Studying the human brain anatomical network via diffusion-weighted MRI and graph theory
Abstract
Our goal is to study the human brain anatomical network. For this, the anatomical connection probabilities (ACP) between 90 cortical and subcortical brain gray matter areas are estimated from diffusion-weighted Magnetic Resonance Imaging (DW-MRI) techniques. The ACP between any two areas gives the probability that those areas are connected at least by a single nervous fiber. Then, the brain is modeled as a non-directed weighted graph with continuous arc weights given by the ACP matrix. Based on this approach, complex networks properties such as small-world attributes, efficiency, degree distribution, vulnerability, betweenness centrality and motifs composition are studied. The analysis was carried out for 20 right-handed healthy subjects (mean age: 31.10, S.D.: 7.43). According to the results, all networks have small-world and broad-scale characteristics. Additionally, human brain anatomical networks present bigger local efficiency and smaller global efficiency than the corresponding random networks. In a vulnerability and betweenness centrality analysis, the most indispensable and critical anatomical areas were identified: putamens, precuneus, insulas, superior parietals and superior frontals. Interestingly, some areas have a negative vulnerability (e.g. superior temporal poles, pallidums, supramarginals and hechls), which suggest that even at the cost of losing in global anatomical efficiency, these structures were maintained through the evolutionary processes due to their…
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A large number of graph theoretical measures have been proposed to study network properties of the brain's connectome.
“A daunting number of graph theoretical measures have been proposed to study the network properties of the brain’s connectome (Bullmore and Sporns, 2009b; Iturria-Medina et al., 2008; Rubinov and Sporns, 2010).”
From Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review (2022) · cites this paper as Iturria-Medina et al., 2008
Cites
Efficiency and Cost of Economical Brain Functional Networks
Achard, S., & Bullmore, E. (2007) · PLoS Computational Biology · doi:10.1371/journal.pcbi.0030017 · Cited by 2,553 · see citing works
Tuch, D. S. (2004) · Magnetic Resonance in Medicine · doi:10.1002/mrm.20279 · Cited by 1,880 · see citing works
Adaptive reconfiguration of fractal small-world human brain functional networks
Bassett, D. S., Meyer-Lindenberg, A., Achard, S., Duke, T., & Bullmore, E. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0606005103 · Cited by 814 · see citing works
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Cited by
Sorted by citations
Complex brain networks: graph theoretical analysis of structural and functional systems
Bullmore, E., & Sporns, O. (2009) · Nature Reviews Neuroscience · doi:10.1038/nrn2575 · Cited by 11,820 · see citing works
Mapping the structural core of human cerebral cortex
Hagmann, P., Cammoun, L., Gigandet, X., Meuli, R., Honey, C. J., Wedeen, V. J., & Sporns, O. (2008) · PLoS Biology · doi:10.1371/journal.pbio.0060159 · Cited by 4,173 · see citing works
Predicting human resting-state functional connectivity from structural connectivity
Honey, C. J., Sporns, O., Cammoun, L., Gigandet, X., Thiran, J. P., Meuli, R., & Hagmann, P. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0811168106 · Cited by 3,307 · see citing works
Network-based statistic: identifying differences in brain networks
Zalesky, A., Fornito, A., & Bullmore, E. T. (2010) · NeuroImage · doi:10.1016/j.neuroimage.2010.06.041 · Cited by 2,750 · see citing works
Experimental and theoretical approaches to conscious processing
Dehaene, S., & Changeux, J.-P. (2011) · Neuron · doi:10.1016/j.neuron.2011.03.018 · Cited by 2,573 · see citing works
Network hubs in the human brain
van den Heuvel, M. P., & Sporns, O. (2013) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2013.09.012 · Cited by 2,123 · see citing works
Whole-brain anatomical networks: does the choice of nodes matter?
Zalesky, A., Fornito, A., Harding, I. H., Cocchi, L., Yücel, M., Pantelis, C., & Bullmore, E. T. (2010) · NeuroImage · doi:10.1016/j.neuroimage.2009.12.027 · Cited by 1,169 · see citing works
Sex differences in the structural connectome of the human brain
Ingalhalikar, M., Smith, A., Parker, D., Satterthwaite, T. D., Elliott, M. A., Ruparel, K., Hakonarson, H., Gur, R. E., Gur, R. C., & Verma, R. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1316909110 · Cited by 1,223 · see citing works
Uğurbil, K., Xu, J., Auerbach, E. J., Moeller, S., Vu, A. T., Duarte-Carvajalino, J. M., Lenglet, C., Wu, X., Schmitter, S., Van de Moortele, P. F., et al. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2013.05.012 · Cited by 812 · see citing works
A Weighted and Directed Interareal Connectivity Matrix for Macaque Cerebral Cortex
Markov, N. T., Ercsey-Ravasz, M. M., Ribeiro Gomes, A. R., Lamy, C., Magrou, L., Vezoli, J., Misery, P., Falchier, A., Quilodran, R., Gariel, M. A., et al. (2014) · Cerebral Cortex · doi:10.1093/cercor/bhs270 · Cited by 857 · see citing works
Brain Anatomical Network and Intelligence
Li, Y., Liu, Y., Li, J., Qin, W., Li, K., Yu, C., & Jiang, T. (2009) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1000395 · Cited by 597 · see citing works
Modeling the impact of lesions in the human brain
Alstott, J., Breakspear, M., Hagmann, P., Cammoun, L., & Sporns, O. (2009) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1000408 · Cited by 561 · see citing works
Disrupted axonal fiber connectivity in schizophrenia
Zalesky, A., Fornito, A., Seal, M. L., Cocchi, L., Westin, C.-F., Bullmore, E. T., Egan, G. F., & Pantelis, C. (2011) · Biological Psychiatry · doi:10.1016/j.biopsych.2010.08.022 · Cited by 439 · see citing works
An anatomical substrate for integration among functional networks in human cortex
van den Heuvel, M. P., & Sporns, O. (2013) · The Journal of Neuroscience · doi:10.1523/jneurosci.2128-13.2013 · Cited by 404 · see citing works
Networks of anatomical covariance
Evans, A. C. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2013.05.054 · Cited by 429 · see citing works
Exploring the network dynamics underlying brain activity during rest
Cabral, J., Kringelbach, M. L., & Deco, G. (2014) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2013.12.005 · Cited by 351 · see citing works
van den Heuvel, M. P., Bullmore, E. T., & Sporns, O. (2016) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2016.03.001 · Cited by 328 · see citing works
Towards quantitative connectivity analysis: reducing tractography biases
Girard, G., Whittingstall, K., Deriche, R., & Descoteaux, M. (2014) · NeuroImage · doi:10.1016/j.neuroimage.2014.04.074 · Cited by 324 · see citing works
Zhang, F., Daducci, A., He, Y., Schiavi, S., Seguin, C., Smith, R. E., Yeh, C.-H., Zhao, T., & O’Donnell, L. J. (2022) · NeuroImage · doi:10.1016/j.neuroimage.2021.118870 · Cited by 302 · see citing works
“A daunting number of graph theoretical measures have been proposed to study the network properties of the brain’s connectome [68, 403, 235].”
BackgroundConnectome sensitivity or specificity: which is more important?
Zalesky, A., Fornito, A., Cocchi, L., Gollo, L. L., van den Heuvel, M. P., & Breakspear, M. (2016) · NeuroImage · doi:10.1016/j.neuroimage.2016.06.035 · Cited by 275 · see citing works
Thalamocortical Connectivity Predicts Cognition in Children Born Preterm
Ball, G., Pazderova, L., Chew, A., Tusor, N., Merchant, N., Arichi, T., Allsop, J. M., Cowan, F. M., Edwards, A. D., & Counsell, S. J. (2015) · Cerebral Cortex · doi:10.1093/cercor/bhu331 · Cited by 234 · see citing works
Optimally controlling the human connectome: the role of network topology
Betzel, R. F., Gu, S., Medaglia, J. D., Pasqualetti, F., & Bassett, D. S. (2016) · Scientific Reports · doi:10.1038/srep30770 · Cited by 247 · see citing works
Tractometer: Towards validation of tractography pipelines
Côté, M.-A., Girard, G., Boré, A., Garyfallidis, E., Houde, J.-C., & Descoteaux, M. (2013) · Medical Image Analysis · doi:10.1016/j.media.2013.03.009 · Cited by 228 · see citing works
Brain anatomical networks in early human brain development
Fan, Y., Shi, F., Smith, J. K., Lin, W., Gilmore, J. H., & Shen, D. (2011) · NeuroImage · doi:10.1016/j.neuroimage.2010.07.025 · Cited by 225 · see citing works
Development Trends of White Matter Connectivity in the First Years of Life
Yap, P.-T., Fan, Y., Chen, Y., Gilmore, J. H., Lin, W., & Shen, D. (2011) · PLoS ONE · doi:10.1371/journal.pone.0024678 · Cited by 190 · see citing works
Scholtens, L. H., Schmidt, R., de Reus, M. A., & van den Heuvel, M. P. (2014) · The Journal of Neuroscience · doi:10.1523/jneurosci.0752-14.2014 · Cited by 160 · see citing works
van den Heuvel, M. P., de Reus, M. A., Feldman Barrett, L., Scholtens, L. H., Coopmans, F. M. T., Schmidt, R., Preuss, T. M., Rilling, J. K., & Li, L. (2015) · Human Brain Mapping · doi:10.1002/hbm.22828 · Cited by 131 · see citing works
Caeyenberghs, K., Leemans, A., Heitger, M. H., Leunissen, I., Dhollander, T., Sunaert, S., Dupont, P., & Swinnen, S. P. (2012) · Brain · doi:10.1093/brain/aws048 · Cited by 129 · see citing works
The brain's connective core and its role in animal cognition
Shanahan, M. (2012) · Philosophical Transactions of the Royal Society B: Biological Sciences · doi:10.1098/rstb.2012.0128 · Cited by 115 · see citing works
Mapping putative hubs in human, chimpanzee and rhesus macaque connectomes via diffusion tractography
Li, L., Hu, X., Preuss, T. M., Glasser, M. F., Damen, F. W., Qiu, Y., & Rilling, J. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2013.04.024 · Cited by 109 · see citing works
MR connectomics: a conceptual framework for studying the developing brain
Hagmann, P., Grant, P. E., & Fair, D. A. (2012) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2012.00043 · Cited by 96 · see citing works
Connecting a Connectome to Behavior: An Ensemble of Neuroanatomical Models of C. elegans Klinotaxis
Izquierdo, E. J., & Beer, R. D. (2013) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1002890 · Cited by 84 · see citing works
Development of cortical anatomical properties from early childhood to early adulthood
Nie, J., Li, G., & Shen, D. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2013.03.021 · Cited by 70 · see citing works
Brain Reserve, Resilience, and Cognitive Stimulation Across the Lifespan
Sorond, F. A., & Gorelick, P. B. (2023) · Clinics in Geriatric Medicine · doi:10.1016/j.cger.2022.08.003 · Cited by 8 · see citing works
- Authors
- Iturria-Medina, Y., Sotero, R. C., Canales-Rodríguez, E. J., Alemán-Gómez, Y., & Melie-García, L.
- Affiliations
- Cuban Neuroscience Center (CU)
- Venue
- NeuroImage
- Publisher
- Elsevier BV
- Published
- 2008-04
- Volume
- 40
- Issue
- 3
- Pages
- 1064-1076
- ISSN
- 1053-8119 (ISSN-L)
- OpenAlex
- W2064125324
- Cited by
- 506
- References
- 3
- Citations by year
- 2026: 9 · 2025: 11 · 2024: 10 · 2023: 21 · 2022: 23 · 2021: 22 · 2020: 27 · 2019: 20 · 2018: 24 · 2017: 36 · 2016: 34 · 2015: 34 · 2014: 40 · 2013: 43 · 2012: 47
- FWCI
- 9.85
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- NeuroImage (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Functional Brain Connectivity Studies
- Health Sciences › Medicine › Radiology, Nuclear Medicine and Imaging › Advanced Neuroimaging Techniques and Applications
- Physical Sciences › Physics and Astronomy › Statistical and Nonlinear Physics › Complex Network Analysis Techniques
- Keywords
- diffusion-weighted imaging, weighted complex networks, small-world property, local efficiency, global efficiency, network vulnerability, betweenness centrality, network motifs, putamen, precuneus, insula
- MeSH terms
- Adult, Algorithms, Brain, Humans, Image Processing, Computer-Assisted, Male, Nerve Fibers, Nerve Net, Neural Pathways, Diffusion Magnetic Resonance Imaging
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