International Journal of Dermatology,
Год журнала:
2023,
Номер
63(1), С. 105 - 107
Опубликована: Ноя. 28, 2023
The
data
that
support
the
findings
of
this
study
are
available
in
PubMed:
https://pubmed.ncbi.nlm.nih.gov/37098171/;
https://pubmed.ncbi.nlm.nih.gov/37012527/;
https://pubmed.ncbi.nlm.nih.gov/35980214/;
https://pubmed.ncbi.nlm.nih.gov/36702810/;
https://pubmed.ncbi.nlm.nih.gov/36660960/;
https://pubmed.ncbi.nlm.nih.gov/36924265/;
https://pubmed.ncbi.nlm.nih.gov/37017620/;
https://pubmed.ncbi.nlm.nih.gov/37016961/;
https://pubmed.ncbi.nlm.nih.gov/36404138/;
https://pubmed.ncbi.nlm.nih.gov/37150301/;
https://pubmed.ncbi.nlm.nih.gov/36794894/;
https://pubmed.ncbi.nlm.nih.gov/36695072/.
Archives of Dermatological Research,
Год журнала:
2024,
Номер
317(1)
Опубликована: Ноя. 30, 2024
Identifying
the
characteristics
of
atopic
dermatitis
(AD)
patients
with
its
comorbidity
has
become
increasingly
crucial.
We
aimed
to
investigate
relevant
factors
associated
comorbidities
in
adults
AD.
analyzed
cross-sectional
data
through
univariate
and
multivariate
regression
analyses,
encompassing
439
adult
cases
AD
from
Clinical
Research
Homogenization
Diagnosis
Treatment
Project
for
Type
2
Inflammatory
Dermatosis.
It
was
found
that
231
developed
at
least
one
comorbidity.
161
had
a
positive
family
history
atopy,
292
exhibited
elevated
IgE
levels.
A
allergic
rhinitis
or
sinusitis
be
concurrent
diseases
(OR
(95%
CI):
2.92
(1.41–6.06)
model
1;
2.71
(1.27–5.77)
2;
3.59
(1.75–7.37)
3;
3.38
(1.62–7.05)
4;
3.60
(1.83–7.08)
5;
3.56
(1.78–7.12)
6).
The
linkage
between
levels
different
classifications
negative
0.51
(0.33–0.79)
(0.33–0.80)
0.52
(0.33–0.81)
0.45
(0.29–0.71)
0.47
(0.30–0.73)
Scores
familial
atopy
1.56
(1.00-2.44)
1.59
(1.03–2.48)
1.84
(1.19–2.84)
6)
were
positively
comorbidities.
Factors
development
included
sinusitis,
scores
indicating
atopy.
These
might
contribute
improved
discrimination
early
intervention
individuals
Current Issues in Molecular Biology,
Год журнала:
2023,
Номер
45(6), С. 5215 - 5231
Опубликована: Июнь 20, 2023
Atopic
dermatitis
(AD)
is
a
chronic
inflammatory
skin
disease
with
high
prevalence
in
the
developed
countries.
It
associated
atopic
and
non-atopic
diseases,
its
close
correlation
comorbidities
has
been
genetically
demonstrated.
One
of
main
roles
genetic
studies
to
comprehend
defects
cutaneous
barrier
due
filaggrin
deficit
epidermal
spongiosis.
Recently,
epigenetic
started
analyze
influence
environmental
factors
on
gene
expression.
The
epigenome
considered
be
superior
second
code
that
controls
genome,
which
includes
alterations
chromatin.
changes
do
not
alter
code,
however,
chromatin
structure
could
activate
or
inhibit
transcription
process
certain
genes
consequently,
translation
new
mRNA
into
polypeptide
chain.
In-depth
analysis
transcriptomic,
metabolomic
proteomic
allow
unravel
detailed
mechanisms
cause
AD.
extracellular
space
lipid
metabolism
are
AD
independent
On
other
hand,
around
45
proteins
as
principal
components
skin.
Moreover,
based
disrupted
can
lead
development
treatments
targeting
inflammation.
Unfortunately,
at
present,
there
no
target
therapies
focus
However,
future,
miR-143
an
important
objective
for
therapies,
it
targets
miR-335:SOX
axis,
thereby
restoring
miR-335
expression,
repairing
defects.
Immunotherapy,
Год журнала:
2023,
Номер
15(18), С. 1521 - 1529
Опубликована: Окт. 18, 2023
Baricitinib
is
a
JAK1-2
inhibitor
recently
approved
in
Europe
and
Japan
for
the
treatment
of
moderate-to-severe
atopic
dermatitis
adult
patients
at
doses
2
4
mg
daily.
The
aim
this
article
to
discuss
safety
profile
baricitinib
using
data
from
clinical
trials
supporting
literature,
with
focus
on
infectious
adverse
events.
An
integrated
analysis
eight
described
infections
as
most
frequent
treatment-emergent
events,
mainly
mild-to-moderate
severity,
notably
upper
respiratory
tract
herpes
simplex
exacerbations.
Real-world
are
still
limited
will
contribute
precisely
that
might
benefit
treatment.Baricitinib
drug
taken
by
mouth,
currently
adults
who
candidates
systemic
therapy,
medication
designed
be
absorbed
into
bloodstream
work
throughout
body.
available
2-
4-mg
tablets
has
been
shown
improve
cutaneous
manifestations,
such
dry
cracked
skin,
redness
symptoms
dermatitis,
especially
itchiness.
generally
well
tolerated.
common
events
have
emerged
include
headache,
nausea
high
cholesterol.
Another
reported
side
effect
an
increased
risk
infections,
nasopharyngitis
(inflammation
nose
throat)
reactivation
zoster,
virus
causes
painful
rash
one
body,
simplex,
which
clustered
blisters
usually
lips
or
genitals.
There
lack
real-world
experience,
important
development
more
precise
may
treatment.
International Journal of Molecular Sciences,
Год журнала:
2023,
Номер
24(8), С. 7557 - 7557
Опубликована: Апрель 20, 2023
Atopic
dermatitis
(AD)
is
a
heterogeneous
disease
in
terms
of
its
phenotypical,
barrier,
and
immunological
presentation.
Emerging
therapies
are
undoubtedly
contributing
to
new
chapter
the
treatment
AD,
bringing
an
excellent
possibility
individualization,
thereby
creating
tailored
approach.
The
two
most
promising
substance
groups
biological
drugs
(dupilumab,
tralokinumab,
lebrikizumab,
nemolizumab)
Janus
kinase
inhibitors
(JAKis)
(baricitinib,
upadacitinib,
abrocitinib).
vision
that
certain
well-defined
phenotypes
endotypes,
as
well
personal
preferences,
may
guide
future
AD
both
tempting
appealing,
but
not
yet
reality.
accessibility
such
biologics
small
molecules
has
opened
up
discussion
regarding
personalized
medicine,
referring
complex
nature
experiences
from
clinical
trials
real-world
evidence.
We
have
now
reached
point
strategies
goals
by
increasing
amount
information
concerning
efficacy
safety
drugs.
This
article
reviewed
novel
options
for
light
heterogeneity
this
proposes
broader
on
strategy
AD.
International Journal of Dermatology,
Год журнала:
2023,
Номер
63(1), С. 105 - 107
Опубликована: Ноя. 28, 2023
The
data
that
support
the
findings
of
this
study
are
available
in
PubMed:
https://pubmed.ncbi.nlm.nih.gov/37098171/;
https://pubmed.ncbi.nlm.nih.gov/37012527/;
https://pubmed.ncbi.nlm.nih.gov/35980214/;
https://pubmed.ncbi.nlm.nih.gov/36702810/;
https://pubmed.ncbi.nlm.nih.gov/36660960/;
https://pubmed.ncbi.nlm.nih.gov/36924265/;
https://pubmed.ncbi.nlm.nih.gov/37017620/;
https://pubmed.ncbi.nlm.nih.gov/37016961/;
https://pubmed.ncbi.nlm.nih.gov/36404138/;
https://pubmed.ncbi.nlm.nih.gov/37150301/;
https://pubmed.ncbi.nlm.nih.gov/36794894/;
https://pubmed.ncbi.nlm.nih.gov/36695072/.