Neurodegenerative Diseases,
Journal Year:
2023,
Volume and Issue:
23(3-4), P. 35 - 42
Published: Jan. 1, 2023
<b><i>Introduction:</i></b>
Progressive
supranuclear
palsy
(PSP)
is
a
four-repeat
tauopathy
characterized
by
multiple
clinicopathologic
subtypes.
Advanced
neuroimaging
techniques
have
shown
an
early
ability
to
distinguish
PSP
subtypes
noninvasively
for
improved
diagnosis.
This
study
utilized
tau
PET
imaging
and
MRI
at
7T
determine
the
profile
of
participant
with
comorbid
amyotrophic
lateral
sclerosis
(ALS).
<b><i>Method:</i></b>
[<sup>18</sup>F]-flortaucipir
was
performed
on
one
PSP-ALS,
typical
(Richardson’s
syndrome;
PSP-RS),
15
healthy
control
volunteers.
Standardized
uptake
value
ratio
(SUVR)
in
each
brain
region
compared
between
participants
controls.
Quantitative
susceptibility
mapping
(QSM)
inflow-based
vascular-space
occupancy
were
two
age-matched
controls
evaluate
differences
regional
iron
content
arteriolar
cerebral
blood
volume
(CBVa),
respectively.
<b><i>Results:</i></b>
In
precentral
gyrus
demonstrated
highest
all
regions
relative
(z-score
1.94).
PSP-RS,
subcortical
regions,
including
pallidum,
thalamus,
hippocampus,
brainstem
(z-scores
1.08,
1.41,
1.49,
1.32,
respectively).
Susceptibility
values
as
measure
higher
globus
pallidus
substantia
nigra
than
midbrain
pons
participant,
regardless
group.
CBVa
tended
be
gray
matter
controls,
although
large
measurement
variability
noted
across
regions.
<b><i>Conclusion:</i></b>
vivo
individual
PSP-ALS
overlap
increased
burden
motor
cortex
that
not
observed
PSP-RS
or
participants.
Consistent
prior
studies,
mainly
basal
ganglia.
QSM
data
suggest
off-target
binding
may
account
some
but
ganglia
PSP-RS.
These
findings
support
existing
evidence
can
among
detecting
distinct
patterns
deposition
brain.
Larger
studies
are
needed
whether
sensitive
changes
microvasculature
PSP.
NeuroImage,
Journal Year:
2023,
Volume and Issue:
282, P. 120401 - 120401
Published: Oct. 5, 2023
Quantitative
susceptibility
mapping
(QSM)
is
a
magnetic
resonance
imaging
(MRI)
technique
that
can
assess
the
properties
of
cerebral
iron
in
vivo.
Although
brain
necessary
for
basic
neurobiological
functions,
excess
content
disrupts
homeostasis,
leads
to
oxidative
stress,
and
ultimately
contributes
neurodegenerative
disease.
However,
some
degree
elevated
present
even
among
healthy
older
adults.
To
better
understand
topographical
pattern
accumulation
its
relation
cognitive
aging,
we
conducted
systematic
review
47
QSM
studies
with
focus
on
five
distinct
themes.
The
first
two
themes
focused
age-related
increases
deep
gray
matter
nuclei
versus
cortex.
overall
level
higher
than
cortical
regions.
Deep
vary
regard
effects,
which
are
most
prominent
putamen,
deposition
also
observed
frontal,
temporal,
parietal
regions
during
aging.
third
theme
behavioral
relevance
indicated
both
was
related
decline
fluid
(speed-dependent)
cognition.
A
handful
multimodal
studies,
reviewed
fourth
theme,
suggest
interacts
measures
function,
white
degradation,
neuropathologies.
final
concerning
modifiers
pointed
potential
roles
cardiovascular,
dietary,
genetic
factors.
relatively
recent
tool
assessing
accumulation,
it
has
significant
promise
contributing
new
insights
into
neurocognitive
International Journal of Molecular Sciences,
Journal Year:
2024,
Volume and Issue:
25(8), P. 4269 - 4269
Published: April 12, 2024
Iron
accumulation
in
the
brain
is
a
common
feature
of
many
neurodegenerative
diseases.
Its
involvement
spans
across
main
proteinopathies
involving
tau,
amyloid-beta,
alpha-synuclein,
and
TDP-43.
Accumulating
evidence
supports
contribution
iron
disease
pathologies,
but
delineation
its
pathogenic
role
yet
challenged
by
complex
multiple
neurotoxicity
mechanisms
supporting
reciprocal
influence
between
protein
pathology.
Here,
we
review
major
proteinopathy-specific
observations
four
distinct
hypotheses:
(1)
deposition
consequence
pathology;
(2)
promotes
(3)
protects
from
or
hinders
(4)
pathology
contribute
parallelly
to
pathogenesis.
an
essential
element
for
physiological
function,
requiring
fine
balance
levels.
Understanding
disease-related
at
more
intricate
systemic
level
critical
advancements
chelation
therapies.
Frontiers in Neuroscience,
Journal Year:
2024,
Volume and Issue:
18
Published: Feb. 26, 2024
Introduction
Alzheimer’s
disease
(AD),
characterized
by
distinctive
pathologies
such
as
amyloid-β
plaques
and
tau
tangles,
also
involves
deregulation
of
iron
homeostasis,
which
may
accelerate
neurodegeneration.
This
meta-analysis
evaluated
the
use
quantitative
susceptibility
mapping
(QSM)
to
detect
accumulation
in
deep
gray
matter
(DGM)
basal
ganglia
AD,
contributing
a
better
understanding
AD
progression,
potentially
leading
new
diagnostic
therapeutic
approaches.
Methods
Using
Preferred
Reporting
Items
for
Systematic
Reviews
Meta-Analyses
(PRISMA)
guidelines,
we
systematically
searched
PubMed,
Scopus,
Web
Sciences,
Google
Scholar
databases
up
October
2023
studies
employing
QSM
research.
Eligibility
criteria
were
based
on
PECO
framework,
included
assessing
alterations
magnetic
indicative
DGM
patients
with
AD.
After
initial
screening
quality
assessment
using
Newcastle-Ottawa
Scale,
was
conducted
compare
levels
between
healthy
controls
(HCs)
random-effects
model.
Results
The
nine
comprising
267
272
HCs.
There
significantly
higher
values,
indicating
greater
deposition,
putamen
(standardized
mean
difference
(SMD)
=
1.23;
95%
CI:
0.62
1.84;
p
0.00),
globus
pallidus
(SMD
0.79;
0.07
1.52;
0.03),
caudate
nucleus
0.72;
0.39
1.06;
0.00)
compared
However,
no
significant
differences
found
thalamus
1.00;
−0.42
2.43;
0.17).
sensitivity
analysis
indicated
that
single
study
impacted
overall
results.
Age
identified
major
contributor
heterogeneity
across
all
nuclei
subgroup
analysis.
Older
age
(>69
years)
lower
male
percentage
(≤30%)
associated
increase
Conclusion
suggests
excessive
deposition
is
linked
especially
putamen.
underscores
complex
nature
pathology
iron,
influenced
age,
sex,
regional
differences,
necessitating
further
research
comprehensive
understanding.
Journal of Magnetic Resonance Imaging,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 28, 2025
Background
As
ferroptosis
is
a
key
factor
in
renal
fibrosis
(RF),
iron
deposition
monitoring
may
help
evaluating
RF.
The
capability
of
quantitative
susceptibility
mapping
(QSM)
for
detecting
RF
remains
uncertain.
Purpose
To
investigate
the
potential
QSM
to
detect
Study
Type
Animal
model.
Model
Eighty
New
Zealand
rabbits
were
randomly
divided
into
control
(N
=
10)
and
70)
groups,
consisting
baseline,
7,
14,
21,
28
days
12
each),
longitudinal
subgroups.
was
induced
via
unilateral
arteria
stenosis.
Field
Strength/Sequence
3
T,
with
gradient
echo,
arterial
spin
labeling
echo.
Assessment
Bilateral
kidney
values
(
χ
)
cortex
CO
outer
medulla
OM
evaluated
histopathology.
Statistical
Tests
Analysis
variance,
Kruskal–Wallis,
Spearman's
correlation,
area
under
receiver
operating
characteristic
curve
(AUC).
P
<
0.05
significant.
Results
In
fibrotic
kidneys,
decreased
at
7
([−6.69
±
0.98]
×
10
−2
ppm)
increased
during
14–28
([−1.85
2.11],
[0.14
0.58],
[1.99
0.60]
ppm,
respectively),
while
had
opposite
trend.
Both
significantly
correlated
histopathology
(|
r
|
0.674–0.849).
AUC
distinguishing
degrees
0.692–0.993.
contralateral
initially
([−6.67
0.84]
then
recovered
baseline
([−4.81
0.89]
ppm),
7–28
([2.58
1.40],
[2.25
1.83],
[2.49
[2.43
1.32]
respectively)
higher
than
([0.54
0.18]
ppm).
Data
Conclusion
Different
patterns
observed
values,
suggesting
Plain
Language
Summary
Renal
(RF)
common
outcome
most
diseases,
leading
scarring
loss
function.
Increasing
evidence
suggests
that
abnormal
metabolism
plays
an
important
role
This
study
used
technique
called
measure
levels
Specifically,
advanced
exhibited
concentrations,
moderate
strong
correlations
between
demonstrated
could
accurately
changes
assess
severity.
Overall,
shows
promise
as
tool
progression.
Evidence
Level
2
Technical
Efficacy
Stage
NeuroImage,
Journal Year:
2024,
Volume and Issue:
290, P. 120555 - 120555
Published: March 5, 2024
Aberrant
susceptibility
due
to
iron
level
abnormality
and
brain
network
disconnections
are
observed
in
Alzheimer's
disease
(AD),
with
disrupted
homeostasis
hypothesized
be
linked
AD
pathology
neuronal
loss.
However,
whether
associations
exist
between
abnormal
quantitative
mapping
(QSM),
atrophy,
altered
connectome
remains
unclear.
Based
on
multi-parametric
imaging
data
from
30
patients
26
healthy
controls
enrolled
at
the
China-Japan
Friendship
Hospital,
we
investigated
of
QSM
signal
volumetric
measure
across
246
regions
patients.
The
structural
functional
connectomes
were
constructed
based
diffusion
MRI
tractography
connectivity,
respectively.
topology
was
quantified
using
graph
theory
analyses.
We
revealed
seven
both
reduced
cortical
thickness
(p<0.05)
AD,
including
right
superior
frontal
gyrus,
left
temporal
fusiform
parietal
lobule,
inferior
precuneus.
Correlations
computed
subjects
specific
group
resulted
statistically
significant
correlations
five
these
regions,
higher
compared
topology.
correlation
topological
metrics,
value
individual
group-averaged
levels,
resulting
a
call
spatial
correlations.
Decreased
global
efficiency
also
found
level.
These
findings
may
provide
insights
into
complex
relationships
among
QSM,
AD.
Biomolecules,
Journal Year:
2024,
Volume and Issue:
14(3), P. 295 - 295
Published: March 1, 2024
Alzheimer’s
disease
(AD)
is
a
prevalent
neurodegenerative
disorder
characterized
by
cognitive
decline
and
neuropathological
hallmarks,
including
β-amyloid
(Aβ)
plaques,
Tau
tangles,
synaptic
dysfunction
neurodegeneration.
Emerging
evidence
suggests
that
abnormal
iron
(Fe)
metabolism
plays
role
in
AD
pathogenesis,
but
the
precise
spatial
distribution
of
Fe
its
transporters,
such
as
ferroportin
(FPN),
within
affected
brain
regions
remains
poorly
understood.
This
study
investigates
FPN
CA1
region
human
hippocampus
patients
with
micrometer
lateral
resolution
using
laser
ablation
inductively
coupled
plasma
mass
spectrometry
(LA-ICP-MS).
For
this
purpose,
we
visualized
quantified
three
separated
layers:
stratum
molecular–radial
(SMR),
pyramidal
(SP)
oriens
(SO).
Additionally,
chromogenic
immunohistochemistry
was
used
to
examine
colocalization
Aβ
proteins.
The
results
show
accumulation
significantly
higher
brains,
particularly
SMR
SO.
However,
did
not
present
changes
AD,
although
it
showed
non-uniform
across
layers,
elevated
levels
SP
Interestingly,
minimal
overlap
observed
between
signals,
none
areas
rich
neurofibrillary
tangles
(NFTs)
or
neuritic
plaques
(NP).
In
conclusion,
lack
correlation
signals
complex
regulatory
mechanisms
deposition.
These
findings
highlight
complexity
dysregulation
potential
progression.
Translational Psychiatry,
Journal Year:
2024,
Volume and Issue:
14(1)
Published: March 26, 2024
Abstract
Quantitative
susceptibility
mapping
is
a
magnetic
resonance
imaging
technique
that
measures
brain
tissues’
susceptibility,
including
iron
deposition
and
myelination.
This
study
examines
the
relationship
between
subcortical
volume
determines
specific
differences
in
these
among
patients
with
major
depressive
disorder
(MDD),
schizophrenia,
healthy
controls
(HCs).
was
cross-sectional
study.
Sex-
age-
matched
MDD
(
n
=
49),
schizophrenia
24),
HCs
50)
were
included.
Magnetic
conducted
using
quantitative
T1-weighted
to
measure
volume.
The
acquired
measurements
compared
groups
analyses
of
variance
post
hoc
comparisons.
Finally,
general
linear
model
examined
susceptibility–volume
relationship.
Significant
group-level
found
nucleus
accumbens
amygdala
p
0.045).
Post-hoc
indicated
for
group
significantly
higher
than
HC
0.0054,
0.0065,
respectively).
However,
no
significant
groups.
interaction
but
not
or
showed
alterations
patients.
A
observed
group’s
accumbens,
which
abnormalities
myelination
dopaminergic
system
related
deposition.
Brain Imaging and Behavior,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Feb. 11, 2025
This
study
aimed
to
evaluate
changes
in
gray
matter
nuclei
iron
deposition
chronic
kidney
disease
(CKD)
patients
using
the
quantitative
susceptibility
mapping
(QSM)
threshold
method,
and
analyze
relationship
between
brain
levels
cognitive
function.
A
total
of
fifty-three
CKD
were
prospectively
recruited,
comprising
35
hemodialysis
(HD,
57.54
±
10.42
years,
21
males)
18
non-hemodialysis
(NHD,
55.06
11.47
10
males
),
compared
43
healthy
controls
(HC,
55.67
7.79
males).
All
participants
underwent
clinical
assessments,
neuropsychological
tests,
QSM
scans.
The
mean
magnetic
value
(MSV)
volume
whole
(MSVM,
VM)
high
region
(MSVRII,
VRII)
measured.
Correlations
data,
scores,
variables
HD
group
analyzed.
Linear
regression
analysis
was
performed
explore
effect
on
cognition
emotional
well-being
group.
statistically
significant
P-value
set
at
0.05.
exhibited
higher
MSVM
right
red
nucleus
(RN)
HCs
(P
=
0.006).
Additionally,
differences
MSVRII
observed
left
caudate
(CN),
bilateral
putamen
(Put),
RN
among
three
groups
(all
P
0.027,
FDR-corrected).
Put
positively
correlated
with
creatinine
uric
acid
levels,
while
negatively
corpuscular
hemoglobin
concentration.
Regression
revealed
that
CN
independently
associated
depression,
delayed
recall
performance.
Conversely,
orientation
ability,
after
controlling
for
age,
sex,
years
education
duration
dialysis.
Brain
is
often
excessive
uneven
patients,
particularly
those
undergoing
hemodialysis.
Assessing
regional
high-iron
can
provide
valuable
insights
into
distribution
iron,
which
dysfunction
disorders.