medRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2023,
Volume and Issue:
unknown
Published: Dec. 17, 2023
Abstract
Importance
Understanding
the
mechanisms
of
major
depressive
disorder
(MDD)
improvement
is
a
key
challenge
to
determine
effective
personalized
treatments.
Objective
To
perform
secondary
analysis
quantifying
neural-to-symptom
relationships
in
MDD
as
function
antidepressant
treatment.
Design
Double
blind
randomized
controlled
trial.
Setting
Multicenter.
Participants
Patients
with
early
onset
recurrent
depression
from
public
Establishing
Moderators
and
Biosignatures
Antidepressant
Response
Clinical
Care
(EMBARC)
study.
Interventions
Either
sertraline
or
placebo
during
8
weeks
(stage
1),
according
response
second
line
treatment
for
additional
2).
Main
Outcomes
Measures
identify
data-driven
pattern
symptom
variations
these
two
stages,
we
performed
Principal
Component
Analysis
(PCA)
on
individual
items
four
clinical
scales
measuring
depression,
anxiety,
suicidal
ideas
manic-like
symptoms,
resulting
univariate
measure
improvement.
We
then
investigated
how
initial
neural
factors
predicted
this
stage
1.
do
so,
extracted
resting-state
global
brain
connectivity
(GBC)
at
baseline
level
using
whole-brain
functional
network
parcellation.
In
turn,
computed
linear
model
each
parcel
scores
1
group.
Results
192
patients
(127
women),
age
37.7
years
old
(standard
deviation:
13.5),
were
included.
The
first
PC
(PC1)
capturing
20%
variation
was
similar
across
groups
2,
suggesting
reproducible
PC1
patients’
significantly
differed
1,
whereas
no
difference
evidenced
between
Global
Impressions
(CGI).
Baseline
GBC
correlated
sertraline,
but
not
Conclusions
Relevance
Using
reduction
symptoms
scales,
identified
common
profile
sertraline.
However,
patterns
that
mapped
onto
distinguished
placebo.
Our
results
underscore
mapping
circuits
vital
detect
treatment-responsive
profiles
may
aid
optimal
patient
selection
future
trials.
Key
Points
Question
What
antidepressants
placebo?
Findings
has
shared
behavioral
geometry
differs
terms
intensity
group
only.
Meaning
There
signature
can
be
more
robustly
by
neurobehavioral
features
when
it
pharmacologically
induced.
Cells,
Journal Year:
2024,
Volume and Issue:
13(10), P. 790 - 790
Published: May 7, 2024
Translational
research
in
neurological
and
psychiatric
diseases
is
a
rapidly
advancing
field
that
promises
to
redefine
our
approach
these
complex
conditions
[...]
bioRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2023,
Volume and Issue:
unknown
Published: Sept. 13, 2023
The
lifespan
growth
of
the
functional
connectome
remains
unknown.
Here,
we
assemble
task-free
and
structural
magnetic
resonance
imaging
data
from
33,250
individuals
aged
32
postmenstrual
weeks
to
80
years
132
global
sites.
We
report
critical
inflection
points
in
nonlinear
curves
mean
variance
connectome,
peaking
late
fourth
third
decades
life,
respectively.
After
constructing
a
fine-grained,
lifespan-wide
suite
system-level
brain
atlases,
show
distinct
maturation
timelines
for
segregation
within
different
systems.
Lifespan
regional
connectivity
is
organized
along
primary-to-association
cortical
axis.
These
connectome-based
normative
models
reveal
substantial
individual
heterogeneities
networks
patients
with
autism
spectrum
disorder,
major
depressive
Alzheimer's
disease.
findings
elucidate
evolution
can
serve
as
reference
quantifying
variation
development,
aging,
neuropsychiatric
disorders.
Nature Communications,
Journal Year:
2024,
Volume and Issue:
15(1)
Published: Aug. 7, 2024
Functional
magnetic
resonance
imaging
in
rodents
holds
great
potential
for
advancing
our
understanding
of
brain
networks.
Unlike
the
human
community,
there
remains
no
standardized
resource
image
processing,
analysis
and
quality
control,
posing
significant
reproducibility
limitations.
Our
software
platform,
Rodent
Automated
Bold
Improvement
EPI
Sequences,
is
a
pipeline
designed
to
address
these
limitations
preprocessing,
confound
correction,
along
with
best
practices
transparency.
We
demonstrate
robustness
preprocessing
workflow
by
validating
performance
across
multiple
acquisition
sites
both
mouse
rat
data.
Building
upon
thorough
investigation
into
data
metrics
sites,
we
introduce
guidelines
control
network
offer
recommendations
addressing
issues.
Taken
together,
this
platform
will
allow
emerging
community
adopt
reproducible
foster
progress
translational
neuroscience.
Background:
Ketamine
has
emerged
as
one
of
the
most
promising
therapies
for
treatment-resistant
depression.
However,
inter-individual
variability
in
response
to
ketamine
is
still
not
well
understood
and
it
unclear
how
ketamine’s
molecular
mechanisms
connect
its
neural
behavioral
effects.
Methods:
We
conducted
a
single-blind
placebo-controlled
study,
with
participants
blinded
their
treatment
condition.
40
healthy
received
acute
(initial
bolus
0.23
mg/kg,
continuous
infusion
0.58
mg/kg/hr).
quantified
resting-state
functional
connectivity
via
data-driven
global
brain
related
individual
ketamine-induced
symptom
variation
cortical
gene
expression
targets.
Results:
found
that:
(i)
both
effects
are
multi-dimensional,
reflecting
robust
variability;
(ii)
principal
gradient
effect
matched
somatostatin
(SST)
parvalbumin
(PVALB)
patterns
humans,
while
mean
did
not;
(iii)
mapped
onto
distinct
gradients
ketamine,
which
were
resolvable
at
single-subject
level.
Conclusions:
These
results
highlight
importance
considering
ketamine.
They
also
have
implications
development
individually
precise
pharmacological
biomarkers
selection
psychiatry.
Funding:
This
study
was
supported
by
NIH
grants
DP5OD012109-01
(A.A.),
1U01MH121766
R01MH112746
(J.D.M.),
5R01MH112189
5R01MH108590
NIAAA
grant
2P50AA012870-11
(A.A.);
NSF
NeuroNex
2015276
(J.D.M.);
Brain
Behavior
Research
Foundation
Young
Investigator
Award
SFARI
Pilot
(J.D.M.,
A.A.);
Heffter
Institute
(Grant
No.
1–190420)
(FXV,
KHP);
Swiss
Neuromatrix
2016–0111)
National
Science
under
framework
Neuron
Cofund
01EW1908)
(KHP);
Usona
(2015
–
2056)
(FXV).
Clinical
trial
number:
NCT03842800
Frontiers in Psychiatry,
Journal Year:
2023,
Volume and Issue:
14
Published: April 25, 2023
Psilocybin
may
help
treat
obsessive-compulsive
disorder
(OCD).
To
date,
only
one
open-label
study
of
psilocybin
for
OCD
exists,
necessitating
further
investigation
with
a
randomized
controlled
design.
The
neural
correlates
psilocybin's
effects
on
have
also
not
been
studied.
Scientific Data,
Journal Year:
2024,
Volume and Issue:
11(1)
Published: Aug. 2, 2024
This
article
describes
primary
data
and
resources
available
from
the
Boston
Adolescent
Neuroimaging
of
Depression
Anxiety
(BANDA)
study,
a
novel
arm
Human
Connectome
Project
(HCP).
Data
were
collected
215
adolescents
(14–17
years
old),
152
whom
had
current
diagnoses
anxiety
and/or
depressive
disorders
at
study
intake.
include
cross-sectional
structural
(T1-
T2-weighted),
functional
(resting
state
three
tasks),
diffusion-weighted
magnetic
resonance
images.
Both
unprocessed
HCP
minimally-preprocessed
imaging
are
within
release
packages.
parent
clinical
interview
data,
as
well
cognitive
neuropsychological
also
included
these
Release
packages
additionally
provide
self-report
measures
assessing
key
features
adolescent
psychopathology,
including:
anxious
symptom
dimensions,
behavioral
inhibition/activation,
exposure
to
stressful
life
events,
risk
behaviors.
Finally,
6-
12-month
longitudinal
acquired
measures.
publicly
accessible
through
National
Institute
Mental
Health
Archive
(ID:
#2505).
Molecular Autism,
Journal Year:
2025,
Volume and Issue:
16(1)
Published: March 26, 2025
Abstract
Background
Autism
spectrum
disorder
(ASD)
is
marked
by
disruptions
in
low-level
sensory
processing
and
higher-order
sociocognitive
functions,
suggesting
a
complex
interplay
between
different
brain
regions
across
the
cortical
hierarchy.
However,
developmental
trajectory
of
this
hierarchical
organization
ASD
remains
underexplored.
Herein,
we
investigated
maturational
abnormalities
hierarchy
among
individuals
with
ASD.
Methods
Resting-state
functional
magnetic
resonance
imaging
data
from
three
large-scale
datasets
were
analyzed:
Brain
Imaging
Data
Exchange
I
II
Lifespan
Human
Connectome
Project
Development
(aged
5–22
years).
The
principal
connectivity
gradient
representing
was
estimated
using
diffusion
map
embedding.
By
applying
normative
modeling
generalized
additive
model
for
location,
scale,
shape
(GAMLSS),
captured
nonlinear
trajectories
developing
gradient,
as
well
individual-level
deviations
typical
development
based
on
centile
scores
measured
curves.
A
whole-brain
summary
metric,
score,
derived
to
measure
extent
abnormal
maturation
Finally,
through
series
mediation
analyses,
examined
potential
role
network-level
connectomic
diagnoses
Results
followed
non-linear
trajectory,
showing
delayed
during
childhood
compared
that
typically
individuals,
an
accelerated
“catch-up”
phase
adolescence
subsequent
decline
young
adulthood.
nature
these
varied
networks,
attention
networks
displaying
most
pronounced
childhood,
while
particularly
default
mode
network
(DMN),
remaining
impaired
adolescence.
Mediation
analyses
revealed
persistent
reduction
DMN
segregation
throughout
key
contributor
atypical
Limitations
uneven
distribution
samples
age
groups,
later
stages
development,
limited
our
ability
fully
capture
older
individuals.
Conclusions
These
findings
highlight
importance
understanding
ASD,
collectively
early
interventions
aimed
at
promoting
may
be
critical
improving
outcomes
bioRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2025,
Volume and Issue:
unknown
Published: April 20, 2025
Abstract
Choices
are
often
affected
by
the
context
of
available
alternatives,
a
phenomenon
termed
choice
effects.
Current
models
effects
require
options
to
be
described
two
explicit
numerical
attributes.
However,
decision-makers
might
represent
these
additional
latent
We
propose
use
participants’
neural
representations
access
full
attribute
set
they
consider
and
predict
without
using
first
estimated
elicited
lotteries
behavioral
sample.
Then
we
recruited
fMRI
samples
with
preregistered
design
estimate
each
lottery
choice.
predicted
only
similarity
in
between
individual
lotteries,
improving
out-of-sample
predictions
14%
explained
variance
20%
compared
traditional
methods.
These
encoded
mixture
attributes,
previously
inaccessible
researchers
Each
cortical
area
has
a
distinct
pattern
of
anatomical
connections
within
the
thalamus,
central
subcortical
structure
composed
functionally
and
structurally
nuclei.
Previous
studies
have
suggested
that
certain
areas
may
more
extensive
target
multiple
thalamic
nuclei,
which
potentially
allows
them
to
modulate
distributed
information
flow.
However,
there
is
lack
quantitative
investigations
into
connectivity
patterns
thalamus.
Consequently,
it
remains
unknown
if
exhibit
systematic
differences
in
extent
their
To
address
this
knowledge
gap,
we
used
diffusion
magnetic
resonance
imaging
(dMRI)
perform
brain-wide
probabilistic
tractography
for
828
healthy
adults
from
Human
Connectome
Project.
We
then
developed
framework
quantify
spatial
each
area’s
Additionally,
leveraged
resting-state
functional
MRI,
myelin,
human
neural
gene
expression
data
test
thalamus
varied
along
hierarchy.
Our
results
revealed
two
cortico-thalamic
motifs:
1)
sensorimotor
motif
characterized
by
focal
targeting
posterolateral
associated
with
fast,
feed-forward
flow;
2)
an
associative
diffuse
anteromedial
slow,
feed-back
These
findings
were
consistent
across
subjects
also
observed
macaques,
indicating
cross-species
generalizability.
Overall,
our
study
demonstrates
association
support
functionally-distinct