Despite
decades
of
research,
we
lack
objective
diagnostic
or
prognostic
biomarkers
mental
health
problems.
A
key
reason
for
this
limited
progress
is
a
reliance
on
the
traditional
case-control
paradigm,
which
assumes
that
each
disorder
has
single
cause
can
be
uncovered
by
comparing
average
phenotypic
values
cases
and
control
samples.
Here,
discuss
problematic
assumptions
paradigm
based
highlight
recent
efforts
seek
to
characterize,
rather
than
minimize,
inherent
clinical
biological
variability
characterizes
psychiatric
populations.
We
argue
embracing
such
will
necessary
understand
pathophysiological
mechanisms
develop
more
targeted
effective
treatments.
Research Square (Research Square),
Journal Year:
2025,
Volume and Issue:
unknown
Published: May 13, 2025
Abstract
Autism
Spectrum
Disorder
(ASD)
is
a
lifelong
neurodevelopmental
condition
characterized
by
atypical
brain
growth.
While
advances
in
neuroimaging
and
openly
sharing
large-sample
datasets
such
as
the
Brain
Imaging
Data
Exchange
(ABIDE)
have
improved
understanding
of
ASD,
most
studies
focus
on
adolescents
adults,
with
early
development-critical
for
diagnosis
intervention-remaining
underexplored.
Existing
research
predominantly
involves
Western
samples,
offering
limited
insight
generalizability
into
non-Caucasian
populations.
We
introduce
China
Consortium
(CABIC)
(https://php.bdnilab.com/resources/),
grassroots
effort
researchers
across
country
to
aggregate
previously
collected
multi-site
structural
MRI
phenotypic
information
from
1,451
autistic
children
1,119
typically
developing
children,
covering
an
age
range
childhood
school
(1.0
-
12.92
years).
Here,
we
present
this
resource
depict
growth
charts
push
forward
more
comprehensive
development
Chinese
autism
children.
constructed
that
reveal
developmental
shift
transitioning
overgrowth
delayed
maturation.
Regional
analyses
identified
distinct
trajectories
specific
regions.
Individual
deviation
scores
quantified
inter-subject
variability,
characterizing
heterogeneity
ASD.
Comparative
between
CABIC
ABIDE
highlighted
differences
potentially
attributable
ethnicity
culture,
advancing
our
cross-population
diversity.
will
be
shared
publicly
foster
investigation
potential
neural
mechanisms
underlying
ASD
non-Western
populations
support
efforts
toward
precision
medicine
individuals
diverse
backgrounds.
Psychological Medicine,
Journal Year:
2023,
Volume and Issue:
54(7), P. 1318 - 1328
Published: Nov. 10, 2023
Abstract
Background
There
is
growing
evidence
that
gray
matter
atrophy
constrained
by
normal
brain
network
(or
connectome)
architecture
in
neuropsychiatric
disorders.
However,
whether
this
finding
holds
true
individuals
with
depression
remains
unknown.
In
study,
we
aimed
to
investigate
the
association
between
and
connectome
at
individual
level
depression.
Methods
297
patients
256
healthy
controls
(HCs)
from
two
independent
Chinese
dataset
were
included:
a
discovery
(105
never-treated
first-episode
matched
130
HCs)
replication
(106
126
HCs).
For
each
patient,
individualized
regional
was
assessed
using
normative
model
regions
whose
structural
profiles
HCs
most
resembled
patterns
identified
as
putative
epicenters
backfoward
stepwise
regression
analysis.
Results
general,
of
disease
significantly
explained
44%
(±16%)
variance
atrophy.
While
demonstrated
tremendous
interindividual
variations
number
distribution
epicenters,
several
higher
participation
coefficient
than
randomly
selected
regions,
including
hippocampus,
thalamus,
medial
frontal
gyrus
shared
Other
strong
connections
exhibited
greater
vulnerability.
addition,
uncovered
distinct
subgroups
different
ages
onset.
Conclusions
These
results
suggest
elucidate
possible
pathological
progression
Molecular Autism,
Journal Year:
2023,
Volume and Issue:
14(1)
Published: Oct. 30, 2023
Abstract
Objective
There
has
been
increasing
evidence
for
atypical
white
matter
(WM)
microstructure
in
autistic
people,
but
findings
have
divergent.
The
development
of
people
early
childhood
is
clouded
by
the
concurrently
rapid
brain
growth,
which
might
lead
to
inconsistent
WM
autism.
Here,
we
aimed
reveal
developmental
nature
children
and
delineate
throughout
while
taking
considerations
into
account.
Method
In
this
study,
diffusion
tensor
imaging
was
acquired
from
two
independent
cohorts,
containing
91
100
typically
developing
(TDC),
aged
4–7
years.
Developmental
prediction
modeling
using
support
vector
regression
based
on
TDC
participants
conducted
estimate
index
children.
Then,
subgroups
were
identified
k-means
clustering
method
compared
each
other
basis
demographic
information,
index,
trait
two-sample
t-test.
Relationship
with
age
estimated
partial
correlation.
Furthermore,
performed
threshold-free
cluster
enhancement-based
t-test
group
comparison
microstructures
subgroup
rematched
subsets
TDC.
Results
We
clustered
according
index.
exhibited
distinct
stages
age-dependent
diversity.
found
negatively
associated
age.
Moreover,
an
inverse
pattern
different
clinical
manifestations
stages,
1
showing
overgrowth
low
level
traits
2
exhibiting
delayed
maturation
high
traits,
revealed.
Conclusion
This
study
illustrated
heterogeneity
delineated
stage-specific
difference
that
ranged
a
pattern.
Trial
registration
registered
at
ClinicalTrials.gov
(Identifier:
NCT02807766)
June
21,
2016
(
https://clinicaltrials.gov/ct2/show/NCT02807766
).
Despite
decades
of
research,
we
lack
objective
diagnostic
or
prognostic
biomarkers
mental
health
problems.
A
key
reason
for
this
limited
progress
is
a
reliance
on
the
traditional
case-control
paradigm,
which
assumes
that
each
disorder
has
single
cause
can
be
uncovered
by
comparing
average
phenotypic
values
cases
and
control
samples.
Here,
discuss
problematic
assumptions
paradigm
based
highlight
recent
efforts
seek
to
characterize,
rather
than
minimize,
inherent
clinical
biological
variability
characterizes
psychiatric
populations.
We
argue
embracing
such
will
necessary
understand
pathophysiological
mechanisms
develop
more
targeted
effective
treatments.