Nature Communications,
Journal Year:
2022,
Volume and Issue:
13(1)
Published: Aug. 10, 2022
Abstract
Numerous
brain
disorders
demonstrate
structural
abnormalities,
which
are
thought
to
arise
from
molecular
perturbations
or
connectome
miswiring.
The
unique
and
shared
contributions
of
these
connectomic
vulnerabilities
remain
unknown,
has
yet
be
studied
in
a
single
multi-disorder
framework.
Using
MRI
morphometry
the
ENIGMA
consortium,
we
construct
maps
cortical
abnormalities
for
thirteen
neurodevelopmental,
neurological,
psychiatric
N
=
21,000
participants
26,000
controls,
collected
using
harmonised
processing
protocol.
We
systematically
compare
multiple
micro-architectural
measures,
including
gene
expression,
neurotransmitter
density,
metabolism,
myelination
(molecular
vulnerability),
as
well
global
measures
number
connections,
centrality,
connection
diversity
(connectomic
vulnerability).
find
relationship
between
vulnerability
white-matter
architecture
that
drives
disorder
profiles.
Local
attributes,
particularly
receptor
profiles,
constitute
best
predictors
both
disorder-specific
morphology
cross-disorder
similarity.
Finally,
consistently
subtended
by
small
subset
network
epicentres
bilateral
sensory-motor,
inferior
temporal
lobe,
precuneus,
superior
parietal
cortex.
Collectively,
our
results
highlight
how
local
attributes
connectivity
jointly
shape
abnormalities.
Advances in bioinformatics and biomedical engineering book series,
Journal Year:
2024,
Volume and Issue:
unknown, P. 246 - 272
Published: March 4, 2024
The
evolutionary
foundations
of
brain
development
represent
point
departure.
It
delves
into
the
depths
history,
unveiling
intricate
journey
that
has
shaped
human
brain.
Comparative
neuroanatomy
and
phylogeny
provide
canvas
upon
which
we
paint
portrait
our
cognitive
evolution.
contemplates
constraints,
both
genetic
epigenetic,
have
sculpted
brain's
architecture.
These
insights
serve
as
bedrock
Evolutionary
Global
Neuroscience
stands.
In
quest
to
unlock
enigmatic
complexities
brain,
emerges
a
transformative
paradigm
transcends
disciplinary
boundaries.
This
expansive
field
explores
profound
interplay
between
heritage
contemporary
challenges
in
cognition,
health,
ever-evolving
landscape
neurotechnology.
Cognition,
quintessential
hallmark
existence,
is
next
claim
attention.
interrogate
adaptive
value
cognition
across
epochs,
deciphering
its
role
survival
prosperity.
Yet,
this
age
rapid
societal
transformation,
concept
“evolutionary
mismatch”
comes
fore.
explore
how
mismatch
underlies
burgeoning
epidemic
disorders,
underscoring
urgent
need
for
new
addressing
health.
paper
illuminates
grim
modernity's
disorders.
Alzheimer's
disease
autism
spectrum
disorders
poignant
exemplars
puzzle
engulfs
us.
From
predispositions
environmental
influences,
it
multifaceted
origins
these
ever
mindful
shadows
cast
by
history.
promise
Neuroscience,
however,
not
confined
diagnosis
treatment.
extends
innovative
approaches
safeguard
well-being.
Drawing
inspiration
from
past,
uncovers
preventive
strategies,
therapeutic
interventions,
personalized
medicine
approaches.
Lifestyle
modifications
adaptations
emerge
potent
tools
preserving
resilience.
Amidst
journey,
neurotechnology
catalyst
innovation.
Neuroimaging,
brain-machine
interfaces,
neuromodulation,
artificial
intelligence
converge
redefine
boundaries
exploration.
fusion
biology
technology
holds
key
unlocking
frontiers
science,
offering
hope
individuals
grappling
with
propels
ourselve
toward
novel
discoveries,
confront
an
array
ethical
challenges.
Questions
enhancement,
informed
consent,
privacy,
equitable
access
neurotechnological
advancements
loom
large.
Our
abstract
engages
considerations,
advocating
responsible
innovation
harmonizes
values.
merely
scientific
endeavor;
call
action.
beckons
us
unite
disciplines,
fostering
interdisciplinary
collaboration
borders
cultures.
urges
invest
longitudinal
cross-cultural
research
expands
understanding
exquisite
diversity.
demands
commitment
health
literacy
thoughtful
policy
recommendations
ensure
fruits
advancement
are
accessible
all.
journeyed
through
realm
begins
past
charts
course
enlightened,
innovative,
future
mind.
Nature Communications,
Journal Year:
2022,
Volume and Issue:
13(1)
Published: Nov. 11, 2022
Abstract
Neuropsychiatric
disorders
are
increasingly
conceptualized
as
overlapping
spectra
sharing
multi-level
neurobiological
alterations.
However,
whether
transdiagnostic
cortical
alterations
covary
in
a
biologically
meaningful
way
is
currently
unknown.
Here,
we
studied
co-alteration
networks
across
six
neurodevelopmental
and
psychiatric
disorders,
reflecting
pathological
structural
covariance.
In
12,024
patients
18,969
controls
from
the
ENIGMA
consortium,
observed
that
patterns
followed
normative
connectome
organization
were
anchored
to
prefrontal
temporal
disease
epicenters.
Manifold
learning
revealed
frontal-to-temporal
sensory/limbic-to-occipitoparietal
gradients,
differentiating
shared
illness
effects
on
thickness
along
these
axes.
The
principal
gradient
aligned
with
covariance
established
transcriptomic
link
cortico-cerebello-thalamic
circuits.
Moreover,
gradients
segregated
functional
involved
basic
sensory,
attentional/perceptual,
domain-general
cognitive
processes,
distinguished
between
regional
cytoarchitectonic
profiles.
Together,
our
findings
indicate
occur
synchronized
fashion
multiple
levels
of
hierarchical
organization.
Nature Communications,
Journal Year:
2022,
Volume and Issue:
13(1)
Published: Aug. 10, 2022
Abstract
Numerous
brain
disorders
demonstrate
structural
abnormalities,
which
are
thought
to
arise
from
molecular
perturbations
or
connectome
miswiring.
The
unique
and
shared
contributions
of
these
connectomic
vulnerabilities
remain
unknown,
has
yet
be
studied
in
a
single
multi-disorder
framework.
Using
MRI
morphometry
the
ENIGMA
consortium,
we
construct
maps
cortical
abnormalities
for
thirteen
neurodevelopmental,
neurological,
psychiatric
N
=
21,000
participants
26,000
controls,
collected
using
harmonised
processing
protocol.
We
systematically
compare
multiple
micro-architectural
measures,
including
gene
expression,
neurotransmitter
density,
metabolism,
myelination
(molecular
vulnerability),
as
well
global
measures
number
connections,
centrality,
connection
diversity
(connectomic
vulnerability).
find
relationship
between
vulnerability
white-matter
architecture
that
drives
disorder
profiles.
Local
attributes,
particularly
receptor
profiles,
constitute
best
predictors
both
disorder-specific
morphology
cross-disorder
similarity.
Finally,
consistently
subtended
by
small
subset
network
epicentres
bilateral
sensory-motor,
inferior
temporal
lobe,
precuneus,
superior
parietal
cortex.
Collectively,
our
results
highlight
how
local
attributes
connectivity
jointly
shape
abnormalities.