scholarly journals Age-related changes in spatial and temporal features of resting state fMRI

2017 ◽  
Author(s):  
Shruti G. Vij ◽  
Jason S. Nomi ◽  
Dina R. Dajani ◽  
Lucina Q. Uddin

AbstractDevelopment and aging are associated with functional changes in the brain across the lifespan. These changes can be detected in spatial and temporal features of resting state functional MRI (rs-fMRI) data. Independent vector analysis (IVA) is a whole-brain multivariate approach that can be used to comprehensively assess these changes in spatial and temporal features. We present a multi-dimensional approach to assessing age-related changes in spatial and temporal features of statistically independent components identified by IVA in a cross-sectional lifespan sample (ages 6-85 years). We show that while large-scale brain network configurations remain consistent throughout the lifespan, changes continue to occur in both local organization and in the spectral composition of these functional networks. We show that the spatial extent of functional networks decreases with age, but with no significant change in the peak functional loci of these networks. Additionally, we show differential age-related patterns across the frequency spectrum; lower frequency correlations decrease across the lifespan whereas higher-frequency correlations increase. These changes indicate an increasing stability of networks with age. In addition to replicating results from previous studies, the current results uncover new aspects of functional brain network changes across the lifespan that are frequency band-dependent.

2021 ◽  
Author(s):  
Heidi Foo ◽  
Anbupalam Thalamuthu ◽  
Jiyang Jiang ◽  
Forrest C Koch ◽  
Karen Mather ◽  
...  

Age and sex have been associated with changes in functional brain network topology, which may in turn affect cognition in older adults. We explored this question further by examining differences in 11 resting-state graph theory measures with respect to age, sex, and their relationships with cognitive performance in 17,127 UK Biobank participants. Age was associated with an overall decrease in the effectiveness of network communication (i.e. integration) and loss of functional specialisation (i.e. segregation) of specific brain regions. Sex differences were also observed, with women showing more efficient networks which were less segregated than in men. Age-related changes were also more apparent in men than women, which suggests that men may be more vulnerable to cognitive decline with age. Interestingly, while network segregation and strength of limbic network were only nominally associated with cognitive performance, the network measures collectively were significantly associated with cognition. This may imply that individual measures may be inadequate to capture much of the variance in neural activity or its output and need further refinement.


2019 ◽  
Author(s):  
Steve Mehrkanoon

AbstractWhen the human brain manifests the birth of organised communication among local and large-scale neuronal populations activity remains undescribed. We report, in resting-state EEG source-estimates of 100 infants at term age, the existence of macro-scale dynamic functional connectivity, which have rich topological organisations, distinct spectral fingerprints and scale-invariance temporal dynamics. These functional networks encompass the default mode, primary sensory-limbic system, thalamo-frontal, thalamo-sensorimotor and visual-limbic system confined in the delta and low-alpha frequency intervals (1-8 Hz). The temporal dynamics of these networks not only are nested within much slower timescale (¡ 0.1 Hz) but also correlated in a hierarchical leading-following organisation. We show that the anatomically constrained richly organised spatial topologies, spectral contents and temporal fluctuations of resting-state networks reflect an established intrinsic dynamic functional connectome in the human brain at term age. The graph theoretical analysis of the spatial architectures of the networks revealed small-world topology and distinct rich-club organisations of interconnected cortical hubs that exhibit rich synchronous dynamics at multiple timescales. The approach opens new avenues to advance our understanding about the early configuration organisation of dynamic networks in the human brain and offers a novel monitoring platform to investigate functional brain network development in sick preterm infants.


2020 ◽  
Author(s):  
Pesoli Matteo ◽  
Rucco Rosaria ◽  
Liparoti Marianna ◽  
Lardone Anna ◽  
D’Aurizio Giula ◽  
...  

AbstractThe topology of brain networks changes according to environmental demands and can be described within the framework of graph theory. We hypothesized that 24-hours long sleep deprivation (SD) causes functional rearrangements of the brain topology so as to impair optimal communication, and that such rearrangements relate to the performance in specific cognitive tasks, namely the ones specifically requiring attention. Thirty-two young men underwent resting-state MEG recording and assessments of attention and switching abilities before and after SD. We found loss of integration of brain network and a worsening of attention but not of switching abilities. These results show that brain network changes due to SD affect switching abilities, worsened attention and induce large-scale rearrangements in the functional networks.


2021 ◽  
Author(s):  
Bo-yong Park ◽  
Casey Paquola ◽  
Richard A.I. Bethlehem ◽  
Oualid Benkarim ◽  
Bratislav Misic ◽  
...  

Adolescence is a time of profound changes in the structural wiring of the brain and maturation of large-scale functional interactions. Here, we analyzed structural and functional brain network development in an accelerated longitudinal cohort spanning 14-25 years (n = 199). Core to our work was an advanced model of cortical wiring that incorporates multimodal MRI features of (i) cortico-cortical proximity, (ii) microstructural similarity, and (iii) diffusion tractography. Longitudinal analyses assessing age-related changes in cortical wiring during adolescence identified increases in cortical wiring within attention and default-mode networks, as well as between transmodal and attention, and sensory and limbic networks, indicative of a continued differentiation of cortico-cortical structural networks. Cortical wiring changes were statistically independent from age-related cortical thinning seen in the same subjects. Conversely, resting-state functional MRI analysis in the same subjects indicated an increasing segregation of sensory and transmodal systems during adolescence, with age-related reductions in their functional connectivity alongside with an increase in structural wiring distance. Our findings provide new insights into adolescent brain network development, illustrating how the maturation of structural wiring interacts with the development of macroscale network function.


2015 ◽  
Vol 7 (10) ◽  
pp. 4111-4122 ◽  
Author(s):  
Xin Xu ◽  
Qifan Kuang ◽  
Yongqing Zhang ◽  
Huijun Wang ◽  
Zhining Wen ◽  
...  

The functional brain network in late adulthood has been found to show a significant difference from that in young adulthood using a variety of network metrics.


2014 ◽  
Vol 36 (3) ◽  
pp. 862-871 ◽  
Author(s):  
Lubin Wang ◽  
Qiang Liu ◽  
Hui Shen ◽  
Hong Li ◽  
Dewen Hu

2019 ◽  
Author(s):  
Alena Damborská ◽  
Camille Piguet ◽  
Jean-Michel Aubry ◽  
Alexandre G. Dayer ◽  
Christoph M. Michel ◽  
...  

AbstractBackgroundNeuroimaging studies provided evidence for disrupted resting-state functional brain network activity in bipolar disorder (BD). Electroencephalographic (EEG) studies found altered temporal characteristics of functional EEG microstates during depressive episode within different affective disorders. Here we investigated whether euthymic patients with BD show deviant resting-state large-scale brain network dynamics as reflected by altered temporal characteristics of EEG microstates.MethodsWe used high-density EEG to explore between-group differences in duration, coverage and occurrence of the resting-state functional EEG microstates in 17 euthymic adults with BD in on-medication state and 17 age- and gender-matched healthy controls. Two types of anxiety, state and trait, were assessed separately with scores ranging from 20 to 80.ResultsMicrostate analysis revealed five microstates (A-E) in global clustering across all subjects. In patients compared to controls, we found increased occurrence and coverage of microstate A that did not significantly correlate with anxiety scores.ConclusionOur results provide neurophysiological evidence for altered large-scale brain network dynamics in BD patients and suggest the increased presence of A microstate to be an electrophysiological trait characteristic of BD.


2019 ◽  
Author(s):  
Moumita Das ◽  
Vanshika Singh ◽  
Lucina Uddin ◽  
Arpan Banerjee ◽  
Dipanjan Roy

AbstractThe human brain undergoes significant structural and functional changes across the lifespan. Our current understanding of the underlying causal relationships of dynamical changes in functional connectivity with age is limited. On average, functional connectivity within resting-state networks (RSNs) weakens in magnitude, while connections between RSNs tend to increase with age. Recent studies show that effective connectivity within and between large scale resting-state functional networks changes over the healthy lifespan. The vast majority of previous studies have focused primarily on characterizing cortical networks, with little work exploring the influence of subcortical nodes such as the thalamus on large-scale network interactions across the lifespan. Using directed connectivity and weighted net causal outflow measures applied to resting-state fMRI data, we examine the age-related changes in both cortical and thalamocortical causal interactions within and between RSNs. The three core neurocognitive networks from the triple network theory (default mode: DMN, salience: SN, and central executive: CEN) were identified independently using ICA and spatial matching of hub regions with these important RSNs previously reported in the literature. Multivariate granger causal analysis (GCA) was performed to test for directional connectivity and weighted causal outflow between selected nodes of RSNs accounting for thalamo-cortical interactions. Firstly, we observe that within-network causal connections become progressively weaker with age, and network dynamics are substantially reconfigured via strong thalamic drive particularly in the young group. Our findings manifest stronger between-network directional connectivity, which is further strongly mediated by the SN in flexible co-ordination with the CEN, and DMN in the old group compared with the young group. Hence, causal within- and between- triple network connectivity largely reflects age-associated effects of resting-state functional connectivity. Thalamo-cortical causality effects on the triple networks with age were next explored. We discovered that left and right thalamus exhibit substantial interactions with the triple networks and play a crucial role in the reconfiguration of directed connections and within network causal outflow. The SN displayed directed functional connectivity in strongly driving both the CEN and DMN to a greater extent in the older group. Notably, these results were largely replicated on an independent dataset of matched young and old individuals. Our findings based on directed functional connectivity and weighted causal outflow measures strengthen the hypothesis that balancing within and between network connectivity is perhaps critical for the preservation and flexibility of cognitive functioning with aging.


2021 ◽  
Vol 5 (Supplement_1) ◽  
pp. 116-116
Author(s):  
Rozalyn Anderson

Abstract Caloric restriction (CR) delays aging and the onset of age-related disease in diverse species. Several diseases of aging including diabetes, cancer, and neurodegeneration, have an established metabolic component. Although the mechanisms of CR remain unknown, numerous factors implicated in longevity regulation by CR converge on regulation of metabolism. The reprograming of metabolism with CR is tissue specific, but mitochondrial activation and changes in redox metabolism are among the shared features. Changes in non-coding miRNA and in processing of transcripts are contributing mechanisms in integrating metabolic and growth pathways. Our studies in simple cell culture shows that small changes in metabolic status can precipitate large-scale multi-modal functional changes across cellular processes. We propose that modest failures in metabolic integrity with age broadly impact homeostasis and adaptation, creating shared vulnerability to diseases and conditions despite differences in their etiology, and that CR harnesses this same axis to promote health and enhanced longevity.


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