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Functionally linked resting‐state networks reflect the underlying structural connectivity architecture of the human brain
Open accessAbstract
During rest, multiple cortical brain regions are functionally linked forming resting‐state networks. This high level of functional connectivity within resting‐state networks suggests the existence of direct neuroanatomical connections between these functionally linked brain regions to facilitate the ongoing interregional neuronal communication. White matter tracts are the structural highways of our brain, enabling information to travel quickly from one brain region to another region. In this study, we examined both the functional and structural connections of the human brain in a group of 26 healthy subjects, combining 3 Tesla resting‐state functional magnetic resonance imaging time‐series with diffusion tensor imaging scans. Nine consistently found functionally linked resting‐state networks were retrieved from the resting‐state data. The diffusion tensor imaging scans were used to reconstruct the white matter pathways between the functionally linked brain areas of these resting‐state networks. Our results show that well‐known anatomical white matter tracts interconnect at least eight of the nine commonly found resting‐state networks, including the default mode network, the core network, primary motor and visual network, and two lateralized parietal‐frontal networks. Our results suggest that the functionally linked resting‐state networks reflect the underlying structural connectivity architecture of the human brain. Hum Brain Mapp 2009. © 2009 Wiley‐Liss, Inc.
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“Anterior and posterior callosal fibres and fibres such as the inferior-fronto-occipital fasciculus provide major connections within the anterior and posterior components of the default mode network regions (van den Heuvel et al., 2009)”
From White matter diffusion alterations precede symptom onset in autosomal dominant Alzheimer’s disease (2018) · cites this paper as van den Heuvel et al., 2009
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“The AIC and ACC are known to be functionally (Taylor et al., 2009) and structurally (van den Heuvel et al., 2009) connected.”
From An Interoceptive Predictive Coding Model of Conscious Presence (2012) · cites this paper as van den Heuvel et al., 2009
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“higher FA has been associated with better functional connectivity between anatomically distant gray matter regions using resting-state fMRI (functional MRI) 35,47,48”
From Physical exercise keeps the brain connected: biking increases white matter integrity in patients with schizophrenia and healthy controls. (2015) · cites this paper as [47]
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Luo, Y., Chen, Q., Li, F., Liang, Y., Xu, P., & Zhang, Y. (2025) · Neural Networks · doi:10.1016/j.neunet.2025.107450 · Cited by 22
An Adaptive Temporal-Causal Network Model for Decision Making Under Acute Stress
Jan Treur, A., & Ziabari, S. S. M. (2018) · Lecture notes in computer science · doi:10.1007/978-3-319-98446-9_2 · Cited by 20
“…energy supplies and consumption is at issue, due to the fact that the brain ’ s vitality utilization (20% of the body ’ s total utilization) is asymmetrical to its size (about 2% of body mass [10]), and the brain has to compete with other body parts to achieving energy and operate for survival [5].”
BackgroundGuo, Z., Fan, C., Li, T., Gesang, L., Yin, W., Wang, N., Weng, X., Gong, Q., Zhang, J., & Wang, J. (2020) · Human Brain Mapping · doi:10.1002/hbm.24954 · Cited by 21
Altered effective connectivity among core brain networks in patients with bipolar disorder
Zhang, Z., Bo, Q., Li, F., Zhao, L., Wang, Y., Liu, R., Chen, X., Wang, C., & Zhou, Y. (2022) · Journal of Psychiatric Research · doi:10.1016/j.jpsychires.2022.06.031 · Cited by 21
Connectivity dynamics and cognitive variability during aging
Jauny, G., Eustache, F., & Hinault, T. (2022) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2022.07.001 · Cited by 21
Application of Partial Directed Coherence to the Analysis of Resting-State EEG-fMRI Data
Biazoli, C. E., Sturzbecher, M. J., White, T. P., Onias, H., Andrade, K. C., de Araújo, D. B., & Sato, J. R. (2013) · Brain Connectivity · doi:10.1089/brain.2012.0135 · Cited by 19
Structural connectivity of the salience-executive loop in schizophrenia
Iwabuchi, S. J., Liddle, P. F., & Palaniyappan, L. K. (2014) · European Archives of Psychiatry and Clinical Neuroscience · doi:10.1007/s00406-014-0547-z · Cited by 20
“Previous studies have established a structural basis for within-network functional connectivity within these large-scale systems [6].”
BackgroundBrain modifications after acute alcohol consumption analyzed by resting state fMRI
Spagnolli, F., Cerini, R., Cardobi, N., Barillari, M., Manganotti, P., Storti, S. F., & Mucelli, R. P. (2013) · Magnetic Resonance Imaging · doi:10.1016/j.mri.2013.04.007 · Cited by 23
“RSNs are reliable and reproducible [12]; they underlie a cortico-cortical structural connectivity visualized with tractography by means of diffusion tensor imaging (DTI) [13–15] and are correlated with electro-encephalographic (EEG) [16,17] rhythms.”
BackgroundZhang, T., Xu, P., Guo, L., Chen, R., Zhang, R., He, H., Xie, Q., Liu, T., Luo, C., & Yao, D. (2015) · Applied Informatics · doi:10.1186/s40535-014-0005-z · Cited by 20
Thomas, F., Moulier, V., Valero‐Cabré, A., & Januel, D. (2016) · Revue Neurologique · doi:10.1016/j.neurol.2016.09.001 · Cited by 21
Probing Intrinsic Resting-State Networks in the Infant Rat Brain
Bajic, D., Craig, M. M., Borsook, D., & Becerra, L. R. (2016) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2016.00192 · Cited by 21
Dang, S., Chaudhury, S., Lall, B., & Roy, P. K. (2017) · IEEE Transactions on Biomedical Engineering · doi:10.1109/tbme.2017.2738035 · Cited by 19
“cortical area is closely related to the pattern of its anatomical connections [27], [28].”
BackgroundHuman cerebral evolution and the clinical syndrome of amyotrophic lateral sclerosis
Henderson, R. D., Garton, F. C., Kiernan, M. C., Turner, M. R., & Eisen, A. (2018) · Journal of Neurology Neurosurgery & Psychiatry · doi:10.1136/jnnp-2017-317245 · Cited by 20
The pathoconnectivity network analysis of the insular cortex: A morphometric fingerprinting
Nani, A., Manuello, J., Mancuso, L., Liloia, D., Costa, T., Vercelli, A., Duca, S., & Cauda, F. (2020) · NeuroImage · doi:10.1016/j.neuroimage.2020.117481 · Cited by 19
Physical exercise keeps the brain connected by increasing white matter integrity in healthy controls
Bashir, S., Alsultan, F., Abujamea, A. H., Almousa, A., Alnafisah, M., Alzahrani, M., Abualait, T., & Yoo, W. (2021) · Medicine · doi:10.1097/md.0000000000027015 · Cited by 19
Structural connectivity of the frontal lobe in children with drug-resistant partial epilepsy
Holt, R. L., Provenzale, J. M., Veerapandiyan, A., Moon, W., Bellis, M. D. D., Leonard, S., Gallentine, W. B., Grant, G. A., EGGER, H. L., Song, A. W., et al. (2011) · Epilepsy & Behavior · doi:10.1016/j.yebeh.2011.03.016 · Cited by 18
“It, thus, interconnects key regions of the default mode network, a network which allows individuals to respond to salient stimuli and to emotionally process and monitor their mental state [9-12].”
BackgroundBrain Connections – Resting State fMRI Functional Connectivity
de la Iglesia-Vayá, M., Molina‐Mateo, J., Jose, M., Ahmad, S., & Martí‐Bonmatí, L. (2013) · InTech eBooks · doi:10.5772/52273 · Cited by 19
Default Mode Network Changes in Moyamoya Disease Before and After Bypass Surgery: Preliminary Report
Sakamoto, Y., Okamoto, S., Maesawa, S., Bagarinao, E., Araki, Y., Izumi, T., Watanabe, H., Sobue, G., & Wakabayashi, T. (2018) · World Neurosurgery · doi:10.1016/j.wneu.2018.01.117 · Cited by 18
Quantification of Structural Brain Connectivity via a Conductance Model
Frau‐Pascual, A., Fogarty, M., Fischl, B. R., Yendiki, A., Aganj, I., & Initiativey, †. T. A. D. N. (2018) · NeuroImage · doi:10.1016/j.neuroimage.2019.01.033 · Cited by 18
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van den Heuvel, M. P., & Pol, H. E. H. (2011) · Psiquiatría Biológica · doi:10.1016/j.psiq.2011.05.001 · Cited by 25
MRI network progression in mesial temporal lobe epilepsy related to healthy brain architecture
Morgan, V. L., Johnson, G. W., Cai, L. Y., Landman, B. A., Schilling, K. G., Englot, D. J., Rogers, B. P., & Chang, C. E. (2021) · Network Neuroscience · doi:10.1162/netn_a_00184 · Cited by 18
“For example, some relate functional relationships across the brain in terms of structural connectivity (van den Heuvel et al., 2009), commu-Structural connectivity: Brain region interaction measured by integrity of diffusion of water across white matter using MRI. nication measures (Goñi et al.,…”
BackgroundPark, H., Kim, M., Kwak, Y. B., Cho, K. I. K., Lee, J., Moon, S., Lho, S. K., & Kwon, J. S. (2022) · Molecular Psychiatry · doi:10.1038/s41380-022-01588-6 · Cited by 20
Baseline activity predicts working memory load of preceding task condition
Pyka, M., Hahn, T., Heider, D., Krug, A., Sommer, J. B., Kircher, T. T. J., & Jansen, A. (2012) · Human Brain Mapping · doi:10.1002/hbm.22121 · Cited by 18
“Long-term rest (15 min) before and after a language task revealed on the group level only slight changes, possibly due to heterogeneous differences on the subject-level [Waites et al., 2005].”
BackgroundMethodInvestigating intrinsic connectivity networks using simultaneous BOLD and CBF measurements
Mayhew, S. D., Mullinger, K. J., Bagshaw, A. P., Bowtell, R. W., & Francis, S. (2014) · NeuroImage · doi:10.1016/j.neuroimage.2014.05.042 · Cited by 17
“Additionally, functional connectivity is localised to grey matter (De Luca et al., 2006) and often reflects the brain's structural connectivity (Greicius et al., 2009; van den Heuvel et al., 2009).”
Koval, M. J., Hutchison, R. M., Lomber, S. G., & Everling, S. (2013) · Journal of Neurophysiology · doi:10.1152/jn.00626.2013 · Cited by 21
Nestor, L. J., Suckling, J., Ersche, K. D., Murphy, A., McGonigle, J., Orbán, C., Paterson, L. M., Reed, L. J., Taylor, E., Flechais, R., et al. (2020) · NeuroImage Clinical · doi:10.1016/j.nicl.2020.102297 · Cited by 18
Avelar‐Pereira, B., Bäckman, L., Wåhlin, A., Nyberg, L. H., & Salami, A. (2020) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2020.08.008 · Cited by 22
“…that FC re fl ects underlying structural connections (Damoiseaux and Greicius, 2009; Honey et al., 2009a; Skudlarski et al., 2008; Uddin, 2013; Van Den Heuvel et al., 2009), with various degrees of structural-functional correspondence across the brain (Vázquez-Rodríguez et al., 2019; Baum et…”
Olivito, G., Lupo, M., Gragnani, A., Saettoni, M., Siciliano, L., Pancheri, C., Panfili, M., Cercignani, M., Bozzali, M., Chiaie, R. D., et al. (2021) · The Cerebellum · doi:10.1007/s12311-021-01317-9 · Cited by 18
Altered structural connectivity and trait anhedonia in patients with schizophrenia
Lee, J. S., Han, K., Lee, S., Seok, J., & Kim, J. (2014) · Neuroscience Letters · doi:10.1016/j.neulet.2014.07.001 · Cited by 20
Developmental Resting State Functional Connectivity for Clinicians
Hulvershorn, L. A., Cullen, K. R., Francis, M., & Schreiner, M. W. (2014) · Current Behavioral Neuroscience Reports · doi:10.1007/s40473-014-0020-3 · Cited by 18
Lehmann, N., Tolentino‐Castro, J. W., Kaminski, E., Ragert, P., Villringer, A., & Taubert, M. (2019) · Human Brain Mapping · doi:10.1002/hbm.24704 · Cited by 16
“Because FA has shown to be associated with functional brain connectivity (van den Heuvel, Mandl, Kahn, & Hulshoff Pol, 2009), one could speculate that the functional meaning of high prefrontal FA values is to support the well-known shifts of functional brain activation occurring during the earliest stage of motor lear…”
BackgroundSolving the “human problem”: The frontal feedback model
Noack, R. A. (2012) · Consciousness and Cognition · doi:10.1016/j.concog.2012.01.011 · Cited by 18
Metadata
- Authors
- van den Heuvel, M. P., Mandl, R. C. W., Kahn, R. S., & Hulshoff Pol, H. E.
- Affiliations
- University Medical Center Utrecht (NL)
- Venue
- Human Brain Mapping
- Publisher
- Wiley
- Published
- 2009-02-23
- Volume
- 30
- Issue
- 10
- Pages
- 3127-3141
- ISSN
- 1065-9471 (ISSN-L)
- 1097-0193
- PMC
- PMC6870902
- OpenAlex
- W2022671987
- Cited by
- 987
- References
- 84
- Citations by year
- 2026: 19 · 2025: 28 · 2024: 28 · 2023: 45 · 2022: 51 · 2021: 47 · 2020: 57 · 2019: 60 · 2018: 69 · 2017: 80 · 2016: 72 · 2015: 79 · 2014: 84 · 2013: 94 · 2012: 74
- FWCI
- 27.75
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Human Brain Mapping (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Pure Amsterdam UMC (submittedVersion)
- Amsterdam UMC (VU Amsterdam) - Institutional Repository (submittedVersion)
- Data Archiving and Networked Services (DANS) (submittedVersion)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Functional Brain Connectivity Studies
- Health Sciences › Medicine › Radiology, Nuclear Medicine and Imaging › Advanced Neuroimaging Techniques and Applications
- Health Sciences › Medicine › Radiology, Nuclear Medicine and Imaging › Advanced MRI Techniques and Applications
- Keywords
- resting-state networks, functional connectivity, structural connectivity, white matter tracts, default mode network, core network, visual network
- MeSH terms
- Adolescent, Adult, Brain, Brain Mapping, Female, Humans, Image Processing, Computer-Assisted, Magnetic Resonance Imaging, Male, Models, Neurological, Nerve Fibers, Myelinated, Nerve Net, Neural Pathways, Oxygen, Rest, Diffusion Magnetic Resonance Imaging, Young Adult
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