Frontiers in Psychology,
Journal Year:
2025,
Volume and Issue:
16
Published: March 11, 2025
Objective
This
study
aimed
to
determine
balance,
fall
risk,
and
kinesiophobia
in
individuals
with
Alzheimer’s
Dementia
(AD).
Methods
The
was
completed
18
AD
healthy
AD-free
control
group
early
or
moderate-stage
diagnosed
by
a
neurologist.
Socio-demographic
characteristics
of
the
were
assessed
using
an
evaluation
form,
their
balance
evaluated
Tinetti
Balance
Gait
Assessment
Test,
Timed
Up
Go
Single
Leg
Standing
Test.
Falls
Risk
Self-Assessment
Scale
(FRSAS)
used
assess
risk
falls.
Kinesiophobia
Tampa
for
(TKS).
Additionally,
participants
underwent
Mini-Mental
State
Examination
(MMSE).
Result
mean
age
lower
than
that
individuals,
means
69
±
3.66
years
65.4
4.10
years,
respectively
(
p
=
0.012).
0.005),
gait
<
0.001),
total
(MMSE)
0,001)
scores
relative
controls.
FRSAS
0.001)
higher
TKS
found
be
similar
between
0.860).
Conclusion
It
disease
(AD)
have
poorer
falls
compared
individuals.
In
light
these
results,
assessments
should
included
when
developing
rehabilitation
protocols
AD.
Treatment
designed
this
patient
must
incorporate
balance-specific
exercise
training
programs.
individual
environmental
preventive
measures
implemented
reduce
Clinical
trial
registration
Trial
Number:
NCT05201768.
Journal of Neurology Neurosurgery & Psychiatry,
Journal Year:
2023,
Volume and Issue:
94(11), P. 954 - 961
Published: June 22, 2023
Alzheimer's
disease
(AD)
is
the
leading
cause
of
dementia.
Currently,
there
are
no
effective
disease-modifying
treatments
for
AD.
Mendelian
randomisation
(MR)
has
been
widely
used
to
repurpose
licensed
drugs
and
discover
novel
therapeutic
targets.
Thus,
we
aimed
identify
targets
AD
analyse
their
pathophysiological
mechanisms
potential
side
effects.A
two-sample
MR
integrating
identified
druggable
genes
was
performed
estimate
causal
effects
blood
brain
expression
quantitative
trait
loci
(eQTLs)
on
A
repeat
study
conducted
using
different
eQTL
data
sources
validate
genes.
Using
markers
with
available
genome-wide
association
studies
data,
evaluated
relationship
between
established
explore
possible
mechanisms.
Finally,
treatment
were
assessed
a
phenome-wide
MR.Overall,
5883
unique
aggregated;
33
in
at
least
one
dataset
(brain
or
blood),
5
validated
dataset.
Among
them,
three
prior
(epoxide
hydrolase
2
(EPHX2),
SERPINB1
SIGLEC11)
reached
significant
levels
both
tissues.
EPHX2
may
mediate
pathogenesis
by
affecting
entire
hippocampal
volume.
Further
analysis
revealed
targeting
EPHX2,
SIGLEC11.This
provides
genetic
evidence
supporting
benefits
treatment,
which
will
be
useful
prioritising
drug
development.
Cells,
Journal Year:
2024,
Volume and Issue:
13(6), P. 511 - 511
Published: March 14, 2024
Neuroinflammatory
and
neurodegenerative
disorders
including
Alzheimer’s
disease
(AD),
Parkinson’s
(PD),
traumatic
brain
injury
(TBI)
Amyotrophic
lateral
sclerosis
(ALS)
are
chronic
major
health
disorders.
The
exact
mechanism
of
the
neuroimmune
dysfunctions
these
pathogeneses
is
currently
not
clearly
understood.
These
show
dysregulated
inflammatory
responses,
activation
neurons,
glial
cells,
neurovascular
unit
damage
associated
with
excessive
release
proinflammatory
cytokines,
chemokines,
neurotoxic
mediators,
infiltration
peripheral
immune
cells
into
brain,
as
well
entry
mediators
through
damaged
endothelial
blood–brain
barrier
tight
junction
proteins.
Activation
leads
to
many
molecules
that
cause
neuroinflammation
neurodegeneration.
Gulf
War
Illness
(GWI)
myalgic
encephalomyelitis/chronic
fatigue
syndrome
(ME/CFS)
also
dysfunctions.
Currently,
there
no
effective
disease-modifying
therapeutic
options
available
for
diseases.
Human
induced
pluripotent
stem
cell
(iPSC)-derived
astrocytes,
microglia,
pericytes
used
models
drug
discovery.
This
review
highlights
certain
recent
trends
in
neuroinflammatory
responses
iPSC-derived
applications
International Journal of Molecular Sciences,
Journal Year:
2024,
Volume and Issue:
25(2), P. 1168 - 1168
Published: Jan. 18, 2024
Alzheimer’s
Disease
(AD)
is
the
most
common
neurodegenerative
disease
which
manifests
with
progressive
cognitive
impairment,
leading
to
dementia.
Considering
noninvasive
collection
of
saliva,
we
designed
systematic
review
answer
question
“Are
salivary
biomarkers
reliable
for
diagnosis
Disease?”
Following
inclusion
and
exclusion
criteria,
30
studies
were
included
in
this
(according
PRISMA
statement
guidelines).
Potential
include
mainly
proteins,
metabolites
even
miRNAs.
Based
on
meta-analysis,
AD
patients,
levels
beta-amyloid42
p-tau
significantly
increased,
t-tau
lactoferrin
decreased
at
borderline
statistical
significance.
However,
according
pooled
AUC,
showed
a
significant
predictive
value
salivary-based
diagnosis.
In
conclusion,
potential
markers
such
as
beta-amyloid42,
tau
can
be
detected
saliva
could
reliably
support
early
disease.
Frontiers in Aging Neuroscience,
Journal Year:
2025,
Volume and Issue:
16
Published: Jan. 3, 2025
Improving
sleep
in
murine
Alzheimer's
disease
(AD)
is
associated
with
reduced
brain
amyloidosis.
However,
the
window
of
opportunity
for
successful
sleep-targeted
interventions,
regarding
reduction
pathological
hallmarks
and
related
cognitive
performance,
remains
poorly
characterized.
Here,
we
enhanced
slow-wave
activity
(SWA)
during
via
sodium
oxybate
(SO)
oral
administration
2
weeks
at
early
(6
months
old)
or
moderately
late
(11
stages
Tg2576
mice
evaluated
resulting
neuropathology
behavioral
performance.
We
observed
that
performance
6-month-old
significantly
improved
upon
SO
treatment,
whereas
no
change
was
11-month-old
mice.
Histochemical
assessment
amyloid
plaques
demonstrated
SO-treated
had
less
plaque
burden
than
placebo-treated
ones,
ELISA
insoluble
protein
fractions
from
brains
indicated
lower
Aβ-42/Aβ-40
ratio
group
vs.
controls.
Altogether,
our
results
suggest
SWA-dependent
amyloidosis
leads
to
alleviated
impairment
only
if
administered
course,
potentially
highlighting
key
importance
sleep-based
interventions
clinical
cohorts.
International Journal of Molecular Sciences,
Journal Year:
2025,
Volume and Issue:
26(2), P. 484 - 484
Published: Jan. 8, 2025
Alzheimer's
disease
(AD)
remains
a
leading
cause
of
cognitive
decline
and
mortality
worldwide,
characterized
by
neurodegeneration,
synaptic
deficiencies,
neuroinflammation.
Despite
advancements
in
early
detection,
diagnosis,
treatment,
AD
presents
substantial
challenges
due
to
its
complex
pathology,
heterogeneity,
the
limited
efficacy
current
therapies.
Consequently,
there
is
pressing
need
for
novel
therapeutic
agents
target
multifaceted
aspects
enhance
treatments,
minimize
adverse
effects.
AdipoRon,
an
adiponectin
receptor
agonist,
has
garnered
interest
potential
neuroprotective
effects,
including
reducing
neuroinflammation,
improving
mitochondrial
function,
mitigating
tau
hyperphosphorylation.
This
review
aimed
evaluate
effects
AdipoRon-based
replacement
therapy
against
AD,
using
comprehensive
approach
grounded
PICO
framework-Population,
Intervention,
Comparison,
Outcomes.
A
total
six
studies
were
reviewed,
vitro
vivo
investigations
examining
AdipoRon's
impact
on
various
models.
These
involved
different
cell
lines
transgenic
mouse
models,
assessing
outcomes
such
as
phosphorylation,
relevant
molecular
pathways.
By
synthesizing
data
from
these
studies,
our
thoroughly
explains
mechanisms
action,
agent
AD.
analysis
aims
highlight
state
knowledge,
identify
gaps
research,
suggest
directions
future
clinical
applications.
Pharmaceutics,
Journal Year:
2025,
Volume and Issue:
17(1), P. 121 - 121
Published: Jan. 16, 2025
In
the
21st
century,
thanks
to
advances
in
biotechnology
and
developing
pharmaceutical
technology,
significant
progress
is
being
made
effective
drug
design.
Drug
targeting
aims
ensure
that
acts
only
pathological
area;
it
defined
as
ability
accumulate
selectively
quantitatively
target
tissue
or
organ,
regardless
of
chemical
structure
active
substance
method
administration.
With
targeting,
conventional,
biotechnological
gene-derived
drugs
body’s
organs,
tissues,
cells
can
be
transported
specific
regions.
These
systems
serve
carriers
regulate
timing
release.
Despite
having
many
advantageous
features,
these
have
limitations
thoroughly
treating
complex
diseases
such
cancer.
Therefore,
combining
with
nanoparticle
technologies
imperative
treat
cancer
at
both
local
systemic
levels
effectively.
The
nanocarrier-based
delivery
involves
encapsulating
target-specific
molecules
into
polymeric
vesicular
systems.
Various
(DDS)
were
investigated
discussed
this
review
article.
first
part
passive
systems,
hydrogels,
thermoplastics,
microdevices
transdermal-based
second
carrier
nanobiotechnology
(carbon
nanotubes,
nanoparticles,
coated,
pegylated,
solid
lipid
nanoparticles
smart
nanogels).
third
part,
advantages
discussed,
finally,
market
research
commercial
used
nanotechnological
approaches
was
included.
Biomedicines,
Journal Year:
2023,
Volume and Issue:
11(6), P. 1752 - 1752
Published: June 18, 2023
Alzheimer’s
disease
(AD)
is
a
deadly,
progressive,
and
irreversible
brain
condition
that
impairs
cognitive
abilities.
Globally,
it
affects
32.6
million
individuals,
if
no
viable
therapies
are
available
by
2050,
figure
might
rise
to
139
million.
The
current
course
of
treatment
enhances
abilities
temporarily
relieves
symptoms,
but
does
not
halt
or
slow
the
disease’s
development.
Additionally,
treatments
primarily
offered
in
conventional
oral
dosage
forms,
lack
specialization
cause
adverse
effects,
resulting
poor
patient
compliance.
A
potential
nanotechnology-based
strategy
can
improve
bioavailability
specificity
drug
targeting
brain.
Furthermore,
this
review
extensively
summarizes
applications
nanomedicines
for
effective
delivery
drugs
used
management
AD.
In
addition,
clinical
progress
AD
also
discussed,
challenges
facing
development
addressed
article.
International Journal of Molecular Sciences,
Journal Year:
2023,
Volume and Issue:
24(19), P. 14794 - 14794
Published: Sept. 30, 2023
Alzheimer's
disease
(AD)
is
one
of
the
most
common
neurodegenerative
disorders
associated
with
age
or
inherited
mutations.
It
characterized
by
severe
dementia
in
late
stages
that
affect
memory,
cognitive
functions,
and
daily
life
overall.
AD
progression
linked
to
accumulation
cytotoxic
amyloid
beta
(Aβ)
hyperphosphorylated
tau
protein
combined
other
pathological
features
such
as
synaptic
loss,
defective
energy
metabolism,
imbalances
protein,
metal
homeostasis.
Several
treatment
options
for
are
under
investigation,
including
antibody-based
therapy
stem
cell
transplantation.
Amyloid
precursor
(APP)
a
membrane
considered
play
main
role
pathology.
known
APP
physiological
conditions
follows
non-amyloidogenic
pathway;
however,
it
can
proceed
an
amyloidogenic
scenario,
which
leads
generation
extracellular
deleterious
Aβ
plaques.
Not
all
steps
biogenesis
clear
so
far,
these
questions
should
be
addressed
future
studies.
complex
chronic
many
factors
contribute
progression.