Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/27754
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dc.contributor.authorOmidvarnia, Amir-
dc.contributor.authorZalesky, Andrew-
dc.contributor.authorMansour L, Sina-
dc.contributor.authorVan De Ville, Dimitri-
dc.contributor.authorJackson, Graeme D-
dc.contributor.authorPedersen, Mangor-
dc.date2021-01-22-
dc.date.accessioned2021-10-18T04:29:56Z-
dc.date.available2021-10-18T04:29:56Z-
dc.date.issued2021-04-15-
dc.identifier.citationNeuroImage 2021; 230: 117760en
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/27754-
dc.description.abstractIt has been hypothesized that resting state networks (RSNs), extracted from resting state functional magnetic resonance imaging (rsfMRI), likely display unique temporal complexity fingerprints, quantified by their multiscale entropy patterns (McDonough and Nashiro, 2014). This is a hypothesis with a potential capacity for developing digital biomarkers of normal brain function, as well as pathological brain dysfunction. Nevertheless, a limitation of McDonough and Nashiro (2014) was that rsfMRI data from only 20 healthy individuals was used for the analysis. To validate this hypothesis in a larger cohort, we used rsfMRI datasets of 987 healthy young adults from the Human Connectome Project (HCP), aged 22-35, each with four 14.4-min rsfMRI recordings and parcellated into 379 brain regions. We quantified multiscale entropy of rsfMRI time series averaged at different cortical and sub-cortical regions. We performed effect-size analysis on the data in 8 RSNs. Given that the morphology of multiscale entropy is affected by the choice of its tolerance parameter (r) and embedding dimension (m), we repeated the analyses at multiple values of r and m including the values used in McDonough and Nashiro (2014). Our results reinforced high temporal complexity in the default mode and frontoparietal networks. Lowest temporal complexity was observed in the subcortical areas and limbic system. We investigated the effect of temporal resolution (determined by the repetition time TR) after downsampling of rsfMRI time series at two rates. At a low temporal resolution, we observed increased entropy and variance across datasets. Test-retest analysis showed that findings were likely reproducible across individuals over four rsfMRI runs, especially when the tolerance parameter r is equal to 0.5. The results confirmed that the relationship between functional brain connectivity strengths and rsfMRI temporal complexity changes over time scales. Finally, a non-random correlation was observed between temporal complexity of RSNs and fluid intelligence suggesting that complex dynamics of the human brain is an important attribute of high-level brain function.en
dc.language.isoeng
dc.subjectFluid intelligenceen
dc.subjectFunctional MRIen
dc.subjectHuman connectome projecten
dc.subjectMultiscale entropyen
dc.subjectReproducibilityen
dc.subjectResting state networken
dc.subjectTemporal complexityen
dc.titleTemporal complexity of fMRI is reproducible and correlates with higher order cognition.en
dc.typeJournal Articleen
dc.identifier.journaltitleNeuroImageen
dc.identifier.affiliationNeurologyen
dc.identifier.affiliationDepartment of Biomedical Engineering, The University of Melbourne, Melbourne, Australiaen
dc.identifier.affiliationThe Florey Institute of Neuroscience and Mental Health, Melbourne Brain Centre, Melbourne, Australiaen
dc.identifier.affiliationInstitute of Bioengineering, Center for Neuroprosthetics, Center for Biomedical Imaging, EPFL, Lausanne, Switzerlanden
dc.identifier.affiliationDepartment of Radiology and Medical Informatics, University of Geneva, Geneva, Switzerlanden
dc.identifier.affiliationFlorey Department of Neuroscience and Mental Health, The University of Melbourne, Melbourne, Australiaen
dc.identifier.affiliationDepartment of Psychology and Neuroscience, Auckland University of Technology, Auckland, New Zealanden
dc.identifier.affiliationMelbourne Neuropsychiatry Centre, Department of Psychiatry, The University of Melbourne, Melbourne, Australiaen
dc.identifier.doi10.1016/j.neuroimage.2021.117760en
dc.type.contentTexten
dc.identifier.pubmedid33486124
local.name.researcherJackson, Graeme D
item.languageiso639-1en-
item.fulltextNo Fulltext-
item.grantfulltextnone-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
item.openairetypeJournal Article-
crisitem.author.deptNeurology-
crisitem.author.deptThe Florey Institute of Neuroscience and Mental Health-
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