Frontiers in Pharmacology,
Journal Year:
2025,
Volume and Issue:
16
Published: March 13, 2025
Background
Alzheimer’s
disease
poses
a
major
public
health
challenge,
with
aducanumab’s
approval
in
2021
as
the
first
disease-modifying
therapy
raising
important
safety
considerations.
This
study
analyzed
Food
Drug
Administration
Adverse
Event
Reporting
System
(FAERS)
database
to
evaluate
real-world
profile
and
identify
potential
risk
factors.
Methods
We
conducted
comprehensive
pharmacovigilance
using
FAERS
from
January
2004
June
2024,
analyzing
510
aducanumab-associated
reports
integrated
databases
containing
over
18
million
demographic
records
66
drug
records.
Safety
signals
were
evaluated
four
complementary
disproportionality
methods:
Odds
Ratio
(ROR),
Proportional
(PRR),
Bayesian
Confidence
Propagation
Neural
Network
(BCPNN),
Multi-item
Gamma
Poisson
Shrinker
(MGPS).
Analyses
stratified
by
age
sex,
adverse
events
examined
at
both
Organ
Class
(SOC)
Preferred
Term
(PT)
levels
SAS
9.4.
Results
Among
event
reports,
predominantly
elderly
patients
(55.49%
aged
≥65
years),
nervous
system
disorders
most
frequent
(53.24%,
n
=
583).
Amyloid
related
imaging
abnormality-oedema/effusion
(ARIA-E)
abnormality-microhaemorrhages
haemosiderin
deposits
(ARIA-H)
emerged
significant
(ROR:
53,538.3
38,187.9,
respectively).
Sex-stratified
analysis
showed
comparable
profiles
between
males
females,
ARIA-E
events,
ARIA-H
maintaining
strong
across
all
groups,
particularly
≥75
years.
The
median
time
onset
was
146.0
days
(IQR:
80.0–195.0).
Temporal
revealed
increasing
signal
strength
for
ARIA-related
2004–2024,
notable
intensification
during
2022–2023.
Conclusion
Our
identified
primary
concern
aducanumab,
typically
occurring
within
146
of
treatment
initiation,
sex
but
heightened
risks
These
findings
support
viability
therapeutic
option
while
emphasizing
critical
importance
rigorous
monitoring
protocols,
ARIA
year
treatment.
Journal of Clinical Medicine,
Journal Year:
2024,
Volume and Issue:
13(3), P. 806 - 806
Published: Jan. 30, 2024
Dementia
is
a
major
cause
of
poor
quality
life,
disability,
and
mortality
in
old
age.
According
to
the
geroscience
paradigm,
mechanisms
that
drive
aging
process
are
also
involved
pathogenesis
chronic
degenerative
diseases,
including
dementia.
The
dissection
such
therefore
instrumental
providing
biological
targets
for
interventions
new
sources
biomarkers.
Within
several
biomarkers
have
been
discovered
can
be
measured
blood
allow
early
identification
individuals
at
risk
cognitive
impairment.
Examples
markers
include
inflammatory
biomolecules,
neuroaxonal
damage,
extracellular
vesicles,
DNA
methylation.
Furthermore,
gait
speed,
usual
fast
pace
as
part
dual
task,
has
shown
detect
future
Here,
we
provide
an
overview
available
may
used
gauge
impairment
apparently
healthy
older
adults.
Further
research
should
establish
which
combination
possesses
highest
predictive
accuracy
toward
incident
implementation
currently
large
share
at-risk
whom
preventive
implemented
maintain
or
increase
reserves,
thereby
reducing
progression
Molecules,
Journal Year:
2024,
Volume and Issue:
29(23), P. 5744 - 5744
Published: Dec. 5, 2024
Gamma-glutamate
is
an
important
excitatory
neurotransmitter
in
the
central
nervous
system
(CNS),
which
plays
role
transmitting
synapses,
plasticity,
and
other
brain
activities.
Nevertheless,
alterations
glutamatergic
signaling
pathway
are
now
accepted
as
a
element
Alzheimer's
disease
(AD)
pathophysiology.
One
of
most
prevalent
types
dementia
older
adults
AD,
progressive
neurodegenerative
illness
brought
on
by
persistent
decline
cognitive
function.
Since
AD
has
been
shown
to
be
multifactorial,
variety
pharmaceutical
targets
may
used
treat
condition.
N-methyl-D-aspartic
acid
receptor
(NMDAR)
antagonists
acetylcholinesterase
inhibitors
(AChEIs)
two
drug
classes
that
Food
Drug
Administration
authorized
for
treatment
AD.
The
AChEIs
approved
galantamine,
donepezil,
rivastigmine.
However,
memantine
only
non-competitive
NMDAR
antagonist
This
review
aims
outline
involvement
glutamate
(GLU)
at
molecular
level
pathways
associated
with
demonstrate
target
therapeutic
potential
its
receptor.
We
will
also
consider
opinion
leading
authorities
working
this
area,
drawback
existing
strategies,
direction
further
investigation.
Expert Opinion on Biological Therapy,
Journal Year:
2024,
Volume and Issue:
24(11), P. 1261 - 1269
Published: Oct. 21, 2024
Introduction
Alzheimer's
disease
can
cause
dementia
through
brain
matter
degradation.
This
study
investigates
the
monoclonal
antibody
usage
for
AD
treatment,
following
PRISMA
2020
guidelines,
and
aims
to
discern
that
offers
optimal
balance
of
efficacy
safety
individuals
with
AD.
The Journal of Prevention of Alzheimer s Disease,
Journal Year:
2025,
Volume and Issue:
12(1), P. 100010 - 100010
Published: Jan. 1, 2025
Declining
motor
abilities
might
be
a
noninvasive
biomarker
for
Alzheimer's
disease
(AD).
Studying
ability
and
AD
progression
in
younger
Latinos
with
autosomal
dominant
(ADAD)
can
provide
insights
into
the
interplay
between
cognition
individuals
minimal
confounding
from
age-normative
changes
comorbid
medical
conditions.
This
study
aimed
to
(1)
examine
as
function
of
years
dementia
diagnosis
(2)
associations
cognitive
performance.
was
cross-sectional
observational
study.
The
took
place
at
University
Southern
California.
39
predominately
Latino
(mean
age
38.6
±
10
old)
known
carry
(carriers;
n=25)
or
50%
risk
inheriting
ADAD
but
not
carrying
mutation
(noncarriers;
n=14).
Individuals
completed
batteries
National
Institute
Health
Toolbox
(NIHTB)
Cognitive
Abilities
Screening
Instrument
(CASI).
All
models
included
effects
age,
education,
primary
language,
sex.
Compared
noncarriers,
carriers
had
significantly
weaker
grip
strength
12
years,
worse
manual
dexterity
slower
gait
speed
seven
before
expected
diagnosis.
Worse
associated
more
severe
stage
CASI
performance,
adjusting
demographic
clinical
variables.
findings
support
utility
precisely
strength,
dexterity,
potential
biomarkers
preclinical
AD.
Theoretical and Natural Science,
Journal Year:
2025,
Volume and Issue:
68(1), P. 221 - 226
Published: Jan. 13, 2025
In
this
society,
Alzheimer's
disease
represents
a
significant
public
health
concern.
Nevertheless,
the
market
offers
only
two
FDA-approved
drugs,
which
are
capable
of
partially
inhibiting
symptoms.
It
is
imperative
that
both
patients
and
researchers
made
aware
mechanism
by
AD
triggered
fundamental
logic
underlying
action
each
drug.
This
should
include
an
understanding
how
drug
reacts
with
body
ingredients
it
contains.
section
primarily
discusses
therapeutic
options
for
disease,
encompassing
drugs
mechanisms
currently
available
on
those
have
not
yet
been
approved
but
theoretically
feasible.
passage
will
introduce
number
potential
treatments
including
Chinese
patent
medicine,
acetylcholinesterase
inhibitors,
NMDA
receptor
antagonists,
Aduhelm,
Leqembi,
anti-amyloid
therapies
A
immunotherapies.
Despite
existence
these
many
years,
still
possible
to
cure
completely
or
delay
prevent
its
progression.
aims
provide
insights
into
future
direction
pharmaceutical
research
selection
appropriate
medications
Journal of Alzheimer s Disease,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 26, 2025
Understanding
the
sequential
progression
of
cognitive
decline
in
autosomal
dominant
Alzheimer's
disease
(ADAD)
Latino
population
is
crucial
for
enhancing
early
identification
targeted
interventions.
Given
tablet-based
administration
and
increasing
frequency
use
epidemiological
research,
validating
this
within
NIH
Toolbox
battery
(NIHTB-CB)
important.
The
first
aim
was
to
utilize
an
innovative
Event-Based
Modeling
(EBM)
analytic
approach
estimate
sequence
declines
persons
at
risk
ADAD
enriched
being
origin.
second
examine
associations
between
EBM-derived
estimates
severity
independent
outcomes
carriers
noncarriers.
This
cross-sectional
observational
study
(N
=
30)
included
16
mutation
14
noncarriers
who
completed
NIHTB-CB
their
primary
language
(n
8
Spanish;
n
22
English).
An
EBM
constructed
compare
on
performance.
We
utilized
linear
regression
cognitive-decline
stage
(e.g.,
performance
Cognitive
Abilities
Screening
Instrument
(CASI)
estimated
years
dementia
diagnosis).
that
tests
assessing
episodic
memory
were
become
abnormal
ADAD-related
decline.
Each
higher
associated
with
approximately
a
three-point
CASI
two
closer
diagnosis.
Findings
support
applied
likely
Latinos
ADAD.
Cells,
Journal Year:
2025,
Volume and Issue:
14(3), P. 229 - 229
Published: Feb. 6, 2025
The
relationship
between
aging,
mitochondrial
dysfunction,
neurodegeneration,
and
the
onset
of
Alzheimer’s
disease
(AD)
is
a
complex
area
study.
Aging
primary
risk
factor
for
AD,
it
associated
with
decline
in
function.
This
dysfunction
believed
to
contribute
neurodegenerative
processes
observed
AD.
Neurodegeneration
AD
characterized
by
progressive
loss
synapses
neurons,
particularly
regions
brain
involved
memory
cognition.
It
hypothesized
that
plays
pivotal
role
disrupting
cellular
energy
metabolism
increasing
production
reactive
oxygen
species
(ROS),
which
can
damage
components
exacerbate
neuronal
loss.
Despite
extensive
research,
precise
molecular
pathways
linking
pathology
are
not
fully
understood.
Various
hypotheses
have
been
proposed,
including
cascade
hypothesis,
suggests
an
early
event
pathogenesis
triggers
events
leading
neurodegeneration.
With
this
narrative
review,
we
aim
summarize
some
specific
issues
literature
on
mitochondria
their
involvement
onset,
focus
development
therapeutical
strategies
targeting
environment
potential
application
treatment
itself.