our results show that connectivity in these functional brain networks varies across infants and maps onto individual differences in behavioral temperament. Specifically, connectivity in the fronto-parietal network was positively associated with regulation and orienting behaviors, whereas connectivity in the default mode network showed the opposite effect on these behaviors. Our analysis also revealed a significant positive association between the homologous-interhemispheric network and infants' negative affect. The current results suggest that variability in long-range intra-hemispheric and cross-hemispheric functional connectivity between frontal, parietal, and temporal cortex is associated with individual differences in affect and behavior. These findings shed new light on the brain origins of individual differences in early-emerging behavioral traits and thus represent a viable novel approach for investigating developmental trajectories in typical and atypical neurodevelopment.


2018 ◽  
Vol 44 (suppl_1) ◽  
pp. S233-S233
Author(s):  
Rebecca Hughes ◽  
Cosima Willi ◽  
Jayde Whittingham-Dowd ◽  
Susan Broughton ◽  
Greg Bristow ◽  
...  

2004 ◽  
Vol 22 (10) ◽  
pp. 1493-1504 ◽  
Author(s):  
Elia Formisano ◽  
Fabrizio Esposito ◽  
Francesco Di Salle ◽  
Rainer Goebel

2019 ◽  
Author(s):  
Yuhui Du ◽  
Zening Fu ◽  
Jing Sui ◽  
Shuang Gao ◽  
Ying Xing ◽  
...  

SummaryIncreasing sharing initiatives on neuroimaging data have provided unprecedented opportunities to study brain disorders. Standardized approaches for capturing reproducible and comparable biomarkers are greatly needed. Here, we propose a method, NeuroMark, which leverages a priori-driven independent component analysis to effectively extract functional brain network biomarkers from functional magnetic resonance imaging (fMRI) data. NeuroMark automatically estimates features adaptable to each individual and comparable across subjects by taking advantage of the replicated brain network templates extracted from 1828 healthy controls as guidance to initialize the individual-level networks. Four studies including 2454 subjects were conducted spanning six brain disorders (schizophrenia, autism spectrum disorder, depression, bipolar disorder, mild cognitive impairment and Alzheimer’s disease) to evaluate the proposed method from different perspectives (replication, cross-study comparison, subtle difference identification, and multi-disorder classification). Results demonstrate the great potential of NeuroMark in its feasibility to link different datasets/studies/disorders and enhance sensitivity in identifying biomarkers for patients with challenging mental illnesses.Significance StatementIncreasing evidence highlights that features extracted from resting fMRI data can be leveraged as potential biomarkers of brain disorders. However, it has been difficult to replicate results using different datasets, translate findings across studies, and differentiate brain disorders sharing similar clinical symptoms. It is important to systematically characterize the degree to which unique and similar impaired patterns are reflective of brain disorders. We propose a fully automated method (called NeuroMark) that leverages priori-driven independent component analysis (ICA) using replicated brain network templates to estimate individual-subject network features. Evaluated by four studies involving six different brain disorders, we show that NeuroMark can effectively link the comparison of biomarkers across different studies/datasets/disorders and enable classification between complex brain disorders, while also providing information about relevant aspects of whole brain functional connectivity.


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