International Journal of Molecular Sciences,
Journal Year:
2025,
Volume and Issue:
26(9), P. 4077 - 4077
Published: April 25, 2025
The
recent
introduction
of
the
term
metabolic-dysfunction-associated
steatotic
liver
disease
(MASLD)
has
highlighted
critical
role
metabolism
in
disease’s
pathophysiology.
This
innovative
nomenclature
signifies
a
shift
from
previous
designation
non-alcoholic
fatty
(NAFLD),
emphasizing
condition’s
progressive
nature.
Simultaneously,
MASLD
become
one
most
prevalent
diseases
worldwide,
highlighting
urgent
need
for
research
to
elucidate
its
etiology
and
develop
effective
treatment
strategies.
review
examines
delineates
revised
definition
MASLD,
exploring
epidemiology
pathological
changes
occurring
at
various
stages
disease.
Additionally,
it
identifies
metabolically
relevant
targets
within
provides
summary
latest
targeted
drugs
under
development,
including
those
clinical
some
preclinical
stages.
finishes
with
look
ahead
future
therapy
goal
summarizing
providing
fresh
ideas
insights.
Medicina,
Journal Year:
2025,
Volume and Issue:
61(1), P. 88 - 88
Published: Jan. 7, 2025
Introduction:
Metabolic
Dysfunction-Associated
Steatotic
Liver
Disease
(MASLD)
stems
from
disrupted
lipid
metabolism
in
the
liver,
often
linked
to
obesity,
type
2
diabetes,
and
dyslipidemia.
In
Mexico,
where
obesity
affects
36.9%
of
adults,
MASLD
prevalence
has
risen,
especially
with
metabolic
syndrome
affecting
56.31%
by
2018.
can
progress
Steatohepatitis
(MASH),
5.27%
globally,
leading
severe
complications
like
cirrhosis
hepatocellular
carcinoma.
Background:
Visceral
fat
distribution
varies
gender,
impacting
development
due
hormonal
influences.
Insulin
resistance
plays
a
central
role
pathogenesis,
exacerbated
high-fat
diets
specific
fatty
acids,
hepatic
steatosis.
Lipotoxicity
saturated
acids
further
damages
hepatocytes,
triggering
inflammation
fibrosis
progression
MASH.
Diagnosing
traditionally
involves
invasive
liver
biopsy,
but
non-invasive
methods
ultrasound
transient
elastography
are
preferred
their
safety
availability.
These
detect
steatosis
reasonable
accuracy,
offering
alternatives
biopsy
despite
varying
sensitivity
specificity.
Conclusions:
as
disorder
underscores
its
impact
on
public
health,
necessitating
improved
awareness
early
management
strategies
mitigate
diseases.
Nutrition Journal,
Journal Year:
2025,
Volume and Issue:
24(1)
Published: Jan. 14, 2025
The
objective
of
this
study
was
to
investigate
the
association
between
sarcopenia
and
liver
fibrosis
in
patients
aged
18–59
years
with
metabolic
dysfunction-associated
steatotic
disease
(MASLD)
assess
potential
as
a
risk
factor
for
progression
fibrosis.
included
821
MASLD
US
cohort
3,405
Chinese
cohort.
Liver
controlled
attenuation
parameters
(CAP)
stiffness
measurements
(LSM)
were
assessed
by
vibration-controlled
transient
elastography
(VCTE)
evaluate
extent
hepatic
steatosis
Sarcopenia
measuring
appendicular
skeletal
muscle
mass
(ASM)
calculating
ASMI.
To
analyze
relationship
sarcopenia,
ASMI,
fibrosis,
logistic
regression
models,
multivariate-adjusted
restricted
cubic
spline
(RCS)
models
employed,
stratification
interaction
analyses.
results
demonstrated
that
exhibited
markedly
elevated
significant
advanced
cirrhosis
compared
those
without
both
cohorts.
After
adjusting
confounding
variables,
identified
an
independent
MASLD.
A
negative
correlation
observed
ASMI
severity
progressive
reduction
associated
increasing
Additionally,
non-linear
feature
evident
some
indicators.
Subgroup
analysis
further
corroborated
finding
harmful
effect
on
consistent
across
all
subgroups.
may
be
Monitoring
assist
identifying
individuals
at
patients.
Background:
The
burden
of
metabolic
dysfunction-associated
steatotic
liver
disease
(MASLD)
is
increasing,
yet
there
little
regional
understanding
in
the
Western
Pacific.
This
study
aims
mainly
to
report
latest
MASLD
and
trends
Pacific
region
for
period
1990-2021.
Background:
Several
randomized
controlled
trials
(RCTs)
have
been
conducted
to
evaluate
treatment
efficacy
for
metabolic
dysfunction-associated
steatotic
liver
disease/steatohepatitis
(MASLD/MASH).
This
network
meta-analysis
compared
the
effectiveness
of
11
promising
targets
under
a
frequentist
framework
(PROSPERO
registration:
CRD42024625681).
International Journal of Molecular Sciences,
Journal Year:
2025,
Volume and Issue:
26(3), P. 1271 - 1271
Published: Jan. 31, 2025
Metabolic-associated
steatotic
liver
disease
(MASLD)
represents
the
most
common
chronic
hepatopathy
worldwide
and
an
independent
risk
factor
for
cardiovascular
mortality,
particularly
when
fibrosis
occurs.
Epigenetic
alterations,
such
as
DNA
methylation,
may
influence
MASLD
susceptibility
progression;
yet
mechanisms
underlying
this
process
are
limited.
This
study
aimed
to
investigate
whether
active
demethylation
in
peripheral
blood
mononuclear
cells
(PBMCs)
from
individuals
with
MASLD,
alongside
methylation
mRNA
levels
of
inflammation-
fibrosis-related
candidate
genes,
is
associated
fibrosis.
For
study,
global
intermediates
(5-hydroxymethylcytosine
[5hmC],
5-formylcytosine
[5fC])
were
quantified
PBMCs
89
with/without
using
ELISA.
Site-specific
SOCS3,
SREBF1,
TXNIP
was
analyzed
by
mass
spectrometry-based
bisulfite
sequencing;
expression
assessed
via
RT-PCR.
Individuals
moderate-to-high
(estimated
non-alcoholic
steatohepatitis
(NASH)
index,
FNI)
progressively
exhibited
greater
5hmC
5fC
levels.
Higher
FNI
reduced
SOCS3
gene
increased
TXNIP,
IL-6,
MCP-1
genes.
In
conclusion,
elevated
demethylation,
well
differential
patterns
which
key
regulators
inflammation
These
epigenetic
alterations
mirror
changes
liver,
potentially
contribute
fibrogenesis
represent
novel
biomarkers
progression
toward
Frontiers in Immunology,
Journal Year:
2025,
Volume and Issue:
16
Published: Feb. 10, 2025
Objective
This
study
aimed
to
investigate
the
association
between
high-sensitivity
C-reactive
protein
(hsCRP)
levels
and
hepatic
fibrosis
in
patients
with
metabolic
dysfunction-associated
steatotic
liver
disease
(MASLD)
assess
its
predictive
efficacy.
Methods
The
included
1,477
participants
from
United
States
1,531
China
diagnosed
MASLD.
Liver
stiffness
measurement
(LSM)
controlled
attenuation
parameter
(CAP)
were
assessed
by
vibration-controlled
transient
elastography
(VCTE)
evaluate
presence
degree
of
steatosis.
relationship
hsCRP
MASLD
was
examined
using
multivariable-adjusted
restricted
cubic
spline
(RCS)
models.
Additionally,
subgroup
analyses
conducted
potential
heterogeneity
among
different
characteristic
subgroups.
Results
results
demonstrated
a
significant
correlation
elevated
an
increased
risk
fibrosis,
advanced
cirrhosis
US
cohort
(OR
2.22,
1.69,
2.85,
respectively;
all
P
<0.05).
Chinese
consistent
those
cohort,
there
positive
2.53,
3.85,
3.78,
respectively,
<0.001).
RCS
analysis
revealed
non-linear
disparate
inflection
point
values
observed
across
cohorts
(approximately
9
mg/L
4
cohort).
impact
on
varied
subgroups
distinct
characteristics.
Conclusion
present
MASLD,
notable
dose-response
relationships
differences.
European Journal of Internal Medicine,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Feb. 1, 2025
It
is
unclear
if
the
risk
of
hepatic
decompensation
or
hepatocellular
carcinoma
(HCC)
differs
between
patients
with
compensated
alcohol-related
liver
disease
(ALD)-
and
metabolic
dysfunction-associated
steatotic
(MASLD)-cirrhosis.
We
investigated
to
develop
HCC
based
on
ALD
MASLD
as
underlying
etiology
cirrhosis.
All
a
new
diagnosis
in
hospital-based
outpatient
care
ALD-
MASLD-cirrhosis
Sweden
2002
2020
were
identified
using
national
registers.
Hepatic
was
analyzed
composite
outcome
HCC.
Cox
regression
employed
compare
rates
HCC,
subsequent
death.
1660
ALD-cirrhosis
943
identified.
The
median
ages
64
years
(IQR
57-70)
69
62-75)
MASLD-cirrhosis,
respectively.
Patients
consisted
69.4
%
males,
compared
47.6
males
group.
581
(35
%)
284
(30
developed
(median
follow-up
time:
25
months),
resulting
an
adjusted
hazard
ratio
1.12
(ALD-
vs.
95
%-confidence
interval=0.88-1.41).
mortality
afterwards
lower
(adjusted
0.62,
interval=0.39-0.97).
comparable
but
after
event
tends
be
higher
MASLD-cirrhosis.