Pro-inflammatory cytokines in stress-induced depression: Novel insights into mechanisms and promising therapeutic strategies
Jun Chang,
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Tingcan Jiang,
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Xiaoqian Shan
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et al.
Progress in Neuro-Psychopharmacology and Biological Psychiatry,
Journal Year:
2024,
Volume and Issue:
131, P. 110931 - 110931
Published: Jan. 2, 2024
Language: Английский
Adverse event reporting of faricimab: a disproportionality analysis of FDA adverse event reporting system (FAERS) database
Chuan He,
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Qin Qiu,
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S L Lu
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et al.
Frontiers in Pharmacology,
Journal Year:
2025,
Volume and Issue:
16
Published: March 12, 2025
Background
Faricimab
is
the
first
and
only
bispecific
antibody
approved
by
U.S.
Food
Drug
Administration
(FDA)
for
intravitreal
injection.
Given
its
increasingly
widespread
use
in
retinal
vascular
diseases,
understanding
adverse
events
(AEs)
real-world
settings
crucial.
This
study
employed
FDA
Adverse
Event
Reporting
System
(FAERS)
database
to
investigate
potential
safety
concerns,
with
aim
of
providing
new
insights
clinical
practice.
Methods
conducted
a
disproportionality
analysis
event
data
from
FAERS
database,
which
faricimab
was
identified
as
primary
suspect,
covering
period
quarter
2022
second
2024.
To
ensure
accuracy
reliability
study,
we
four
types
analyses:
reporting
odds
ratio
(ROR),
proportional
(PRR),
multi-item
gamma
Poisson
shrinker
(MGPS),
Bayesian
confidence
propagation
neural
network
(BCPNN).
Additionally,
Weibull
distribution
utilized
model
risk
over
time.
Results
A
total
2,735
reaction
reports,
were
retrieved
database.
The
showed
that
faricimab-induced
AEs
occurred
across
25
system
organ
classes
(SOCs),
eye
disorders
meeting
positive
threshold
all
algorithms.
Significant
mapped
preferred
terms
(PT),
identifying
reactions
listed
on
drug
label:
endophthalmitis,
elevated
intraocular
pressure,
cataract,
pigment
epithelial
tear,
vitreous
floaters,
vasculitis,
artery
occlusion,
vein
occlusion.
In
addition
label,
several
previously
unreported
identified,
including
blindness,
cerebral
infarction,
hemorrhage,
occlusive
glaucoma,
dry
eye,
metamorphopsia,
unilateral
blindness.
Conclusion
provided
valuable
evidence
faricimab,
suggesting
clinicians
should
place
greater
emphasis
monitoring
effects
during
use.
Language: Английский
Agonism of β3-Adrenoceptors Inhibits Pathological Retinal Angiogenesis in the Model of Oxygen-Induced Retinopathy
Investigative Ophthalmology & Visual Science,
Journal Year:
2024,
Volume and Issue:
65(10), P. 34 - 34
Published: Aug. 26, 2024
Purpose:
In
response
to
hypoxia,
sympathetic
fibers
the
retina
activate
β-adrenoceptors
(β-ARs)
that
play
an
important
role
in
regulation
of
vascular
and
neuronal
functions.
We
investigated
β3-AR
using
mouse
model
oxygen-induced
retinopathy
(OIR).
Methods:
Mouse
pups
were
exposed
75%
oxygen
at
postnatal
day
7
(PD7)
followed
by
a
return
room
air
PD12.
The
preferential
agonist
BRL37344
was
subcutaneously
administered
once
daily
different
times
after
air.
At
PD17,
OIR
mice
underwent
flash
pattern
electroretinogram.
After
sacrifice,
retinal
wholemounts
used
for
vessel
staining
or
immunohistochemistry
astrocytes,
Müller
cells,
ganglion
cells
(RGCs).
homogenates,
levels
markers
associated
with
neovascularization
(NV),
blood–retinal
barrier
(BRB),
astrocytes
determined
western
blot,
quantitative
reverse-transcription
polymerase
chain
reaction
assess
messenger.
Administration
antagonist
SR59230A
performed
verify
selectivity.
Results:
expression
is
upregulated
but
its
increase
prevented
BRL37344,
which
counteracts
NV
inhibiting
pro-angiogenic
pathway,
activating
anti-angiogenic
recovering
BRB-associated
markers,
triggering
nitric
oxide
production,
favoring
revascularization
central
through
recovered
density
ultimately
midperiphery.
Vasculature
rescue
prevents
dysfunctional
activity
OIR-associated
cell
loss.
Conclusions:
has
emerged
as
crucial
intermediary
hypoxia-dependent
NV,
suggesting
agonists
treatment
proliferative
retinopathies.
Language: Английский
Ophthalmic corticosteroids-related adverse events: the FDA adverse event reporting system (FAERS) database pharmacovigilance study
Frontiers in Pharmacology,
Journal Year:
2024,
Volume and Issue:
15
Published: Dec. 11, 2024
Corticosteroids
are
extensively
used
in
ophthalmology,
particularly
for
treating
various
inflammatory
conditions.
Despite
their
effectiveness,
prolonged
or
high-dose
corticosteroid
use
is
associated
with
significant
adverse
drug
reactions
(ADRs),
such
as
increased
intraocular
pressure,
cataract
formation,
and
secondary
infections.
However,
there
currently
no
systematic
study
comparing
the
side
effects
of
ophthalmic
corticosteroids.
This
aims
to
investigate
safety
profiles
corticosteroids
through
pharmacovigilance
analysis
using
FDA
Adverse
Event
Reporting
System
(FAERS)
database.
Language: Английский