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
).
Abstract
Diffusion
magnetic
resonance
imaging
is
an
important
tool
for
mapping
tissue
microstructure
and
structural
connectivity
non‐invasively
in
the
vivo
human
brain.
Numerous
diffusion
signal
models
are
proposed
to
quantify
microstructural
properties.
Nonetheless,
accurate
estimation
of
model
parameters
computationally
expensive
impeded
by
image
noise.
Supervised
deep
learning‐based
approaches
exhibit
efficiency
superior
performance
but
require
additional
training
data
may
be
not
generalizable.
A
new
DIffusion
Model
OptimizatioN
framework
using
physics‐informed
self‐supervised
Deep
learning
entitled
“DIMOND”
address
this
problem.
DIMOND
employs
a
neural
network
map
input
optimizes
minimizing
difference
between
acquired
synthetic
generated
via
parametrized
outputs.
produces
tensor
results
generalizable
across
subjects
datasets.
Moreover,
outperforms
conventional
methods
fitting
sophisticated
including
kurtosis
NODDI
model.
Importantly,
reduces
time
from
hours
minutes,
or
seconds
leveraging
transfer
learning.
In
summary,
manner,
high
efficacy,
increase
practical
feasibility
adoption
clinical
neuroscientific
applications.
Abstract
The
human
brain
undergoes
age‐related
microstructural
alterations
across
the
lifespan.
Soma
and
Neurite
Density
Imaging
(SANDI),
a
novel
biophysical
model
of
diffusion
MRI,
provides
estimates
cell
body
(soma)
radius
density,
neurite
density
in
gray
matter.
goal
this
cross‐sectional
study
was
to
assess
sensitivity
high‐gradient
MRI
toward
cortical
microstructure
adult
lifespan
using
SANDI.
Seventy‐two
cognitively
unimpaired
healthy
subjects
(ages
19–85
years;
40
females)
were
scanned
on
3T
Connectome
scanner
with
maximum
gradient
strength
300mT/m
multi‐shell
protocol
incorporating
8
b
‐values
time
19
ms.
Intra‐soma
signal
fraction
obtained
from
SANDI
model‐fitting
data
strongly
correlated
age
all
major
lobes
(
r
=
−0.69
−0.60,
FDR‐
p
<
0.001).
0.48–0.63,
0.001)
soma
0.28–0.40,
0.04)
significantly
volume
prefrontal
cortex,
frontal,
parietal,
temporal
lobes.
relationship
between
metrics
greater
than
or
comparable
regions,
particularly
occipital
lobe
anterior
cingulate
gyrus.
In
contrast
metrics,
associations
tensor
imaging
(DTI)
kurtosis
low
moderate.
These
results
suggest
that
may
be
more
sensitive
underlying
substrates
neurodegeneration
aging
DTI
traditional
macroscopic
measures
such
as
thickness.
NeuroImage,
Год журнала:
2022,
Номер
254, С. 119137 - 119137
Опубликована: Март 23, 2022
Diffusion
MRI
(dMRI)
has
become
one
of
the
most
important
imaging
modalities
for
noninvasively
probing
tissue
microstructure.
Diffusional
Kurtosis
(DKI)
quantifies
degree
non-Gaussian
diffusion,
which
in
turn
been
shown
to
increase
sensitivity
towards,
e.g.,
disease
and
orientation
mapping
neural
tissue.
However,
specificity
DKI
is
limited
as
different
sources
can
contribute
total
intravoxel
diffusional
kurtosis,
including:
variance
diffusion
tensor
magnitudes
(Kiso),
due
anisotropy
(Kaniso),
microscopic
kurtosis
(μK)
related
restricted
microstructural
disorder,
and/or
exchange.
Interestingly,
μK
typically
ignored
signal
modelling
it
assumed
be
negligible
tissues.
recently,
Correlation
Tensor
(CTI)
based
on
Double-Diffusion-Encoding
(DDE)
was
introduced
source
separation,
revealing
non
preclinical
imaging.
Here,
we
implemented
CTI
first
time
a
clinical
3T
scanner
investigated
healthy
subjects.
A
robust
framework
separation
humans
introduced,
followed
by
estimation
(and
other
sources)
brain.
Using
this
approach,
find
that
significantly
contributes
both
grey
white
matter
but,
expected,
not
ventricles.
The
maps
human
brain
are
presented,
spatial
distribution
provides
unique
contrast,
appearing
from
isotropic
anisotropic
counterparts.
Moreover,
group
average
templates
these
have
generated
time,
corroborated
our
findings
at
underlying
individual-level
maps.
We
further
show
common
practice
ignoring
assuming
multiple
Gaussian
component
approximation
introduces
significant
bias
and,
perhaps
even
worse,
compromises
their
interpretation.
Finally,
twofold
acceleration
discussed
context
potential
future
applications.
conclude
much
vivo
characterizations
pathological
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
).