Deleted Journal,
Journal Year:
2025,
Volume and Issue:
8(1)
Published: Jan. 1, 2025
ABSTRACT
Background
Pemafibrate,
a
selective
peroxisome
proliferator‐activated
receptor
alpha
(PPARα)
modulator
(SPPARMα),
has
positive
effects
on
liver‐related
markers
(e.g.,
liver
stiffness
determined
by
magnetic
resonance
elastography
and
alanine
aminotransferase)
in
the
PEMA‐FL
study
patients
with
metabolic
dysfunction‐associated
steatotic
disease
(MASLD).
Patients
MASLD
reportedly
have
high
rate
of
muscle
mass
loss;
hence,
prevention
treatment
sarcopenia
is
important
for
MASLD.
PPARα
may
be
involved
expression
carnitine
myostatin,
which
are
known
muscle‐related
markers.
We
conducted
post‐hoc
analysis
to
investigate
pemafibrate
myostatin
levels.
Methods
The
study,
double‐blind,
placebo‐controlled,
randomized,
multicenter,
Phase
2
trial,
randomized
118
either
Pemafibrate
0.4
mg/day
or
placebo
(1:1)
group
(orally,
twice
daily
72
weeks).
This
examined
percentage
change
total
carnitine,
free
acylcarnitine,
compared
those
group.
correlation
between
changes
Results
Pmafibrate
significantly
increased
serum
levels
from
baseline
at
Week
48
(treatment
difference
24.2%;
p
<
0.001,
27.3%;
respectively)
similar
trends
acylcarnitine
10.7%).
reduced
plasma
−11.0%;
0.01)
baseline.
Analysis
significant
subgroups
showed
almost
all
subgroups.
percent
12
weeks
demonstrated
no
obvious
correlations
(
r
=
0.337,
0.358,
0.077,
respectively).
Conclusions
decreased
MASLD,
potential
application
development
progression
sarcopenia,
but
there
results
effect
mass.
Further
research
warranted
determine
whether
these
physiology
can
lead
clinical
benefits
Trial
Registration:
ClinicalTrials.gov
identifier:
NCT03350165.
Life,
Journal Year:
2025,
Volume and Issue:
15(2), P. 288 - 288
Published: Feb. 12, 2025
Metabolic
dysfunction-associated
steatotic
liver
disease
(MASLD)
challenges
traditional
paradigms
by
manifesting
in
lean
individuals.
The
link
between
MASLD
and
inflammatory
bowel
(IBD)
underscores
the
importance
of
gut-liver
axis
progression
chronic
inflammation.
This
study
evaluates
prevalence,
clinical
characteristics,
diagnostic
predictors
individuals
with
without
IBD.
prospective
included
387
patients.
Hepatic
steatosis
fibrosis
were
assessed
using
vibration-controlled
transient
elastography
(VCTE).
Anthropometric,
biological
data
compared.
subgroup
analyses
focused
on
patients
was
present
34.1%
46.3%
those
who
had
increased
visceral
adiposity
(CUN-BAE:
31.21
±
5.42
vs.
24.57
6.49,
p
<
0.001)
metabolic
dysfunction,
including
dyslipidemia
elevated
fasting
glucose.
IBD-MASLD
exhibited
greater
hepatic
systemic
CUN-BAE
outperformed
FLI
HSI
predicting
steatosis,
especially
IBD
(AUC
=
0.806).
Lean
MASLD,
particularly
patients,
highlights
need
for
tailored
management
strategies.
plays
a
key
role
progression,
index
demonstrates
superior
accuracy
identifying
steatosis.
MedComm,
Journal Year:
2025,
Volume and Issue:
6(2)
Published: Feb. 1, 2025
Abstract
We
aimed
to
compare
the
association
of
metabolic
dysfunction‐associated
fatty
liver
disease
(MAFLD),
steatotic
(MASLD),
alcohol‐related
(ALD),
dysfunction
and
ALD
(MetALD),
MASLD
with
viral
hepatitis
(MASLD‐Viral)
risks
cirrhosis,
cancer,
mortality.
The
data
464,556
adults
from
UK
Biobank
(UKB),
13,526
National
Health
Nutrition
Examination
Survey
(NHANES),
2554
BeijngFH
Cohort
Study
(FHCS)
were
included.
Adjusted
hazard
ratios
(aHR)
odds
calculated
using
Cox
Logistic
regression
models,
respectively.
Compared
non‐SLD,
risk
cancer
increased
MetALD
(aHR
1.70
[95%
CI
1.37,
2.09]),
(1.91
[1.66,
2.21]),
MAFLD
(2.01
[1.76,
2.29]),
(3.16
[2.54,
3.93]),
MASLD‐Viral
(22.0
[10.8,
44.4])
in
a
stepwise
manner
UKB;
all‐cause
mortality
MetALD,
MASLD,
MAFLD,
ALD,
NHANES.
ratio
fibrosis
FHCS.
In
patients
diabetes,
metformin
plus
other
drugs
associated
higher
or
MAFLD.
Prevention
rather
than
antiglycemic
treatment
is
important
for
diabetic
Exploration of Medicine,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Feb. 17, 2025
Metabolic
dysfunction-associated
steatotic
liver
disease
(MASLD)
is
an
emerging
and
rapidly
growing
health
problem
that
currently
affects
more
than
one-third
of
the
world
general
population
two-thirds
patients
with
obesity
or
type
2
diabetes.
MASLD
associated
one
cardio-metabolic
risk
factors
(CMRFs)
determine
complexity
its
natural
history
management.
Although
term
encompasses
a
single
disease,
each
CMRF
has
different
impact
on
MASLD,
number
overlapping
CMRFs
results
in
rate
progression
outcomes
both
systemic
disease.
Its
pathogenesis
characterized
by
insulin
resistance,
lipotoxicity
complex
cross-talk
between
liver,
adipose
tissue,
muscle,
intestine
through
release
hepatokines,
cytokines,
myokines
inflammatory
products.
The
stage
fibrosis
best
predictor
outcomes,
such
as
failure
mortality,
also
predicts
high
all-cause
mortality
In
many
cases,
development
hepatocellular
carcinoma
(HCC)
advanced
cirrhosis,
although
it
can
occur
at
all
stages
making
prevention
difficult.
increasing
very
low-density
lipoprotein
(VLDL)
secretion
chronic
low-grade
inflammation,
which
increase
cardio-vascular,
renal,
endocrine
diseases
extrahepatic
cancer.
Thus,
management
requires
holistic
approach
treatment
multispecialty
collaboration.
Currently,
diet
physical
activity
are
effective
first-line
approaches.
There
no
approved
drugs
for
apart
from
resmetirom,
percentage
cases
improves
metabolic
steatohepatitis
(MASH)
fibrosis.
We
summarize
wide
varied
recent
literature
etiopathogenetic,
clinical
therapeutic
aspects
connecting
interpreting
to
facilitate
Journal of Human Nutrition and Dietetics,
Journal Year:
2025,
Volume and Issue:
38(2)
Published: Feb. 27, 2025
ABSTRACT
Background
Metabolic
dysfunction‐associated
steatotic
liver
disease
(MASLD)
is
a
growing
global
health
concern.
Effective
management
of
this
condition
relies
heavily
on
lifestyle
modifications
and
dietary
interventions.
In
study,
we
sought
to
evaluate
the
plans
for
MASLD
generated
by
ChatGPT
(GPT‐4o)
according
current
guideline
recommendations.
Methods
was
used
create
single‐day
meal
48
simulated
patients
with
MASLD,
tailored
individual
characteristics
such
as
age,
gender,
height,
weight
transient
elastography
parameters.
The
were
assessed
appropriateness
disease‐specific
guidelines.
Results
mean
energy
content
menus
planned
1596.9
±
141.5
kcal
accuracy
91.3
11.0%,
fibre
22.0
0.6
g
88.1
2.5%.
However,
they
exhibited
elevated
levels
protein,
fat
saturated
acids.
Conversely,
carbohydrate
lower.
recommended
loss
obese
but
did
not
extend
advice
normal‐weight
overweight
individuals.
Notably,
recommendations
Mediterranean
diet
physical
activity
absent.
Conclusions
shows
potential
in
developing
management.
discrepancies
macronutrient
distributions
omission
key
evidence‐based
highlight
need
further
refinement.
To
enhance
effectiveness
AI
tools
recommendations,
alignment
established
guidelines
must
be
improved.
Livers,
Journal Year:
2025,
Volume and Issue:
5(1), P. 11 - 11
Published: March 4, 2025
Non-alcoholic
fatty
liver
disease
(NAFLD),
recently
redefined
as
metabolic
dysfunction-associated
steatotic
(MASLD),
is
the
most
common
cause
of
chronic
worldwide.
Characterized
by
excessive
hepatic
fat
accumulation,
this
encompasses
a
spectrum
from
simple
steatosis
to
more
severe
forms,
including
steatohepatitis,
fibrosis,
and
cirrhosis.
Emerging
evidence
highlights
pivotal
role
gut
dysbiosis
in
pathogenesis
MASLD.
Dysbiosis
disrupts
gut–liver
axis,
an
intricate
communication
network
that
regulates
metabolic,
immune,
barrier
functions.
Alterations
microbiota
composition,
increased
permeability,
translocation
pro-inflammatory
metabolites/factors
have
been
shown
trigger
inflammatory
fibrotic
cascades,
exacerbating
inflammation
injury.
Recent
studies
identified
microbiome
signatures
associated
with
MASLD,
offering
promise
non-invasive
diagnostic
biomarkers
paving
way
for
new
potential
therapeutic
strategies
targeting
dysbiosis.
This
review
explores
crucial
MASLD
need
further
targeted
research
field
validate
microbial
optimize
strategies.
Comprehensive
understanding
axis
may
enable
innovative
approaches,
transforming
clinical
management
Metabolism and Target Organ Damage,
Journal Year:
2025,
Volume and Issue:
5(1)
Published: March 8, 2025
The
transition
from
non-alcoholic
fatty
liver
disease
(NAFLD)
to
metabolic
dysfunction-associated
steatotic
(MASLD)
represents
a
significant
evolution
in
the
nomenclature
of
disease.
This
updated
terminology
emphasizes
dysfunction
as
central
criterion,
offering
greater
precision
and
improved
risk
stratification.
MASLD
broadens
scope
classification
by
incorporating
individuals
with
diverse
profiles,
including
lean
patients
hepatic
steatosis,
aligns
clinical
practice
multifactorial
nature
this
condition.
global
adoption
creates
opportunities
for
standardization
research
settings,
facilitating
multicenter
collaborations
enhancing
development
diagnostic
tools
therapeutic
strategies.
However,
new
poses
challenges,
potential
confusion
during
implementation,
cultural
linguistic
barriers,
integration
MetALD,
need
educational
initiatives
targeting
healthcare
providers
patients.
Further
efforts
are
required
refine
criteria,
address
implementation
seamlessly
incorporate
into
international
coding
systems.
review
evaluates
key
advantages
ongoing
challenges
associated
MASLD,
providing
comprehensive
analysis
its
impact
on
practice,
research,
health