bioRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2022,
Volume and Issue:
unknown
Published: July 27, 2022
Abstract
Temporal
Diffusion
Ratio
(TDR)
is
a
recently
proposed
dMRI
technique
(Dell’Acqua,
2019)
which
provides
contrast
between
areas
with
restricted
diffusion
and
either
without
or
length
scales
too
small
for
characterisation.
Hence,
it
has
potential
mapping
pore
sizes,
in
particular
large
axon
diameters
other
cellular
structures.
TDR
employs
the
signal
from
two
acquisitions
obtained
same,
large,
b-value
but
different
times
gradient
settings.
advantageous
as
standard
acquisition
sequences,
does
not
make
any
assumptions
on
underlying
tissue
structure
require
model
fitting,
avoiding
issues
related
to
degeneracy.
This
work
first
time
optimises
sequences
simulation
range
of
tissues
scanner
constraints.
We
extend
original
(which
considers
substrates
containing
cylinders)
by
additionally
considering
spherical
structures,
representing
cell
soma
tissue.
Our
results
show
that
contrasting
an
short
duration
long
improves
wide
configurations.
Additionally,
presence
Rician
noise,
computing
subset
(50%
fewer)
acquired
gradients
rather
than
entire
shell
originally
further
contrast.
In
last
part
are
demonstrated
experimentally
rat
spinal
cord.
line
simulations,
experimental
data
shows
optimised
compared
non-optimised
TDR.
Furthermore,
we
find
strong
correlation
histology
measurements
diameter.
conclusion,
great
very
promising
alternative
(or
potentially
complement)
model-based
approaches
sizes
general.
Highlights
2-seq
approach
maps
Optimised
waveform
pair
is:
δ
+
low
G
high
If
noisy
calculating
using
HARDI
subsets
increases
accuracy
demonstrate
pre-clinically
cord
Pre-clinical
values
strongly
correlated
diameter
Magnetic Resonance in Medicine,
Journal Year:
2022,
Volume and Issue:
89(3), P. 1160 - 1172
Published: Oct. 11, 2022
To
develop
a
denoising
strategy
leveraging
redundancy
in
high-dimensional
data.The
SNR
fundamentally
limits
the
information
accessible
by
MRI.
This
limitation
has
been
addressed
host
of
techniques,
recently
including
so-called
MPPCA:
principal
component
analysis
signal
followed
automated
rank
estimation,
exploiting
Marchenko-Pastur
distribution
noise
singular
values.
Operating
on
matrices
comprised
data
patches,
this
popular
approach
objectively
identifies
components
and,
ideally,
allows
to
be
removed
without
introducing
artifacts
such
as
image
blurring,
or
nonlocal
averaging.
The
MPPCA
however,
relies
large
number
values
relative
avoid
ill
effects.
condition
is
unlikely
met
when
patches
and
therefore
are
small,
for
example
due
spatially
varying
noise.
Here,
we
introduce
tensor
(tMPPCA)
purpose
multidimensional
data,
from
multicontrast
acquisitions.
Rather
than
combining
dimensions
matrices,
tMPPCA
uses
each
dimension
data's
inherent
tensor-structure
better
characterize
noise,
recursively
estimate
components.Relative
matrix-based
MPPCA,
requires
no
additional
assumptions,
comparing
two
numerical
phantom
multi-TE
diffusion
MRI
set,
dramatically
improves
performance.
particularly
true
small
suggesting
that
can
especially
beneficial
cases.The
technique
extended
with
improved
performance
smaller
patch
sizes.
Magnetic Resonance in Medicine,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Feb. 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.
Scientific Reports,
Journal Year:
2024,
Volume and Issue:
14(1)
Published: April 29, 2024
Abstract
Pathological
data
showed
focal
inflammation
and
regions
of
diffuse
neuronal
loss
in
the
cortex
people
with
multiple
sclerosis
(MS).
In
this
work,
we
applied
a
novel
model
(“soma
neurite
density
imaging
(SANDI)”)
to
multishell
diffusion-weighted
MRI
acquired
healthy
subjects
(pwMS),
order
investigate
degeneration-related
changes
cortical
tissue
pwMS.
We
aimed
(i)
establish
whether
SANDI
is
applicable
vivo
clinical
data;
(ii)
inflammatory
degenerative
using
soma
fraction
(
f
)—a
marker
cellularity—in
both
lesions
normal-appearing-cortex
(iii)
correlate
biological
measures
simplified
version
scanners.
then
provided
evidence
that
pwMS
exhibited
an
overall
decrease
compared
subjects,
suggesting
global
processes
compatible
loss.
On
other
hand,
have
found
progressive
higher
outer
part
relapsing–remitting
pwMS,
possibly
supporting
current
pathological
knowledge
increased
innate
cells
these
regions.
A
similar
finding
was
obtained
subpial
patients,
reflecting
existing
lesion
types.
significant
correlation
between
serum
neurofilament
light
chain—a
biomarker
axonal
damage—suggesting
relationship
again.
Overall,
our
show
promising
monitor
cellularity
neurodegeneration
neuroinflammation
MS
patients.
Human Brain Mapping,
Journal Year:
2023,
Volume and Issue:
44(13), P. 4792 - 4811
Published: July 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
Aging Cell,
Journal Year:
2024,
Volume and Issue:
23(11)
Published: Aug. 8, 2024
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,
Journal Year:
2023,
Volume and Issue:
269, P. 119930 - 119930
Published: Feb. 5, 2023
Temporal
Diffusion
Ratio
(TDR)
is
a
recently
proposed
dMRI
technique
(Dell'Acqua
et
al.,
proc.
ISMRM
2019)
which
provides
contrast
between
areas
with
restricted
diffusion
and
either
without
or
length
scales
too
small
for
characterisation.
Hence,
it
has
potential
informing
on
pore
sizes,
in
particular
the
presence
of
large
axon
diameters
other
cellular
structures.
TDR
employs
signal
from
two
acquisitions
obtained
same,
large,
b-value
but
different
gradient
waveforms.
advantageous
as
standard
acquisition
sequences,
does
not
make
any
assumptions
underlying
tissue
structure
require
model
fitting,
avoiding
issues
related
to
degeneracy.
This
work
first
time
introduces
optimises
method
simulation
range
tissues
scanner
constraints
validates
pre-clinical
demonstration.
We
consider
both
substrates
containing
cylinders
spherical
structures,
representing
cell
soma
tissue.
Our
results
show
that
contrasting
an
short
duration,
high
strength
long
low
strength,
maximises
wide
configurations.
Additionally,
Rician
noise,
computing
subset
(50%
fewer)
acquired
gradients
rather
than
entire
shell
originally
further
improves
contrast.
In
last
part
are
demonstrated
experimentally
rat
spinal
cord.
line
simulations,
experimental
data
shows
optimised
compared
non-optimised
TDR.
Furthermore,
we
find
strong
correlation
histology
measurements
diameter.
conclusion,
great
very
promising
alternative
(or
potentially
complement)
model-based
approaches
sizes
general.
Science Advances,
Journal Year:
2025,
Volume and Issue:
11(18)
Published: May 1, 2025
Atlases
of
the
brain
are
critical
resources
that
make
it
possible
to
share
data
in
a
common
reference
frame.
Unexpectedly,
there
is
no
three-dimensional
(3D)
stereotaxic
atlas
mouse
provides
whole
coverage
at
macro
single-cell
levels.
Diffusion
tensor
images
from
five
perfusion-fixed
(in
skull)
specimens
were
acquired
15
micrometers,
highest
resolution
ever
reported.
imaging
yields
multiple
3D
volumes,
each
which
highlights
unique
cytoarchitecture.
The
averages
mapped
into
micro-computed
tomography
skull
create
external
landmarks
(bregma
and
lambda).
Light
sheet
same
brains
coregistered,
providing
cell
maps
space.
Allen
Reference
Atlas
was
registered
volume
correct
geometric
distortion
bring
resulting
multiscalar
(13
terabytes)
spatial
framework
anneal
across
molecular,
structural,
functional
studies
mice.