Frontiers in Public Health,
Journal Year:
2025,
Volume and Issue:
12
Published: Jan. 7, 2025
Metabolic-associated
steatohepatitis
and
liver
fibrosis
(MASLD)
is
a
growing
public
health
concern,
with
environmental
factors
potentially
playing
role
in
its
development.
This
study
aimed
to
investigate
the
associations
between
serum
cadmium
mercury
levels
risk
of
MASLD
nationally
representative
sample
from
United
States.
Data
National
Health
Nutrition
Examination
Survey
1999
2018
were
analyzed.
Serum
concentrations
measured,
was
defined
based
on
established
criteria.
Logistic
regression
models
used
assess
metal
MASLD,
adjustments
for
potential
confounders.
Stratified
analyses
restricted
cubic
spline
curves
employed
examine
subgroup
differences
nonlinear
relationships.
The
revealed
significant
inverse
likelihood
MASLD.
Individuals
highest
quartiles
had
lower
odds
compared
those
lowest
(Model
3:
Cadmium
Q4
vs.
Q1,
Mercury
Q1).
showed
stronger
older
adults,
males,
never
smokers
cadmium,
females
individuals
without
diabetes
mercury.
Nonlinear
dose-response
indicated
critical
thresholds
beyond
which
dynamics
changed.
Higher
associated
notable
variations
across
subgroups.
These
findings
challenge
conventional
understanding
these
heavy
metals
as
universally
harmful
highlight
need
further
research
unravel
complex
interplay
exposures
pathophysiology.
Liver International,
Journal Year:
2024,
Volume and Issue:
44(7), P. 1526 - 1536
Published: April 5, 2024
Abstract
The
rising
prevalence
of
metabolic
dysfunction‐associated
steatotic
liver
disease
(MASLD)
poses
a
significant
global
health
challenge,
affecting
over
30%
adults
worldwide.
MASLD
is
linked
to
increased
mortality
rates
and
substantial
healthcare
costs,
primarily
driven
by
its
progression
steatohepatitis
(MASH),
which
can
lead
severe
complications
including
cirrhosis
hepatocellular
carcinoma.
Despite
growing
burden,
effective
pharmacotherapy
for
MASLD/MASH
has
been
lacking
until
the
recent
conditional
approval
resmetirom
FDA.
Resmetirom,
liver‐targeted
thyroid
hormone
receptor‐β
selective
drug,
shown
promise
in
clinical
trials
treating
non‐cirrhotic
MASH
with
moderate
advanced
fibrosis.
It
demonstrated
efficacy
reducing
hepatic
fat
content,
improving
histology
(both
resolution
fibrosis
improvement),
ameliorating
biomarkers
damage
without
effects
on
body
weight
or
glucose
metabolism.
Notably,
also
exhibits
favourable
circulating
lipids,
potentially
cardiovascular
risk
patients.
safety
profile
appears
acceptable,
gastrointestinal
adverse
events
being
most
common,
though
generally
mild
moderate.
However,
long‐term
surveillance
warranted
monitor
potential
risks
related
thyroid,
gonadal,
bone
diseases.
Clinical
implementation
faces
challenges
patient
selection
monitoring
treatment
response,
will
heavily
rely
non‐invasive
tests
assessment.
Nonetheless,
represents
landmark
breakthrough
treatment,
paving
way
future
therapeutic
strategies
aiming
mitigate
multifaceted
associated
this
complex
disease.
Clinical and Molecular Hepatology,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Aug. 19, 2024
As
the
rates
of
obesity
and
type
2
diabetes
(T2D)
continue
to
increase
globally,
so
does
prevalence
metabolic
dysfunction
associated
steatotic
liver
disease
(MASLD).
Currently,
38%
all
adults
7-14%
children
adolescents
have
MASLD.
By
2040,
MASLD
rate
for
is
projected
over
55%.
Although
many
with
will
not
develop
progressive
disease,
given
vast
number
patients
MASLD,
it
has
now
become
top
indication
transplant
in
United
States
those
hepatocellular
carcinoma
(HCC)
women.
However,
most
common
cause
mortality
among
remains
death
cardiovascular
diseases.
In
addition
outcomes
(cirrhosis
HCC),
increased
risk
developing
de-novo
T2D,
chronic
kidney
sarcopenia
extrahepatic
cancers.
Furthermore,
decreased
health
related
quality
life,
work
productivity,
fatigue
healthcare
resource
utilization
substantial
economic
burden.
Similar
other
lifestyle
interventions
heathy
diet
physical
activity
remain
cornerstone
managing
these
patients.
a
T2D
drugs
are
available
treat
co-morbid
Resmetirom
only
MASH-targeted
medication
that
was
recently
approved
by
Federal
Drug
Administration
use
stage
2-3
fibrosis.
The
following
review
provides
an
overview
epidemiology,
its
factors
demonstrates
without
further
global
initiatives,
may
increase.
Gut,
Journal Year:
2024,
Volume and Issue:
73(11), P. 1893 - 1908
Published: Sept. 25, 2024
The
understanding
that
changes
in
microbiome
composition
can
influence
chronic
human
diseases
and
the
efficiency
of
therapies
has
driven
efforts
to
develop
microbiota-centred
such
as
first
next
generation
probiotics,
prebiotics
postbiotics,
microbiota
editing
faecal
transplantation.
Central
research
is
how
disease
impacts
vice
versa,
yet
there
a
problematic
issue
with
term
'dysbiosis',
which
broadly
links
microbial
imbalances
various
illnesses
without
precision
or
definition.
Another
significant
discussions
defining
'healthy
individuals'
ascertain
what
characterises
healthy
microbiome.
This
involves
questioning
who
represents
healthiest
segment
our
population-whether
it
those
free
from
illnesses,
athletes
at
peak
performance,
individuals
living
healthily
through
regular
exercise
good
nutrition
even
elderly
adults
centenarians
have
been
tested
by
time
achieved
remarkable
longevity.This
review
advocates
for
delineating
'what
defines
microbiome?'
considering
broader
range
factors
related
health
environmental
influences
on
microbiota.
A
undoubtedly
linked
gut
health.
Nevertheless,
very
difficult
pinpoint
universally
accepted
definition
'gut
health'
due
complexities
measuring
functionality
besides
composition.
We
must
take
into
account
individual
variabilities,
diet,
lifestyle,
host
factors.
Moreover,
challenge
distinguishing
causation
correlation
between
overall
presented.The
also
highlights
resource-heavy
nature
comprehensive
assessments,
hinders
their
practicality
broad
application.
Finally,
we
call
continued
nuanced
approach
better
understand
intricate
evolving
concept
health,
emphasising
need
more
precise
inclusive
definitions
methodologies
studying
Frontiers in Cell and Developmental Biology,
Journal Year:
2024,
Volume and Issue:
12
Published: July 16, 2024
Metabolic
dysfunction-associated
steatotic
liver
disease
(MASLD),
previously
known
as
non-alcoholic
fatty
(NAFLD),
is
the
most
common
disorder
worldwide,
with
an
estimated
global
prevalence
of
more
than
31%.
steatohepatitis
(MASH),
formerly
(NASH),
a
progressive
form
MASLD
characterized
by
hepatic
steatosis,
inflammation,
and
fibrosis.
This
review
aims
to
provide
comprehensive
analysis
extrahepatic
manifestations
MASH,
focusing
on
chronic
diseases
related
cardiovascular,
muscular,
renal
systems.
A
systematic
published
studies
literature
was
conducted
summarize
findings
systemic
impacts
MASH.
The
focused
association
MASH
metabolic
comorbidities,
cardiovascular
mortality,
sarcopenia,
kidney
disease.
Mechanistic
insights
into
concept
lipotoxic
inflammatory
"spill
over"
from
MASH-affected
were
also
explored.
are
highly
associated
(50%-80%)
other
comorbidities
such
impaired
insulin
response,
type
2
diabetes,
dyslipidemia,
hypertriglyceridemia,
hypertension.
Furthermore,
90%
obese
patients
diabetes
have
Data
suggest
that
in
middle-aged
individuals
(especially
those
aged
45-54),
independent
risk
factor
for
plays
crucial
role
mediating
pathological
effects
observed.
Understanding
multifaceted
impact
heart,
muscle,
early
detection
stratification.
knowledge
timely
implementing
management
strategies
addressing
multi-organ
involvement
pathogenesis.
International Journal of Molecular Sciences,
Journal Year:
2024,
Volume and Issue:
25(11), P. 5640 - 5640
Published: May 22, 2024
The
epidemiological
burden
of
liver
steatosis
associated
with
metabolic
diseases
is
continuously
growing
worldwide
and
in
all
age
classes.
This
condition
generates
possible
progression
damage
(i.e.,
inflammation,
fibrosis,
cirrhosis,
hepatocellular
carcinoma)
but
also
independently
increases
the
risk
cardio-metabolic
cancer.
In
recent
years,
terminological
evolution
from
“nonalcoholic
fatty
disease”
(NAFLD)
to
“metabolic
dysfunction-associated
(MAFLD)
and,
finally,
steatotic
(MASLD)
has
been
paralleled
by
increased
knowledge
mechanisms
linking
local
hepatic)
systemic
pathogenic
pathways.
As
a
consequence,
need
for
an
appropriate
classification
individual
phenotypes
oriented
investigation
innovative
therapeutic
tools.
Besides
well-known
role
lifestyle
change,
number
pharmacological
approaches
have
explored,
ranging
antidiabetic
drugs
agonists
acting
on
gut–liver
axis
at
level
(mainly
farnesoid
X
receptor
(FXR)
agonists,
PPAR
thyroid
hormone
agonists),
anti-fibrotic
anti-inflammatory
agents.
intrinsically
complex
pathophysiological
history
MASLD
makes
selection
single
effective
treatment
major
challenge,
so
far.
this
evolving
scenario,
cooperation
between
different
stakeholders
(including
subjects
risk,
health
professionals,
pharmaceutical
industries)
could
significantly
improve
management
disease
implementation
primary
secondary
prevention
measures.
high
healthcare
search
new,
effective,
safe
pressing
need,
together
accurate
characterization
phenotypes.
Recent
promising
advances
indicate
that
we
may
soon
enter
era
precise
personalized
therapy
MASLD/MASH.
Gut,
Journal Year:
2024,
Volume and Issue:
73(11), P. 1883 - 1892
Published: Aug. 1, 2024
Background
Statins
have
multiple
benefits
in
patients
with
metabolic-associated
steatotic
liver
disease
(MASLD).
Aim
To
explore
the
effects
of
statins
on
long-term
risk
all-cause
mortality,
liver-related
clinical
events
(LREs)
and
stiffness
progression
MASLD.
Methods
This
cohort
study
collected
data
MASLD
undergoing
at
least
two
vibration-controlled
transient
elastography
examinations
16
tertiary
referral
centres.
Cox
regression
analysis
was
performed
to
examine
association
between
statin
usage
mortality
LREs
stratified
by
compensated
advanced
chronic
(cACLD):
baseline
measurement
(LSM)
≥10
kPa.
Liver
defined
as
an
LSM
increase
≥20%
for
cACLD
from
<10
kPa
or
non-cACLD.
reduction
decrease
cACLD.
Results
We
followed
up
7988
5.9
(IQR
4.6–8.2)
a
median
4.6
years.
At
baseline,
40.5%
used
statins,
present
17%.
Statin
significantly
associated
lower
(adjusted
HR=0.233;
95%
CI
0.127
0.426)
HR=0.380;
0.268
0.539).
also
rates
(HR=0.542;
0.389
0.755)
non-cACLD
HR=0.450;
0.342
0.592),
but
not
HR=0.914;
0.778
1.074).
Conclusions
relatively
Cardiovascular Diabetology,
Journal Year:
2024,
Volume and Issue:
23(1)
Published: June 1, 2024
Abstract
Backgrounds
Insulin
resistance
(IR)
plays
a
vital
role
in
the
pathogenesis
of
metabolic
dysfunction-associated
steatotic
liver
disease
(MASLD).
However,
it
remains
unclear
whether
triglyceride–glucose
(TyG)
related
parameters,
which
serve
as
useful
biomarkers
to
assess
IR,
have
prognostic
effects
on
mortality
outcomes
MASLD.
Methods
Participants
National
Health
and
Nutrition
Examination
Survey
(NHANES)
database
from
1999
2018
years
were
included.
TyG
its
parameters
[TyG-waist
circumference
(TyG-WC)
TyG-waist
height
ratio
(TyG-WHtR)]
calculated.
Kaplan–Meier
curves,
Cox
regression
analysis,
restricted
cubic
splines
(RCS)
conducted
evaluate
association
between
TyG-related
indices
with
all-cause
cardiovascular
adults
The
concordance
index
(C-index)
was
used
prediction
accuracy
indices.
Results
A
total
8208
(4209
men
3999
women,
median
age
49.00
years)
MASLD
included
this
study.
Multivariate-adjusted
analysis
revealed
that
high
quartile
levels
significantly
associated
participants
[
adjusted
hazard
(aHR)
=
1.25,
95%
confidence
interval
(CI)
1.05–1.50,
P
0.014;
TyG-WC
aHR
for
1.28,
CI
1.07–1.52,
0.006;
TyG-WHtR
1.50,
1.25–1.80,
<
0.001;
1.81,
1.28–2.55,
2.22,
1.55–3.17,
0.001].
C-index
predicting
0.563
index,
0.579
0.585
respectively.
Regarding
mortality,
0.561
0.607
0.615
Nonlinear
trends
observed
(
0.001
0.012,
respectively).
non-linear
relationship
0.025).
Subgroup
suggested
aged
65
old
those
without
comorbidities
more
sensitive
Conclusion
Findings
study
highlight
predictive
value
indices,
especially
would
be
surrogate
clinical
management