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.
Magnetic Resonance in Medicine,
Journal Year:
2023,
Volume and Issue:
90(1), P. 150 - 165
Published: March 20, 2023
Purpose
Tensor‐valued
diffusion
encoding
can
probe
more
specific
features
of
tissue
microstructure
than
what
is
available
by
conventional
weighting.
In
this
work,
we
investigate
the
technical
feasibility
tensor‐valued
at
high
b
‐values
with
q‐space
trajectory
imaging
(QTI)
analysis,
in
human
heart
vivo.
Methods
Ten
healthy
volunteers
were
scanned
on
a
3T
scanner.
We
designed
time‐optimal
gradient
waveforms
for
(linear
and
planar)
second‐order
motion
compensation.
Data
analyzed
QTI.
Normal
values
repeatability
investigated
mean
diffusivity
(MD),
fractional
anisotropy
(FA),
microscopic
FA
(μFA),
isotropic,
anisotropic
total
kurtosis
(MKi,
MKa,
MKt),
orientation
coherence
(
C
c
).
A
phantom,
consisting
two
fiber
blocks
adjustable
angles,
was
used
to
evaluate
sensitivity
parameters
dispersion
time.
Results
QTI
data
left
ventricular
myocardium
MD
=
1.62
±
0.07
μm
2
/ms,
0.31
0.03,
μFA
0.43
0.07,
MKa
0.20
MKi
0.13
MKt
0.33
0.09,
0.56
0.22
(mean
SD
across
subjects).
Phantom
experiments
showed
that
depends
dispersion,
whereas
insensitive
effect.
Conclusion
demonstrated
first
analysis
vivo,
along
measurements
myocardial
μFA,
MKi,
.
The
methodology
technically
feasible
provides
promising
novel
biomarkers
characterization.
NMR in Biomedicine,
Journal Year:
2024,
Volume and Issue:
37(11)
Published: July 4, 2024
Filter
exchange
imaging
(FEXI)
is
a
double
diffusion-encoding
(DDE)
sequence
that
specifically
sensitive
to
between
sites
with
different
apparent
diffusivities.
FEXI
uses
filtering
block
followed
by
detection
at
varying
mixing
times
map
the
rate.
Long
enhance
sensitivity
exchange,
but
they
pose
challenges
for
applications
require
stimulated
echo
crusher
gradients.
Thin
slices
strong
crushers,
which
can
introduce
significant
diffusion
weighting
and
bias
rate
estimates.
Here,
we
treat
crushers
as
an
additional
encoding
consider
triple
sequence.
This
allows
be
corrected
in
case
of
multi-Gaussian
diffusion,
not
easily
presence
restricted
diffusion.
Our
approach
addresses
relies
on
ability
independently
gauge
sensitivities
arbitrary
gradient
waveforms.
It
follows
two
principles:
(i)
effects
are
included
forward
model
using
signal
cumulant
expansion;
(ii)
timing
parameters
gradients
filter
blocks
adjusted
maintain
same
level
restriction
regardless
time.
results
tuned
(TEXI)
protocol.
The
accuracy
mapping
TEXI
was
assessed
through
Monte
Carlo
simulations
spheres
identical
sizes
gamma-distributed
sizes,
parallel
hexagonally
packed
cylinders.
demonstrate
provides
consistent
rates
slice
thickness
size,
even
crushers.
However,
depends
b-values,
times,
geometry.
constraints
limitations
discussed,
including
suggestions
protocol
adaptations.
Further
studies
needed
optimize
precision
assess
experimentally
realistic,
heterogeneous
substrates.
Magnetic Resonance in Medicine,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Oct. 29, 2024
Abstract
Purpose
The
nonmonotonic
dependence
of
diffusion
kurtosis
on
time
has
been
observed
in
biological
tissues,
yet
its
relation
to
membrane
integrity
and
cellular
geometry
remains
be
clarified.
Here
we
establish
explain
the
characteristic
asymmetric
shape
peak.
We
also
derive
between
peak
,
when
reaches
maximum,
tissue
parameters.
Methods
position
qualitatively
follow
from
adiabatic
extension
Kärger
model
onto
case
intra‐cellular
diffusivity
time‐dependence.
This
intuition
is
corroborated
by
effective
medium
theory‐based
calculation,
as
well
Monte
Carlo
simulations
exchange
randomly
densely
packed
spheres
for
various
values
permeability,
cell
fractions
sizes,
intrinsic
diffusivity.
Results
that
proportional
geometric
mean
two
scales:
extra‐cellular
correlation
(determined
size)
residence
permeability).
When
barrier‐limited,
approaches
a
universal
scaling
form
determined
ratio
.
Conclusion
Numerical
theory
provide
an
interpretation
specific
feature
time‐dependence,
offering
potential
biomarker
vivo
evaluation
pathology
disentangling
functional
(permeability)
structural
(cell
tissues.
relevant
time‐dependent
cumulants
are
sensitive
pathological
changes
structure
diseases,
such
ischemic
stroke,
tumors,
Alzheimer's
disease.
NeuroImage Clinical,
Journal Year:
2023,
Volume and Issue:
38, P. 103419 - 103419
Published: Jan. 1, 2023
Structural
brain
MRI
has
proven
invaluable
in
understanding
movement
disorder
pathophysiology.
However,
most
work
focused
on
grey/white
matter
volumetric
(macrostructural)
and
white
microstructural
effects,
limiting
of
frequently
implicated
grey
differences.
Using
ultra-strong
spherical
tensor
encoding
diffusion-weighted
MRI,
a
persistent
signal
was
seen
healthy
cerebellar
even
at
high
diffusion-weightings
(b
≥
10,000
s/mm2).
Quantifying
the
proportion
this
(denoted
fs),
previously
ascertained
to
originate
from
inside
small
spaces,
provides
potential
proxy
for
cell
body
density.
In
work,
approach
applied
first
time
clinical
cohort,
including
patients
with
diagnosed
disorders
which
cerebellum
been
symptom
Five
control
participants
(control
group
1,
median
age
24.5
years
(20–39
years),
imaged
two
timepoints,
demonstrated
consistency
measurement
all
three
measures
-
MD
(Mean
Diffusivity)
fs,
Ds
(dot
diffusivity)-
intraclass
correlation
coefficients
(ICC)
0.98,
0.86
0.76,
respectively.
Comparison
an
older
2
(n
=
5),
51
(43–58
years))
found
no
significant
differences,
neither
morphometric
nor
(MD
(p
0.36),
fs
0.17)
0.22))
measures.
The
cohort
(Parkinson's
Disease,
n
5,
dystonia,
5.
Spinocerebellar
Ataxia
6,
5)
when
compared
age-matched
(Control
Group
2)
identified
significantly
lower
<
0.0001
p
0.0001)
higher
values
SCA6
dystonia
cohorts
Lobar
division
these
same
differences
superior
inferior
posterior
lobes,
while
were
either
anterior
lobes
or
measurements.
contrast
more
conventional
diffusion
imaging,
framework
enhanced
specificity
restricted
spaces
(including
cells)
by
eliminating
signals
cerebrospinal
fluid
axons.
context
human
animal
histopathology
studies,
findings
potentially
implicate
Purkinje
granule
cells
as
contributors
observed
both
types
having
several
neurological
through
postmortem
model
studies.
This
novel
imaging
shows
promise
improving
diagnosis,
prognosis,
treatment.
Magnetic Resonance Letters,
Journal Year:
2023,
Volume and Issue:
3(3), P. 232 - 247
Published: June 18, 2023
Water
exchange
between
the
different
compartments
of
a
heterogeneous
specimen
can
be
characterized
via
diffusion
magnetic
resonance
imaging
(dMRI).
Many
analysis
frameworks
using
dMRI
data
have
been
proposed
to
describe
exchange,
often
double
encoding
(DDE)
stimulated
echo
sequence.
Techniques
such
as
weighted
(DEWI)
and
filter
rapid
models,
use
specific
subset
full
space
DDE
signal.
In
this
work,
general
representation
signal
was
employed
with
sampling
schemes
(namely
constant
b1,
diagonal
anti-diagonal)
from
reduction
models
estimate
exchange.
A
near-uniform
scheme
compared
other
schemes.
The
were
also
applied
their
own
subsampling
These
on
both
simulated
experimental
acquired
benchtop
MR
scanner.
synthetic
data,
performed
best
due
consistency
estimates
ground
truth.
shifted
outperformed
others,
yielding
most
consistent
estimation.
results
suggest
feasibility
measuring
along
variable
future
studies,
algorithms
could
further
developed
for
optimization
schemes,
well
incorporating
additional
properties,
geometry
anisotropy,
into
frameworks.
Physics in Medicine and Biology,
Journal Year:
2024,
Volume and Issue:
69(10), P. 105013 - 105013
Published: April 12, 2024
In
Magnetic
Resonance
(MR)
parallel
imaging
with
virtual
channel-expanded
Wave
encoding,
limitations
are
imposed
on
the
ability
to
comprehensively
and
accurately
characterize
background
phase.
These
primarily
attributed
calibration
process
relying
solely
center
low-frequency
Auto-Calibration
Signals
(ACS)
data
for
calibration.
Research Square (Research Square),
Journal Year:
2024,
Volume and Issue:
unknown
Published: July 29, 2024
Abstract
Double
diffusion
encoding
(DDE)
makes
MRI
sensitive
to
a
wide
range
of
microstructural
features,
and
the
acquired
data
can
be
analysed
using
different
approaches.
Correlation
tensor
imaging
(CTI)
uses
DDE
resolve
three
components
diffusional
kurtosis:
isotropic,
anisotropic,
microscopic.
The
microscopic
kurtosis
is
estimated
from
contrast
between
single
(SDE)
parallel
signals
at
same
b-value.
Another
approach
multi-Gaussian
exchange
(MGE),
which
employs
measure
exchange.
Sensitivity
obtained
by
contrasting
SDE
CTI
MGE
exploit
signal
quantify
exchange,
this
study
investigates
interplay
these
two
quantities.
We
perform
Monte-Carlo
simulations
in
geometries
with
varying
levels
behaviour
parameters
MGE.
conclude
that
rate.
In
an
attempt
separate
we
propose
heuristic
representation
referred
as
µMGE
(MGE
incorporating
kurtosis)
accounts
for
both
effects,
exploiting
distinct
signatures
mixing
time:
causes
dependence
on
time
while
does
not.
find
applying
multiple
times
orthogonal
allows
estimation
well
all
sources
kurtosis.
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.