Journal of Magnetic Resonance Imaging,
Год журнала:
2024,
Номер
unknown
Опубликована: Май 20, 2024
Background
Accurately
fitting
diffusion‐time‐dependent
diffusion
MRI
(
t
d
‐dMRI)
models
poses
challenges
due
to
complex
and
nonlinear
formulas,
signal
noise,
limited
clinical
data
acquisition.
Purpose
Introduce
a
Bayesian
methodology
refine
microstructural
within
the
IMPULSED
(Imaging
Microstructural
Parameters
Using
Limited
Spectrally
Edited
Diffusion)
model
optimize
prior
distribution
framework.
Study
Type
Retrospective.
Population
Involving
69
pediatric
patients
(median
age
6
years,
interquartile
range
[IQR]
3–9
61%
male)
with
41
low‐grade
28
high‐grade
gliomas,
of
which
76.8%
were
identified
brainstem
or
cerebellum.
Field
Strength/Sequence
3
T,
oscillating
gradient
spin‐echo
(OGSE)
pulsed
(PGSE).
Assessment
The
method's
performance
in
cell
diameter
(),
intracellular
volume
fraction
extracellular
coefficient
()
was
compared
against
NLLS
method,
considering
simulated
experimental
data.
tumor
region‐of‐interest
(ROI)
manually
delineated
on
b
0
images.
diagnostic
distinguishing
high‐
gliomas
assessed,
accuracy
validated
H&E‐stained
pathology.
Statistical
Tests
T‐test,
receiver
operating
curve
(ROC),
area
under
(AUC)
DeLong's
test
conducted.
Significance
considered
at
P
<
0.05.
Results
manifested
increased
robust
estimates
simulation
(RMSE
decreased
by
29.6%,
40.9%,
13.6%,
STD
29.2%,
43.5%,
24.0%,
respectively
for
,
NLLS),
indicating
fewer
outliers
reduced
error.
Diagnostic
grade
similar
both
methods,
however,
method
generated
smoother
maps
(outliers
ratio
45.3%
±
19.4%)
marginal
enhancement
correlation
H&E
staining
result
r
=
0.721
0.698
using
NLLS,
0.5764).
Data
Conclusion
proposed
substantially
enhances
robustness
estimation,
suggesting
its
potential
utility
characterizing
cellular
microstructure.
Evidence
Level
Technical
Efficacy
Stage
1
NeuroImage,
Год журнала:
2022,
Номер
251, С. 118976 - 118976
Опубликована: Фев. 7, 2022
Diffusion
MRI
(dMRI)
provides
contrast
that
reflect
diffusing
spins'
interactions
with
microstructural
features
of
biological
systems,
but
its
specificity
remains
limited
due
to
the
ambiguity
relation
underlying
microstructure.
To
improve
specificity,
biophysical
models
white
matter
(WM)
typically
express
dMRI
signals
according
Standard
Model
(SM)
and
have
more
recently
in
gray
(GM)
attempted
incorporate
cell
soma
(the
SANDI
model).
The
validity
assumptions
these
models,
however,
largely
undetermined,
especially
GM.
Observing
models'
unique,
functional
properties,
such
as
$b^{-1/2}$
power-law
associated
1d
diffusion,
has
emerged
a
fruitful
strategy
for
experimental
validation.
absence
this
signature
GM
been
explained
by
neurite
water
exchange,
non-linear
morphology,
and/or
obscuring
signal
contributions.
Here,
we
present
simulations
realistic
neurons
demonstrating
curvature
branching
does
not
destroy
stick
impermeable
neurites,
their
is
drowned
under
typical
conditions:
Nevertheless,
identify
an
attainable
regime
which
dominates.
Furthermore,
find
exchange-driven
time
dependence
produces
behavior
opposite
expected
from
restricted
thereby
providing
disambiguating
two
effects.
We
data
experiments
ex
vivo
rat
brain
at
ultrahigh
field
observe
consistent
substantial
exchange
power-law.
first
finding
suggests
significant
while
second
small
sub-population
neurites.
quantify
our
observations,
harness
K\"arger
model
corresponding
SM
SANDI.
Imaging Neuroscience,
Год журнала:
2024,
Номер
2, С. 1 - 19
Опубликована: Фев. 20, 2024
Abstract
Biophysical
models
of
diffusion
tailored
to
quantify
gray
matter
microstructure
are
gathering
increasing
interest.
The
two-compartment
Neurite
EXchange
Imaging
(NEXI)
model
has
been
proposed
recently
account
for
neurites,
extra-cellular
space,
and
exchange
across
the
cell
membrane.
NEXI
parameter
estimation
requires
multi-shell
multi-diffusion
time
data
so
far
only
implemented
experimentally
on
animal
collected
a
preclinical
magnetic
resonance
imaging
(MRI)
set-up.
In
this
work,
translation
human
cortex
in
vivo
was
achieved
using
3
T
Connectom
MRI
system
with
300
mT/m
gradients,
that
enables
acquisition
broad
range
b-values
(0
–
7.5
ms/µm²)
window
covering
short
intermediate
times
(20
49
ms)
suitable
characteristic
(10
50
ms).
Microstructure
estimates
four
variants:
NEXI,
NEXIdot
(its
extension
addition
dot
compartment),
their
respective
versions
correct
Rician
noise
floor
(NEXIRM
NEXIdot,RM)
particularly
impacts
high
b-value
signal,
were
compared.
reliability
each
variant
evaluated
synthetic
data.
latter,
intra-subject
(scan-rescan)
versus
between-subjects
variability
compared
cortex.
better
performance
NEXIRM
highlights
importance
correcting
bias
obtain
accurate
parameters
cortex,
sensitivity
framework
individual
differences
cortical
microstructure.
This
application
humans
represents
significant
step,
unlocking
new
avenues
studying
neurodevelopment,
aging,
various
neurodegenerative
disorders.
NMR in Biomedicine,
Год журнала:
2024,
Номер
37(9)
Опубликована: Май 7, 2024
Abstract
Cerebrospinal
fluid
(CSF)
plays
a
critical
role
in
metabolic
waste
clearance
from
the
brain,
requiring
its
circulation
throughout
various
brain
pathways,
including
ventricular
system,
subarachnoid
spaces,
para‐arterial
interstitial
and
para‐venous
spaces.
The
complexity
of
CSF
has
posed
challenge
obtaining
noninvasive
measurements
dynamics.
assessment
dynamics
circulatory
pathways
is
possible
using
diffusion
magnetic
resonance
imaging
(MRI)
with
optimized
sensitivity
to
incoherent
water
movement
across
brain.
This
review
presents
an
overview
both
established
emerging
MRI
techniques
designed
measure
their
potential
clinical
applications.
discussion
offers
insights
into
optimization
acquisition
parameters
enhance
specificity
metrics
on
underlying
Lastly,
we
emphasize
importance
cautious
interpretations
diffusion‐based
imaging,
especially
when
differentiating
between
tissue‐
fluid‐related
changes
or
elucidating
structural
versus
functional
alterations.
Nature Communications,
Год журнала:
2024,
Номер
15(1)
Опубликована: Май 18, 2024
Abstract
After
contracting
COVID-19,
a
substantial
number
of
individuals
develop
Post-COVID-Condition,
marked
by
neurologic
symptoms
such
as
cognitive
deficits,
olfactory
dysfunction,
and
fatigue.
Despite
this,
biomarkers
pathophysiological
understandings
this
condition
remain
limited.
Employing
magnetic
resonance
imaging,
we
conduct
comparative
analysis
cerebral
microstructure
among
patients
with
healthy
controls,
that
contracted
COVID-19
without
long-term
symptoms.
We
reveal
widespread
alterations
in
microstructure,
attributed
to
shift
volume
from
neuronal
compartments
free
fluid,
associated
the
severity
initial
infection.
Correlating
these
cognition,
olfaction,
fatigue
unveils
distinct
affected
networks,
which
are
close
anatomical-functional
relationship
respective
Imaging Neuroscience,
Год журнала:
2024,
Номер
2, С. 1 - 14
Опубликована: Март 18, 2024
Abstract
Water
diffusion-weighted
MRI
is
a
very
powerful
tool
for
probing
tissue
microstructure,
but
disentangling
the
contribution
of
compartment-specific
structural
disorder
from
cellular
restriction
and
inter-compartment
exchange
remains
an
open
challenge.
In
this
work,
we
use
MR
spectroscopy
(dMRS)
water
metabolite
as
function
diffusion
time
in
vivo
mouse
gray
matter
to
shed
light
on:
i)
which
these
concomitant
mechanisms
(structural
disorder,
restriction,
exchange)
dominates
measurements
ii)
with
specific
signature.
We
report
time-dependence
excellent
SNR
conditions
provided
by
dMRS,
up
long
(500
ms).
kurtosis
decreases
increasing
time,
showing
influence
both
exchange.
However,
despite
experimental
conditions,
were
not
able
clearly
identify
nature
(i.e.,
1D
versus
2D/3D
short-range
disorder).
Measurements
purely
intracellular
metabolites
(up
500
ms)
show
opposite
behavior
water,
time.
that
signature
restricted
space,
microstructural
features
such
soma’s
cell
projections’
size
can
be
estimated.
Finally,
comparing
time-dependencies,
attempt
disentangle
effect
intra/extracellular
extracellular
space
(both
impacting
only).
Our
results
suggest
relatively
short
(~1-50
(still
unclear
if
or
2D/3D)
most
likely
coming
compartment.
This
work
provides
novel
insights
help
interpret
diffusion-time
dependent
terms
underlying
microstructure
suggests
may
offer
new
way
quantify
restrictions
matter.
Magnetic Resonance in Medicine,
Год журнала:
2025,
Номер
unknown
Опубликована: Янв. 29, 2025
Abstract
Purpose
Filter‐exchange
imaging
(FEXI)
and
diffusion
time
(t)‐dependent
kurtosis
(DKI(t))
are
two
diffusion‐based
methods
that
have
been
proposed
for
in
vivo
measurements
of
water
exchange
rates.
Few
studies
directly
compared
these
methods.
We
aimed
to
investigate
whether
FEXI
DKI(t)
yield
comparable
the
human
brain
vivo.
Methods
Eight
healthy
volunteers
underwent
multiple‐direction
acquisitions
on
a
3T
scanner.
performed
region
interest
(ROI)
analysis
determine
correlations
between
FEXI‐derived
apparent
rate
(AXR)
DKI(t)‐derived
reciprocal
().
Results
In
both
white
matter
(WM)
gray
(GM),
revealed
substantial
diffusion‐time
dependence
diffusivity
kurtosis.
However,
at
t
≥
100
ms,
showed
weak
dependence.
WM,
this
may
be
due
myelin
“free”
with
different
T
1
values,
although
other
factors,
such
as
remaining
restrictive
effects
from
microstructural
barriers,
cannot
excluded.
found
significant
correlation
AXR
axial
direction
within
WM.
No
was
present
GM,
values
similar
ranges.
Conclusion
These
results
suggest
could
sensitive
same
process
only
when
is
sufficiently
long,
GM
effect
microstructure
non‐negligible,
especially
short
times
(<100
ms).
Magnetic Resonance in Medicine,
Год журнала:
2025,
Номер
unknown
Опубликована: Фев. 26, 2025
Abstract
Small‐animal
diffusion
MRI
(dMRI)
has
been
used
for
methodological
development
and
validation,
characterizing
the
biological
basis
of
phenomena,
comparative
anatomy.
The
steps
from
animal
setup
monitoring,
to
acquisition,
analysis,
interpretation
are
complex,
with
many
decisions
that
may
ultimately
affect
what
questions
can
be
answered
using
resultant
data.
This
work
aims
present
selected
considerations
recommendations
community
on
best
practices
preclinical
dMRI
in
vivo
animals.
We
describe
general
foundational
knowledge
must
considered
when
designing
experiments.
briefly
differences
species
disease
models
discuss
why
some
more
or
less
appropriate
different
studies.
We,
then,
give
acquisition
protocols,
including
hardware,
preparation,
imaging
sequences,
followed
by
advice
data
processing
preprocessing,
model‐fitting,
tractography.
Finally,
we
provide
an
online
resource
lists
publicly
available
datasets
software
packages
promote
responsible
reproducible
research.
In
each
section,
attempt
guides
recommendations,
but
also
highlight
areas
which
no
guidelines
exist
(and
why),
where
future
should
focus.
Although
mainly
cover
central
nervous
system
(on
most
studies
focused),
provide,
possible
applicable,
other
organs
interest.
An
overarching
goal
is
enhance
rigor
reproducibility
small
acquisitions
analyses,
thereby
advance
biomedical
knowledge.
Abstract
Strong
gradient
systems
can
improve
the
signal-to-noise
ratio
of
diffusion
MRI
measurements
and
enable
a
wider
range
acquisition
parameters
that
are
beneficial
for
microstructural
imaging.
We
present
comprehensive
dataset
26
healthy
participants
acquired
on
MGH-USC
3
T
Connectome
scanner
equipped
with
300
mT/m
maximum
strength
custom-built
64-channel
head
coil.
For
each
participant,
one-hour
long
systematically
sampled
accessible
measurement
space,
including
two
times
(19
49
ms),
eight
strengths
linearly
spaced
between
30
290
time,
32
or
64
uniformly
distributed
directions.
The
data
were
preprocessed
to
correct
nonlinearity,
eddy
currents,
susceptibility
induced
distortions.
In
addition,
scan/rescan
from
subset
seven
individuals
also
provided.
MGH
Diffusion
Microstructure
Dataset
(CDMD)
may
serve
as
test
bed
development
new
analysis
methods,
such
fiber
orientation
estimation,
tractography
modelling.
NeuroImage,
Год журнала:
2023,
Номер
282, С. 120338 - 120338
Опубликована: Авг. 19, 2023
Diffusion
MRI
uses
the
random
displacement
of
water
molecules
to
sensitize
signal
brain
microstructure
and
properties
such
as
density
shape
cells.
Microstructure
modeling
techniques
aim
estimate
these
from
acquired
data
by
separating
between
virtual
tissue
'compartments'
intra-neurite
extra-cellular
space.
A
key
challenge
is
that
diffusion
relatively
featureless
compared
with
complexity
tissue.
Another
wildly
different
within
gray
white
matter
brain.
In
this
review,
we
use
results
multidimensional
encoding
discuss
challenges
their
tentative
solutions.
Multidimensional
increases
information
content
varying
not
only
b-value
direction
but
also
additional
experimental
parameters
b-tensor
echo
time.
Three
main
insights
have
emerged
encoding.
First,
contradict
common
model
assumptions
on
T2
relaxation
illustrates
how
cause
erroneous
interpretations
in
both
healthy
pathology.
Second,
many
can
be
dispensed
if
are
The
necessary
easily
vivo
using
protocols
optimized
minimize
Cramér-Rao
lower
bounds.
Third,
microscopic
anisotropy
reflects
presence
axons
dendrites.
This
insight
stands
contrast
current
'neurite
models'
tissue,
which
assume
dendrites
feature
highly
similar
diffusion.
Nevertheless,
an
axon-based
contrast,
differentiate
when
myelin
alterations
confound
conventional
contrasts.
For
its
size,
the
brain
is
most
metabolically
active
organ
in
body.
Most
of
energy
demand
used
to
maintain
stable
homeostatic
physiological
conditions.
Altered
homeostasis
and
states
are
hallmarks
many
diseases
disorders.
Yet
there
currently
no
direct
reliable
method
assess
absolute
basal
activity
cells
tissue
noninvasively
without
exogenous
tracers
or
contrast
agents.
We
propose
a
novel
low-field,
high-gradient
diffusion
exchange
nuclear
magnetic
resonance
(NMR)
capable
directly
measuring
cellular
metabolic
via
rate
constant
for
water
across
cell
membranes.
Exchange
rates
140±16
s
-1
under
normal
conditions
viable
ex
vivo
neonatal
mouse
spinal
cords.
High
repeatability
samples
suggest
that
values
intrinsic
tissue.
Using
temperature
drug
(ouabain)
perturbations,
we
find
majority
coupled
transport
by
sodium-potassium
pump.
show
this
sensitive
primarily
provides
distinct
functional
information.
In
contrast,
apparent
coefficient
(ADC)
measured
with
submillisecond
times
microstructure
but
not
activity.
Water
appears
independently
regulated
from
microstructural
oxygenation
changes
reported
ADC
T1
relaxation
measurements
an
oxygen-glucose
deprivation
model
stroke;
remain
30-40
min
before
dropping
levels
similar
effect
ouabain
never
completely
recovering
when
oxygen
glucose
restored.