Rheumatology Science and Practice,
Journal Year:
2024,
Volume and Issue:
62(5), P. 445 - 464
Published: Oct. 31, 2024
The
main
indications
for
colchicine
treatment
until
recently
were
gout,
pericarditis,
familial
Mediterranean
fever
and
some
other
auto-inflammatory
diseases.
expansion
of
(repositioning)
the
use
in
direction
prevention
cardiovascular
complications
should
be
considered
as
one
major
events
medicine
XXI
century.
Deciphering
role
inflammation
most
important
mechanism
development
atherosclerosis
has
created
prerequisites
concept
anti-inflammatory
therapy
atherosclerosis,
which
low-dose
can
take
an
place,
complementing
effects
aspirin,
statins
antihypertensive
therapy.
analysis
materials
from
randomized
placebo-controlled
studies
indicates
a
decrease
frequency
patients
with
coronary
heart
disease
(by
31%)
who
have
suffered
myocardial
infarction
23%),
well
33%),
stroke,
need
revascularization
mortality.
low
dose
(0.5
mg/day)
is
approved
by
U.S.
Food
Drug
Administration
disease.
It
assumed
that
future
will
place
pathology
associated
atherosclerotic
vascular
BMC Medicine,
Journal Year:
2025,
Volume and Issue:
23(1)
Published: Jan. 6, 2025
Patients
with
systemic
lupus
erythematosus
(SLE)
suffered
from
an
increasing
risk
of
cardiovascular
diseases.
In
this
multi-center
prospective
study,
we
aimed
to
determine
the
association
between
antiphospholipid
antibodies
(aPLs)
and
future
atherosclerotic
disease
(ASCVD)
in
SLE.
total,
1573
SLE
patients
were
recruited
based
on
Chinese
Treatment
Research
group
(CSTAR)
registry.
aPLs
profile,
including
anticardiolipin
(aCL)
IgG/IgM,
anti-β2
glycoprotein
I
(aβ2GPI)
anticoagulant
(LA),
measured
each
center.
Future
ASCVD
events
defined
as
new-onset
myocardial
infarction,
stroke,
artery
revascularization,
or
death.
Among
patients,
525
(33.4%)
had
positive
aPLs.
LA
highest
prevalence
(324
[20.6%]),
followed
by
aCL
IgG
(249
[15.8%]),
aβ2GPI
(199
[12.7%]).
116
(7.37%)
developed
during
mean
follow-up
4.51
±
2.32
years
92
positive.
univariate
Cox
regression
analysis,
both
(HR
=
7.81,
95%
CI
5.00–12.24,
p
<
0.001)
traditional
factors
associated
events.
multiple
1.95,
1.25–3.00,
0.003),
IgM
1.83,
1.03–3.20,
0.039),
5.13,
3.23–8.20,
positivity
remained
ASCVD;
for
ASCVD,
smoking,
gender,
age
hypertension,
also
play
independent
role
patients.
More
importantly,
Aspirin
can
reduce
0.57
CI,
0.25–0.93,
P
0.026).
aPLs,
especially
IgG/IgM
LA,
warrant
more
care
surveillance
follow-up.
may
have
a
protective
effect
ASCVD.
International Journal of Molecular Sciences,
Journal Year:
2025,
Volume and Issue:
26(1), P. 334 - 334
Published: Jan. 2, 2025
The
first
part
of
this
review
highlighted
the
evolving
landscape
atherosclerosis,
noting
emerging
cardiometabolic
risk
factors,
growing
impact
exposomes,
and
social
determinants
health.
prominent
role
atherosclerosis
in
bidirectional
relationship
between
cardiovascular
disease
cancer
was
also
discussed.
In
second
part,
we
examine
complex
interplay
multimorbid
cardio-oncologic
patients,
harmful
environments
that
lend
a
“syndemic”
nature
to
these
chronic
diseases.
We
summarize
management
strategies
targeting
disordered
factors
mitigate
explore
molecular
mechanisms
enabling
more
tailored
therapies.
Importantly,
emphasize
early
interception
through
multifactorial
interventions
detect
subclinical
signs
(via
biomarkers
imaging)
treat
modifiable
prevent
clinical
events.
A
concerted
preventive
effort—referred
by
some
as
“preventome”—is
essential
reduce
burden
atherosclerosis-driven
diseases,
shifting
from
mere
proactive
promotion
“chronic
health”.
Journal of the American Chemical Society,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 21, 2025
The
presence
of
a
substantial
necrotic
core
in
atherosclerotic
plaques
markedly
heightens
the
risk
rupture,
consequence
elevated
iron
levels
that
exacerbate
oxidative
stress
and
lipid
peroxidation,
thereby
sustaining
detrimental
cycle
ferroptosis
inflammation.
Concurrently
targeting
both
inflammation
is
crucial
for
effective
treatment
vulnerable
plaques.
In
this
study,
we
introduce
gallium
hexacyanoferrate
nanoabsorption
catalysts
(GaHCF
NACs)
designed
to
disrupt
pathological
cycle.
GaHCF
NACs
function
as
highly
efficient
chelators
with
robust
antiferroptosis
properties.
Through
situ
capture
within
plaques,
these
enhance
reactive
oxygen
species
scavenging,
initiating
an
amplified
therapeutic
response.
significantly
advance
plaque
regression,
stabilization,
vascular
functional
recovery
by
inhibiting
MAPK13
(p38-δ
MAPK)
signaling,
key
mediator
cell
death.
Importantly,
process
generates
detectable
photoacoustic
signal,
offering
notable
diagnostic
advantage
allows
real-time
monitoring
plague
status.
This
multifunctional
nanocatalytic
platform
transforms
toxic
into
agent,
adapting
dynamically
microenvironment
representing
promising
strategy
reducing
vulnerability
preventing
rupture.
European Journal of Clinical Investigation,
Journal Year:
2025,
Volume and Issue:
unknown
Published: March 8, 2025
Targeting
inflammation
offers
a
unique
possibility
to
address
residual
cardiovascular
risk
in
almost
two
thirds
of
all
patients
with
prevalent
atherosclerotic
disease
(ASCVD).
However,
despite
FDA
approval
and
the
ESC
2024
Guidelines
for
Management
Chronic
Coronary
Syndrome
recommendations
implement
low-dose
colchicine
(0.5
mg
daily)
secondary
prevention
ASCVD
inflammatory
risk,
its
clinical
adoption
is
still
limited.
In
this
regard,
simple
screening
elevated
high-sensitive
C-reactive
protein
(hsCRP)
on
routine
basis
might
help
recognize
low-grade
as
an
important
therapeutic
target.
Within
present
review,
we
first
provide
recently
published
epidemiologic
evidence
that
hsCRP
at
least
strong
predictor
future
events
traditional
lipoproteins.
Furthermore,
summarize
our
recent
knowledge
currently
available
strategies
modulate
process
critically
discuss
open
issues
regarding
benefit
therapy
acute
coronary
setting
or
stroke
prevention.
addition,
also
briefly
touch
upon
some
specific
safety
related
long-term
use
colchicine.
Finally,
next
diagnostic
frontiers
targeting
such
detection
vascular/coronary
by
pericoronary
fat
attenuation
ziltivekimab,
human
monoclonal
antibody
interleukin-6.
Thus,
integration
interventions
aimed
lowering
burden
combination
aggressive
lipid-modifying
may
hold
potential
further
reduce
substantial
ASCVD.
EClinicalMedicine,
Journal Year:
2024,
Volume and Issue:
76, P. 102835 - 102835
Published: Oct. 1, 2024
Summary
Background
Guidelines
recommend
low-dose
colchicine
for
secondary
prevention
in
cardiovascular
disease,
but
uncertainty
remains
concerning
its
efficacy
stroke,
key
subgroups
and
about
uncommon
serious
safety
outcomes.
Methods
In
this
trial-level
meta-analysis,
we
searched
bibliographic
databases
trial
registries
form
inception
to
May
16,
2024.
We
included
randomised
trials
of
ischaemic
stroke
major
adverse
events
(MACE:
myocardial
infarction,
coronary
revascularisation,
or
death).
Secondary
outcomes
were
mortality.
A
fixed-effect
inverse-variance
model
was
used
generate
a
pooled
estimate
relative
risk
(RR)
with
95%
confidence
intervals
(CI).
This
study
is
registered
PROSPERO,
CRD42024540320.
Findings
Six
involving
14,934
patients
prior
disease
included.
all
patients,
compared
placebo
no
reduced
the
by
27%
(132
[1.8%]
versus
186
[2.5%]
events,
RR
0.73
[95%
CI
0.58–0.90])
MACE
(505
[6.8%]
693
[9.4%]
[0.65–0.81]).
Efficacy
consistent
(females
males,
age
below
above
70,
without
diabetes,
statin
non-statin
users).
Colchicine
not
associated
an
increase
outcomes:
hospitalisation
pneumonia
(109
[1.5%]
106
[1.5%],
0.99
[0.76–1.30]),
cancer
(247
[3.5%]
255
[3.6%],
0.97
[0.82–1.15]),
gastro-intestinal
(153
[2.1%]
135
[1.9%]),
1.15
[0.91–1.44].
There
difference
all-cause
death
(201
[2.7%]
181
[2.4%],
1.09
[0.89–1.33]),
(70
[0.9%]
80
[1.1%],
0.89
[0.65–1.23]),
non-cardiovascular
(131
101
[1.4%],
1.26
[0.98–1.64]).
Wiener klinische Wochenschrift,
Journal Year:
2025,
Volume and Issue:
137(S1), P. 1 - 33
Published: Feb. 1, 2025
Zusammenfassung
Colchicin
ist
ein
entzündungshemmender
pflanzlicher
Arzneistoff
mit
einer
jahrtausendealten
Geschichte.
Es
wird
seit
jeher
erfolgreich
in
der
Akuttherapie
und
Prophylaxe
Gicht
eingesetzt
konnte
sich
einen
festen
Platz
im
pharmakologischen
Standardrepertoire
bei
familiärem
Mittelmeerfieber,
Perikarditis,
neutrophilen
Dermatosen,
Morbus
Behçet
oralen
therapierefraktären
schweren
Aphthosen
sichern.
Rezent
hat
die
US-amerikanische
Food
and
Drug
Administration
(FDA)
zugelassen,
um
das
Risiko
von
Myokardinfarkt,
Schlaganfall,
koronarer
Revaskularisation
kardiovaskulärem
Tod
erwachsenen
Patienten
bestehender
atherosklerotischer
Erkrankung
oder
mehreren
Risikofaktoren
für
eine
kardiovaskuläre
zu
verringern.
Der
Empfehlungsgrad
zur
kardiovaskulären
wurde
den
aktuellen
ESC-Leitlinien
2024
IIb
auf
IIa
angehoben.
Klinische
Studien
vergangenen
Jahre
belegen
ferner
Effekt
beim
akuten
Koronarsyndrom
Vorhofflimmern.
Diese
Übersichtsarbeit
beleuchtet
Wirksamkeits-
Sicherheitsprofil
bietet
Einblick
rezente
mögliche
zukünftige
evidenzbasierte
Anwendungsgebiete.
Current Cardiology Reports,
Journal Year:
2025,
Volume and Issue:
27(1)
Published: Feb. 19, 2025
Abstract
Purpose
of
Review
The
inclusion
immunomodulatory
strategies
as
supportive
therapies
in
ischemic
heart
disease
(IHD)
has
garnered
significant
support
over
recent
years.
Several
such
approaches
appear
to
be
unified
through
their
ultimate
target,
the
NLRP3
inflammasome.
This
review
presents
a
brief
update
on
continuum
conditions
constituting
and
emphasising
seemingly
unifying
mechanism
activation
well
modulation
across
these
conditions.
Recent
Findings
inflammasome
is
multiprotein
complex
assembled
upon
inflammatory
stimulation,
causing
release
pro-inflammatory
cytokines
initiating
pyroptosis.
pathway
relevant
signalling
cardiac
immune
cells
non-immune
myocardium,
including
cardiomyocytes,
fibroblasts
endothelial
cells.
In
addition
focus
clinical
outcome
efficacy
trials
targeting
NLRP3-related
pathways,
potential
connection
between
immunomodulation
cardiology
currently
being
explored
preclinical
trials.
Colchicine,
cytokine-based
SGLT2
inhibitors
have
emerged
promising
agents.
However,
comprising
IHD
atherosclerosis,
coronary
artery
(CAD),
myocardial
infarction
(MI)
cardiomyopathy/heart
failure
(iCMP/HF)
are
not
equally
amenable
with
respective
drugs.
Atherosclerosis,
cardiomyopathy
affected
by
chronic
inflammation,
but
approach
acute
inflammation
post-MI
setting
remains
pharmacological
challenge,
detrimental
regenerative
effects
initiated
unison.
Summary
lies
at
center
cell
mediated
IHD.
trial
evidence
highlighted
anti-inflammatory
colchicine,
interleukin-based
therapy
SGLT2i
that
drugs
modulate