Frontiers in Immunology,
Journal Year:
2024,
Volume and Issue:
15
Published: Dec. 23, 2024
Introduction
The
critical
role
played
by
vascular
dysfunction
and
ineffective
angiogenesis
in
the
pathophysiology
of
systemic
sclerosis
(SSc)
suggests
that
circulating
biomarkers
reflecting
these
alterations
may
be
useful
clinical
evaluation
this
patient
group.
We
sought
to
address
issue
conducting
a
systematic
review
meta-analysis
studies
investigating
such
candidate
biomarker,
endostatin,
an
endogenous
glycoprotein
exerting
anti-angiogenic
effects,
SSc
patients
healthy
controls.
Methods
A
literature
search
was
conducted
electronic
databases
Web
Science,
PubMed,
Scopus
from
inception
27
May
2024.
Risk
bias
certainty
evidence
were
assessed
using
JBI
checklist
for
analytical
GRADE,
respectively.
Results
In
19
eligible
studies,
endostatin
concentrations
significantly
higher
than
controls
(standard
mean
difference,
SMD=0.90,
95%
CI
0.56
1.23,
p<0.001;
low
evidence).
Endostatin
also
with
digital
ulcers
those
without
(SMD=0.43,
0.24
0.62,
very
evidence)
pulmonary
arterial
hypertension
(SMD=1.21,
0.67
1.76,
By
contrast,
no
significant
differences
observed
between
limited
vs.
diffuse
disease
different
video
capillaroscopy
patterns.
There
regarding
interstitial
lung
disease,
telangiectasias,
gastrointestinal
manifestations.
associations
meta-regression
subgroup
analysis
effect
size
various
study
characteristics.
Discussion
Therefore,
results
suggest
measuring
can
assessing
presence
specific
complications,
i.e.,
hypertension,
patients.
Systematic
registration
https://www.crd.york.ac.uk/prospero/
,
identifier
CRD42024558174.
Scientific Reports,
Journal Year:
2024,
Volume and Issue:
14(1)
Published: March 18, 2024
Abstract
We
aimed
to
evaluate
the
association
between
systemic
sclerosis
(SSc)
and
major
cerebrovascular/cardiovascular
risks
through
a
systematic
approach.
Databases
were
systematically
searched
from
their
inception
October
10,
2023
for
studies
comparing
event
rates
patients
with
SSc
controls.
The
primary
outcome
was
stroke
risk
in
SSc.
Secondary
outcomes
included
of
myocardial
infarction
(MI),
cardiovascular
disease
(CVD),
peripheral
vascular
(PVD),
venous
thromboembolism
(VTE).
Seventeen
6,642,297
participants
included.
associated
significantly
increased
(HR,
1.64;
95%
confidence
interval
[CI],
1.35–2.01),
CVD
2.12;
CI,
1.36–3.3),
MI
2.15;
1.23–3.77),
VTE
2.75;
1.77–4.28),
PVD
5.23;
4.25–6.45).
Subgroup
analysis
revealed
non-Asian
group
1.55;
1.26–1.9),
while
Asian
displayed
higher
but
not
statistically
significant
1.86;
0.97–3.55).
study
found
that
is
events.
These
findings
highlight
importance
vasculopathy
suggest
need
enhanced
clinical
monitoring
preventive
measures
this
high-risk
population.
International Journal of Molecular Sciences,
Journal Year:
2025,
Volume and Issue:
26(2), P. 535 - 535
Published: Jan. 10, 2025
Individuals
with
chronic
inflammatory
and
immune
disorders
are
at
an
increased
risk
of
atherosclerotic
events
premature
cardiovascular
(CV)
disease.
Despite
extensive
literature
exploring
the
relationship
between
"non-traditional"
conditions
CV
risk,
many
aspects
remain
unresolved,
including
underlying
mechanisms
promoting
"non-traditional
risk",
development
innovative
comprehensive
assessment
tool,
recommendations
for
tailored
interventions.
This
review
aims
to
evaluate
available
evidence
on
key
risk-enhancer
conditions,
a
focus
assessing
managing
factors.
We
conducted
412
original
articles,
narrative
systematic
reviews,
meta-analyses
addressing
associated
conditions.
The
analysis
examined
these
relationships
identified
strategies
mitigating
elevated
risk.
A
major
challenge
highlighted
is
difficulty
in
quantifying
contribution
individual
factors
disease-specific
elements
While
supports
benefits
statins
beyond
lipid
lowering,
such
as
pleiotropic
endothelial
effects,
current
guidelines
lack
specific
use
or
other
therapies
targeting
non-traditional
Additionally,
absence
validated
scores
that
incorporate
hinders
accurate
evaluation
management.
growing
prevalence
conditions"
underscores
need
improved
awareness
thorough
understanding
all
contributing
factors,
elements,
crucial
prediction
disease
(CVD)
represents
essential
foundation
informed
decision-making
primary
secondary
prevention.
advocate
future
research
developing
innovative,
tools
recognizing
this
promising
avenue
translational
clinical
outcome
research.
Frontiers in Immunology,
Journal Year:
2025,
Volume and Issue:
16
Published: Feb. 19, 2025
To
investigate
alterations
in
blood
lipid
profiles
and
T
cell
subsets
among
systemic
sclerosis
(SSc)
patients,
to
assess
their
potential
utility
predicting
cardiovascular
disease
(CVD)
risk.
105
SSc
patients
80
age-
sex-matched
healthy
controls
(HCs)
were
enrolled.
Flow
cytometry
was
employed
quantify
subsets.
Multivariate
logistic
regression
analysis
investigated
the
association
between
profile,
subsets,
occurrence,
CVD
Additionally,
a
prediction
model
developed
predictive
value
of
In
low-density
lipoprotein
cholesterol
(LDL-C)
(OR
=
3.212,
95%CI
1.132-9.113,
p=
0.028),
ESR
1.218,
1.086-1.367,
0.001),
CRP
2.156,
95%
CI
1.393-3.338,
p
helper
(Th)cells
1.004,
1.001-1.008,
0.034)
positively
correlated
with
risk
SSc.
Further
studies
found
that
absolute
increases
Th
cells
associated
(OR=1.002,
95%CI=1.001-1.005,
=0.011)
independent
predictors
When
exceeded
866.53
cells/μL,
greatly
increased
(p<0.001).
Altered
dysregulated
expression
significant
elevation
specifically
noted
SSc-CVD
suggesting
may
serve
as
biomarker
for
thereby
aiding
early
diagnosis.
The
underlying
mechanism
this
requires
further
investigation.
Frontiers in Immunology,
Journal Year:
2025,
Volume and Issue:
16
Published: April 16, 2025
Systemic
Sclerosis
(SSc)
is
a
systemic
autoimmune
disease
of
unknown
etiology
characterized
by
the
development
frequently
progressive
cutaneous
and
internal
organ
fibrosis
accompanied
severe
vascular
alterations.
The
pathogenesis
SSc
highly
complex
and,
despite
extensive
investigation,
has
not
been
fully
elucidated.
Numerous
studies
have
suggested
that
etiologic
factors
cause
multiple
alterations
in
genetically
receptive
hosts,
leading
to
progression.
These
events
may
be
functionally
pathologically
interconnected
include:
1)
Structural
functional
microvascular
endothelial
cell
abnormalities;
2)
Severe
oxidative
stress
high
reactive
oxygen
species
(3);
Frequently
visceral
fibrosis;
4)
Transdifferentiation
various
types
into
activated
myofibroblasts,
cells
ultimately
responsible
for
fibrotic
process;
5)
Establishment
chronic
inflammatory
process
affected
tissues;
6)
Release
cytokines,
chemokines,
growth
from
cells;
7)
Abnormalities
humoral
cellular
immunity
with
production
specific
autoantibodies;
8)
Epigenetic
including
changes
non-coding
RNAs.
manifest
different
levels
intensity
organs
display
remarkable
individual
variability,
resulting
wide
heterogeneity
extent
severity
clinical
manifestations.
Here,
we
will
review
some
recent
related
pathogenesis.
Frontiers in Immunology,
Journal Year:
2024,
Volume and Issue:
15
Published: Nov. 7, 2024
The
hypoxic
microenvironment,
characterized
by
significantly
reduced
oxygen
levels
within
tissues,
has
emerged
as
a
critical
factor
in
the
pathogenesis
and
progression
of
various
autoimmune
diseases
(AIDs).
Central
to
this
process
is
hypoxia-inducible
factor-1
(HIF-1),
which
orchestrates
wide
array
cellular
responses
under
low
conditions.
This
review
delves
into
multifaceted
roles
microenvironment
modulating
immune
cell
function,
particularly
highlighting
its
impact
on
activation,
metabolic
reprogramming,
angiogenesis.
Specific
focus
given
mechanisms
hypoxia
contributes
development
exacerbation
such
rheumatoid
arthritis
(RA),
systemic
lupus
erythematosus
(SLE),
multiple
sclerosis
(MS),
dermatomyositis
(DM).
In
these
conditions,
not
only
disrupts
tolerance
but
also
enhances
inflammatory
promotes
tissue
damage.
discusses
emerging
therapeutic
strategies
aimed
at
targeting
pathways,
including
application
HIF-1α
inhibitors,
mTOR
other
modulators
response.
By
providing
comprehensive
overview
interplay
between
dysfunction
AIDs,
offers
new
perspectives
underlying
highlights
potential
avenues
for
intervention.
Genes,
Journal Year:
2024,
Volume and Issue:
15(4), P. 393 - 393
Published: March 22, 2024
Autoimmunity
is
defined
as
the
inability
to
regulate
immunological
activities
in
body,
especially
response
external
triggers,
leading
attack
of
tissues
and
organs
host.
Outcomes
include
onset
autoimmune
diseases
whose
effects
are
primarily
due
dysregulated
immune
responses.
In
past
years,
there
have
been
cases
that
show
an
increased
susceptibility
other
disorders
patients
who
already
experiencing
same
type
disease.
Research
this
field
has
started
analyzing
potential
molecular
cellular
causes
interconnectedness,
bearing
mind
possibility
advancing
drugs
therapies
for
treatment
autoimmunity.
With
that,
study
aimed
determine
correlation
four
diseases,
which
1
diabetes
(T1D),
psoriasis
(PSR),
systemic
sclerosis
(SSc),
lupus
erythematosus
(SLE),
by
identifying
highly
preserved
co-expressed
genes
among
datasets
using
WGCNA.
Functional
annotation
was
then
employed
characterize
these
sets
based
on
their
relationship
a
whole
elucidate
biological
processes,
components,
functions
pathways
they
involved
in.
Lastly,
drug
repurposing
analysis
performed
screen
candidate
repositioning
could
abnormal
expression
diseases.
A
total
thirteen
modules
were
obtained
from
analysis,
majority
associated
with
transcriptional,
post-transcriptional,
post-translational
modification
processes.
Also,
evaluation
KEGG
suggested
possible
role
TH17
differentiation
simultaneous
Furthermore,
clomiphene
top
regulating
overexpressed
hub
genes;
meanwhile,
prilocaine
under-expressed
genes.
This
geared
towards
utilizing
transcriptomics
approaches
assessment
microarray
data,
different
use
traditional
genomic
analyses.
Such
research
design
investigating
correlations
may
be
first
its
kind.
Journal of Clinical Medicine,
Journal Year:
2024,
Volume and Issue:
13(10), P. 2738 - 2738
Published: May 7, 2024
Background:
Systemic
sclerosis
is
a
complex
autoimmune
disease
characterized
by
vasculopathy,
fibrosis,
and
immune
dysregulation.
Ocular
manifestations
in
these
patients
are
increasingly
recognized,
suggesting
potential
correlations
between
systemic
vascular
abnormalities
ocular
microvascular
changes.
Advancements
molecular
immunology
imaging
technology
using
coherence
tomography
(OCT)
have
unveiled
intricate
pathways
underlying
possible
pathogenesis.
Understanding
the
interplay
retinal
parameters
could
provide
insights
into
mechanisms
biomarkers.
Purpose:
The
aim
of
this
study
was
to
investigate
abnormalities,
detected
with
optical
angiography
(OCT-A),
find
severity
findings
OCT-A
parameters.
Methods:
A
group
32
were
compared
9
healthy
controls.
Ganglion
cell
thickness
(GCC),
retina
fovea
parafovea,
nerve
fiber
layer
(RNFL)
cup/disc
area
ratio
investigated
OCT.
Vessel
density
(VD)
superficial
(SCP)
deep
capillary
plexus
(DCP)
whole
macular
ETDRS
grid,
size
foveal
avascular
zone
(FAZ)
vessel
radial
peripapillary
(RPCP)
evaluated
OCT-A.
Modified
Rodnan
skin
score
(mRSS),
capillaroscopy
duration
used
stage
severity.
Results:
There
statistically
significant
reduction
VD
DCP,
SCP
DCP
grid
patient
controls
(p
<
0.001).
presented
enlargement
FAZ
0.005).
No
correlation
OCT
scores
found.
Conclusions:
represent
non-invasive
tool
detect
damage
sclerosis.
Current Issues in Molecular Biology,
Journal Year:
2024,
Volume and Issue:
46(7), P. 7486 - 7504
Published: July 15, 2024
Systemic
sclerosis
(SSc)
is
a
connective
tissue
disorder
characterized
by
microvascular
injury,
extracellular
matrix
deposition,
autoimmunity,
inflammation,
and
fibrosis.
The
clinical
complexity
high
heterogeneity
of
the
disease
make
discovery
potential
therapeutic
targets
difficult.
However,
recent
progress
in
comprehension
its
pathogenesis
encouraging.
Growth
Arrest-Specific
6
(Gas6)
Tyro3,
Axl,
MerTK
(TAM)
receptors
are
involved
multiple
biological
processes,
including
modulation
immune
response,
phagocytosis,
apoptosis,
fibrosis,
cancer
development,
autoimmune
disorders.
In
present
manuscript,
we
review
current
evidence
regarding
SSc
role
Gas6/TAM
system
several
human
diseases,
suggesting
likely
contribution
highlighting
areas
where
further
research
necessary
to
fully
comprehend
TAM
this
condition.
Indeed,
understanding
involvement
SSc,
which
currently
unknown,
could
provide
valuable
insights
for
novel
targets.