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Objective: The aim of this study was to explore the relationship between global brain activity, changes in whole-brain connectivity, and changes in brain states across subjects using resting-state functional magnetic resonance imaging.
Methods: We extended current methods that use a sparse set of coactivation patterns to extract critical time points in global brain activity. Critical activity time points were defined as points where the global signal is greater than one standard deviation above or below the average global signal. Four categories of critical points were defined along dimensions of global signal intensity and trajectory. Voxel-based methods were used to interrogate differences in connectivity between these critical points.
Results: Several differences in connectivity were found in functional resting-state networks (RSNs) as a function of global activity. RSNs associated with cognitive functions in frontal, parietal, and subcortical regions exhibited greater whole-brain connectivity during lower global activity states. Meanwhile, RSNs associated with sensory functions exhibited greater whole-brain connectivity during the higher global activity states. Moreover, we present evidence that these results depend in part upon the standard deviation threshold used to define the critical points, suggesting critical points at different thresholds represent unique brain states.
Conclusion: Overall, the findings support the hypothesis that the brain oscillates through different states over the course of a resting-state study reflecting differences in RSN connectivity associated with global brain activity.
Significance: Increased understanding of brain dynamics may help to elucidate individual differences in behavior and dysfunction.
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http://dx.doi.org/10.1109/TBME.2016.2600248 | DOI Listing |
Nat Aging
September 2025
Goizueta Alzheimer's Disease Research Center, Emory University School of Medicine, Atlanta, GA, USA.
Clinical Alzheimer's disease is currently characterized by cerebral β-amyloidosis associated with cognitive impairment. However, most cases of Alzheimer's disease are associated with multiple neuropathologies at autopsy. The peripheral protein changes associated with these disease endophenotypes are poorly understood.
View Article and Find Full Text PDFNat Aging
September 2025
Department of Neurology, Division of Cerebrovascular Medicine and Neurology, National Cerebral and Cardiovascular Center (NCVC), Suita, Japan.
Thorax
September 2025
Department of Clinical Sciences, Liverpool School of Tropical Medicine, Liverpool, UK.
Introduction: Breathlessness is a common cause of hospital admission globally and is associated with high mortality, particularly in low-income countries. In sub-Saharan Africa, there is a paucity of data on breathlessness, with existing data focused on individual diseases. There is a need for patient-centred approaches to understand interactions between multiple conditions to address population needs and inform health system responses.
View Article and Find Full Text PDFBiol Pharm Bull
September 2025
Computational and Biological Learning Laboratory, University of Cambridge, Cambridge CB21PZ, United Kingdom.
Neuroimaging in rodents holds promise for advancing our understanding of the central nervous system (CNS) mechanisms that underlie chronic pain. Employing two established, but pathophysiologically distinct rodent models of chronic pain, the aim of the present study was to characterize chronic pain-related functional changes with resting-state functional magnetic resonance imaging (fMRI). In Experiment 1, we report findings from Lewis rats 3 weeks after Complete Freund's adjuvant (CFA) injection into the knee joint (n = 16) compared with the controls (n = 14).
View Article and Find Full Text PDFJ Neurotrauma
September 2025
Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland, USA.
Mean apparent propagator MRI (MAP-MRI) quantifies subtle alterations in tissue microstructure noninvasively and provides a more nuanced and comprehensive assessment of tissue architectural and structural integrity compared with other diffusion MRI techniques. We investigate the sensitivity of MAP-MRI-derived quantitative imaging biomarkers to detect previously unseen microstructural damage in patients with mild traumatic brain injuries (mTBI), whose clinical scans otherwise appeared normal. We developed and validated an MAP-MRI data processing pipeline for analyzing diffusion-weighted images for use in healthy controls and mTBI patients whose longitudinal scans were obtained from the GE/NFL/mTBI MRI database.
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