Lipids in Health and Disease,
Journal Year:
2025,
Volume and Issue:
24(1)
Published: March 7, 2025
The
incidence
of
heart
failure
(HF),
a
cardiovascular
disease,
has
been
widely
reported
to
be
gradually
increasing.
Although
the
triglyceride-glucose
(TyG)
index
is
associated
with
risk
HF,
this
relationship
may
affected
by
differences
in
nutritional
status
among
individuals
varying
levels
obesity.
Waist
circumference
combined
TyG
more
accurately
HF.
This
study
analyzed
data
from
8769
participants
2011–2020
National
Health
and
Nutrition
Examination
Survey
(NHANES).
After
weighting
data,
multivariable
logistic
regressions
were
used
calculate
associations
between
HF
TyG-waist
(TyG-WC)
indices
adults
different
body
mass
(BMIs).
Restricted
cubic
splines
employed
assess
for
linear
or
nonlinear
relationships.
Receiver
operating
characteristic
(ROC)
curves
demonstrate
efficacy
models
indices.
Net
Reclassification
Index
(NRI)
was
measure
improvement
TyG-WC
relative
models.
Integrated
Discriminant
Improvement
(IDI)
supports
conclusion.
positively
(TyG:
odds
ratio
[OR],
1.765;
95%
CI],
1.390–2.242;
P
<
0.001;
TyG-WC:
OR,
1.003;
CI,
1.002–1.004;
0.001),
except
In
Model
4
(OR,
1.238;
0.941–1.629;
=
0.124).
BMI
categorize
population
into
normal
underweight
overweight
obese
groups.
groups,
(OR)
increased
as
value
increased.
However,
high
low
ORs.
According
ROC,
NRI,
IDI
analyses,
weight
groups
(area
under
curve
[AUC]:
0.6724;
CI:
0.4991-0.6400),
whereas
alone
not
(AUC:
0.5695;
0.6115–0.7334).
4,
adjusted
all
covariates,
had
slightly
better
ability
than
(NRI:
-0.4112;
-0.6818-
-0.1406;
0.05;
IDI:
-0.0072;
95%CI:
-0.0228-0.0083;
0.36256).
populations,
0.3089;
0.1726–0.4451;
0.0084;
0.0017–0.0151;
0.05).
sensitivity
only
41.8%.
association
these
two
influenced
BMI.
normal-weight
higher
imply
improved
status.
Therefore,
should
WC
both
can
HF;
however,
less
sensitive
when
alone.
International Journal of Molecular Sciences,
Journal Year:
2024,
Volume and Issue:
25(2), P. 1211 - 1211
Published: Jan. 19, 2024
This
comprehensive
review
explores
the
critical
role
of
fatty
acid
(FA)
metabolism
in
cardiac
diseases,
particularly
heart
failure
(HF),
and
implications
for
therapeutic
strategies.
The
heart’s
reliance
on
ATP,
primarily
sourced
from
mitochondrial
oxidative
metabolism,
underscores
significance
metabolic
flexibility,
with
oxidation
(FAO)
being
a
dominant
source.
In
HF,
shifts
occur
an
altered
FA
uptake
FAO,
impacting
function
contributing
to
disease
progression.
Conditions
like
obesity
diabetes
also
lead
disturbances,
resulting
cardiomyopathy
marked
by
over-reliance
dysfunction,
lipotoxicity.
Therapeutic
approaches
targeting
diseases
have
evolved,
focusing
inhibiting
or
stimulating
FAO
optimize
energetics.
Strategies
include
using
CPT1A
inhibitors,
PPARα
agonists,
enhancing
biogenesis
function.
However,
effectiveness
varies,
reflecting
complexity
remodeling
HF.
Hence,
treatment
strategies
should
be
individualized,
considering
that
energy
is
intricate
tightly
regulated.
aim
overall
function,
recognizing
pivotal
FAs
need
further
research
develop
effective
therapies,
promising
new
improve
Frontiers in Pharmacology,
Journal Year:
2025,
Volume and Issue:
15
Published: Jan. 10, 2025
Sustained
production
of
reactive
oxygen
species
(ROS)
and
an
imbalance
in
the
antioxidant
system
have
been
implicated
development
cardiovascular
diseases
(CVD),
especially
when
combined
with
diabetes,
hypercholesterolemia,
other
metabolic
disorders.
Among
them,
NADPH
oxidases
(NOX),
including
NOX1-5,
are
major
sources
ROS
that
mediate
redox
signaling
both
physiological
pathological
processes,
fibrosis,
hypertrophy,
remodeling.
Recent
studies
demonstrated
mitochondria
produce
more
proteins
energy
response
to
adverse
stress,
corresponding
increase
superoxide
radical
anions.
Novel
NOX4-mediated
modulatory
mechanisms
considered
crucial
for
maintaining
metabolism
homeostasis
during
states.
In
this
review,
we
integrate
latest
data
elaborate
on
interactions
between
oxidative
stress
various
CVD,
aiming
elucidate
higher
incidence
CVD
individuals
Furthermore,
correlations
NOX
ferroptosis,
based
metabolism,
preliminarily
discussed.
Further
discoveries
these
might
promote
novel
therapeutic
drugs
targeting
their
crosstalk
potentially
offering
efficient
management
strategies
CVD.
Circulation Research,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Feb. 14, 2025
BACKGROUND:
Pathological
cardiac
hypertrophy
can
result
in
heart
failure.
Protein
dephosphorylation
plays
a
primary
role
the
mediation
of
various
cellular
processes
cardiomyocytes.
Here,
we
investigated
effects
protein
tyrosine
phosphatase,
PRL2
(phosphatase
regenerative
liver
2),
on
pathological
hypertrophy.
METHODS:
The
knockout
mice
were
subjected
to
angiotensin
II
infusion
or
transverse
aortic
constriction
induce
myocardial
and
dysfunction.
RNA-sequencing
analysis
was
performed
explore
underlying
mechanisms.
Mass
spectrometry
bio-layer
interferometry
assays
used
identify
AMPKα2
(AMP-activated
kinase
α2)
as
an
interacting
PRL2.
Mutant
plasmids
clarify
how
interacts
dephosphorylates
AMPKα2.
RESULTS:
A
significant
upregulation
observed
hypertrophic
myocardium
tissues
patients
with
deficiency
alleviated
hypertrophy,
fibrosis,
dysfunction
challenged
constriction.
Transcriptomic
biochemical
analyses
showed
that
silence
maintained
AMPK
T172
phosphorylation
subsequent
mitochondrial
integrity
II-challenged
spectrometry-based
interactome
assay
indicated
subunit
substrate
Mechanistically,
binds
C-terminal
domain
then
via
its
active
site
C46.
Adeno-associated
virus
9-mediated
cardiomyocyte
also
protected
function
cardioprotective
mice,
but
these
benefits
not
−/−
mice.
CONCLUSIONS:
This
study
reveals
PRL2,
novel
AMPK-regulating
promotes
instability
injury
cardiomyocytes
provides
PLR2
potential
target
for
future
drug
development
treating
Archiv der Pharmazie,
Journal Year:
2025,
Volume and Issue:
358(2)
Published: Feb. 1, 2025
Abstract
Cardiovascular
diseases
(CVDs),
the
leading
cause
of
human
death
worldwide,
are
that
affect
heart
and
blood
vessels
include
arrhythmias,
coronary
atherosclerotic
disease,
hypertension,
so
on.
Resveratrol
(RSV)
is
a
natural
nonflavonoid
phenolic
compound
with
antioxidant,
anti‐inflammatory,
anticancer,
cardiovascular
protection
functions.
RSV
has
shown
significant
protective
effects
against
CVD.
However,
RSV's
clinical
application
limited
by
its
tendency
to
be
oxidized
metabolized
easily.
Therefore,
it
necessary
optimize
structure.
This
review
will
introduce
activity,
synthesis,
structure–activity
relationships
derivatives,
mechanism
action
in
CVDs
recent
years.
Neurobiology of Disease,
Journal Year:
2024,
Volume and Issue:
unknown, P. 106415 - 106415
Published: Jan. 1, 2024
The
prevalence
of
depression
is
higher
in
heart
failure
(HF)
patients.
Early
screening
depressive
symptoms
HF
patients
and
timely
intervention
can
help
improve
patients'
quality
life
prognosis.
This
study
aims
to
explore
biomarkers
for
disease
diagnosis
by
examining
the
expression
profile
serum
exosomal
miRNAs
with
symptoms.
Serum
RNA
was
isolated
extracted
from
6
(HF-DS)
without
(HF-NDS).
High-throughput
sequencing
performed
obtain
miRNA
profiles
target
genes
were
predicted
screened
differentially
expressed
miRNAs.
Biological
functions
analyzed
through
Gene
Ontology
(GO)
Kyoto
Encyclopedia
Genes
Genomes
(KEGG).
Subsequently,
we
collected
RNAs
HF-DS
(n
=
20)
HF-NDS
20).
selected
results
validated
using
reverse
transcription
quantitative
polymerase
chain
reaction
(RT-qPCR).
Finally,
diagnostic
efficacy
predicting
evaluated
receiver
operating
characteristic
(ROC)
curves.
A
total
19
significantly
high-throughput
sequencing,
consisting
12
up-regulated
7
down-regulated
RT-qPCR
validation
demonstrated
that
level
exo-miR-144-3p
group,
levels
exo-miR-625-3p
exo-miR-7856-5p
up-regulated.
negatively
correlated
severity
patients,
area
under
curve
(AUC)
diagnosing
0.763.
In
this
study,
examined
found
lower
associated
more
severe
Exo-miR-144-3p
a
potential
biomarker
Biomedicine & Pharmacotherapy,
Journal Year:
2024,
Volume and Issue:
175, P. 116650 - 116650
Published: April 27, 2024
Sodium-glucose
cotransporter
2
inhibitors
(SGLT2i),
a
new
class
of
glucose-lowering
drugs
traditionally
used
to
control
blood
glucose
levels
in
patients
with
type
diabetes
mellitus,
have
been
proven
reduce
major
adverse
cardiovascular
events,
including
death,
heart
failure
irrespective
ejection
fraction
and
independently
the
hypoglycemic
effect.
Because
their
favorable
effects
on
kidney
outcomes,
use
has
expanded
all
any
combination
mellitus
2,
chronic
disease
failure.
Although
mechanisms
explaining
these
system
are
not
well
understood,
effectiveness
conditions
suggests
that
they
act
at
intersection
metabolic,
renal
cardiac
axes,
thus
disrupting
maladaptive
vicious
cycles
while
contrasting
direct
organ
damage.
In
this
systematic
review
we
provide
state
art
randomized
controlled
trials
investigating
effect
SGLT2i
outcomes
and/or
diabetes.
We
also
discuss
molecular
targets
signaling
pathways
potentially
pharmacological
agents,
from
clinical
experimental
perspective.