Expert Opinion on Pharmacotherapy,
Год журнала:
2023,
Номер
24(18), С. 2153 - 2159
Опубликована: Ноя. 29, 2023
Introduction
New
biologic
and
small
molecule
therapeutics
have
emerged
for
the
treatment
of
moderate-to-severe
atopic
dermatitis
(AD),
including
oral
Janus
kinase
(JAK)
inhibitors
such
as
baricitinib.
While
JAK
are
commonly
used
to
treat
rheumatoid
arthritis
inflammatory
bowel
disease,
these
agents
relatively
new
in
field
dermatology.
Dermatology and Therapy,
Год журнала:
2024,
Номер
14(4), С. 919 - 932
Опубликована: Март 21, 2024
Several
systemic
therapies
have
been
approved
for
the
treatment
of
severe
AD.
In
particular,
Janus
kinase
inhibitors
(JAKi),
including
abrocitinib,
baricitinib,
and
upadacitinib,
recently
received
approval
patients
with
AD
after
being
evaluated
in
several
clinical
trials.
However,
a
few
concerns
raised
regarding
their
long-term
safety
management
these
drugs
real-world
practice.
this
article
we
described
results
Delphi
consensus
aimed
at
describing
knowledge
on
JAKi
focusing,
providing
recommendations
dermatologists
daily
practice
use
drugs.
Twelve
Italian
reviewed
most
recent
literature
efficacy
profiles
proposed
24
statements.
Agreement
was
reached
statements
focusing
three
main
topics:
(1)
place
therapy
moderate-to-severe
AD;
(2)
effectiveness
JAK
different
phenotypes;
(3)
approaches
to
treated
The
panel
all
Given
wide
practice,
it
is
crucial
establish
specific
follow-up
each
patient's
phenotype
order
achieve
best
possible
outcome
minimize
potential
adverse
events.
Clinical Therapeutics,
Год журнала:
2025,
Номер
unknown
Опубликована: Фев. 1, 2025
To
compare
the
risk
of
cardiovascular
disease
(CVD)
and
common
solid
cancers
between
JAK
inhibitors
(JAKi)
versus
TNF
or
IL-17
inhibitors,
among
people
with
psoriatic
arthritis
(PsA)
axial
spondyloarthritis
(axSpA).
We
used
real-world
electronic
health
records
data
from
a
predominantly
North
American
population
PsA
axSpA.
Initiators
JAKi
(tofacitinib
upadacitinib)
TNFi
were
1:1
propensity
score
matched.
Cox
models
to
time
CVD
(acute
myocardial
infarction,
stroke
revascularization)
(breast,
colorectal,
lung
prostate)
over
3
years.
Analyses
repeated
for
IL-17i.
performed
sensitivity
analyses
follow-up
1
5
years,
in
those
aged
≥65
initiating
treatment
before
2021.
The
vs
comparison
included
2,200
matched
individuals
each
group
3,092
4,618
person-years,
respectively.
Compared
TNFi,
was
not
associated
higher
(HR
0.977;
95%
0.632,
1.510)
cancer
0.710;
0.462,
1.091)
years'
follow-up.
IL-17i
2,287
3,190
4,312
IL-17i,
1.114;
0.720,1.722)
0.737;
0.484,1.122).
Results
across
stratified
directionally
concordant.
These
results
are
reassuring
that
large
axSpA,
increased
cancers,
compared
initiators.
Ongoing
monitoring
risks
is
needed.
Current Allergy and Asthma Reports,
Год журнала:
2024,
Номер
24(5), С. 289 - 301
Опубликована: Апрель 18, 2024
Historically,
systemic
treatments
for
atopic
dermatitis
(AD)
primarily
consisted
of
immunosuppressive
agents
such
as
corticosteroids
and
Disease
Modifying
Antirheumatic
Drugs
(DMARDS),
which
provided
symptomatic
relief
but
often
had
long-term
adverse
effects.
Newer
have
shown
significant
efficacy
with
less
side
effects
in
clinical
trials.
This
review
discusses
compares
conventional
newer
AD.
ABSTRACT
Background
Janus
kinase
inhibitors
(JAKis)
are
an
integral
aspect
of
the
management
myeloproliferative
neoplasms
(MPNs).
Part
clinical
benefit
derived
from
JAKis
may
be
due
to
reductions
in
thrombosis,
a
potentially
life‐threatening
complication
MPNs.
However,
evidence
has
emerged
adverse
cardiovascular
effects
secondary
JAKis.
We
conducted
first‐of‐a‐kind
meta‐analysis
safety
treatment
Methods
This
study
was
according
Preferred
Reporting
Items
for
Systematic
Reviews
and
Meta‐Analysis
(PRISMA).
searches
studies
comparing
JAKi
control
group
were
conducted.
Studies
reporting
hypertension,
major
events
(MACE)
thromboembolic
included
using
random‐effects
model
primary
analysis,
fixed‐effects
any
subgroup
analyses
performed.
Results
A
total
23
publications,
consisting
nine
trials
one
retrospective
met
inclusion
criteria.
resulted
pooled
population
2198
patients
(JAKi
n
=
1145,
Control
1053).
In
(
9),
analysis
revealed
significantly
lower
rate
(incidence
ratio
(IRR):
0.52,
95%
CI:
0.28–0.98,
p
0.04).
primarily
driven
by
ruxolitinib
myelofibrosis
(MF)
polycythemia
vera
(PV)
as
when
these
performed
7),
even
more
significant
reduction
with
found
(IRR:
0.41,
95%CI:
0.26–0.64,
<
0.001).
There
no
difference
MACE
or
hypertension
between
groups.
Conclusion
suggests
that
MPN
associated
reduced
risk
events;
PV
MF.
Further
prospective
warranted
confirm
findings
characterise
profile
other
types
Frontiers in Immunology,
Год журнала:
2024,
Номер
15
Опубликована: Фев. 23, 2024
Background
Clinicians
and
healthcare
policymakers
have
been
drenched
with
a
deluge
of
overlapping
meta-analyses
(MAs),
the
necessity
for
comprehensive
clearly
defined
evidence
Janus
kinase
inhibitors
(JKIs)
in
atopic
dermatitis
(AD)
is
urgent.
Methods
Six
databases
were
searched
MAs
published
until
October
2023.
Qualitative
description
was
mainly
used,
Investigator's
Global
Assessment
response
(IGA
response),
75%
improvement
Eczema
Area
Severity
Index
(the
EASI75),
peak
pruritus
Numerical
rating
score
(PP-NRS),
adverse
effects
cited
to
describe
efficacy
safety
JKIs.
The
methodological
quality
included
assessed
by
A
Measurement
Tool
Assess
Systematic
Reviews
II
(AMSTAR
II),
evaluated
grading
recommendations,
assessment,
development,
evaluation
(GRADE).
Results
Sixteen
pooled
this
review,
which
five
studies
appraised
JKIs,
systemic
papers
abrocitinib
only,
one
baricitinib.
Two
“high”
14
“moderate”
quality.
Eleven
integrated
results
JKIs
reported
that
provide
faster
onset
IGA
(RR=2.83,
95%
CI
[2.25,
3.56],
high-quality
evidence).
Similarly,
10
showed
JAK
more
effective
improving
EASI75
(RR=2.84,
[2.2,
3.67],
from
12
active
reducing
PP-NRS
(SMD=-0.49,
[-0.67,
-0.32]).
All
affirmed
added
no
leading
discontinuation
serious
events
(P<0.05).
However,
200mg
had
higher
risk
acne
(RR=4.34,
[1.61,
11.71),
herpes
zoster
(RR=1.64,
[0.42,
6.39]),
headache
(RR=1.76,
[1.03,
3]),
nausea
(RR=7.81,
[3.84,
15.87]).
Upadacitinib
known
increase
(RR=6.23,
[4.08,
9.49]),
nasopharyngitis
(RR=1.36,
1.8])
blood
creatine
phosphokinase
(blood
CPK)
(RR=2.41,
[1.47,
3.95]).
Baricitinib
at
2mg
associated
increased
CPK
(RR=2.25,
[1.1,
2.97]).
Conclusion
Compared
placebo
or
dupilumab,
administration
can
ameliorate
effectively,
improve
EASI75,
relieve
without
severe
effect,
while
accompanied
acne,
nasopharyngitis,
headache,
digestive
disturbances.
curative
effect
200
mg
significant
caution
should
be
given
patients
gastrointestinal
dysfunction,
zoster,
those
who
are
acne-prone.
upadacitinib
avoided
populations
high
cardiovascular
events.
review
registration
https://www.crd.york.ac.uk/prospero/display_record.php?RecordID=369369
,
PROSPERO
(CRD42022369369).
Clinical and Experimental Dermatology,
Год журнала:
2024,
Номер
49(11), С. 1405 - 1412
Опубликована: Май 4, 2024
Abstract
Background
Atopic
dermatitis
(AD)
is
a
chronic
relapsing
inflammatory
skin
disease
characterized
by
intense
itch,
and
impacting
heavily
on
patients’
caregivers’
quality
of
life.
Its
clinical
presentation
accompanied
variety
comorbidities
associated
with
type
2
inflammation,
such
as
asthma,
hay
fever
food
allergies.
However,
current
data
cardiovascular
are
inconsistent.
Objectives
To
identify
the
risk
diseases
(CVDs)
in
patients
AD.
Methods
Data
from
electronic
health
records
1
070
965
AD
equally
distributed
propensity-score
matched
controls
were
retrieved
US
Collaborative
Network,
part
federated
TriNetX
network.
Hazard
ratios
(HRs)
for
onset
CVDs
prevalence
≥
1%
both
cohorts
within
20
years
after
diagnosis
determined.
Results
In
total,
55
belonging
to
8
major
groups
identified.
Of
those,
53
diagnoses
displayed
significantly
increased
Different
heart
failure
found
most
often,
followed
valve
insufficiencies,
arrhythmia,
tachycardia,
atrial
fibrillation
flutter,
but
also
adverse
events
venous
thromboembolism.
The
highest
HRs
individual
insufficiency,
atherosclerosis
native
arteries
extremities,
unspecified
diastolic
(congestive)
failure.
Conclusions
an
multiple
CVDs.
Biomedicines,
Год журнала:
2023,
Номер
11(8), С. 2284 - 2284
Опубликована: Авг. 17, 2023
Inflammation
has
a
critical
role
in
the
development
and
progression
of
atherosclerosis.
On
molecular
level,
inflammatory
pathways
negatively
impact
endothelial
barrier
properties
thus,
tissue
homeostasis.
Conformational
changes
destruction
glycocalyx
further
promote
pro-inflammatory
also
contributing
to
pro-coagulability
prothrombotic
state.
In
addition,
extracellular
matrix
composition
lead
(peri-)vascular
remodelling
alterations
vessel
wall,
e.g.,
aneurysm
formation.
Moreover,
progressive
fibrosis
leads
reduced
perfusion
due
loss
functional
capillaries.
The
present
review
aims
at
discussing
clinical
effects
processes
on
micro-
macrovasculature
with
focus
peripheral
artery
disease.