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.
The
accumulation
of
adipose
tissue
is
associated
with
metabolic
disorders,
including
insulin
resistance,
type
2
diabetes
(T2D),
dyslipidemia,
syndrome,
and
cardiovascular
diseases
(CVD).
Menopause
might
predispose
women
to
increase
body
weight
tissue,
decrease
lean
muscle
mass.
Furthermore,
postmenopausal
display
fat
mass
redistribution
greater
in
the
visceral
area
mainly
due
hormonal
shifts
that
result
a
higher
testosterone/estradiol
ratio.
These
effects
are
less
favorable
adipokine
profile,
cardiac
dysfunction
after
menopause.
Fat
determined
by
balance
between
storage
triacylglycerol
(TAG)
(lipogenesis)
removal
stored
TAG
(lipolysis)
combination
differentiation
new
adipocytes
(adipogenesis).
Disturbances
dynamics
lead
an
lipogenesis
(hypertrophy)
and/or
adipogenesis
(hyperplasia)
accommodate
excess
energy
intake.
While
large
dysfunctional
have
secretion
inflammatory
adipocytokines,
small
healthier
improvements.
Different
strategies
can
be
used
prevent
or
reduce
gain
mass,
as
well
maintain
healthy
tissue;
however,
robust
evidence,
lifestyle
interventions
should
pillars
this
process.
This
review
provides
comprehensive
summary
findings
on
role
balanced
diet
physical
exercise
improving
composition
promoting
women.
Internal and Emergency Medicine,
Journal Year:
2025,
Volume and Issue:
unknown
Published: March 14, 2025
Abstract
Sodium-glucose
co-transporter
type-2
(SGLT2)
inhibitors
have
been
identified
to
a
crucial
hepatoprotective
role
in
patients
with
type
2
diabetes
(T2DM)
and
metabolic-associated
steatotic
liver
disease
(MASLD).
Thus,
we
aimed
assess
the
effect
of
SGLT2
on
hepatic
steatosis
T2DM
MASLD
added
standard
care
(SOC)
treatment.
Our
study
was
single-arm
clinical
trial
no
ISRCTN85961860.
Thirty
were
recruited
from
outpatient
endocrinology
clinic
Internal
Medicine
Department
at
Kasr
Al-Aini
Hospital,
Cairo
University,
Egypt.
Patients
received
Empagliflozin
10
mg
daily
which
SOC
treatment
followed
up
for
24
weeks.
Magnetic
resonance
imaging
proton
density
fat
fraction
(MRI-PDFF)
done
baseline
after
weeks
percentage
change
mass.
Also
changes
Fib-4
NAFLD
fibrosis
scores
calculated.
showed
statistically
significant
decrease
mean
MRI-PDFF
measurement
adding
empagliflozin
(13.297
±
7.15)
compared
(15.288
8.72),
P
=
0.006
overall
about
13.16%
steatosis.
There
decreases
BMI,
fasting
blood
glucose,
Alanine
transaminase,
(
<
0.001,
0.03,
0.01)
respectively.
differences
or
scores.
Adding
could
reduce
mass
significantly
practice
guidelines
be
therapeutic
agent
T2DM.
Hepatoma Research,
Journal Year:
2025,
Volume and Issue:
unknown
Published: March 14, 2025
Surveillance
for
hepatocellular
carcinoma
(HCC)
improves
early
tumor
detection,
increases
access
to
curative
therapies,
and
reduces
mortality
by
about
40%.
Early
diagnosis
through
surveillance
is
essential
should
be
extended
as
many
at-risk
patients
possible
maximize
the
benefits
of
multidisciplinary
board
evaluations.
Current
guidelines
recommend
semi-annual
abdominal
ultrasonography
(US),
with/without
serum
alpha-fetoprotein
measurement,
with
cirrhosis
certain
subgroups
individuals
pre-cirrhotic
chronic
liver
disease.
However,
populations
eligible
include
subsets
varying
degrees
HCC
risk,
which
may
change
over
time
in
some
individuals.
As
risk
level
a
key
determinant
cost-effectiveness,
rigid,
“one-size-fits-all”
strategy
appears
inadequate.
Moreover,
non-cirrhotic
-
particularly
those
advanced
fibrosis
are
currently
excluded
from
but
benefit
stratification
identify
whom
would
cost-effective.
strategies
must
also
consider
potential
harms,
limitations
US
screening
test.
In
response,
alternative
approaches
such
biomarkers-based
tests
abbreviated
magnetic
resonance
imaging
under
investigation.
This
article
reviews
literature
advocating
transition
current
approach
programs
tailored
individual
oncological
(risk-stratified
surveillance)
or
that
main
factors
(sex,
etiology,
phenotype)
influence
test
performance
(precision
surveillance).
Additionally,
it
presents
seminal
proposal
risk-stratified
algorithm
designed
optimize
cost-effectiveness
risk-benefit
balance
integrating
variable
intervals
modality
selection.
Diabetes Obesity and Metabolism,
Journal Year:
2025,
Volume and Issue:
unknown
Published: March 13, 2025
Abstract
Background
and
aim
We
assessed
the
prevalence
of
metabolic
dysfunction‐associated
steatotic
liver
disease
(MASLD)
significant
fibrosis
in
adults
with
type
1
diabetes
mellitus
(T1DM)
association
MASLD
insulin
sensitivity
continuous
glucose
monitoring
metrics.
Methods
consecutively
enrolled
198
T1DM
undergoing
vibration‐controlled
transient
elastography
stiffness
measurement
(LSM)
controlled
attenuation
parameter
(CAP).
All
participants
had
a
(CGM)
device.
Insulin
was
evaluated
by
estimated
disposal
rate
(eGDR).
defined
as
CAP
≥
248
db/m
presence
at
least
one
cardiometabolic
risk
factor.
Significant
LSM
7
kPa.
Results
Patients
mean
age
56
years,
BMI
26.0
±
5.9
kg/m
2
,
eGDR
7.1
2.3
mg/kg/min.
73
(37%)
patients
(using
threshold
274
dB/m),
16
(8.1%)
whom
fibrosis.
associated
significantly
lower
(beta
coefficient
=
−0.367,
95%
confidence
interval
−0.472
to
−0.261;
p
<
0.001).
This
remained
significant,
even
after
adjustment
for
age,
sex,
body
mass
index,
plasma
triglycerides,
duration,
daily
dose,
time
above
range
levels,
chronic
kidney
disease.
No
observed
between
CGM‐derived
These
results
were
not
different
when
we
used
dB/m
diagnosing
MASLD.
Conclusion
In
T1DM,
inversely
biomarkers
resistance
but
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.