Magnetic Resonance in Medicine,
Год журнала:
2022,
Номер
89(4), С. 1441 - 1455
Опубликована: Ноя. 20, 2022
Purpose
Filter
exchange
imaging
(FEXI)
and
diffusion
time
(
t
)‐dependent
kurtosis
(DKI(
))
are
both
sensitive
to
water
between
tissue
compartments.
The
restrictive
effects
of
microstructure,
however,
introduce
bias
the
rate
obtained
by
these
two
methods,
as
their
interpretation
conventionally
rely
on
Kärger
model
barrier
limited
Gaussian
Here,
we
investigated
whether
FEXI
DKI(
)
can
provide
comparable
rates
in
ex
vivo
mouse
brains.
Theory
Methods
data
were
acquired
from
brains
a
preclinical
MRI
system.
Phase
cycling
negative
slice
prewinder
gradients
used
minimize
interferences
gradients.
Results
In
corpus
callosum,
apparent
(AXR)
correlated
with
(the
inverse
time,
1/
τ
along
radial
direction.
comparison,
discrepancies
found
cortex
due
low
filter
efficiency
confounding
microstructure.
Conclusion
results
suggest
that
same
processes
white
matter
when
separated
complex
microstructure
gray
matter,
potential
among
multiple
compartments
still
pose
challenge
for
).
NeuroImage,
Год журнала:
2022,
Номер
256, С. 119277 - 119277
Опубликована: Май 3, 2022
Biophysical
models
of
diffusion
in
white
matter
are
based
on
what
is
now
commonly
referred
to
as
the
"Standard
Model"
(SM)
non-exchanging
anisotropic
Gaussian
compartments.
In
this
work,
we
focus
MRI
gray
matter,
which
requires
rethinking
basic
microstructure
modeling
blocks.
particular,
at
least
three
contributions
beyond
SM
need
be
considered:
water
exchange
across
cell
membrane
-
between
neurites
and
extracellular
space;
non-Gaussian
along
neuronal
glial
processes
resulting
from
structural
disorder;
signal
contribution
soma.
For
first
contribution,
propose
Neurite
Exchange
Imaging
(NEXI)
an
extension
diffusion,
builds
K\"arger
model
two
exchanging
Using
datasets
acquired
multiple
weightings
(b)
times
(t)
rat
brain
vivo,
show
that
for
investigated
time
window
(~10-45
ms)
there
minimal
diffusivity
time-dependence
more
pronounced
kurtosis
decay
with
well
fit
by
model.
Moreover,
observe
lower
longer
high
b.
light
these
observations,
identify
mechanism
best
explains
signatures
both
low-b
high-b
regime,
thereby
NEXI
mapping.
We
finally
highlight
multi-b
multi-t
acquisitions
protocols
being
suited
estimate
parameters
reliably.
approach,
inter-compartment
15
60
ms
cortex
hippocampus
same
order
or
shorter
than
typical
acquisitions.
This
suggests
essential
component
interpreting
measurements
matter.
The
glymphatic
system
is
a
fluid
transport
network
of
cerebrospinal
(CSF)
entering
the
brain
along
arterial
perivascular
spaces,
exchanging
with
interstitial
(ISF),
ultimately
establishing
directional
clearance
solutes.
CSF
facilitated
by
expression
aquaporin-4
(AQP4)
water
channels
on
endfeet
astrocytes.
Mice
genetic
deletion
AQP4
(AQP4
KO)
exhibit
abnormalities
in
structure
and
molecular
transport.
Yet,
no
studies
have
systematically
examined
how
these
correlate
function.
Here,
we
used
high-resolution
3D
magnetic
resonance
(MR)
non-contrast
cisternography,
diffusion-weighted
MR
imaging
(MR-DWI)
intravoxel-incoherent
motion
(IVIM)
DWI,
while
evaluating
function
using
standard
dynamic
contrast-enhanced
to
better
understand
disrupted
after
AQP4.
KO
mice
had
larger
spaces
total
volumes
resulting
higher
content
reduced
space
volumes,
despite
similar
production
rates
vascular
density
compared
wildtype
mice.
volume
likely
resulted
increased
slow
but
not
fast
diffusion
measures
coincided
influx.
This
markedly
altered
may
result
from
reduction
clearance,
leading
enlargement
stagnation
space.
Overall,
useful
tool
evaluate
serve
as
valuable
translational
biomarker
study
glymphatics
human
disease.
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.
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).
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.
Human Brain Mapping,
Год журнала:
2023,
Номер
44(13), С. 4792 - 4811
Опубликована: Июль 17, 2023
Abstract
Soma
and
neurite
density
image
(SANDI)
is
an
advanced
diffusion
magnetic
resonance
imaging
biophysical
signal
model
devised
to
probe
in
vivo
microstructural
information
the
gray
matter
(GM).
This
requires
acquisitions
that
include
b
values
are
at
least
six
times
higher
than
those
used
clinical
practice.
Such
high
required
disentangle
contribution
of
water
diffusing
soma
from
neurites
extracellular
space,
while
keeping
time
as
short
possible
minimize
potential
bias
due
exchange.
These
requirements
have
limited
use
SANDI
only
preclinical
or
cutting‐edge
human
scanners.
Here,
we
investigate
impact
neglecting
exchange
present
a
10‐min
acquisition
protocol
enables
characterize
both
GM
white
(WM)
on
3
T
We
implemented
analytical
simulations
(i)
evaluate
stability
fitting
parameters
when
diminishing
number
shells;
(ii)
estimate
between
space
such
reduced
scheme,
comparing
it
with
experimental
noise.
Then,
demonstrated
feasibility
assessed
repeatability
reproducibility
our
approach
by
computing
metrics
AMICO
toolbox
other
state‐of‐the‐art
models
five
healthy
subjects.
Finally,
applied
multiple
sclerosis
patients.
Results
suggest
practical
method
WM
tissues
performant