JACC Advances,
Journal Year:
2024,
Volume and Issue:
4(1), P. 101459 - 101459
Published: Dec. 12, 2024
Estimation
of
long-term
risk
for
cardiovascular
events
using
the
SMART
(Secondary
Manifestations
Arterial
Disease)
score
can
be
potentially
valuable
in
devising
mitigation
strategies.
American Journal of Preventive Cardiology,
Journal Year:
2024,
Volume and Issue:
19, P. 100702 - 100702
Published: June 23, 2024
The
inhibition
of
intestinal
cholesterol
absorption
by
ezetimibe
improves
outcomes
after
myocardial
infarction
(MI),
yet
real-world
data
on
is
scarce.
We
studied
the
usage
and
association
with
outcome
MI.
Consecutive
MI
patients
in
Finland
(2010-2018)
were
retrospectively
(N
=
57,505;
65%
men;
mean
age
69
years).
study
collected
from
national
registries.
median
follow-up
was
4.5
(IQR
2.8-7.1)
years.
Between-group
differences
adjusted
for
using
multivariable
regression.
Ezetimibe
use
competing
risk
analyses.
cumulative
incidence
3.7%
at
90
days,
13.4%
5
years,
19.8%
10
Younger
one
strongest
predictors
(adj.sHR
6.67;
CI
5.88-7.69
aged
<60
vs
≥80
Women
more
likely
to
during
than
men.
average
proportion
6.8%.
(11.7%
discontinued
43.6%
follow-up.
Patients
early
therapy
had
lower
all-cause
mortality
(33.6%
45.1%;
adj.HR
0.77;
0.69-0.86;
P<0.0001).
Early
associated
irrespective
sex,
age,
atrial
fibrillation,
diabetes,
heart
failure,
malignancy,
revascularization,
or
statin
use.
Ongoing
a
time-dependent
analysis
(adj.HR
0.53;
0.48-0.59;
death
MI,
its
therapeutic
limited,
discontinuation
frequent.
Reducing
levels
of
low-density-lipoprotein-cholesterol
(LDL-C)
below
recommended
thresholds
is
a
core
component
cardiovascular
prevention
strategies.
We
hypothesized
that
the
addition
bempedoic
acid
to
patients
already
on
statin-ezetimibe
therapy
was
more
effective
than
titrating
statin
dose
in
reducing
LDL-C.
The
study
enrolled
120
at
high
risk,
and
with
LDL-C
above
70
mg/dl.
They
were
randomly
divided
two
groups:
(BA)
group,
taking
plus
ezitimibe,
titration
(ST)
group
including
who
doubled
statin.
At
12-weeks,
BA
presented
greater
significant
decrease
compared
ST
(-22.9%
vs
7.5%
p
0.002).
Total-cholesterol
decreased
significantly
(-14.8%
vs-4.7%
;
0.013)
No
between-groups
changes
HDL
triglycerides
occurred.
12
weeks
number
reached
lower
mg/dl
38
(63%)
versus
22
(37%)
(between
0.034).
In
LDL
lowering
effect
similar
between
atorvastatin
rosuvastatin.
side
effects
occurred
during
follow
up
period.
conclusion,
Bempedoic
statin/ezetimibe
combined
treatment
doubling
increased
reaching
goal.
International Journal of Smart and Nano Materials,
Journal Year:
2024,
Volume and Issue:
15(3), P. 610 - 651
Published: July 2, 2024
Atherosclerosis
is
a
severe
cardiovascular
disease
followed
by
the
accumulation
of
atherosclerotic
plaques
within
lumen
blood
vessels
resulting
in
reduced
flow
thus
initiating
series
events.
Conventional
therapies
for
atherosclerosis
encounter
multiple
challenges,
especially
difficulty
precisely
concentrating
certain
affected
regions
and
potential
unwanted
side
effects.
Consequently,
scientists
are
focused
on
developing
nanoformulations
diagnosis
therapy.
Peptide-based
nanomedicines
improve
conventional
offering
improved
structural
therapeutic
stability
enabling
target-specific
delivery.
Their
inherent
biocompatibility
biodegradability
additionally
render
them
desirable
materials
intended
vivo
use.
This
review
manuscript
aims
to
provide
an
in-depth
overview
peptide-based
atherosclerosis,
focusing
targeted
cells
like
endothelial
cells,
macrophages,
monocytes
their
interaction
with
different
plaque
components.
Moreover,
also
highlights
latest
progress
multimodal
techniques
provides
comprehensive
limitations
associated
practical
implementation.
Pharmaceuticals,
Journal Year:
2024,
Volume and Issue:
17(12), P. 1581 - 1581
Published: Nov. 25, 2024
This
paper
investigates
the
therapeutic
use
of
PCSK9
inhibitors,
particularly
Evolocumab,
as
monoclonal
antibodies
for
treatment
atherosclerosis
based
on
recent
literature
reviews.
is
an
outstanding
example
a
breakthrough
in
medical
science,
with
advancements
understanding
its
biological
function
driving
substantial
progress
treatment.
Atherosclerotic
cardiovascular
disease
(ASCVD)
leading
global
cause
mortality,
imposing
financial
burdens
healthcare
systems.
Elevated
low-density
lipoprotein
cholesterol
(LDL-C),
modifiable
risk
factor,
plays
pivotal
role
development
ASCVD.
Emerging
treatments
such
inhibitors
are
now
being
introduced
to
combat
this
issue,
goal
reducing
ASCVD
by
directly
targeting
LDL-C
levels.
discovery
highlighted
potential
inhibit
PCSK9,
thereby
enhancing
receptor
activity.
led
Alirocumab
and
Evolocumab
which
typically
reduce
levels
approximately
50%.
research
underscores
importance
treating
ASCVD,
drawing
evidence
from
various
randomized
controlled
trials
FOURIER,
ODYSSEY
OUTCOMES,
VESALIUS-CV.
These
have
also
shown
that
effective
safe
several
disorders.
therefore
useful
patients
who
do
not
reach
their
target
when
highest
doses
statins
or
very
high
cannot
tolerate
at
all.
Diagnostics,
Journal Year:
2024,
Volume and Issue:
14(12), P. 1241 - 1241
Published: June 13, 2024
Low-density
lipoprotein
cholesterol
(LDL-C),
which
makes
up
about
70%
of
the
in
blood,
is
critical
formation
arteriosclerotic
plaques,
increasing
risk
heart
disease.
LDL-C
levels
are
estimated
using
Friedewald,
Martin
and
Sampson
equations,
though
they
have
limitations
with
high
triglycerides.
Our
aim
to
compare
effectiveness
these
equations
versus
ultracentrifugation
technique
individuals
without
dyslipidemia
identify
precision.
There
were
113
participants,
59
healthy
controls
54
dyslipidemic
patients.
Samples
collected
after
fasting.
was
equations.
The
purified
LDL-C,
ultracentrifugated
dialysized
control
group
vs.
patients
coronary
artery
disease
(CAD)
showed
differences
age,
HDL-C,
triglycerides
glucose
non-HDL-C
(
PLoS ONE,
Journal Year:
2024,
Volume and Issue:
19(8), P. e0309470 - e0309470
Published: Aug. 22, 2024
Low-Density
Lipoprotein
(LDL)
cholesterol
is
one
of
the
main
target
for
cardiovascular
(CV)
prevention
and
therapy.
In
last
years,
Proprotein
Convertase
Subtilisin–Kexin
type
9
inhibitors
(PCSK9-i)
has
emerged
as
a
key
therapeutic
to
lower
LDL
were
introduced
CV
events.
Recently
(June
2022)
Italian
Medicines
Agency
(AIFA)
modified
eligibility
criteria
use
PCSK9-i.
We
designed
an
observational
study
estimate
prevalence
eligible
subjects
evaluate
effectiveness
PCSK9-i
applying
Target
Trial
Emulation
(TTE)
approach
based
on
Electronic
Health
Records
(EHR).
Subjects
meeting
identified
from
July
2017
(when
became
available)
December
2020.
Outcomes
all-cause
death
first
hospitalization.
Among
subjects,
we
those
treated
at
date
prescription.
Inverse
Probability
Treatment
Weights
(IPTW)
estimated
including
demographic
clinical
covariates,
history
treatment
with
statins
month/year
date.
Competing
risk
models
weighted
cohorts
used
derive
Average
Effect
(ATE)
Conditional
(CATE)
in
subgroups
interest.
Out
1976
161
(8%)
received
Treated
individuals
slightly
younger,
predominantly
male,
had
more
severe
conditions,
often
statin
compared
untreated
subjects.
The
latter
exhibited
higher
non-CV
comorbidities.
A
significant
absolute
relative
reduction
hospitalization
was
observed.
confirmed
CATE
analysis.
PCSk9-i
prescribed
minority
Within
TTE
framework,
analysis
association
between
events,
aligning
findings
randomized
trials
(RCTs).
our
study,
provided
protection
specifically
against
death,
expanding
upon
evidence
RCTs
that
primarily
focused
composite
outcomes.
Journal of Cardiovascular Development and Disease,
Journal Year:
2024,
Volume and Issue:
11(9), P. 286 - 286
Published: Sept. 14, 2024
Reducing
levels
of
low-density
lipoprotein
cholesterol
(LDL-C)
below
recommended
thresholds
is
a
core
component
cardiovascular
prevention
strategies.
We
hypothesized
that
the
addition
bempedoic
acid
to
patients
already
on
statin–ezetimibe
therapy
was
more
effective
than
titrating
statin
dose
in
reducing
LDL-C.
The
study
enrolled
120
at
high
risk
and
with
LDL-C
above
70
mg/dL.
They
were
randomly
divided
into
two
groups:
(BA)
group,
taking
plus
ezitimibe,
titration
(ST)
including
who
doubled
statin.
At
12
weeks,
BA
group
presented
significant
decrease
compared
ST
(−22.9%
vs.
7.5%
p
0.002).
total
decreased
significantly
(−14.8%
vs.−4.7%;
0.013)
No
between-group
changes
HDL
triglycerides
occurred.
number
reached
lower
mg/dL
38
(63%)
versus
22
(37%)
(between
groups,
0.034).
In
LDL-lowering
effect
similar
between
atorvastatin
rosuvastatin.
side
effects
occurred
during
follow
up
period.
conclusion,
combined
treatment
doubling
increased
reaching
goal.
Pharmacotherapy The Journal of Human Pharmacology and Drug Therapy,
Journal Year:
2024,
Volume and Issue:
44(11), P. 861 - 869
Published: Oct. 23, 2024
Abstract
Background
Proprotein
convertase
subtilisin/kexin
type
9
inhibitors
(PCSK9i)
have
been
shown
to
improve
cardiovascular
outcomes
by
reducing
low‐density
lipoprotein
cholesterol
(LDL‐C).
However,
sex
differences
in
the
efficacy
of
evolocumab
remain
unclear.
This
study
aimed
investigate
using
real‐world
data.
Method
Data
were
collected
from
First
Affiliated
Hospital
Guangxi
Medical
University.
A
total
416
eligible
patients
selected
1463
treated
with
for
secondary
prevention.
Clinical
data,
including
individual
characteristics
and
lipids
profiles,
recorded.
Propensity
score
matching
(PSM)
was
used
control
potential
confounders,
covariates
age,
body
mass
index,
smoking
status,
diabetes.
All
participants
propensity‐matched
1:1
female
versus
male
a
match
tolerance
0.02.
The
females
males
compared
PSM‐adjusted
analysis.
Results
In
PSM
analysis,
significant
difference
found
relative
percentage
reduction
LDL‐C
between
(−42.7%
vs.
−54.4%,
p
<
0.001).
addition,
absolute
lower
(interquartile
range:
−1.5
[−2.2,
−0.8]
mmol/L
−1.9
[−2.5,
−1.0]
mmol/L,
=
0.018).
rate
target
attainment
than
after
treatment
(21.6%
39.8%,
0.009).
Conclusion
These
results
suggest
that
better
response
term
females.