Diabetes Obesity and Metabolism,
Journal Year:
2024,
Volume and Issue:
27(2), P. 683 - 696
Published: Nov. 11, 2024
Metabolic
dysfunction-associated
steatotic
liver
disease
(MASLD)
and
obesity
increases
risk
of
cardiovascular
disease.
This
cohort
study
examines
the
prognostic
value
MASLD,
across
body
weight
categories,
in
a
secondary
preventative
acute
myocardial
infarction
(AMI)
cohort.
European Journal of Preventive Cardiology,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Sept. 13, 2024
Abstract
Aims
The
prediction
of
future
trends
in
cardiovascular
disease
(CVD)
mortality
and
their
risk
factors
can
assist
policy-makers
healthcare
planning.
This
study
aims
to
project
geospatial
CVDs
underlying
from
2025
2050.
Methods
results
Using
historical
data
on
disability-adjusted
life
years
(DALYs)
the
Global
Burden
Disease
(GBD)
2019
study,
encompassing
period
1990
2019,
Poisson
regression
was
performed
model
DALYs
associated
with
CVD
its
Subgroup
analysis
based
GBD
super-regions.
Between
2050,
a
90.0%
increase
prevalence,
73.4%
crude
mortality,
54.7%
are
projected,
an
expected
35.6
million
deaths
2050
(from
20.5
2025).
However,
age-standardized
prevalence
will
be
relatively
constant
(−3.6%),
decreasing
(−30.5%)
(−29.6%).
In
ischaemic
heart
remain
leading
cause
(20
deaths)
while
high
systolic
blood
pressure
main
factor
driving
(18.9
deaths).
Central
Europe,
Eastern
Asia
super-region
is
set
incur
highest
rate
(305
per
100
000
population).
Conclusion
coming
decades,
global
suggests
that
net
effect
summative
preventative
efforts
likely
continue
unchanged.
fall
reflects
improvement
medical
care
following
diagnosis.
systems
expect
rapid
rise
driven
by
ageing
populace.
continued
burden
largely
attributed
atherosclerotic
diseases.
Registration
Not
applicable.
Cardiovascular Diabetology,
Journal Year:
2025,
Volume and Issue:
24(1)
Published: Feb. 7, 2025
Emerging
evidence
has
demonstrated
the
unfavourable
cardiovascular
risk
of
individuals
with
lean
type
2
diabetes
mellitus
(T2DM).
Our
study
aims
to
investigate
prognostic
value
T2DM
in
patients
acute
myocardial
infarction
(AMI),
stratified
by
sex.
The
cohort
examines
clinical
characteristics
and
long-term
outcomes
AMI,
four
phenotypes
based
on
body
category—lean
T2DM,
non-lean
non-T2DM
non-T2DM.
primary
outcome
was
all-cause
mortality.
Cox
regression
model
constructed
associations
mortality,
adjusted
for
age,
ethnicity,
previous
AMI
type,
chronic
kidney
disease,
angiotensin
converting
enzyme
inhibitor
or
receptor
blockers,
beta-blockers,
smoking
status.
A
9545
examined,
a
mean
follow-up
duration
3.4
±
2.4
years.
Majority
had
phenotype
(40.4%),
followed
(29.8%),
(15.9%),
(13.9%).
In
group,
one-quarter
(N
=
1324),
while
vast
majority
(74.5%)
non-lean.
Individuals
tended
be
female
older.
Patients
highest
rates
heart
failure
(23.3%,
p
<
0.001),
cardiogenic
shock
(9.1%,
0.036),
mortality
(32.6%,
0.001).
that
an
independent
predictor
(adjusted
hazard
ratio
[aHR]
1.171,
95%
CI
1.040–1.319,
0.009)
after
adjustment.
presence
higher
following
present
males
(aHR
1.201,
1.037–1.391,
0.015),
but
not
females
1.066,
0.869–1.308,
0.538).
T2DM.
although
this
association
stronger
than
females.
Diabetes Obesity and Metabolism,
Journal Year:
2024,
Volume and Issue:
26(8), P. 3328 - 3338
Published: May 23, 2024
Abstract
Aim
Patients
with
metabolic
dysfunction‐associated
steatotic
liver
disease
(MASLD)
are
at
increased
risk
of
incident
cardiovascular
disease.
However,
the
clinical
characteristics
and
prognostic
importance
MASLD
in
patients
presenting
acute
myocardial
infarction
(AMI)
have
yet
to
be
examined.
Methods
This
study
compared
outcomes
without
AMI
a
tertiary
centre
Singapore.
was
defined
as
hepatic
steatosis,
least
one
five
criteria.
Hepatic
steatosis
determined
using
Steatosis
Index.
Propensity
score
matching
performed
adjust
for
age
sex.
The
Kaplan‐Meier
curve
constructed
long‐term
all‐cause
mortality.
Cox
regression
analysis
used
investigate
independent
predictors
Results
In
this
4446
AMI,
2223
were
matched
propensity
scores.
mean
follow‐up
duration
3.4
±
2.4
years.
group
had
higher
rates
obesity,
diabetes
chronic
kidney
than
their
counterparts.
early
excess
mortality
(6.8%
vs.
3.6%,
p
<
.001)
30
days,
unfavourable
sustained
(18.3%
14.5%,
=
those
MASLD.
After
adjustment,
remained
independently
associated
(hazard
ratio
1.330,
95%
confidence
interval
1.106‐1.598,
.002).
Conclusion
embodies
burden
dysfunction
is
an
predictor
population.
Its
identification
may
beneficial
stratification
provide
therapeutic
targets
secondary
preventive
strategies
AMI.
BMJ Open,
Journal Year:
2024,
Volume and Issue:
14(12), P. e089047 - e089047
Published: Dec. 1, 2024
Purpose
Coronary
CT
angiography
(CCTA)
is
well
established
for
the
diagnostic
evaluation
and
prognostication
of
coronary
artery
disease
(CAD).
The
growing
burden
CAD
in
Asia
emergence
novel
CT-based
risk
markers
highlight
need
an
automated
platform
that
integrates
patient
data
with
CCTA
findings
to
provide
tailored,
accurate
cardiovascular
assessments.
This
study
aims
develop
artificial
intelligence
(AI)-driven
assessment
using
Singapore’s
multiethnic
population.
We
will
conduct
a
hybrid
retrospective-prospective
recruitment
patients
who
have
undergone
as
part
workup
CAD,
along
prospective
follow-up
clinical
endpoints.
images
be
analysed
locally
by
core
lab
stenosis
grading,
Agatston
scoring,
epicardial
adipose
tissue
plaque
analysis.
analyses
also
uploaded
AI
deidentification,
integration
reporting,
generating
precision
toolkits
each
parameter.
Participants
baseline
characteristics
been
collected
verified
4196
recruited
patients,
comprising
75%
Chinese,
6%
Malay,
10%
Indian
9%
from
other
ethnic
groups.
Among
participants,
41%
are
female,
mean
age
55±11
years.
Additionally,
hypertension,
51%
dyslipidaemia,
15%
diabetes
22%
history
smoking.
Findings
date
cohort
used
four
modules
training,
testing
validation.
During
development
process,
preprocessing
standardised
format,
resolution
relevant
attributes
images.
Future
plans
on
track
endpoints,
including
events,
hospitalisations
mortality.
we
monitor
long-term
impact
AI-driven
outcomes
healthcare
delivery.
Trial
registration
number
NCT05509010
.