Network neuroscience is an approach to understanding the structure and function of the human brain through an approach of network science, through the paradigm of graph theory. A network is a connection of many brain regions that interact with each other to give rise to a particular function.
Network Neuroscience is a broad field that studies the brain in an
integrative way by recording, analyzing, and mapping the brain in
various ways.
The field studies the brain at multiple scales of analysis to
ultimately explain brain systems, behavior, and dysfunction of behavior
in psychiatric and neurological diseases.
Network neuroscience provides an important theoretical base for
understanding neurobiological systems at multiple scales of analysis.
Multiple scales of analysis for the brain
Microscale
On the microscale (nanometer to micrometer), network analysis is performed on individual neurons and synapses.
Due to the incredible number of neurons in a brain network, it is
extremely difficult to construct a complete network at the microscale.
Specifically, data collection is too slow to resolve all of the billions
of neurons, machine vision tools to annotate the collected data are
insufficient, and we lack the mathematical algorithms to properly
analyze the resulting networks. Mapping the brain at the cellular level
in vertebrates
currently requires post-mortem (after death) microscopic analysis of
limited portions of brain tissue. Non-optical techniques that rely on
high-throughput DNA sequencing have been proposed recently by Anthony Zador (CSHL).
Mesoscale
On the mesoscopic scale (micrometer to millimeter), mesoscale analysis seeks to capture anatomically distinct populations of typically 80-120 neurons (e.g. cortical columns)
across different brain regions. Mesoscale analysis allows integration
of both microscale and macroscale studies, and thus allows multiscale
and structural-functional integration.
This scale still presents a very ambitious technical challenge at this
time and can only be probed on a small scale with invasive techniques or
very high field magnetic resonance imaging (MRI) on a local scale.
Macroscale
On the macroscale (millimeter),
large brain areas can be analyzed for anatomical distinctions, their
structure and interactions. The macroscopic scale is best suited for
mapping and annotating human connectomes, a comprehensive map of neural
connections, with cognitive and behavioral associations since in vivo
imaging of the human connectome is only available at the macroscale.
Additionally, macroscale analysis permits more compact and comprehensive
mapping. Magnetic resonance imaging, functional magnetic resonance imaging (fMRI), and diffusion-weighted magnetic resonance imaging
(DW-MRI) are the most popular tools for building macroscale data sets
due to their availability and resolution, among fMRI's and dMRI's
abilities to parce structural and functional connectivities,
respectively.
Mapping brain networks
Brain
networks can be mapped at multiple scales using both structural
connectivity and functional connectivity imaging techniques. Structural
descriptions of the components of neuronal networks are described as the
connectome.
Structural connectivity
Structural
connectivity describes how regions in the brain can communicate through
anatomical pathways such as synaptic coupling between cells and axonal
projections between neurons at the micro-scale and meso-scale and white matter fiber bundles at the macro scale. Diffusion-weighted MRI data is used to measure white-matter bundles.
Functional connectivity
Functional
connectivity measures the commonality in function between anatomically
separated brain regions and is usually measured at the macroscopic
level.
This commonality of function is inferred from similar activation
patterns in imaging techniques such as functional magnetic resonance
imaging (fMRI). Many of these fMRI experiments are known as resting-state experiments and measure spontaneous brain activity when the participant is told to relax. Similar (Blood-Oxygen Level Dependent) BOLD signals between different regions represent co-activation between these regions.
There are many new methods that have emerged for extracting functional
connectivity from fMRI data including Granger causality and dynamic
causal modeling (DCM).
Even though fMRI is the preferred method for measuring large-scale functional networks, electroencephalography (EEG) has also shown some progress in measuring resting state functional brain networks.
In a simultaneous fMRI-EEG study, a statistically significant
correlation was observed between the fMRI data and the EEG data thus
showing that EEG can be a new and promising method to measure functional
brain networks. The advantage of using EEG over fMRI includes its large temporal resolution.
There are novel methods to study functional connectivity.
Polarized Light Imaging (PLI) allows high-resolution quantitative
analysis of fiber orientations and can be used to bridge the microscopic
and macroscopic levels of analysis.
Optogenetic functional MRI (ofMRI) allows selective mapping of brain
regions based on genetic markers, anatomic location, and axonal
projections. Optogenetics can connect cellular activity with BOLD fMRI signals.
Functional networks differ from structural networks in that they
have additional properties not evident by studying the structural
network alone. There are new methods using linear algebra such as the eignenmode approach that seek to explain the complicated connection between functional and structural networks.
Analyzing brain networks
Graph theory
The
utilization of graph theory in neuroscience studies has been actively
applied after the discovery of functional brain networks. In graph
theory, an N × N adjacency matrix (also called a connection matrix) with
the elements of zero or non-zero indicates the absence or presence of a
relationship between the vertices of a network with N nodes. By
analyzing different metrics from these connection matrices from the
network, one can obtain a topological analysis of the desired graph; and
this is referred to as the human brain network in the field of
neuroscience.
One of the core architectures in brain network models is the
"small-world" architecture. It interprets models to be regular networks,
while they occasionally experience random activity. In small-world
networks, the clustering coefficient (i.e., transitivity) is high, and
the average path distance is short. These two characteristics reflect
the central maxim in the natural biological process: the balance between
minimizing the resource cost and maximizing the flow of information
among the network components. Given the complex structure of the human
brain, measures that can represent the small-world properties of the
brain network are of great importance since it simplifies the systems
and becomes decipherable.
Graph theoretical approaches have set up a mathematical framework
to model the pairwise communications between elements of a network. In human neuroscience, graph theory is generally applied to either functional or effective connectivity.
Graph theory methods, when applied properly, can offer important new
insights into the structure and function of networked brain systems,
including their architecture, evolution, development, and clinical
disorders.
It describes meaningful information about the topological architecture
of human brain networks, such as small-worldness, modular organization,
and highly connected or centralized hubs.
For example, in a study hypothesizing that aging processes modulate
brain connectivity networks, 170 healthy elderly volunteers were
submitted to EEG recordings in order to define age-related normative
limits.
Graph theory functions were applied to exact low-resolution
electromagnetic tomography on cortical sources in order to evaluate the
small-world parameter as a representative model of network architecture.
It is based on the strength of synchronization in the time-varying
oscillatory electromagnetic activity of different brain regions as
measured by EEG or MEG.
Key components of network analysis
Key components include:
Node degree, distribution and assortativity
The
degree of a node is the number of connections that link with the rest
of the network, which is one of the fundamental measures for defining
the model. The degrees of all the network's nodes form a degree
distribution. In random networks, all connections are equally probable,
resulting in a Gaussian and symmetrically centered degree distribution.
Complex networks generally have non-Gaussian degree distributions. By
convention, the degree distributions of scale-free networks follow a
power law. Lastly, assortativity is the correlation between the degrees
of connected nodes. Positive assortativity indicates that high-degree
nodes tend to connect to each other.
Clustering coefficients and motifs
The
clustering coefficient is a measure of the degree to which each node in
a graph tends to cluster together. Random networks have low average
clustering whereas complex networks have high clustering (associated
with high local efficiency of information transfer and robustness).
Interactions between neighboring nodes can also be quantified by
counting the occurrence of small motifs of interconnected nodes. The
distribution of different motifs in a network provides information about
the types of local interactions that the network can support.
Path length and efficiency
Path
length is the minimum number of edges that must be traversed between
two nodes. Random and complex networks have short mean path lengths
(high global efficiency of parallel information transfer) whereas
regular lattices have long mean path lengths. Efficiency is the
inversely related metric related to the path length. It is more actively
utilized than the path length due to its easier numerical use and
interpretation - for instance, estimating topological distances between
elements of disconnected graphs.
Connection density or cost
Connection
density is the actual number of edges in the graph as a proportion of
the total number of possible edges. It is the simplest estimator of the
physical cost of a network — for example, the energy or other resource
requirements.
Hubs, centrality, and robustness
Hubs
are nodes with high degree, or high centrality. The centrality of a
node measures how many of the shortest paths between all other node
pairs in the network pass through it. A node with high centrality is
thus crucial to efficient communication. The importance of an individual
node to network efficiency can be evaluated by deleting (i.e.,
lesioning) the certain hubs and estimating the efficiency of that
'lesioned' network. Robustness refers either to the structural integrity
of the network following deletion of nodes or edges or to the effects
of perturbations on local or global network states.
Modularity
Many
complex networks consist of a number of modules. There are various
algorithms that estimate the modularity of a network, and one of the
widely utilized algorithms is based on hierarchical clustering. Each
module contains several densely interconnected nodes, and there are
relatively few connections between nodes in different modules. Hubs can
therefore be described in terms of their roles in this community
structure. Provincial hubs are connected mainly to nodes in their own
modules, whereas connector hubs are connected to nodes in other modules.
Models
Dynamic networks
Brain
networks are not immutable, static constructs; rather those networks
are highly variable based on multiple time scales. Data on time-varying
brain graphs generally takes the form of time series (or stacks) of
graphs that form an ordered series of snapshots, for example data
recorded in the course of learning or across developmental stages. This
dynamicity can be represented through tracking the changes in network
topology utilizing the graph measures on each time point.
Multilayer networks
The
arrival of multi-omic data has enabled the joint analysis of networks
between elements of neurobiological systems at different levels of
organization. Prime examples are recent studies that combine maps of
anatomical and functional networks, as well as studies that combine
large-scale brain connectivity data with spatially registered data on
patterns of gene expression.
Algebraic topology
Network
science is largely built on the tools of graph theory, which focuses on
the dyad (a single connection between two nodes) as the fundamental
unit of interest. However, recent evidence suggests that sensor
networks, technological networks, and even neural networks display
higher-order interactions that simply cannot be reduced to pairwise
relationships. To address this, network science started to incorporate
algebraic topology. Algebraic topology reframes the problem of
relational data in terms of simplices or collections of vertices, rather
than pairs. IN other words, simplices represent the relational data in
terms of collections of vertices: a 0-simplex is a node, a 1-simplex is
an edge, and a 2-simplex is a filled (connected) triangle. Due to the
macroscopic scale to re-define the network systems through "simplicies",
topological data analysis can detect, quantify and compare mesoscale
structure present in complex network data.
Network of networks
Analyzing
similarity between brain networks - also referred to as the network of
network - can be useful for several applications in cognitive and
clinical neuroscience. In cognitive neuroscience experiments, similarity
analysis of brain networks can be used to build a "semantic map": nodes
represent the estimated networks of visual/auditory objects, and edges
denote the similarity between these networks. In clinical neuroscience, a
potential application of network distance measures is the mapping of a
"disease network". Here, the nodes may represent each brain disease and
the edges can represent the similarity between the different networks
associated with each disease - for example, Parkinson's, Alzheimer's,
and epilepsy. Another potential application of the network of networks
approach is to construct a similarity network across species
connectomes, in which nodes can denote species and edges the similarity
between them. However, the major difficulty of this cross-species
network analysis is devising the measure to access the different
connectome data from a range of species as each specimen has a unique
biological baseline or structure. Yet, this may help to better
understand cross-species communalities and differences in terms of brain
structure and function.
Large-scale brain networks
When Blood-Oxygen-Level-Dependent (BOLD)
signal activity in different areas of our brains co-occur, during tasks
or rest, those areas are considered to have varying degrees of functional connectivity between them. Large Scale Brain Networks
occur when various different areas in the brain are showing
co-activation and functional connectivity with each other, either during
rest or when a certain task is performed.
Current large scale brain networks include the Default Mode Network,
the Salience Network, the FrontoParietal Network, the Attention Network,
the Sensorimotor Network, the Visual Network and the Cingulo-Opercular
Network.
Default mode
The Default Mode Network (DMN) is a large-scale brain network that is active while the brain is at wakeful rest.
It was initially noticed to be deactivated during external goal
oriented tasks, specifically tasks involving visual attention or
cognitive working memory. Because of this, it was referred to as a task-negative network.
However, when tasks are internally goal-oriented, the default mode
network is activated and positively correlated with other brain
networks. Similarly, this network has also been shown to be active when individuals are focused on their internal mental-state processes.
Internal mental-state processes can include daydreaming, thinking of
the future, remembering past memories, thinking of others and ourselves,
mind wandering and introspection.
Some of the main anatomical features of this network include the
medial prefrontal cortex, posterior cingulate cortex and areas of the
inferior parietal lobule, such as the angular gyrus. Abnormalities in the DMN have been associated with Autism Spectrum Disorders, Alzheimer's and Schizophrenia.
Salience
The Salience Network is thought to be made up of primarily the anterior insula and the anterior cingulate cortex.
This network functions not only to complete bottom-up recognition of
salient stimuli, such as sensory and emotional occurrences, but also
aids in switching between various other large scale brain networks such
as the Default Mode Network and the Frontal-Parietal Network. In this way, the Salience Network allows us to generate and perform the correct behavioral response to a given salient stimuli.
The salience network also integrates the ventral attention network in
its function to respond to unexpected salient behavioral stimuli. Salience Network dysfunction has been associated with schizophrenia, anxiety disorders, and Autism Spectrum Disorders.
Attention
During tasks that require attention, certain regions become more active while others become less active.
This is because there are different networks in the brain that are
responsible for different types of activity and are activated by
different types of stimuli. There are two main systems that modulate
different aspects of attention: the dorsal frontoparietal system and the
ventral frontoparietal system.
The Dorsal frontoparietal system primarily functions in
goal-oriented control over visuospatial attention. This network
increases activity with attention-demanding tasks; it guides "top-down
voluntary allocation of attention to locations or features."
It is composed primarily of the intraparietal sulcus (IPS) and the
frontal eye fields (FEF). Researchers have used tools such as fMRI and
MRI to locate these regions by monitoring the brain while people perform
various cognitive tasks.
The Ventral frontoparietal system, on the other hand, is responsible
for triggering shifts of attentions. The system is implicated in
detecting unexpected stimuli and guiding where attention should be
directed.
While there are two relatively distinct systems involved in
attention, they must interact in a dynamic way to give rise to flexible
and fluid attention. The way they interact is thought to be determined
by the type of task that is at hand.
Frontoparietal
The frontoparietal network,
also known as the Central Executive Network, is one of the large-scale
brain networks involved in manipulating and maintaining information in
working memory.
It also plays a role in decision making and problem solving regarding
goal-directed behavior. The major anatomical parts of this network are
the dorsolateral prefrontal cortex and the posterior parietal cortex.
Brain imaging research has shown this network becomes more active during
cognitively demanding tasks, unlike other networks such as the Default
Mode Network, which reduces activity during cognitive tasks.
Despite the distinct network systems in terms of cognitive tasks, these
two networks are theorised to interact via the Salience Network. The
Salience Network, which is involved in bottom-up processing, modulates
between the Default Mode Network and the Frontoparietal Network.
Sensorimotor
The sensorimotor, or somatomotor, network is a large-scale brain network that is activated during motor tasks.
It includes the somatosensory and motor regions and extends to the
supplementary motor areas and auditory cortex. Sensorimotor performance
declines with age. This may be due to age-related reduction in GABA
levels, leading to less segregated networks that then affects
sensorimotor performance.
Visual
The
visual network's function is to receive, integrate, and process visual
information relayed from the retinas. The visual cortex, located in the
occipital lobe, handles this process. It is divided into five different
areas, V1-V5, each with different functions and structures. V1 processes
simple visual components such as orientation and direction. V2 received
the information from V1 and further interpreted that data through
differences in color, spatial frequency, moderately complex patterns,
and object orientation before sending feedback connections to V1 and
feedforward connections with V3-V5.
Regions like the occipital and lingual gyri are stable for visual
feature binding in the visual system network. The parietal lobe is also
identified as crucial for the binding process of color and shape
features and the fusiform and inferior temporal gyri for processing
color and shape information. The further the information travels, the more specialized cells there are to receive and interpret the data.
Cingulo-opercular
The
cingulo-opercular (CO) network fundamentally functions to maintain
tonic alertness which is the effortful process of making cognitive
faculties available for processing requirements.
The network is composed of the anterior insula/operculum, dorsal
anterior cingulate cortex, and thalamus. The CO network is frequently
co-activated with other control-related networks such as the
frontoparietal (FP) network. Both play a role in executive functions but
are also vulnerable to decline in non-pathological aging. At rest in
older adults, average CO connectivity is associated with better working
memory, inhibition, and set-shifting performance whereas FP connectivity
is associated with only working memory.
Newer Theories
Artificial Neural Networks
Neural
networks (i.e., artificial neural networks (ANNs) or simulated neural
networks (SNNs)), are a subset of machine learning and are widely used
as deep learning algorithms. Gleaned from the terminology itself, the
name and structure of the models are inspired by the mechanism of human
brain, which simulates the way that neurons signal to one another.
Three major types of ANNs are (1) feedforward neural networks (i.e.,
Multi-Layer Perceptrons (MLPs)), (2) convolutional neural networks
(CNNs), and (3) recurrent neural networks (RNNs).
Overlapping Networks
Recently,
it has come to light that the same brain regions can be part of
multiple networks and networks can have significant overlap between
them.
The most common methods for measuring brain networks are
"winner-takes-all" approaches where each region is only assigned to one
network. However, the organization of the brain makes it unlikely that the networks are actually nonoverlapping.
One study used novel methods such as Latent Dirichlet Association (LDA)
combined with Independent Components Analysis (ICA) to generate
multiple overlapping networks.
These networks were consistent with the nonoverlapping networks
previously generated. Another study showed that overlapping networks
occur in high frequency throughout the cerebral cortex.
The Default Mode Network (DMN) and the subjective value network (SVN)
both share regions in the central ventromedial prefrontal cortex
(cVMPFC) and dorsal posterior cingulate cortex (dPCC).
Emotion
Affective neuroscience theory
Affective
neuroscience (AN) theory aims to understand the material basis of
emotions and examines how the brain constructs emotional responses.
It postulates that seven primary emotional controls encompass the human
emotional experience. These seven systems include: seeking, lust, care,
play, fear, anger/rage, and panic/sadness.
Thorough studies of these systems have been performed in animals, yet
this data must be translated to human applications. Applications of
tools from network neuroscience and psychometry are used to map and
correlate connectivity patterns between the seven circuits.
Constructed emotion
The
theory of constructed emotion (TCE) offers an explanation of the basis
of emotion by formulating the brain as a running internal model that
controls central pattern generators in order to maintain allostasis.
This theory argues that the computational goal of the brain is to
minimize the prediction error, unpredicted events, that arise in a
particular sensory environment. Once prediction error is minimized, the
brain's predictions become experiences and perceptions and the brain
categorizes sensory events. In this manner, the brain continually
updates and constructs its categorizations and predictions. When the
brain's internal model constructs an emotion concept, the subsequent
categorization elicits an emotion. It is hypothesized that the brain's
default mode network is necessary to the generation its internal model
while the salience network tunes the internal model by minimizing
prediction error.
Emotions as functionally integrated systems
Emotional
representation in the brain has been proposed to be a functionally
integrated system that involve large-scale cortical-subcortical
networks tuned by bodily signals.
A functionally integrated emotional system is consistent with analysis
of fMRI data indicating emotional states are highly distributed and
predicts that brain "signatures" of affective dimensions, such as
arousal and fear, strongly depend on the sensory and contextual
environment, which may not generalize well across environments and
tasks.
This model also explains why structures, such as the amygdala, are so
important to emotions, as they are important hubs of distributed
cortical-subcortical functionally integrated systems.
Cognitive function
Theories
Cognitive
function is a term that encompasses mental processes involved in the
acquisition of knowledge, manipulation of information, and reasoning.
The typical domains categorized as cognitive function are perception
(including sensory perception), memory, learning, attention, decision
making, and language abilities.
One of the objectives in cognitive science is to reduce cognitive
systems to models of representations paired with processes. In
cognitive neuroscience, brain structures composed of complex
organizations of neurons are assumed to support cognitive functions; and
thus, the field actively utilizes neural localization techniques (such
as neuroimaging) to describe and identify the cognitive processes in the
brain. The variables in neural localization protocols are used to
predict behavioral indices to make inferences about the operations of
the underlying neural substrate. In contrast to these traditional
approaches, cognitive network neuroscience focuses on complex
interactions between spatially discrete brain regions, represented by
graphs, and seeks to link these patterns of interaction to measured
behavioral variables. The key consequence of using network
representations is that they can describe and uncover higher-level
complexity in terms of the interaction perspective and further identify
the overall processes of neural-behavioral activity.
Applications
Sensory perception and learning
With
respect to sensory perception, network studies have shown that the
strengthening of key functional connections underlies tasks that demand
sensory integration. For instance, the spatial distribution of network
modules in auditory and visual cortex and of hub-like areas became more
constrained to traditional anatomical boundaries in a multisensory task
and displayed less variability across subjects.
Network approaches can therefore contextualize the local functions of
primary sensory areas within systems that support dynamic sensory
integration and consolidation. Such approaches suggest that tasks with a
heavy emphasis on sensory processing and integration appear to depend
on tightly communicating cognitive hubs and sensorimotor regions.
Recent studies in learning have begun to capture dynamic patterns
of functional connectivity at finer temporal scales, from temporal
networks extracted from contiguous 2–3 min windows of fMRI experiments
to long-term scale experiments. Using these fMRI data, dynamic community
detection techniques can uncover changes in clusters of brain regions
linked by strong functional connectivity (i.e., putative functional
modules).
One possible interpretation of the dynamicity of fMRI data obtained
from learning experiments is based on the flexibility of brain network
dynamics. Brain network dynamics is commonly defined as the frequencies
of a brain region when it changes its allegiances to network modules
over time. his provides an index to individual differences in learning:
more flexible individuals learn better than less flexible individuals.
Human intelligence
Spearman's enigmatic g
Research
in the psychological and brain sciences has long sought to understand
the nature of individual differences in human intelligence, examining
the stunning breadth and diversity of intellectual abilities and the
remarkable cognitive and neurobiological mechanisms from which they
emerge.
These early findings motivated Spearman's two-factor model which held
that performance on tests of mental ability jointly reflect (i) a
specific factor, s, that is unique to each test, and (ii) a general
factor, g, that is common across all tests. Contemporary research has
further elaborated Spearman's model to include an intermediate level of
broad abilities that account for the variance that is shared across
similar domains of cognitive ability. elucidate how g – reflected in the
positive manifold and the hierarchical pattern of correlations among
tests – emerges from individual differences in the network topology and
dynamics of the human brain.
Intelligence models
Spearman's
model of general intelligence has been elaborated in modern theories to
include an intermediate level of cognitive domains that are broader
than specific abilities 's', but are less comprehensive than g.
These intermediate level abilities include (i) crystallized
intelligence, which underlies performance on tests of previously
acquired knowledge, and (ii) fluid intelligence, which reflects the
capacity for adaptive reasoning in novel environments. From a network
neuroscience perspective, the formation of broad abilities reflects the
competing forces of local versus global efficiency. Such competing
forces in terms of efficiency conclude the existence of modules that
create a broader set of cognitive abilities whose topology enables a
more globally efficient, small-world network.
Network neuroscience further adopts a new perspective, proposing
that g originates from individual differences in the system-wide
topology and dynamics of the human brain. In this viewpoint, the
small-world topology of brain networks enables the rapid reconfiguration
of their modular community structure, creating globally coordinated
mental representations of a desired goal-state and the sequence of
operations required to achieve it.
The capacity to flexibly transition between network states therefore
provides the foundation for individual differences in g which consists
of two states: (i) easy-to-reach network states to construct mental
representations for crystallized intelligence based on prior knowledge
and experience, and (ii) difficult-to-reach network states to construct
mental representations for fluid intelligence based on cognitive control
functions that guide adaptive reasoning and problem-solving. Thus,
network flexibility and dynamics provide the foundation for general
intelligence – enabling rapid information exchange across networks and
capturing individual differences in information processing at a global
level.
Theories on personality
Personality
is the characteristic patterns of thinking, feeling, and behaving. Its
psychological foundation lies in the observation that individual
differences follow principles–traits or dispositions–that are
sufficiently stable within individuals, consistent between individuals,
and invariant to situational context to explain past and to predict
future behavior.
In science, personality traits are often investigated using the
five-factor-model, a set of personality factors that are empirically
defined and stable over time. They are useful in explaining specific
types of behavior. The five-factor-model includes neuroticism, extraversion, openness/intellect, agreeableness and conscientiousness.
Previous studies have identified the connection between personality
factors and certain structures, functional brain networks and regions
and how these interactions are crucial to emotional and cognitive
processes.
Individuals are classified along the trait continuum and with
traits producing consistent behaviors across situations and times, a
person scoring at the upper end of a trait will respond consistently
stronger to relevant stimuli as opposed to a person scoring at the lower
end. Because each situation is associated with a certain brain state
(functional connectivity, network state), such states bear trait-like
connectivity across situations and times as well, representing the
neural trait system.
This correlates to the trait theory that personality traits are
biophysical entities that actually exist in the brain as conceptual
nervous systems.
From the concept of personality and network neuroscience sprouts
the field of personality network neuroscience (PNN). The goal of
personality network neuroscience is to identify and to integrate neural
systems (or biophysical entities) associated with psychological trait
conceptions within an integrated framework for human personality. It
promises an integrative, network level account of brain-personality
relationships. PNN utilizes techniques from affective and cognitive
neuroscience to relate brain processes to personality characteristics.
MRI is the backbone technology of this field. It is a medical technology
that has enabled researchers to non-invasively assess neural processes
in the awake human brain and has allowed for the discovery of marvelous
insights into the neural foundation of psychological processes.
One study on personality and network neuroscience selected
regions-of-interest based on their inclusion within the default mode
network (DMN), the salience network (SN), the cognitive executive
network (CEN), or on their strong relation with these networks to
investigate the relationship between personality domains and brain
activity. Personality profiles were generated from the NEO Five-Factor
Inventory that contains 60 questions related to five different
personality domains (personality factors): neuroticism, extraversion,
openness/intellect, agreeableness and conscientiousness. The results
from this test showed that there were strong and significant
correlations between several of the domains: neuroticism was negatively
correlated to agreeableness, extraversion and conscientiousness;
agreeableness was positively correlated to openness, extraversion and
conscientiousness; extraversion was positively correlated to
conscientiousness.
The study concluded that personality profiles allow for personality
factors to be observed in the context of all other traits and two of
them were found to be associated with patterns of co-activation in the
brain during rest in regions involved with emotion and cognition.
These findings could be proved useful in linking personality to
increased risk for psychiatric disorders and better understanding of
normal and pathological processes.
Psychiatric Disorders
Autism spectrum disorder
Autism spectrum disorder
(ASD) is a neuro developmental disorder, most commonly diagnosed in
childhood, and is characterized by deficits in social and communication
skills.
Symptoms include social impairments, hyper-fixations, repetitive
behaviors and hypersensitivity. ASD severity falls on a spectrum, which
means some individuals may have very severe symptoms and social
impairments and might need substantial assistance, while others require
less support. ASD individuals have been shown to have abnormal reduced intrinsic functional connectivity in their Default Mode Network (DMN) as well as disruptions in their Frontoparietal Network (FPN or CEN) and Salience Network (SN).
Most notably for the SN, ASD patients have been shown to have
hypoactivity in the anterior insula, one of the anchoring points of the
SN in the brain.
It is thought that these disruptions within networks result in
disrupted interactions between networks, resulting in the ASD pathology.
More specifically, the reduced activity in the SN leads to deficient
signaling to the FPN and the DMN, leading to a "disengagement of
cognitive systems important for attending to salient external stimuli or
internal mental events.".
Schizophrenia
Schizophrenia
is a psychiatric disorder that is most commonly diagnosed in adulthood.
It is usually characterized by psychotic symptoms, such as
hallucinations and delusions, disorganized speech and motor behavior,
deficits in attention, concentration and memory, as well as negative
symptoms, such as social isolation, loss of motivation and enjoyment in
previous fulfilling activities and loss of emotional expression.
Primary networks implicated in Schizophrenia include the Frontoparietal
Network (FPN), Default mode Network (DMN) and the Salience Network
(SN).
In one study participants with schizophrenia showed significant
deficits in functional connectivity in the FPN when compared to healthy
controls.
Schizophrenia patients have shown hyperconnectivity as well as
hypoconnectivity in the DMN. One study found that schizophrenia patients
had hyperconnectivity from the Posterior Cingulate Cortex (PCC) to the
Medial PreFrontal Cortex (mPFC), when compared to healthy controls.
Other studies have shown hypoconnectivity and reduced anatomical
connectivity in the DMN, with mPFC dysfunction playing a leading role.
These connection deficits in the DMN can be associated with the
positive symptoms experienced in schizophrenia such as hallucinations
and delusions.
There are also functional and structural abnormalities in the Salience
Network in individuals with schizophrenia. Structurally, main nodes of
the SN such as the anterior insula and Anterior Cingulate Cortex (ACC)
have been shown to have a bilateral volume reduction when compared to
healthy controls; and this reduced volume has been correlated with the
severity of reality distortion experienced by schizophrenic patients.
Studies have also shown that increased activation in the anterior
insula and the frontal operculum in the SN is correlated with
experiences of auditory verbal hallucinations in schizophrenic patients.
Similar to ASD, it is thought that these disruptions within networks
result in disrupted interactions between networks, such as reduced
functional connectivity between the SN and the DMN which results in the schizophrenia pathology.
Addiction
Addiction
is a complicated disorder and one that can strongly be influenced by
environmental, societal and genetic factors and there are many risk
factors that put certain people at a greater likelihood of developing an
addiction. There are two types of addiction to be considered: substance use disorder (SUD), usually characterized by uncontrolled drug seeking and taking, and behavioral addictions (BA), characterized by a compulsion or need to perform certain behaviors or practices, such as gambling.
The compulsion that accompanies the action, either performing the
behavior or taking the drug, as well as negative emotions if not allowed
to complete compulsion and lack of self control are all indicators of
both disorders.
The networks most associated with addiction are the Frontoparietal
Network, the Reward Network, the Salience Network and the Memory and
Habit networks.
In individuals with addiction, there seems to be a general theme of
hyper-activation of these networks when exposed to drug cues.
During resting state, it appears that in chronic stimulant users there
is a tight coupling and connection between the Reward, Salience, Memory
and Habit networks, and these networks all have enhanced connection with
the Frontoparietal Network.
Bipolar disorder
Bipolar disorder (BD) is a mood disorder usually characterized by extreme mood swings and oscillating periods of intense emotion, such as mania and depression.
The cycling between manic and depressive episodes is the main hallmark
of bipolar disorder. In BD, there seems to be a disconnect between the
Frontoparietal Network (FPN) and Defualt Mode Network (DMN), in which
the FPN is unable "to suppress task irrelevant DMN activity during
cognitive performance" which leads to BD's cognitive impairments.
It also appears that in BD, there is a disruption in the recruitment of
the salience network which contributes to cognitive dysregulation.
Bipolar disorder is also thought to be characterized by abnormal
functional connectivity between the FPN and motivational networks, with
the DMN playing a mediation role. All these aberrant connectivity and dysregulation leads to the BD pathology witnessed in patients with this mood disorder.
Anxiety disorders
Anxiety
disorders is a category of various mental disorders characterized by
uncontrollable fear and anxiety. The most common of these is generalized
anxiety disorder.
Studies show many different brain regions and networks implicated in
this group of disorders, as well as similar differences seen across
disorders. For example, dysfunction in the central executive network is
implicated in most major psychiatric disorders, including depression and
anxiety.
Abnormalities regarding the functional connectivity of the default mode
network have also been identified in most major psychiatric disorders.
More specifically related to anxiety, studies show that they are
associated with hyperactivity in the cingulo-opercular and central
attention networks. There is also decreased activity within the
fronto-parietal and default mode networks in those with anxiety. Within the Salience Network, hyperactivity in the anterior insula has been linked to anxiety disorders and negative thoughts.
Post-traumatic stress disorder
Post-traumatic stress disorder (PTSD) is a mental disorder triggered by a specific event that causes flashbacks, nightmares, and severe anxiety.
Similar to other psychiatric disorders, there are multiple brain
networks implicated in this disorder. Studies have shown that the
Central Executive Network has decreased connectivity during cognitive
tasks in those with PTSD compared to controls.
Examples of these types of tasks include emotional processing or
working memory tasks. There is also decreased connectivity within the
Salience Network in the brains of people who suffer from PTSD. The
Default Mode Network, on the other hand, shows higher connectivity. In a
healthy brain, the Salience Network modulates between the activation of
the Central Executive Network and the Default Mode Network. The
alternating network systems functioned by the anterior insula is not
done as effectively in those with PTSD, which could account for the
differences in activation.
Depression
Depression,
or major depressive disorder, is a mood disorder characterized by
persistent feelings of sadness. It affects the way one thinks, feels,
and acts. The Central Executive Network, which helps maintain
information in working memory and aids in decision making and problem
solving, has been shown to be hypoactive in individuals with depression.
Hyperconnectivity between the Central Executive Network and areas of
the Default Mode Network has also been observed. Within the Default Mode
Network, depressed individuals exhibit hyperconnectivity. This network
is believed to be involved in internally oriented thought.
Psychopathy
Psychopathy
is a personality disorder that is characterized by antisocial behavior,
lack of remorse and empathy, and impaired decision making.
Studies that examine the neural correlates of this disorder find
similar dysfunction across the large-scale brain networks that can be
seen in other psychiatric disorders such as depression and anxiety.
These studies discovered functional differences within the Default Mode
Network (DMN) and the Central Executive Network (CEN), as well as across
networks. Many individuals exhibit hyperactivity in the Default Mode
Network, as well as decreased activity in the Dorsal Anterior Cingulate
Cortex (dorsal ACC).
The Dorsal ACC is one of the major nodes of the Salience Network, which
is the network that is supposed to modulate between the DMN and the
CEN. This decreased activation is hypothesized to be one of the reasons
for the increased activation in the DMN due to the lack of alternating
activation patterns from DMN to the Salience Network.
One study done with a group of incarcerated individuals with
psychopathy also showed that higher levels of psychopathy were linked to
a more efficient organisation within the dorsal attention network.
Neurological disorders
ALS
Amyotrophic Lateral Sclerosis
(ALS) is a neurodegenerative disease of upper and lower motor neurons,
leading to respiratory issues and death in 3–5 years. Multiple networks
can be impacted in ALS showing that it is a multisystem network
disorder. Connectivity in motor regions, somatosensory regions, and
extra-motor regions are altered in patients with ALS. Connectivity in
visual areas are also altered. Further, both motor and cognitive networks show decreased activation in ALS patients.
The specific impaired networks include the Default Mode Network (DMN),
sensorimotor network (SMN), fronto-parietal network (FPN), and salience
network (SN). There is specifically decreased connectivity between the DMN and the SMN.
Resting state functional connectivity (rsFC) in ALS patients is
decreased and resting state networks interact with each other less.
Parkinson's disease
Parkinson's disease
(PD) is a movement disorder that also causes cognitive decline in some
cases. Parkison's patients have changed connectivity in the sensorimotor
network (SMN), the visual network, the putamen in the subcortical
network, and the cerebellum.
Severity of symptoms in PD was also associated with temporal
variability between the subcortical networks and the visual network,
ventral, and dorsal attention networks. Primary motor cortex and supplementary motor areas are also less active in patients with PD.
The frontoparietal (FP) network in patients with Parkinson's disease
but without cognitive decline is more robust and resilient to network
perturbation compared to those with cognitive decline.
This suggests that the FP network can be a predictor of cognitive
decline in Parkinson's patients. The FP control network also shows
decreased network connectivity with other resting-state networks.
PD patients with amnestic disturbances (processing speed and memory
impairments) are more at risk of developing dementia. Network
connectivity is decreased in patients with amnestic disturbances
compared to those without.
There is also evidence that a special PD network forms in patients with
PD linking metabolically active areas in the cerebellum, pons, frontal
cortex, and limbic regions. Thus, PD patients have increased small-world
network connectivity.
Huntington's disease
Huntington's disease (HD) is an inherited neurological disorder which causes progressive motor, behavior, and cognitive decline. Patients with the gene causing HD have different connections in their default mode network (DMN).
These patients have decreased connectivity between the anterior medial
prefrontal cortex, the left inferior parietal and the posterior
cingulate cortex. They also have increased connectivity between the two DMN subsystems.
Decreased connectivity within the sensorimotor network (SMN) exists in
early stages of HD and the visual network and attentional networks are
affected later.
Sleep disorders
There are many types of sleep disorders. Sleep restriction (SR) is a consequence of not getting sufficient sleep and causes changes in structural network connectivity.
Specifically, it targets the bilateral orbital part of the frontal
gyri, superior occipital gyri, left insula, fusiform, right
supplementary motor area, and cingulate gyrus.
A study conducted on young males with less sleep also showed that there
was increased connectivity within the somatomotor network (SMN) during
rest. Insomnia
is a condition where patients have difficulty falling asleep or staying
asleep. There is evidence that insomnia involves distributed brain
networks and causes increased structural connectivity around the right
angular gyrus.
A subnetwork that was centralized at the right angular gyrus and
included frontal, temporal, and subcortical regions, showed enhanced
connectivity in patients with insomnia.
Further, the lapse in cognitive abilities after a certain period of
total sleep deprivation is associated with increased coupling between
the default mode network (DMN) and the salience network (SN). Sleep disturbances in adolescents may also be caused by increased grey matter volume in several large-scale networks.
Dementia
Dementia
is a general term for loss of memory, language, problem-solving and
other thinking abilities that are severe enough to interfere with daily
life.
Dementia is a general term like heart disease is a general term.
Dementia is caused by damage to brain cells. This damage interferes with
the ability of brain cells to communicate with each other. When brain
cells cannot communicate normally, thinking, behavior and feelings can
be affected.
There are many signs of dementia. These signs can manifest as
short-term memory, problems keeping track of items, and more. Usually,
dementia is provoked by a "disconnection event" (e.g., a stroke) which
disconnects one or more functional areas from a task-associated ensemble
of functionally connected regions, resulting in a clinically observable
"disconnection" syndrome.
The most common form of dementia is Alzheimer's disease.
Alzheimer's disease (AD) is a progressive, neurodegenerative disease
that can be clinically characterized by impaired memory and many other
cognitive functions.
Several recent studies have suggested that AD patients have disruptive
neuronal integrity in large-scale structural and functional brain
systems underlying high-level cognition, as demonstrated by a loss of
small-world network characteristics.
In Alzheimer's disease, high levels of certain proteins inside and
outside brain cells make it hard for brain cells to stay healthy and to
communicate with each other.
The brain region first affected is the hippocampus. It begins
specifically in the lateral entorhinal cortex, or LEC. The LEC is
considered to be a gateway to the hippocampus, which plays a key role in
the consolidation of long-term memory, among other functions. If the
LEC is affected, other aspects of the hippocampus will also be affected.
The hippocampus is the center of learning and memory in the brain, and
the brain cells in this region are often the first to be damaged. That's
why memory loss is often one of the earliest symptoms of Alzheimer's.
Epilepsy
Epilepsy is a brain network disorder. It is a brain disorder that causes recurring, unprovoked seizures.
In an epileptic brain, certain networks have abnormal parameters at the
molecular and cellular levels, due to genetic or to acquired pathogenic
factors, rendering some essential parameters that control network
stability extremely vulnerable to the influence of exogenous and
endogenous factors.
At the local neuronal network level, some hubs constituted by neurons
and associated glia constitute oscillatory systems that became
increasingly coupled at the transition to a seizure, thereby recruiting
more distant neuronal networks, constituting complex oscillatory
circuits, which can be recognized by EEG or MEG recordings.
Structural epilepsies in older children and adults most commonly
present with focal seizures and have very similar symptoms from event to
event.
Focal seizures can be simple or complex. Simple focal seizures, also
known as auras, occur in one area on one side of the brain, but may
spread from there. The person does not lose consciousness during a
simple focal seizure.
Simple focal seizures with motor symptoms will affect muscle activity,
causing jerking movements of a foot, the face, an arm or another part of
the body.
It may cause sensory symptoms affecting the senses, such as: hearing
problems, hallucinations and olfactory or other distortions; as well as,
affect the senses by causing hearing problems, hallucinations and
olfactory or other distortions.
It can also strike parts of the brain that trigger emotions or memories
of previous experiences, causing feelings of fear, anxiety, or déjà vu
(the illusory feeling that something has been experienced before).
Complex focal seizures are often preceded by a simple focal seizure
(aura). When experiencing a complex focal seizure, patients may stare
blankly into space, or experience automatisms (non-purposeful,
repetitive movements such as lip smacking, blinking, grunting, gulping
or shouting).
In some cases, seizures can spread to both sides of the brain, leading to a generalized tonic-clonic seizure.
Tonic-clonic seizures are seizures that affect the muscles. Tonic
seizures cause a stiffening of muscles while clonic seizures are
characterized by jerking or twitching.
They are seizures that originate in both halves (hemispheres) of the
brain simultaneously, causing stiffness or twitching throughout the
body, known as a tonic or clonic seizure. A tonic or clonic seizure can
also begin in one area of the brain (called a partial or focal seizure),
affecting only one part of the body such as an arm or a leg. They can be partial or generalized.
A simple partial seizure is when the person knows what is
happening and is somewhat aware of his or her surroundings and may be
able to describe what happened.
A complex partial seizure is when the person does not know what is
happening, not aware of their surroundings, and does not know anything
unusual has happened.
Some reports state that some epilepsy seizures are generalized,
which means that the seizure starts in one area of the brain and then
spreads but this is an outdated term because in cases of idiopathic
generalised epilepsies (IGE) and childhood absence epilepsy (CAE) there
is now compelling evidence that the seizures start in a well defined
brain area and spread at great speed to connected brain areas recruiting
specific neuronal networks into typical oscillatory behavior.
Stroke
A stroke, also known as transient ischemic attack or cerebrovascular accident, happens when blood flow to the brain is blocked.
This prevents the brain from getting oxygen and nutrients from the
blood. Without oxygen and nutrients, brain cells begin to die within
minutes.
Stroke causes focal brain lesions that disrupt functional connectivity
(FC), a measure of activity synchronization, throughout distributed
brain networks. The disruption in FC regions is caused by damage to
cortical regions in the brain, which are various regions in the cerebral
cortex. Strokes also cause a disconnection in the white matter of one's
brain. It is shown that neurological deficits do not only arise from
focal tissue damage but also from local and remote changes in
white-matter tracts and in neural interactions among wide-spread
networks.
Aphasia
Aphasia
is a language disorder caused by damage in a specific area of the brain
that controls language expression and comprehension.
Aphasia can be the result of a stroke, head injury, brain tumor,
dementia, etc. Aphasia can occur after a subacute stroke where there are
alterations in the two distinct phase synchrony networks.
There are many types of aphasia but the main types fall into three
categories: Broca aphasia, Wernicke aphasia, and Global aphasia. In
stroke patients, lesions affecting the Broca's area (inferior frontal
gyrus or IFG), Wernicke's area (superior temporal gyrus or STG) and
connecting white matter tracts, can lead to aphasia.
Broca aphasia is when there is damage to the front portion of the language-dominant side of the brain.
It is the failure to express language. This region, located in the
posterior inferior frontal gyrus of the dominant hemisphere at Brodmann
areas 44 (pars opercularis) and 45 (pars triangularis), and the frontal
lobe make up the Broca region.
The Broca area is vital for language and also necessary for language
repetition, gesture production, sentence grammar and fluidity, and the
interpretation of others' actions.
Lesions in the Broca's area in the IFG, the lower part of the
precentral gyrus, and the opercular and insular regions are associated
with naming difficulties and overall expressive language deficits in
individuals with Broca's aphasia.
Wernicke aphasia is when there is damage to the side portion of the language-dominant part of the brain.
Wernicke's aphasia is the failure to comprehend language. It is when
there has been damage to the temporal lobe of the brain that it may
result in Wernicke's aphasia, the most common type of fluent aphasia.
People with Wernicke's aphasia may speak in long, complete sentences
that have no meaning, adding unnecessary words and even creating made-up
words. The most common cause of Wernicke's aphasia is an ischemic
stroke affecting the posterior temporal lobe of the dominant hemisphere.
Global aphasia is when there is damage to a large portion of the language-dominant side of the brain.
It is the result of damage to extensive portions of the language areas
of the brain. Individuals with global aphasia have severe communication
difficulties and may be extremely limited in their ability to speak or
comprehend language.
They may be unable to say even a few words or may repeat the same words
or phrases over and over again. They may have trouble understanding
even simple words and sentences. This aphasia is usually associated with
a large lesion in the perisylvian area. The perisylvian area is the
region around the lateral sulcus (Sylvian fissure) of the left
hemisphere and includes Broca's area and Wernicke's area.
Global aphasia is most commonly the result of a stroke in the middle
cerebral artery that supplies blood to the lateral surface of the left
hemisphere of the brain
Personality Disorders
Borderline Personality Disorder
Borderline
Personality Disorder (BPD) is a relatively rare personality disorder,
making up around 1.4% of the adult U.S. population, with women being
disproportionately affected.
BPD can be characterized by instability in self image, mood and
behavior. Impulsivity, rapid mood swings, and unstable relationships
with others are all indicators of BPD.
Similar to other disorders, BPD can be influenced by many things such
as genetic, environmental and societal factors, but researchers have
been slowly uncovering potential neurobiological explanations for
personality disorders as well. Current theories point to deficits in
connectivity between three large scale brain networks, the Default Mode
Network (DMN), the Salience Network (SN), and the medial temporal lobe
network, which is associated with memory and processing of negative
emotions.
In particular in BPD, there appears to be aberrant connectivity between
detection of salient stimuli as well as "self referential encoding"
which results in "misidentification with neutral stimuli as well as a
failure to integrate salience information with internal
representations".
Studies have also shown increased connectivity within the medial
temporal lobe as well as between areas in the medial temporal lobe and
areas in the salience network.
The frontolimbic system also shows importance in preliminary studies,
with researchers associating severity of BPD systems with severity of
deficits in frontolimbic structures and connections.
Research on neural correlates of BPD is very preliminary and more
research needs to be done on how our brains connections can inform
understanding on this disorder.
Obsessive Compulsive Personality Disorder
Obsessive
Compulsive Personality Disorder(OCPD) is a personality type where the
need for perfectionism in all aspects of life takes precedence.
Despite the fact that OCPD is the most common personality disorder in
the general population, published studies looking at the brain
correlates of this disorder are practically nonexistent.
In a recent study, ten individuals diagnosed with OCPD and ten healthy
controls underwent a clinical assessment interview and a resting-state
functional magnetic resonance imaging (fMRI) acquisition. The results
show that OCPD patients presented an increased functional connectivity
in the precuneus (i.e., a posterior node of the DMN), known to be
involved in the retrieval manipulation of past events in order to solve
current problems and develop plans for the future.
These results suggest that this key node of the DMN may play an
important role in OCPD. OCPD patients exhibit altered spontaneous neural
activity as compared to healthy controls in multiple brain regions,
which may reflect different characteristic symptoms of OCPD
pathophysiology, including cognitive inflexibility, excessive
self-control, lower empathy, and visual attention bias.