NeuroImage Clinical,
Journal Year:
2021,
Volume and Issue:
32, P. 102811 - 102811
Published: Jan. 1, 2021
Our
current
understanding
of
autism
is
largely
based
on
clinical
experiences
and
research
involving
male
individuals
given
the
male-predominance
in
prevalence
under-inclusion
female
due
to
small
samples,
co-occurring
conditions,
or
simply
being
missed
for
diagnosis.
There
a
significantly
biased
‘male
lens’
this
field
with
autistic
females
insufficiently
understood.
We
therefore
conducted
systematic
review
examine
how
sex
gender
modulate
brain
structure
function
individuals.
Findings
from
past
20
years
are
yet
converge
specific
regions/networks
consistent
sex/gender-modulating
effects.
Despite
at
least
three
well-powered
studies
identifying
patterns
significant
sex/gender-modulation
autism-control
differences,
many
other
likely
underpowered,
suggesting
critical
need
future
investigation
into
sex/gender-based
heterogeneity
better-powered
designs.
Future
should
also
formally
investigate
effects
gender,
beyond
biological
sex,
which
mostly
absent
literature.
Understanding
roles
development
an
imperative
step
extend
field.
Science,
Journal Year:
2022,
Volume and Issue:
376(6597), P. 1070 - 1074
Published: June 2, 2022
Autism
spectrum
disorder
(ASD)
is
highly
heterogeneous.
Identifying
systematic
individual
differences
in
neuroanatomy
could
inform
diagnosis
and
personalized
interventions.
The
challenge
that
these
are
entangled
with
variation
because
of
other
causes:
unrelated
to
ASD
measurement
artifacts.
We
used
contrastive
deep
learning
disentangle
ASD-specific
neuroanatomical
from
shared
typical
control
participants.
correlated
symptoms.
structure
this
also
addresses
a
long-standing
debate
about
the
nature
ASD:
At
least
terms
neuroanatomy,
individuals
do
not
cluster
into
distinct
subtypes;
instead,
they
organized
along
continuous
dimensions
affect
sets
regions.
Communications Biology,
Journal Year:
2022,
Volume and Issue:
5(1)
Published: Sept. 27, 2022
It
is
increasingly
recognized
that
multiple
psychiatric
conditions
are
underpinned
by
shared
neural
pathways,
affecting
similar
brain
systems.
Here,
we
carried
out
a
multiscale
contextualization
of
alterations
cortical
morphology
across
six
major
(autism
spectrum
disorder,
attention
deficit/hyperactivity
depression
obsessive-compulsive
bipolar
and
schizophrenia).
Our
framework
cross-referenced
morphological
anomalies
with
respect
to
myeloarchitecture
cytoarchitecture,
as
well
connectome
neurotransmitter
organization.
Pooling
disease-related
effects
on
MRI-based
thickness
measures
ENIGMA
working
groups,
including
total
28,546
participants
(12,876
patients
15,670
controls),
identified
cortex-wide
dimension
changes
described
sensory-fugal
pattern,
paralimbic
regions
showing
the
most
consistent
conditions.
The
disease
was
closely
related
gradients
microstructure
axes,
specifically
variations
in
serotonin
dopamine.
Multiple
sensitivity
analyses
confirmed
robustness
slight
analytical
choices.
findings
embed
common
structure
scales
organization,
may
provide
insights
into
mechanisms
transdiagnostic
vulnerability.
BMC Medicine,
Journal Year:
2024,
Volume and Issue:
22(1)
Published: March 4, 2024
Abstract
Background
Autism
spectrum
disorder
(ASD)
and
attention-deficit/hyperactivity
(ADHD)
are
neurodevelopmental
disorders
with
overlapping
behavioral
features
genetic
etiology.
While
brain
cortical
thickness
(CTh)
alterations
have
been
reported
in
ASD
ADHD
separately,
the
degree
to
which
associated
common
distinct
patterns
of
CTh
changes
is
unclear.
Methods
We
searched
PubMed,
Web
Science,
Embase,
Science
Direct
from
inception
8
December
2023
included
studies
comparing
youth
(age
less
than
18)
or
typically
developing
controls
(TDC).
conducted
a
comparative
meta-analysis
vertex-based
identify
ADHD.
Results
Twelve
datasets
involving
458
individuals
10
383
were
analysis.
Compared
TDC,
showed
increased
bilateral
superior
frontal
gyrus,
left
middle
temporal
right
parietal
lobule
(SPL)
decreased
temporoparietal
junction
(TPJ).
precentral
gyri,
postcentral
TPJ
relative
TDC.
Conjunction
analysis
both
shared
reduced
located
default
mode
network
(DMN).
Comparative
analyses
indicated
had
greater
SPL
dorsal
attention
thinner
ventral
Conclusions
These
results
suggest
DMN
an
neurobiological
feature
This
alteration
together
might
be
related
altered
biological
motion
processing
ASD,
while
abnormalities
sensorimotor
systems
may
contribute
control
problems
The
disorder-specific
disparate
networks
provides
novel
insight
into
symptoms
attentional
deficits
two
disorders.
Trial
registration
PROSPERO
CRD42022370620.
Registered
on
November
9,
2022.
Molecular Psychiatry,
Journal Year:
2024,
Volume and Issue:
29(11), P. 3440 - 3451
Published: May 16, 2024
Abstract
Previous
studies
have
reported
alterations
in
cortical
thickness
autism.
However,
few
included
enough
autistic
females
to
determine
if
there
are
sex
specific
differences
structure
This
longitudinal
study
aimed
investigate
and
trajectory
of
thinning
across
childhood.
Participants
290
(88
females)
139
nonautistic
(60
individuals
assessed
at
up
4
timepoints
spanning
~2–13
years
age
(918
total
MRI
timepoints).
Estimates
early
late
childhood
as
well
the
were
modeled
using
spatiotemporal
linear
mixed
effects
models
age-by-sex-by-diagnosis.
Additionally,
spatial
correspondence
between
maps
sex-by-diagnosis
neurotypical
evaluated.
Relative
their
peers,
had
more
extensive
than
males.
These
involved
multiple
functional
networks,
mainly
characterized
by
thicker
cortex
~3
faster
females.
Cortical
regions
which
different
sexes
significantly
overlapped
with
that
differed
development.
Autistic
males
demonstrated
some
shared
rate
relative
however
these
areas
relatively
small
compared
widespread
observed
sexes.
results
support
evidence
sex-specific
neurobiology
autism
suggest
processes
regulate
differentiation
brain
contribute
etiology
medRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 17, 2025
Abstract
Autism
is
a
heterogeneous
condition,
and
functional
magnetic
resonance
imaging-based
studies
have
advanced
understanding
of
neurobiological
correlates
autistic
features.
Nevertheless,
little
work
has
focused
on
the
optimal
brain
states
to
reveal
brain-phenotype
relationships.
In
addition,
there
need
better
understand
relevance
attentional
abilities
in
mediating
Using
connectome-based
predictive
modelling,
we
interrogate
three
datasets
determine
scanning
conditions
that
can
boost
prediction
clinically
relevant
phenotypes
assess
generalizability.
dataset
one,
sample
youth
with
autism
neurotypical
participants,
find
sustained
attention
task
(the
gradual
onset
continuous
performance
task)
results
high
traits
compared
free-viewing
social
resting-state
condition.
two,
observe
network
model
generated
from
generalizes
predict
measures
adults.
three,
show
same
one
further
responsiveness
data
Brain
Imaging
Data
Exchange.
sum,
our
suggest
an
in-scanner
challenge
help
delineate
robust
markers
support
continued
investigation
under
which
psychiatric
conditions.
Autism Research,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 30, 2025
Of
the
1
in
36
individuals
United
States
who
are
diagnosed
with
autism
spectrum
disorder,
nearly
40%
also
have
intellectual
disability
(ID).
The
cortex
has
been
widely
implicated
neural
processes
underlying
autistic
behaviors
as
well
ability.
Thus,
neuroimaging
features
such
cortical
thickness
of
particular
interest
a
possible
biomarkers
condition.
However,
studies
often
fail
to
include
ID.
As
result,
there
few
across
entire
range
abilities.
This
study
used
MRI
evaluate
young
children
(n
=
88,
mean
age
5.37
years)
large
ability
(IQ
19-133)
nonautistic,
nondevelopmentally
delayed
(referred
here
typically
developing
[TD])
peers
53,
5.29
years).
We
first
investigated
associations
between
full
scale
IQ
and
both
TD
children.
Autistic
had
significant
negative
(i.e.,
thinner
cortex,
higher
IQ)
bilateral
entorhinal
right
fusiform
gyrus,
superior,
middle
inferior
temporal
gyri,
pole
that
were
not
present
Significantly
thicker
was
observed
these
regions
for
ID
≤
70)
compared
those
without.
Last,
given
reported
correspondence
severity
symptoms
ability,
we
ADOS
Calibrated
Severity
Scores
found
patterns
overlapped
degree
cortex.
Molecular Psychiatry,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Feb. 24, 2025
Abstract
Genetic
variants
linked
to
autism
are
thought
change
cognition
and
behaviour
by
altering
the
structure
function
of
brain.
Although
a
substantial
body
literature
has
identified
structural
brain
differences
in
autism,
it
is
unknown
whether
autism-associated
common
genetic
changes
cortical
macro-
micro-structure.
We
investigated
this
using
neuroimaging
data
from
adults
(UK
Biobank,
N
=
31,748)
children
(ABCD,
4928).
Using
polygenic
scores
correlations
we
observe
robust
negative
association
between
for
magnetic
resonance
imaging
derived
phenotype
neurite
density
(intracellular
volume
fraction)
general
population.
This
result
consistent
across
both
adults,
cortex
white
matter
tracts,
confirmed
correlations.
There
were
no
sex
association.
Mendelian
randomisation
analyses
provide
evidence
causal
relationship
intracellular
fraction,
although
should
be
revisited
better
powered
instruments.
Overall,
study
provides
shared
variant
genetics
density.