Brain,
Journal Year:
2024,
Volume and Issue:
147(7), P. 2483 - 2495
Published: May 3, 2024
Network
neuroscience
offers
a
unique
framework
to
understand
the
organizational
principles
of
human
brain.
Despite
recent
progress,
our
understanding
how
brain
is
modulated
by
focal
lesions
remains
incomplete.
Resection
temporal
lobe
most
effective
treatment
control
seizures
in
pharmaco-resistant
epilepsy
(TLE),
making
this
syndrome
powerful
model
study
lesional
effects
on
network
organization
young
and
middle-aged
adults.
Here,
we
assessed
downstream
consequences
lesion
its
surgical
resection
brain's
structural
connectome,
explored
reorganization
relates
clinical
variables
at
individual
patient
level.
We
included
adults
with
TLE
(n
=
37)
who
underwent
anterior
lobectomy
between
two
imaging
time
points,
as
well
age-
sex-matched
healthy
controls
comparable
31).
Core
analysis
was
projection
high-dimensional
connectome
data-derived
from
diffusion
MRI
tractography
each
subject-into
lower-dimensional
gradients.
then
compared
gradients
patients
relative
before
surgery,
tracked
surgically-induced
reconfiguration
pre-
postoperative
examined
associations
patient-specific
phenotypes.
Before
individuals
presented
marked
changes
bilateral
temporo-parietal
regions,
reflecting
an
increased
segregation
ipsilateral
rest
Surgery-induced
localized
subnetwork,
but
primarily
involved
integration
contralateral
regions
Using
partial
least-squares
analysis,
uncovered
latent
signature
underlying
reorganization,
showing
that
displayed
fronto-occipital
cortices
also
had
greater
preoperative
hippocampal
atrophy,
lower
seizure
frequency
secondarily
generalized
seizures.
Our
results
bridge
their
resections
large-scale
interindividual
variability,
thus
offering
new
avenues
examine
fundamental
malleability
JAMA Neurology,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Sept. 30, 2024
Importance
Drug-resistant
temporal
lobe
epilepsy
(TLE)
has
been
associated
with
hippocampal
pathology.
Most
surgical
treatment
strategies,
including
resection
and
responsive
neurostimulation
(RNS),
focus
on
this
disease
epicenter;
however,
imaging
alterations
distant
from
the
hippocampus,
as
well
emerging
data
trials,
suggest
conceptualizing
TLE
a
network
disorder.
Objective
To
assess
whether
brain
networks
connected
to
areas
of
atrophy
in
hippocampus
align
topography
neuroimaging
RNS
response.
Design,
Setting,
Participants
This
retrospective
case-control
study
was
conducted
between
July
2009
June
2022.
Data
collection
for
multicenter,
population-based
took
place
across
4
tertiary
referral
centers
Montréal,
Canada;
Querétaro,
México;
Nanjing,
China;
Salt
Lake
City,
Utah.
Eligible
patients
were
diagnosed
according
International
League
Against
Epilepsy
criteria
received
either
or
hippocampus.
Patients
encephalitis,
traumatic
injury,
bilateral
excluded.
Main
Outcomes
Measures
Spatial
alignment
topographies.
Results
Of
110
eligible
patients,
94
individuals
analyzed
(51
[54%]
female;
mean
[SD]
age,
31.3
[10.9]
years).
Hippocampal
thickness
maps
compared
120
healthy
control
(66
[55%]
29.8
[9.5]
years),
identified.
Using
an
atlas
normative
connectivity
(n
=
1000),
2
identified
that
functionally
atrophy.
The
first
defined
by
positive
correlations
temporolimbic,
medial
prefrontal,
parietal
regions,
whereas
second
negative
frontoparietal
regions.
White
matter
changes
colocalized
(
t
93
–3.82;
P
2.44
×
10
−4
).
In
contrast,
cortical
localized
3.54;
6.29
−3
additional
38
(20
[53%]
35.8
[11.3]
years)
treated
RNS,
stimulation
site
atrophied
regions
within
seizure
reduction
212
−2.74;
.007).
Conclusions
Relevance
findings
indicate
distributed
pathology
may
occur
epicenter.
Connectivity
these
same
improvement
following
RNS.
A
approach
reveal
therapeutic
targets
outside
traditional
target
Network Neuroscience,
Journal Year:
2024,
Volume and Issue:
8(4), P. 1009 - 1031
Published: Jan. 1, 2024
Abstract
The
study
of
large-scale
brain
connectivity
is
increasingly
adopting
unsupervised
approaches
that
derive
low-dimensional
spatial
representations
from
high-dimensional
connectomes,
referred
to
as
gradient
analysis.
When
translating
this
approach
interindividual
variations
in
connectivity,
one
technical
issue
pertains
the
selection
an
appropriate
group-level
template
which
individual
gradients
are
aligned.
Here,
we
compared
different
construction
strategies
using
functional
and
structural
connectome
data
neurotypical
controls
individuals
with
autism
spectrum
disorder
(ASD)
identify
between-group
differences.
We
studied
multimodal
magnetic
resonance
imaging
obtained
Autism
Brain
Imaging
Data
Exchange
(ABIDE)
Initiative
II
Human
Connectome
Project
(HCP).
designed
six
varied
whether
(1)
they
included
typical
addition
ASD;
or
(2)
mapped
dataset
onto
another.
found
aligning
a
combined
subject
ASD
control
subjects
ABIDE
HCP
exhibited
most
pronounced
effect
size.
This
strategy
showed
robust
identification
ASD-related
regions
for
both
across
settings.
Replicating
findings
on
focal
epilepsy
demonstrated
generalizability
our
approach.
Our
will
contribute
improving
gradient-based
research.
bioRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2024,
Volume and Issue:
unknown
Published: June 14, 2024
Abstract
It
is
increasingly
common
to
statistically
compare
macroscopic
brain
maps
assess
how
spatially
similar
they
are.
Due
the
presence
of
spatial
autocorrelation,
statistical
inference
can
be
challenging;
address
this,
random
permutation
approaches
based
on
null
models
are
widely
used.
Here,
we
show
that
heterogeneity
in
autocorrelation
across
may
affect
for
correlated
maps.
In
response,
highlight
need
explicitly
model
processes,
including
non-stationarity,
more
accurate
inference.
We
illustrate
a
Bayesian
regression
approach
applied
functional
and
structural
cortical
maps,
even
heterogeneity.
By
modelling
processes
underlying
data,
much
wider
sophisticated
range
neurobiological
questions
answered
about
relationship
between
than
with
current
approaches.
Brain,
Journal Year:
2024,
Volume and Issue:
unknown
Published: June 23, 2024
Abstract
Considering
the
growing
age
of
world
population,
incidence
epilepsy
in
older
adults
is
expected
to
increase
significantly.
It
has
been
suggested
that
late-onset
temporal
lobe
(LO-TLE)
may
be
neurodegenerative
origin
and
overlap
with
Alzheimer’s
disease
(AD).
Herein,
we
aimed
characterize
pattern
cortical
atrophy
CSF
biomarkers
AD
(total
phosphorylated
tau
amyloid-β)
a
selected
population
LO-TLE
unknown
origin.
We
prospectively
enrolled
individuals
onset
after
50
no
cognitive
impairment.
They
underwent
structural
MRI
scan
measurement.
Imaging
data
were
compared
three
retrospectively
collected
groups:
(i)
age-sex-matched
healthy
controls;
(ii)
patients
mild
impairment
(MCI)
abnormal
(MCI-AD);
(iii)
MCI
normal
(MCI-noAD).
From
pool
52
patients,
20
consecutive
eligible
mean
duration
1.8
years
recruited.
As
control
populations,
25
MCI-AD,
MCI-noAD
controls
enrolled.
returned
values
LO-TLE,
significantly
different
from
due
AD.
There
differences
cortico-subcortical
between
controls,
while
demonstrated
widespread
injuries
structures.
Individuals
characterized
by
short
amyloid-β
protein
levels,
showed
patterns
thickness
subcortical
volumes
not
but
highly
MCI,
either
or
not.
Advanced Science,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 13, 2025
Abstract
Excitation‐inhibition
(E/I)
imbalance
is
theorized
as
a
key
mechanism
in
the
pathophysiology
of
epilepsy,
with
ample
research
focusing
on
elucidating
its
cellular
manifestations.
However,
few
studies
investigate
E/I
at
macroscale,
whole‐brain
level,
and
microcircuit‐level
mechanisms
clinical
significance
remain
incompletely
understood.
Here,
Hurst
exponent,
an
index
ratio,
computed
from
resting‐state
fMRI
time
series,
microcircuit
parameters
are
simulated
using
biophysical
models.
A
broad
decrease
exponent
observed
pharmaco‐resistant
temporal
lobe
epilepsy
(TLE),
suggesting
more
excitable
network
dynamics.
Connectome
decoders
point
to
temporolimbic
frontocentral
cortices
plausible
epicenters
imbalance.
Furthermore,
computational
simulations
reveal
that
enhancing
cortical
excitability
TLE
reflects
atypical
increases
recurrent
connection
strength
local
neuronal
ensembles.
Mixed
cross‐sectional
longitudinal
analyses
show
stronger
ratio
elevation
patients
longer
disease
duration,
frequent
electroclinical
seizures
well
interictal
epileptic
spikes,
worse
cognitive
functioning.
exponent‐informed
classifiers
discriminate
healthy
controls
high
accuracy
(72.4%
[57.5%–82.5%]).
Replicated
independent
dataset,
this
work
provides
vivo
evidence
macroscale
shift
balance
points
progressive
functional
imbalances
relate
decline.
bioRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 17, 2025
A
bstract
Temporal
lobe
epilepsy
with
hippocampal
sclerosis
(TLE-HS)
is
associated
a
complex
genetic
architecture,
but
the
translation
from
risk
factors
to
brain
vulnerability
remains
unclear.
Here,
we
examined
associations
between
epilepsy-related
polygenic
scores
for
HS
(PRS-HS)
and
structure
in
large
sample
of
neurotypical
children,
correlated
these
signatures
case-control
findings
multicentric
cohorts
patients
TLE-HS.
Imaging-genetic
analyses
revealed
PRS-related
cortical
thinning
temporo-parietal
fronto-central
regions,
strongly
anchored
distinct
functional
structural
network
epicentres.
Compared
disease-related
effects
derived
cohorts,
correlates
PRS-HS
mirrored
atrophy
epicentre
patterns
By
identifying
potential
pathway
disease
mechanisms,
our
provide
new
insights
into
underpinnings
alterations
TLE-HS
highlight
imaging-genetic
biomarkers
early
stratification
personalized
interventions.
Frontiers in Neuroscience,
Journal Year:
2025,
Volume and Issue:
19
Published: March 17, 2025
Age-related
hearing
loss
(ARHL)
is
a
common
sensory
disability
among
older
adults
and
considered
risk
factor
for
the
development
of
dementia.
Previous
work
has
shown
altered
brain
connectome
topology
in
ARHL,
including
abnormal
nodal
strength
clustering
coefficient.
However,
whether
ARHL
affects
hierarchical
organization
structural
how
these
alterations
relate
to
transcriptomic
signatures
remain
unknown.
Here,
we
apply
gradient
mapping
framework
derived
from
diffusion
magnetic
resonance
imaging.
We
focus
on
first
three
gradients
that
reflect
distinct
connectome,
assess
ARHL-related
changes.
find
that,
compared
controls,
patients
exhibit
widespread
disruptions
organization,
spanning
primary
areas
(e.g.,
somatomotor
network)
high-order
association
default
mode
network).
Subsequently,
by
employing
subcortical-weighted
weighting
cortical
subcortical-cortical
connectivity,
observe
show
significantly
connectivity
left
caudate,
nucleus
accumbens,
right
hippocampus,
amygdala.
Finally,
investigate
relationship
between
gene
expression
gradients.
are
associated
with
weighted
profiles,
relevant
genes
preferentially
enriched
inorganic
ion
transmembrane
transport
terms
related
regulating
biological
processes.
Taken
together,
findings
highlight
hierarchy
reveal
relevance
abnormalities,
contributing
richer
understanding
neurobiological
substrates
ARHL.
The
zona
incerta
(ZI)
is
a
deep
brain
region
originally
described
by
Auguste
Forel
as
an
“immensely
confusing
area
about
which
nothing
can
be
said.”
Despite
the
elusive
nature
of
this
structure,
mounting
evidence
supports
role
ZI
and
surrounding
regions
across
diverse
range
functions
candidate
target
for
neuromodulatory
therapies.
Using
in
vivo
diffusion
MRI
data-driven
connectivity,
we
identify
topographic
organization
between
neocortex.
Specifically,
our
methods
rostral-caudal
gradient
predominantly
connecting
frontopolar
ventral
prefrontal
cortices
with
rostral
ZI,
primary
sensorimotor
caudal
ZI.
Moreover,
demonstrate
how
clustering
approaches
build
complementary
including
facilitating
mapping
central
connected
dorsal
cortex.
These
results
were
shown
to
replicable
multiple
datasets
at
individual
subject
level,
building
important
mediating
frontal
lobe-associated
tasks,
ranging
from
motor
cognitive
emotional
control.
Finally,
consider
impact
on
refinement
targets.
pave
way
increasingly
detailed
understanding
substructures,
considerations
targeting
neuromodulation.
The
zona
incerta
(ZI)
is
a
deep
brain
region
originally
described
by
Auguste
Forel
as
an
“immensely
confusing
area
about
which
nothing
can
be
said.”
Despite
the
elusive
nature
of
this
structure,
mounting
evidence
supports
role
ZI
and
surrounding
regions
across
diverse
range
functions
candidate
target
for
neuromodulatory
therapies.
Using
in
vivo
diffusion
MRI
data-driven
connectivity,
we
identify
topographic
organization
between
neocortex.
Specifically,
our
methods
rostral-caudal
gradient
predominantly
connecting
frontopolar
ventral
prefrontal
cortices
with
rostral
ZI,
primary
sensorimotor
caudal
ZI.
Moreover,
demonstrate
how
clustering
approaches
build
complementary
including
facilitating
mapping
central
connected
dorsal
cortex.
These
results
were
shown
to
replicable
multiple
datasets
at
individual
subject
level,
building
important
mediating
frontal
lobe-associated
tasks,
ranging
from
motor
cognitive
emotional
control.
Finally,
consider
impact
on
refinement
targets.
pave
way
increasingly
detailed
understanding
substructures,
considerations
targeting
neuromodulation.