Medical Physics,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Oct. 10, 2024
Abstract
Background
Quantitative
imaging
biomarkers
(QIBs)
can
characterize
tumor
heterogeneity
and
provide
information
for
biological
guidance
in
radiotherapy
(RT).
Time‐dependent
diffusion
MRI
(TDD‐MRI)
derived
parameters
are
promising
QIBs,
as
they
describe
tissue
microstructure
with
more
specificity
than
traditional
diffusion‐weighted
(DW‐MRI).
Specifically,
TDD‐MRI
about
both
restricted
diffusional
exchange,
which
the
two
time‐dependent
effects
affecting
tissue,
relevant
tumors.
However,
exhaustive
modeling
of
require
long
acquisitions
complex
model
fitting.
Furthermore,
several
introduced
measurements
high
gradient
strengths
and/or
waveforms
that
possibly
not
available
RT
settings.
Purpose
In
this
study,
we
investigated
feasibility
a
simple
analysis
framework
detection
exchange
signal.
To
promote
clinical
applicability,
use
standard
on
conventional
1.5
T
system
moderate
strength
(
G
max
=
45
mT/m),
hybrid
MRI‐Linac
low
15
mT/m).
Methods
Restricted
were
simulated
geometries
mimicking
to
investigate
DW‐MRI
signal
behavior
determine
optimal
experimental
parameters.
was
implemented
using
pulsed
field
spin
echo
optimized
MRI‐Linac.
Experiments
green
asparagus
10
patients
brain
lesions
performed
evaluate
(TDD)
contrast
source
DW‐images.
Results
Simulations
demonstrated
how
TDD
able
differentiate
only
dominating
smaller
cells
from
larger
cells.
The
maximal
simulations
typical
cancer
cell
sizes
exceeded
5%
but
remained
below
particular,
r
5–10
µm)
or
around
2%
strength.
measured
MRI,
found
sub‐regions
reflecting
either
compared
noisy
appearing
white
matter.
Conclusions
On
system,
maps
showed
consistent
indicating
different
effects,
potentially
providing
spatial
heterogeneity.
MRI‐Linac,
same
trends
close
measurement
noise
levels
when
common
sizes.
systems
strengths,
could
be
used
tool
identify
include
choosing
biophysical
specific
characterization.
NMR in Biomedicine,
Journal Year:
2024,
Volume and Issue:
37(4)
Published: Jan. 2, 2024
The
increasing
availability
of
high‐performance
gradient
systems
in
human
MRI
scanners
has
generated
great
interest
diffusion
microstructural
imaging
applications
such
as
axonal
diameter
mapping.
Practically,
sensitivity
to
axon
is
attained
at
strong
weightings
,
where
the
deviation
from
expected
scaling
white
matter
yields
a
finite
transverse
diffusivity,
which
then
translated
into
an
estimate.
While
axons
are
usually
modeled
perfectly
straight,
impermeable
cylinders,
local
variations
(caliber
variation
or
beading)
and
direction
(undulation)
known
influence
estimates
have
been
observed
microscopy
data
axons.
In
this
study,
we
performed
Monte
Carlo
simulations
reconstructed
three‐dimensional
electron
temporal
lobe
specimen
using
simulated
sequence
parameters
matched
maximal
strength
next‐generation
Connectome
2.0
scanner
(
500
mT/m).
We
show
that
estimation
accurate
for
nonbeaded,
nonundulating
fibers;
however,
fibers
with
caliber
undulations,
heavily
underestimated
due
variations,
effect
overshadows
overestimation
undulations.
This
unexpected
underestimation
may
originate
coarse‐grained
axial
diffusivity
variations.
Given
increased
beading
undulations
pathological
tissues,
traumatic
brain
injury
ischemia,
interpretation
alterations
pathology
be
significantly
confounded.
Magnetic Resonance in Medicine,
Journal Year:
2025,
Volume and Issue:
unknown
Published: April 28, 2025
Abstract
Purpose
To
experimentally
evaluate
the
change
in
radial
diffusivity
with
diffusion
time
()
as
a
simple
estimate
of
axon
diameter.
Methods
Ex
vivo
ferret
spinal
cords
were
imaged
via
MRI
and
scanning
electron
microscopy.
Region‐of‐interest
comparisons
made
between
area‐weighted
mean
diameter,
,
derived
from
Additional
quantitative
myelin
metrics.
Results
A
strong
linear
correlation
was
found
.
Negative
correlations
water
fraction
well
bound
pool
Conclusion
The
value
is
shown
to
be
good
size
ex
regardless
variations
content,
indicated
by
MRI.
This
work
proposes
µGUIDE:
a
general
Bayesian
framework
to
estimate
posterior
distributions
of
tissue
microstructure
parameters
from
any
given
biophysical
model
or
signal
representation,
with
exemplar
demonstration
in
diffusion-weighted
magnetic
resonance
imaging.
Harnessing
new
deep
learning
architecture
for
automatic
feature
selection
combined
simulation-based
inference
and
efficient
sampling
the
distributions,
µGUIDE
bypasses
high
computational
time
cost
conventional
approaches
does
not
rely
on
acquisition
constraints
define
model-specific
summary
statistics.
The
obtained
allow
highlight
degeneracies
present
definition
quantify
uncertainty
ambiguity
estimated
parameters.
Frontiers in Neuroinformatics,
Journal Year:
2023,
Volume and Issue:
17
Published: Aug. 1, 2023
Monte-Carlo
diffusion
simulations
are
a
powerful
tool
for
validating
tissue
microstructure
models
by
generating
synthetic
diffusion-weighted
magnetic
resonance
images
(DW-MRI)
in
controlled
environments.
This
is
fundamental
understanding
the
link
between
micrometre-scale
properties
and
DW-MRI
signals
measured
at
millimetre-scale,
optimizing
acquisition
protocols
to
target
of
interest,
exploring
robustness
accuracy
estimation
methods.
However,
accurate
require
substrates
that
reflect
main
microstructural
features
studied
tissue.
To
address
this
challenge,
we
introduce
novel
computational
workflow,
CACTUS
(Computational
Axonal
Configurator
Tailored
Ultradense
Substrates),
white
matter
substrates.
Our
approach
allows
constructing
with
higher
packing
density
than
existing
methods,
up
95%
intra-axonal
volume
fraction,
larger
voxel
sizes
500μm3
rich
fibre
complexity.
generates
bundles
angular
dispersion,
bundle
crossings,
variations
along
fibres
their
inner
outer
radii
g-ratio.
We
achieve
introducing
global
cost
function
radial
growth
match
predefined
targeted
characteristics
mirror
those
reported
histological
studies.
improves
development
complex
substrates,
paving
way
future
applications
imaging.
This
work
proposes
µGUIDE:
a
general
Bayesian
framework
to
estimate
posterior
distributions
of
tissue
microstructure
parameters
from
any
given
biophysical
model
or
signal
representation,
with
exemplar
demonstration
in
diffusion-weighted
magnetic
resonance
imaging.
Harnessing
new
deep
learning
architecture
for
automatic
feature
selection
combined
simulation-based
inference
and
efficient
sampling
the
distributions,
µGUIDE
bypasses
high
computational
time
cost
conventional
approaches
does
not
rely
on
acquisition
constraints
define
model-specific
summary
statistics.
The
obtained
allow
highlight
degeneracies
present
definition
quantify
uncertainty
ambiguity
estimated
parameters.
bioRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2024,
Volume and Issue:
unknown
Published: Aug. 6, 2024
Abstract
Water
exchange
is
increasingly
recognized
as
an
important
biological
process
that
can
affect
the
study
of
tissue
using
diffusion
MR.
Methods
to
measure
exchange,
however,
remain
immature
opposed
those
used
characterize
restriction,
with
no
consensus
on
optimal
pulse
sequence(s)
or
signal
model(s).
In
general,
trend
has
been
towards
data-intensive
fitting
highly
parameterized
models.
We
take
opposite
approach
and
show
a
judicious
sub-sample
spectroscopy
(DEXSY)
data
be
robustly
quantify
well
in
data-efficient
manner.
This
sampling
produces
ratio
two
points
per
mixing
time:
(i)
one
point
equal
weighting
both
encoding
periods,
which
gives
maximal
contrast,
(ii)
same
total
just
first
period,
for
normalization.
call
this
quotient
Diffusion
EXchange
Ratio
(DEXR).
Furthermore,
we
it
probe
time-dependent
by
estimating
velocity
autocorrelation
function
(VACF)
over
intermediate
long
times
(∼
2
−
500
ms).
provide
comprehensive
theoretical
framework
design
DEXR
experiments
case
static
constant
gradients.
Data
from
Monte
Carlo
simulations
acquired
fixed
viable
ex
vivo
neonatal
mouse
spinal
cord
permanent
magnet
system
are
presented
test
validate
approach.
cord,
report
following
apparent
parameters
6
points:
τ
k
=
17
±
4
ms,
f
NG
0.71
0.01,
R
eff
1.10
0.01
μ
m,
0.21
0.06
m/ms,
correspond
time,
restricted
non-Gaussian
fraction,
effective
spherical
radius,
permeability,
respectively.
For
VACF,
long-time,
power-law
scaling
≈
t
2.4
,
approximately
consistent
disordered
domains
3-D.
Overall,
method
shown
efficient,
capable
providing
valuable
quantitative
metrics
minimal
MR
data.
This
work
proposes
μGUIDE:
a
general
Bayesian
framework
to
estimate
posterior
distributions
of
tissue
microstructure
parameters
from
any
given
biophysical
model
or
signal
representation,
with
exemplar
demonstration
in
diffusion-weighted
MRI.
Harnessing
new
deep
learning
architecture
for
automatic
feature
selection
combined
simulationbased
inference
and
efficient
sampling
the
distributions,
μGUIDE
bypasses
high
computational
time
cost
conventional
approaches
does
not
rely
on
acquisition
constraints
define
model-specific
summary
statistics.
The
obtained
allow
highlight
degeneracies
present
definition
quantify
uncertainty
ambiguity
estimated
parameters.
This
work
proposes
μGUIDE:
a
general
Bayesian
framework
to
estimate
posterior
distributions
of
tissue
microstructure
parameters
from
any
given
biophysical
model
or
signal
representation,
with
exemplar
demonstration
in
diffusion-weighted
MRI.
Harnessing
new
deep
learning
architecture
for
automatic
feature
selection
combined
simulationbased
inference
and
efficient
sampling
the
distributions,
μGUIDE
bypasses
high
computational
time
cost
conventional
approaches
does
not
rely
on
acquisition
constraints
define
model-specific
summary
statistics.
The
obtained
allow
highlight
degeneracies
present
definition
quantify
uncertainty
ambiguity
estimated
parameters.
Human Brain Mapping,
Journal Year:
2023,
Volume and Issue:
44(14), P. 4859 - 4874
Published: July 20, 2023
Assessing
axonal
morphology
in
vivo
opens
new
avenues
for
the
combined
study
of
brain
structure
and
function.
A
novel
approach
has
recently
been
introduced
to
estimate
fibers
from
combination
magnetic
resonance
imaging
(MRI)
data
electroencephalography
(EEG)
measures
interhemispheric
transfer
time
(IHTT).
In
original
study,
IHTT
were
computed
EEG
averaged
across
a
group,
leading
bias
estimates.
Here,
we
seek
individual
IHTT,
obtained
acquired
visual
evoked
potential
experiment.
Subject-specific
IHTTs
are
data-driven
framework
with
minimal
priori
constraints,
based
on
maximal
peak
neural
responses
stimuli
within
periods
statistically
significant
activity
inverse
solution
space.
The
subject-specific
estimates
ranged
8
29
ms
except
one
participant
between-session
variability
was
comparable
between-subject
variability.
mean
radius
distribution,
MRI
data,
0
1.09
μm
subjects.
change
g-ratio
0.62
0.81
μm-α
.
single-subject
measurement
yields
that
consistent
histological
values.
However,
improvement
repeatability
is
required
improve
specificity