Imaging Neuroscience,
Journal Year:
2024,
Volume and Issue:
2, P. 1 - 22
Published: Jan. 1, 2024
Abstract
The
brain’s
biological
age
has
been
considered
as
a
promising
candidate
for
neurologically
significant
biomarker.
However,
recent
results
based
on
longitudinal
magnetic
resonance
imaging
(MRI)
data
have
raised
questions
its
interpretation.
A
central
question
is
whether
an
increased
of
the
brain
indicative
pathology
and
if
changes
in
correlate
with
diagnosed
(state
hypothesis).
Alternatively,
could
discrepancy
be
stable
characteristic
unique
to
each
individual
(trait
hypothesis)?
To
address
this
question,
we
present
comprehensive
study
aging
clinical
Electroencephalography
(EEG),
which
complementary
previous
MRI-based
investigations.
We
apply
state-of-the-art
temporal
convolutional
network
(TCN)
task
regression.
train
recordings
Temple
University
Hospital
EEG
Corpus
(TUEG)
explicitly
labeled
non-pathological
evaluate
subjects
well
pathological
recordings,
both
examinations
at
single
point
time
TUH
Abnormal
(TUAB)
repeated
over
time.
Therefore,
created
four
novel
subsets
TUEG
that
include
multiple
recordings:
(RNP):
all
non-pathological;
(RP):
pathological;
transition
non-patholoigical
(TNPP):
least
one
recording
followed
by
(TPNP):
similar
TNPP
but
opposing
(first
then
non-pathological).
show
our
TCN
reaches
performance
decoding
TUAB
mean
absolute
error
6.6
years
R2
score
0.73.
Our
extensive
analyses
demonstrate
model
underestimates
subjects,
latter
significantly
(-1
-5
years,
paired
t-test,
p
=
0.18
6.6e−3).
Furthermore,
there
exist
differences
average
gap
between
(RNP
vs.
RP)
(-4
-7.48
permutation
test,
1.63e−2
1e−5).
find
mixed
regarding
significance
classification
While
it
datasets
RNP
versus
RP
(61.12%
60.80%
BACC,
1.32e−3
1e−5),
not
TPNP
(44.74%
47.79%
0.086
0.483).
Additionally,
these
scores
are
clearly
inferior
ones
obtained
from
direct
86%
BACC
higher.
evidence
change
status
within
relates
(0.46
1.35
0.825
0.43;
Wilcoxon-Mann-Whitney
Brunner-Munzel
0.13).
findings,
thus,
support
trait
rather
than
state
hypothesis
estimates
derived
EEG.
In
summary,
findings
indicate
neural
underpinnings
likely
more
multifaceted
previously
thought,
taking
into
account
will
benefit
interpretation
empirically
observed
dynamics.
Human Brain Mapping,
Journal Year:
2022,
Volume and Issue:
44(3), P. 1118 - 1128
Published: Nov. 8, 2022
Abstract
Machine
learning
has
been
increasingly
applied
to
neuroimaging
data
predict
age,
deriving
a
personalized
biomarker
with
potential
clinical
applications.
The
scientific
and
value
of
these
models
depends
on
their
applicability
independently
acquired
scans
from
diverse
sources.
Accordingly,
we
evaluated
the
generalizability
two
brain
age
that
were
trained
across
lifespan
by
applying
them
three
distinct
early‐life
samples
participants
aged
8–22
years.
These
chosen
based
size
diversity
training
data,
but
they
also
differed
greatly
in
processing
methods
predictive
algorithms.
Specifically,
one
model
was
built
gradient
tree
boosting
(GTB)
extracted
features
cortical
thickness,
surface
area,
volume.
other
2D
convolutional
neural
network
(DBN)
minimally
preprocessed
slices
T1‐weighted
scans.
Additional
variants
created
understand
how
changed
when
each
became
more
similar
test
terms
acquisition
protocols.
Our
results
illustrated
numerous
trade‐offs.
GTB
predictions
relatively
accurate
overall
yielded
reliable
lower
quality
In
contrast,
DBN
displayed
most
utility
detecting
associations
between
gaps
cognitive
functioning.
Broadly
speaking,
largest
limitations
affecting
protocol
differences
biased
estimates.
If
such
confounds
could
eventually
be
removed
without
post‐hoc
corrections,
may
have
greater
as
biomarkers
healthy
aging.
Human Brain Mapping,
Journal Year:
2023,
Volume and Issue:
44(10), P. 4101 - 4119
Published: May 17, 2023
Unveiling
the
details
of
white
matter
(WM)
maturation
throughout
ageing
is
a
fundamental
question
for
understanding
brain.
In
an
extensive
comparison
brain
age
predictions
and
age-associations
WM
features
from
different
diffusion
approaches,
we
analyzed
UK
Biobank
magnetic
resonance
imaging
(dMRI)
data
across
midlife
older
(N
=
35,749,
44.6-82.8
years
age).
Conventional
advanced
dMRI
approaches
were
consistent
in
predicting
age.
WM-age
associations
indicate
steady
microstructure
degeneration
with
increasing
to
ages.
Brain
was
estimated
best
when
combining
showing
aspects
contributing
Fornix
found
as
central
region
complement
forceps
minor
another
important
region.
These
regions
exhibited
general
pattern
positive
intra
axonal
water
fractions,
axial,
radial
diffusivities,
negative
relationships
mean
fractional
anisotropy,
kurtosis.
We
encourage
application
multiple
detailed
insights
into
WM,
further
investigation
fornix
potential
biomarkers
ageing.
Sensors,
Journal Year:
2023,
Volume and Issue:
23(7), P. 3622 - 3622
Published: March 30, 2023
Machine
learning
(ML)
has
transformed
neuroimaging
research
by
enabling
accurate
predictions
and
feature
extraction
from
large
datasets.
In
this
study,
we
investigate
the
application
of
six
ML
algorithms
(Lasso,
relevance
vector
regression,
support
extreme
gradient
boosting,
category
boost,
multilayer
perceptron)
to
predict
brain
age
for
middle-aged
older
adults,
which
is
a
crucial
area
in
neuroimaging.
Despite
plethora
proposed
models,
there
no
clear
consensus
on
how
achieve
better
performance
prediction
population.
Our
study
stands
out
evaluating
impact
both
image
modalities
using
cohort
cognitively
normal
adults
aged
44.6
82.3
years
old
(N
=
27,842)
with
modalities.
We
found
that
predictive
more
reliant
used
than
employed.
Specifically,
our
highlights
superior
T1-weighted
MRI
diffusion-weighted
imaging
demonstrates
multi-modality-based
significantly
enhances
compared
unimodality.
Moreover,
identified
Lasso
as
most
algorithm
predicting
age,
achieving
lowest
mean
absolute
error
single-modality
multi-modality
predictions.
Additionally,
also
ranked
highest
comprehensive
evaluation
relationship
between
BrainAGE
five
frequently
mentioned
BrainAGE-related
factors.
Notably,
shows
ensemble
outperforms
when
computational
efficiency
not
concern.
Overall,
provides
valuable
insights
into
development
reliable
models
significant
implications
clinical
practice
research.
findings
highlight
importance
modality
selection
emphasize
promising
prediction.
Molecular Psychiatry,
Journal Year:
2023,
Volume and Issue:
28(7), P. 3111 - 3120
Published: May 10, 2023
Abstract
The
difference
between
chronological
age
and
the
apparent
of
brain
estimated
from
imaging
data—the
gap
(BAG)—is
widely
considered
a
general
indicator
health.
Converging
evidence
supports
that
BAG
is
sensitive
to
an
array
genetic
nongenetic
traits
diseases,
yet
few
studies
have
examined
architecture
its
corresponding
causal
relationships
with
common
disorders.
Here,
we
estimate
using
state-of-the-art
neural
networks
trained
on
scans
53,542
individuals
(age
range
3–95
years).
A
genome-wide
association
analysis
across
28,104
(40–84
years)
UK
Biobank
revealed
eight
independent
genomic
regions
significantly
associated
(
p
<
5
×
10
−8
)
implicating
neurological,
metabolic,
immunological
pathways
–
among
which
seven
are
novel.
No
significant
correlations
or
were
found
for
Parkinson’s
disease,
major
depressive
disorder,
schizophrenia,
but
two-sample
Mendelian
randomization
indicated
influence
AD
=
7.9
−4
bipolar
disorder
1.35
−2
BAG.
These
results
emphasize
polygenic
provide
insights
into
relationship
selected
neurological
neuropsychiatric
disorders
Human Brain Mapping,
Journal Year:
2024,
Volume and Issue:
45(4)
Published: March 1, 2024
Abstract
Estimated
age
from
brain
MRI
data
has
emerged
as
a
promising
biomarker
of
neurological
health.
However,
the
absence
large,
diverse,
and
clinically
representative
training
datasets,
along
with
complexity
managing
heterogeneous
data,
presents
significant
barriers
to
development
accurate
generalisable
models
appropriate
for
clinical
use.
Here,
we
present
deep
learning
framework
trained
on
routine
(
N
up
18,890,
range
18–96
years).
We
five
separate
prediction
(all
mean
absolute
error
≤4.0
years,
R
2
≥
.86)
across
different
sequences
(T
‐weighted,
T
‐FLAIR,
1
diffusion‐weighted,
gradient‐recalled
echo
*‐weighted).
Our
offer
dual
functionality.
First,
they
have
potential
be
directly
employed
data.
Second,
can
used
foundation
further
refinement
accommodate
other
(and
therefore
scenarios
which
employ
such
sequences).
This
adaptation
process,
enabled
by
transfer
learning,
proved
effective
in
our
study
scan
orientations,
including
those
differed
considerably
original
datasets.
Crucially,
findings
suggest
that
this
approach
remains
viable
even
limited
availability
(as
low
=
25
fine‐tuning),
thus
broadening
application
estimation
more
diverse
contexts
patient
populations.
By
making
these
publicly
available,
aim
provide
scientific
community
versatile
toolkit,
promoting
research
related
areas.
Human Brain Mapping,
Journal Year:
2024,
Volume and Issue:
45(5)
Published: March 23, 2024
Abstract
While
neurological
manifestations
are
core
features
of
Fabry
disease
(FD),
quantitative
neuroimaging
biomarkers
allowing
to
measure
brain
involvement
lacking.
We
used
deep
learning
and
the
brain‐age
paradigm
assess
whether
FD
patients'
brains
appear
older
than
normal
validate
brain‐predicted
age
difference
(brain‐PAD)
as
a
possible
severity
biomarker.
MRI
scans
patients
healthy
controls
(HCs)
from
single
Institution
were,
retrospectively,
studied.
The
stabilization
index
(FASTEX)
was
recorded
severity.
Using
minimally
preprocessed
3D
T1‐weighted
subjects
eight
publicly
available
sources
(
N
=
2160;
mean
33
years
[range
4–86]),
we
trained
model
predicting
chronological
based
on
DenseNet
architecture
it
generate
predictions
in
internal
cohort.
Within
linear
modeling
framework,
brain‐PAD
tested
for
age/sex‐adjusted
associations
with
diagnostic
group
(FD
vs.
HC),
FASTEX
score,
both
global
voxel‐level
measures.
studied
52
(40.6
±
12.6
years;
28F)
58
HC
(38.4
13.4
28F).
achieved
accurate
out‐of‐sample
performance
(mean
absolute
error
4.01
years,
R
2
.90).
had
significantly
higher
(estimated
marginal
means:
3.1
−0.1,
p
.01).
Brain‐PAD
associated
score
B
0.10,
.02),
parenchymal
fraction
−153.50,
.001),
white
matter
hyperintensities
load
0.85,
.01),
tissue
volume
reduction
throughout
brain.
demonstrated
that
normal.
correlates
FD‐related
multi‐organ
damage
is
influenced
by
hyperintensities,
offering
comprehensive
biomarker
(neurological)
NeuroImage,
Journal Year:
2023,
Volume and Issue:
269, P. 119911 - 119911
Published: Jan. 30, 2023
To
learn
multiscale
functional
connectivity
patterns
of
the
aging
brain,
we
built
a
brain
age
prediction
model
measures
at
seven
scales
on
large
fMRI
dataset,
consisting
resting-state
scans
4186
individuals
with
wide
range
(22
to
97
years,
an
average
63)
from
five
cohorts.
We
computed
individual
subjects
using
personalized
network
computational
method,
harmonized
multiple
datasets
in
order
build
model,
and
finally
evaluated
how
gap
correlated
cognitive
subjects.
Our
study
has
revealed
that
were
more
informative
than
those
any
single
scale
for
prediction,
data
harmonization
significantly
improved
performance,
measures'
tangent
space
worked
better
their
original
space.
Moreover,
scores
derived
clinical
measures.
Overall,
these
results
demonstrated
learned
large-scale
multi-site
rsfMRI
dataset
characterizing
was
associated
npj Digital Medicine,
Journal Year:
2024,
Volume and Issue:
7(1)
Published: May 2, 2024
Deep
learning
approaches
for
clinical
predictions
based
on
magnetic
resonance
imaging
data
have
shown
great
promise
as
a
translational
technology
diagnosis
and
prognosis
in
neurological
disorders,
but
its
impact
has
been
limited.
This
is
partially
attributed
to
the
opaqueness
of
deep
models,
causing
insufficient
understanding
what
underlies
their
decisions.
To
overcome
this,
we
trained
convolutional
neural
networks
structural
brain
scans
differentiate
dementia
patients
from
healthy
controls,
applied
layerwise
relevance
propagation
procure
individual-level
explanations
model
predictions.
Through
extensive
validations
demonstrate
that
deviations
recognized
by
corroborate
existing
knowledge
aberrations
dementia.
By
employing
explainable
classifier
longitudinal
dataset
with
mild
cognitive
impairment,
show
spatially
rich
complement
prediction
when
forecasting
transition
help
characterize
biological
manifestation
disease
individual
brain.
Overall,
our
work
exemplifies
potential
artificial
intelligence
precision
medicine.