Cardiometabolic Risk in Psoriatic Arthritis: A Hidden Burden of Inflammation and Metabolic Dysregulation
Metabolites,
Journal Year:
2025,
Volume and Issue:
15(3), P. 206 - 206
Published: March 18, 2025
Psoriatic
arthritis
(PsA)
is
a
chronic
inflammatory
disease
that
extends
beyond
musculoskeletal
and
dermatologic
involvement
to
elevate
cardiometabolic
risk.
Emerging
evidence
highlights
the
critical
role
of
systemic
inflammation
in
metabolic
dysregulation,
accelerating
insulin
resistance,
dyslipidemia,
oxidative
stress,
all
which
contribute
increased
burden
cardiovascular
PsA.
This
review
explores
intricate
interplay
between
mediators—such
as
tumor
necrosis
factor-alpha
(TNF-α),
interleukin-6
(IL-6),
interleukin-17
(IL-17),—adipokine
imbalances,
lipid
metabolism
abnormalities,
foster
endothelial
dysfunction
atherosclerosis.
The
dysregulation
adipokines,
including
leptin,
adiponectin,
resistin,
further
perpetuates
cascades,
exacerbating
Additionally,
alterations
seen
PsA,
particularly
resistance
dysfunction,
not
only
comorbidities
but
also
impact
severity
therapeutic
response.
Understanding
these
mechanistic
links
imperative
for
refining
risk
stratification
strategies
tailoring
interventions.
By
integrating
targeted
immunomodulatory
therapies
with
management,
more
comprehensive
approach
PsA
treatment
can
be
achieved.
Future
research
must
focus
on
elucidating
shared
pathways,
enabling
development
innovative
mitigate
both
complications
Language: Английский
Impact of a High-Fat Diet on the Gut Microbiome: A Comprehensive Study of Microbial and Metabolite Shifts During Obesity
Cells,
Journal Year:
2025,
Volume and Issue:
14(6), P. 463 - 463
Published: March 20, 2025
Over
the
last
few
decades,
prevalence
of
metabolic
diseases
such
as
obesity,
diabetes,
non-alcoholic
fatty
liver
disease,
hypertension,
and
hyperuricemia
has
surged,
primarily
due
to
high-fat
diet
(HFD).
The
pathologies
these
show
disease-specific
alterations
in
composition
function
their
gut
microbiome.
How
HFD
alters
microbiome
its
metabolite
mediate
adipose
tissue
(AT)
inflammation
obesity
is
not
well
known.
Thus,
this
study
aimed
identify
changes
metabolomic
signatures
induced
by
an
alter
obesity.
To
explore
microbiota
metabolites,
16S
rRNA
gene
amplicon
sequencing
analyses
were
performed
after
normal
(ND)
feeding.
We
noticed
that,
at
taxonomic
levels,
number
operational
units
(OTUs),
along
with
Chao
Shannon
indexes,
significantly
shifted
HFD-fed
mice
compared
those
fed
a
ND.
Similarly,
phylum
level,
increase
Firmicutes
decrease
Bacteroidetes
mice.
At
genus
Lactobacillus
Ruminococcus
was
observed,
while
Allobaculum,
Clostridium,
Akkermansia
markedly
reduced
group.
Many
bacteria
from
impair
bile
acid
metabolism
restrict
weight
loss.
are
efficient
breaking
down
complex
carbohydrates
into
short-chain
acids
(SCFAs)
other
whereas
involved
more
balanced
or
energy
extraction.
over
enhances
absorption
calories
food,
which
may
contribute
Taken
together,
altered
metabolites
trigger
AT
inflammation,
contributes
dysregulation
disease
progression.
highlights
potential
development
therapeutic
strategies
for
related
disorders.
Language: Английский
Life’s Crucial 9 and psoriasis: a mediation analysis of systemic inflammation response index using NHANES cohort data
Xinyan Liu,
No information about this author
Qirui Deng,
No information about this author
Hongfeng Tang
No information about this author
et al.
Frontiers in Immunology,
Journal Year:
2025,
Volume and Issue:
16
Published: April 15, 2025
Background
Psoriasis
is
a
chronic,
recurrent,
inflammatory
disease.
The
aim
of
this
study
was
to
investigate
the
association
between
Life’s
Crucial
9
(LC9)
score
and
risk
psoriasis
examine
mediating
role
system
inflammation
response
index
(SIRI).
Methods
Utilizing
data
from
National
Health
Nutrition
Examination
Survey
(NHANES)
spanning
2009
2014,
employed
multifactor
logistic
regression,
restricted
triple
spline
analysis,
various
subgroup
analyses
evaluate
correlation
LC9
scores
occurrence
psoriasis.
Furthermore,
mediation
were
executed
SIRI’s
possible
intermediary
effect
in
linkage
Results
This
included
11,499
US
adults
with
345
patients.
In
fully
adjusted
models,
notable
inverse
relationship
identified
prevalence
(OR
=
0.90,
95%
CI:
0.80,
0.99).
After
adjusting
for
all
covariates,
no
significant
interactions
found
analyses.
addition,
analysis
showed
that
SIRI
mediated
(mediation
ratio:
7.02%,
p
0.004).
Conclusions
Higher
reduce
And,
by
SIRI.
suggests
we
should
actively
regulate
our
lifestyles
improve
cardiovascular
health,
thereby
preventing
delaying
onset
Language: Английский
The Role of Metabolic Syndrome in Psoriasis Treatment Response: A One-Year Comparative Analysis of PASI Progression
Maria-Lorena Mustață,
No information about this author
Mihaela Ionescu,
No information about this author
Lucreţiu Radu
No information about this author
et al.
Diagnostics,
Journal Year:
2024,
Volume and Issue:
14(24), P. 2887 - 2887
Published: Dec. 23, 2024
Background/Objectives:
Psoriasis
is
a
chronic
dermatological
condition
with
systemic
implications,
especially
metabolic
syndrome
(MS).
This
study
evaluated
the
vicious
cycle
where
obesity
and
MS
exacerbate
inflammation
that
complicates
efficacy
of
psoriasis
therapies
by
examining
PASI
score
over
one-year
period.
Patients
were
classified
into
two
subgroups:
those
alone
(PSO)
both
(PSO-MS).
Methods:
A
total
150
patients,
half
whom
also
concomitantly
presented
syndrome,
received
biologic
comprising
anti-IL-17,
anti-IL-23,
anti-TNF-a,
or
methotrexate,
scores
assessed
at
baseline
3,
6,
12
months.
Results:
All
treatments
showed
significant
reductions
in
PASI;
however,
patients
PSO
more
marked
than
PSO-MS
group.
Anti-IL-17
produced
greatest
sustained
long-term
improvements,
whereas
anti-IL-23
prompt
early
improvements.
Increases
BMI
leptin
concentrations
associated
modest
rate
reduction
score,
underlining
impact
dysfunction
on
treatment
efficacy.
Conclusions:
highlights
importance
managing
comorbidities
such
as
psoriasis,
interplay
between
health
further
therapeutic
outcomes.
Language: Английский