Is the brain really a small-world network?

It is commonly assumed that the brain is a small-world network (e.g., Sporns and Honey 2006). Indeed, one of the present authors claimed as much 15 years ago (Hilgetag et al. 2000). The small-worldness is believed to be a crucial aspect of efficient brain organization that confers significant advantages in signal processing (e.g., LagoFernandez et al. 2000). Correspondingly, the small-world organization is deemed essential for healthy brain function, as alterations of small-world features are observed in patient groups with Alzheimer’s disease (Stam et al. 2007), autism (Barttfeld et al. 2011) or schizophrenia spectrum diseases (Liu et al. 2008; Wang et al. 2012; Zalesky et al. 2011). While the colloquial idea of a small, interconnected world has a long tradition (e.g., Klemperer 1938), the present concept of small-world features of networks is frequently associated with the Milgram experiment (Milgram 1967) that demonstrated surprisingly short paths across social networks (‘six degrees of separation’). The concept was formalized by Watts and Strogatz (1998), who derived small-world networks from regular networks by including a small proportion of random network shortcuts. Such an organization results in short paths across the whole network—almost as small as in random networks—combined with local ‘cliquishness’ (or clustering) of neighboring nodes, due to dense local interconnections. These features can be mathematically summarized by the smallworld coefficient (Humphries et al. 2006), which is defined as the clustering coefficient of a given network (normalized by the clustering coefficient of a same-size random network) divided by the network’s normalized average shortest pathlength. While any network that has a smallworld coefficient larger than one is formally a small-world network, for many researchers, the term has become associated with the specific Watts and Strogatz model that is based on the partial random rewiring of a regular network (Fig. 1a). Indeed, the estimation of the rewiring probability has been used to directly associate real-world networks with the Watts and Strogatz model (Humphries and Gurney 2008). Incidentally, the small-world coefficient might not faithfully capture the small-world property as originally described by Watts and Strogatz (1998). Therefore, an alternative coefficient has been proposed that compares the clustering of the network to a lattice instead of a random network (Telesford et al. 2011). A large number of empirical network data conform to the small-world features of short paths combined with high clustering, including many neural networks—but do these Electronic supplementary material The online version of this article (doi:10.1007/s00429-015-1035-6) contains supplementary material, which is available to authorized users.

[1]  Woodrow L. Shew,et al.  The Functional Benefits of Criticality in the Cortex , 2013, The Neuroscientist : a review journal bringing neurobiology, neurology and psychiatry.

[2]  S. Herculano‐Houzel The remarkable, yet not extraordinary, human brain as a scaled-up primate brain and its associated cost , 2012, Proceedings of the National Academy of Sciences of the United States of America.

[3]  Marcus Kaiser,et al.  Criticality of spreading dynamics in hierarchical cluster networks without inhibition , 2007, 0802.2508.

[4]  Mariano Sigman,et al.  A small world of weak ties provides optimal global integration of self-similar modules in functional brain networks , 2011, Proceedings of the National Academy of Sciences.

[5]  Marcus Kaiser,et al.  Optimal Hierarchical Modular Topologies for Producing Limited Sustained Activation of Neural Networks , 2009, Front. Neuroinform..

[6]  M. A. Muñoz,et al.  Griffiths phases and the stretching of criticality in brain networks , 2013, Nature Communications.

[7]  T. Prescott,et al.  The brainstem reticular formation is a small-world, not scale-free, network , 2006, Proceedings of the Royal Society B: Biological Sciences.

[8]  Henry Kennedy,et al.  Cortical High-Density Counterstream Architectures , 2013, Science.

[9]  G. Edelman,et al.  Reentry: a key mechanism for integration of brain function , 2013, Front. Integr. Neurosci..

[10]  K. Gurney,et al.  Network ‘Small-World-Ness’: A Quantitative Method for Determining Canonical Network Equivalence , 2008, PloS one.

[11]  O. Sporns,et al.  Rich-Club Organization of the Human Connectome , 2011, The Journal of Neuroscience.

[12]  Andrew Zalesky,et al.  A DTI-Derived Measure of Cortico-Cortical Connectivity , 2009, IEEE Transactions on Medical Imaging.

[13]  Thomas Nowotny,et al.  Influence of Wiring Cost on the Large-Scale Architecture of Human Cortical Connectivity , 2014, PLoS Comput. Biol..

[14]  Nikola T. Markov,et al.  A Weighted and Directed Interareal Connectivity Matrix for Macaque Cerebral Cortex , 2012, Cerebral cortex.

[15]  Marcus Kaiser,et al.  Hierarchy and Dynamics of Neural Networks , 2010, Front. Neuroinform..

[16]  M P Young,et al.  Anatomical connectivity defines the organization of clusters of cortical areas in the macaque monkey and the cat. , 2000, Philosophical transactions of the Royal Society of London. Series B, Biological sciences.

[17]  Marc-Thorsten Hütt,et al.  Perspective: network-guided pattern formation of neural dynamics , 2014, Philosophical Transactions of the Royal Society B: Biological Sciences.

[18]  Paul J. Laurienti,et al.  The Ubiquity of Small-World Networks , 2011, Brain Connect..

[19]  Olaf Sporns,et al.  Small worlds inside big brains , 2006, Proceedings of the National Academy of Sciences.

[20]  O. Sporns,et al.  Identification and Classification of Hubs in Brain Networks , 2007, PloS one.

[21]  Duncan J. Watts,et al.  Collective dynamics of ‘small-world’ networks , 1998, Nature.

[22]  Edward T. Bullmore,et al.  Whole-brain anatomical networks: Does the choice of nodes matter? , 2010, NeuroImage.

[23]  Alex S. Ferecskó,et al.  The fractions of short- and long-range connections in the visual cortex , 2009, Proceedings of the National Academy of Sciences.

[24]  D. J. Felleman,et al.  Distributed hierarchical processing in the primate cerebral cortex. , 1991, Cerebral cortex.

[25]  Yuan Zhou,et al.  Anatomical insights into disrupted small-world networks in schizophrenia , 2012, NeuroImage.

[26]  H. Markram The Blue Brain Project , 2006, Nature Reviews Neuroscience.

[27]  L F Lago-Fernández,et al.  Fast response and temporal coherent oscillations in small-world networks. , 1999, Physical review letters.

[28]  O. Sporns,et al.  Organization, development and function of complex brain networks , 2004, Trends in Cognitive Sciences.

[29]  D. Modha,et al.  Network architecture of the long-distance pathways in the macaque brain , 2010, Proceedings of the National Academy of Sciences.

[30]  Yong He,et al.  Disrupted small-world networks in schizophrenia. , 2008, Brain : a journal of neurology.

[31]  M. Young,et al.  Advanced database methodology for the Collation of Connectivity data on the Macaque brain (CoCoMac). , 2001, Philosophical transactions of the Royal Society of London. Series B, Biological sciences.

[32]  Sharon L. Milgram,et al.  The Small World Problem , 1967 .

[33]  Gorka Zamora-López,et al.  Cortical Hubs Form a Module for Multisensory Integration on Top of the Hierarchy of Cortical Networks , 2009, Front. Neuroinform..

[34]  M. Sigman,et al.  A big-world network in ASD: Dynamical connectivity analysis reflects a deficit in long-range connections and an excess of short-range connections , 2010, Neuropsychologia.

[35]  G Tononi,et al.  Theoretical neuroanatomy: relating anatomical and functional connectivity in graphs and cortical connection matrices. , 2000, Cerebral cortex.

[36]  Changsong Zhou,et al.  Sustained Activity in Hierarchical Modular Neural Networks: Self-Organized Criticality and Oscillations , 2010, Front. Comput. Neurosci..

[37]  Bin He,et al.  A weighted small world network measure for assessing functional connectivity , 2013, Journal of Neuroscience Methods.

[38]  Abhishek Mathur,et al.  Efficient system-wide coordination in noisy environments. , 2004, Proceedings of the National Academy of Sciences of the United States of America.

[39]  Nikola T. Markov,et al.  Weight Consistency Specifies Regularities of Macaque Cortical Networks , 2010, Cerebral cortex.

[40]  Martin Suter,et al.  Small World , 2002 .

[41]  Alex Arenas,et al.  From Modular to Centralized Organization of Synchronization in Functional Areas of the Cat Cerebral Cortex , 2010, PloS one.

[42]  P Riley,et al.  Dynamical reconnection and stability constraints on cortical network architecture. , 2009, Physical review letters.

[43]  M. A. Muñoz,et al.  Griffiths phases on complex networks. , 2010, Physical review letters.

[44]  H E Stanley,et al.  Classes of small-world networks. , 2000, Proceedings of the National Academy of Sciences of the United States of America.

[45]  Xiaoping Hu,et al.  Quantitative assessment of a framework for creating anatomical brain networks via global tractography , 2012, NeuroImage.

[46]  Egon Wanke,et al.  Mapping brains without coordinates , 2005, Philosophical Transactions of the Royal Society B: Biological Sciences.

[47]  M. A. O'Neil,et al.  The connectional organization of the cortico-thalamic system of the cat. , 1999, Cerebral cortex.

[48]  Peter Stiers,et al.  Comparative Analysis of the Macroscale Structural Connectivity in the Macaque and Human Brain , 2014, PLoS Comput. Biol..

[49]  Olaf Sporns,et al.  Complex network measures of brain connectivity: Uses and interpretations , 2010, NeuroImage.

[50]  Marc-Thorsten Hütt,et al.  Building Blocks of Self-Sustained Activity in a Simple Deterministic Model of Excitable Neural Networks , 2012, Front. Comput. Neurosci..

[51]  O. Sporns,et al.  Complex brain networks: graph theoretical analysis of structural and functional systems , 2009, Nature Reviews Neuroscience.

[52]  Prof. Dr. Dr. Valentino Braitenberg,et al.  Cortex: Statistics and Geometry of Neuronal Connectivity , 1998, Springer Berlin Heidelberg.

[53]  Marc-Thorsten Hütt,et al.  Organization of Excitable Dynamics in Hierarchical Biological Networks , 2008, PLoS Comput. Biol..

[54]  C. Stam,et al.  Small-world networks and functional connectivity in Alzheimer's disease. , 2006, Cerebral cortex.

[55]  Edward T. Bullmore,et al.  Modular and Hierarchically Modular Organization of Brain Networks , 2010, Front. Neurosci..

[56]  Marcus Kaiser,et al.  Clustered organization of cortical connectivity , 2007, Neuroinformatics.

[57]  S. Brenner,et al.  The structure of the nervous system of the nematode Caenorhabditis elegans. , 1986, Philosophical transactions of the Royal Society of London. Series B, Biological sciences.

[58]  Edward T. Bullmore,et al.  Neuroinformatics Original Research Article , 2022 .

[59]  O. Sporns Small-world connectivity, motif composition, and complexity of fractal neuronal connections. , 2006, Bio Systems.

[60]  Marc-Thorsten Huett,et al.  Similar impact of topological and dynamic noise on complex patterns , 2006 .

[61]  D. Leopold,et al.  Anatomical accuracy of brain connections derived from diffusion MRI tractography is inherently limited , 2014, Proceedings of the National Academy of Sciences.

[62]  G A Orban,et al.  Functional impact of cerebral connections. , 1997, Proceedings of the National Academy of Sciences of the United States of America.

[63]  Olaf Sporns,et al.  Weight-conserving characterization of complex functional brain networks , 2011, NeuroImage.

[64]  C. Hilgetag,et al.  Hierarchical modular brain connectivity is a stretch for criticality , 2014, Trends in Cognitive Sciences.

[65]  E. Bullmore,et al.  Disrupted Axonal Fiber Connectivity in Schizophrenia , 2011, Biological Psychiatry.