Compared
to
the
history
of
NAFLD
briefly
summarized
above,
notions
that
and
NAFLD-related
metabolic
conditions
could
also
be
a
risk
factor
for
development
primary
liver
cancer
(PLC)
in
limited
proportion
individuals
are
more
recent
(Table
1)
[8-13].While
it
is
logical
somewhat
foreseeable
PLC
may
eventually
develop
some
with
NAFLD,
observations
substantiate
probably
unexpected
theory
that,
further
PLCs,
Journal of Hepatology,
Journal Year:
2023,
Volume and Issue:
79(6), P. 1524 - 1541
Published: Sept. 18, 2023
While
the
links
between
metabolic
dysfunction
associated
steatotic
liver
disease
(MASLD)
and
obesity,
insulin
resistance
are
widely
appreciated,
there
a
host
of
complex
interactions
other
endocrine
axes.
it
can
be
difficult
to
definitively
distinguish
direct
causal
relationships
those
attributable
increased
adipocyte
mass,
is
substantial
evidence
indirect
specific
dysregulation
severity
MASLD.
Strong
effects
exists
for
low
levels
growth
hormone,
sex
hormones,
thyroid
hormone
with
development
disease.
The
impact
steroid
e.g.
cortisol
dehydropepiandrosterone,
adipokines
much
more
divergent.
Thoughtful
assessment,
based
on
individual
risk
factors
findings,
also
management
non-insulin
axes
should
performed
in
evaluation
Multiple
therapeutic
pharmaceutical
targets
have
emerged
that
leverage
various
reduce
fibroinflammatory
cascade
steatohepatitis
(MASH).
Internal and Emergency Medicine,
Journal Year:
2023,
Volume and Issue:
18(4), P. 993 - 1006
Published: Feb. 17, 2023
Abstract
The
term
non-alcoholic
fatty
liver
disease
(NAFLD)
has
rapidly
become
the
most
common
type
of
chronic
disease.
NAFLD
points
to
excessive
hepatic
fat
storage
and
no
evidence
secondary
accumulation
in
patients
with
“no
or
little
alcohol
consumption”.
Both
etiology
pathogenesis
are
largely
unknown,
a
definitive
therapy
is
lacking.
Since
very
often
closely
associated
metabolic
dysfunctions,
consensus
process
ongoing
shift
acronym
MAFLD,
i.e.,
metabolic-associated
change
terminology
likely
improve
classification
affected
individuals,
awareness,
comprehension
pathophysiological
aspects
involved,
choice
more
personalized
therapeutic
approaches
while
avoiding
intrinsic
stigmatization
due
“non-alcoholic”.
Even
recently,
other
sub-classifications
have
been
proposed
concentrate
heterogeneous
causes
under
one
umbrella.
While
awaiting
additional
validation
studies
this
field,
we
discuss
main
reasons
underlying
important
paradigm.
Metabolites,
Journal Year:
2024,
Volume and Issue:
14(1), P. 40 - 40
Published: Jan. 8, 2024
This
narrative
review
aims
to
illustrate
the
notion
that
nonalcoholic
steatohepatitis
(NASH),
recently
renamed
metabolic
dysfunction-associated
(MASH),
is
a
systemic
disorder
featuring
both
adverse
hepatic
and
extrahepatic
outcomes.
In
recent
years,
several
NASH
trials
have
failed
identify
effective
pharmacological
treatments
and,
therefore,
lifestyle
changes
are
cornerstone
of
therapy
for
NASH.
with
this
context,
we
analyze
epidemiological
burden
possible
pathogenetic
factors
involved.
These
include
genetic
factors,
insulin
resistance,
lipotoxicity,
immuno-thrombosis,
oxidative
stress,
reprogramming
metabolism,
hypoxia,
all
which
eventually
culminate
in
low-grade
chronic
inflammation
increased
risk
fibrosis
progression.
The
explanations
underlying
failure
also
accurately
examined.
We
conclude
high
heterogeneity
NASH,
resulting
from
variable
backgrounds,
exposure,
responses
different
stresses,
susceptibility
hepatocyte
differences
repair-response,
calls
personalized
medicine
approaches
involving
research
on
noninvasive
biomarkers.
Future
should
aim
at
achieving
complete
assessment
determinants,
modifiers,
correlates
thus
adopting
more
holistic
unbiased
approach,
notably
including
cardiovascular–kidney–metabolic
outcomes,
without
restricting
therapeutic
perspectives
histological
surrogates
liver-related
outcomes
alone.
Liver International,
Journal Year:
2024,
Volume and Issue:
44(7), P. 1513 - 1525
Published: April 3, 2024
Abstract
Background
Recent
observational
studies
examining
the
association
between
Helicobacter
pylori
infection
and
risk
of
metabolic
dysfunction‐associated
steatotic
liver
disease
(MASLD)
have
reported
conflicting
results.
We
performed
a
meta‐analysis
to
quantify
magnitude
H.
MASLD.
Methods
systematically
searched
three
large
electronic
databases
identify
eligible
(published
up
30
November
2023)
in
which
biopsy,
imaging
methods
or
blood‐based
biomarkers/scores
were
used
for
diagnosing
Data
from
selected
extracted,
was
using
common
random‐effects
modelling.
Statistical
heterogeneity
among
published
studies,
subgroup
analyses,
meta‐regression
analyses
publication
bias
assessed.
Results
A
total
28
(24
cross‐sectional
4
longitudinal
studies)
identified,
including
231
291
middle‐aged
individuals
predominantly
Asian
ethnicity
(~95%).
Meta‐analysis
showed
that
significantly
associated
with
small
increase
prevalent
MASLD
(
n
=
24
studies;
odds
ratio
1.11,
95%
CI
1.05–1.18;
I
2
63%).
data
an
increased
developing
incident
over
mean
5‐year
follow‐up
1.20,
95%CI
1.08–1.33;
44%).
Sensitivity
did
not
modify
these
The
funnel
plot
reveal
any
significant
bias.
Conclusions
is
mildly
Further
well‐designed
prospective
mechanistic
are
required
better
decipher
complex
link
Metabolism and Target Organ Damage,
Journal Year:
2024,
Volume and Issue:
4(2)
Published: April 7, 2024
Chronic
kidney
disease
(CKD)
and
nonalcoholic
fatty
liver
(NAFLD),
metabolic
dysfunction-associated
(MAFLD)
steatotic
(MASLD)
account
for
substantial
financial
burden
worldwide.
These
alarming
features
call
enhanced
efforts
to
prevent
manage
the
development
progression
of
CKD.
Accumulating
evidence
supporting
a
causal
role
NAFLD/MAFLD/MASLD-in
CKD
opens
new
horizons
achieve
this
aim.
Recent
epidemiological
studies
meta-analyses
exploring
association
NAFLD/MAFLD/MASLD
with
characteristics
associated
odds
incident
are
discussed.
The
involved
pathomechanisms,
including
common
soil
hypothesis,
genetics,
gut
dysbiosis,
portal
hypertension,
examined
in
detail.
Finally,
lifestyle
changes
(diet
physical
exercise),
direct
manipulation
microbiota,
drug
approaches
involving
statins,
renin-angiotensin-aldosterone
system
inhibitors,
GLP-1
Receptor
Agonists,
Sodium-glucose
cotransporter-2,
pemafibrate,
vonafexor
within
context
prevention
management
among
those
NAFLD/MAFLD/MASLD.
evolving
nomenclature
may
generate
confusion
practicing
clinicians
investigators.
However,
comparative
investigating
pros
contra
different
nomenclatures
identify
most
useful
definitions
strategies
identify,
prevent,
halt
onset
Liver International,
Journal Year:
2024,
Volume and Issue:
44(3), P. 848 - 864
Published: Jan. 23, 2024
Abstract
Background
and
Aims
Thyroid
axis
is
currently
under
investigation
as
a
therapeutic
target
in
metabolic
dysfunction‐associated
steatotic
liver
disease
(MASLD).
function
was
examined
herein
the
full
spectrum
of
disease.
Methods
Subjects
were
recruited
had
biopsies
two
Gastroenterology‐Hepatology
Clinics
(Greece
Australia)
one
Bariatric‐Metabolic
Surgery
Clinic
(Italy).
The
main
working
sample
n
=
677
subjects
with
MASLD
after
excluding
abnormal
free
thyroxine
levels.
Participants
classified
according
to
thyroid‐stimulating
hormone
(TSH)
standard
criteria:
Subclinical
hyperthyroidism
(<0.4
uIU/mL);
Euthyroidism
relatively
low
(0.4
<2.5
euthyroidism
high
(2.5–4.0
subclinical
hypothyroidism
(>4
uIU/mL).
Results
TSH
continuous
variable
positively
associated
significant
fibrosis
(
F
≥
2),
steatohepatitis
(MASH)
at‐risk
MASH.
2
(odds
ratio
[OR]
3.47,
95%
confident
interval
[CI]
[1.50,
8.05],
p
.02),
MASH
(OR
3.44,
CI
[1.48,
7.98]
.001)
3.88,
[1.76,
8.55],
.001),
before
controlling
for
adiposity,
central
obesity,
insulin
resistance.
When
leptin,
adiponectin,
or
growth
differentiation
factor‐15
moderators,
significance
lost.
Sex‐specific
analysis
revealed
strong
association
between
presence
among
women,
eliminated
only
when
adipokines/mitokines
adjusted
for.
Restricted
cubic
spline
associations
outcomes
‐values
<
.01)
inflection
points
being
2.49,
2.67
6.96.
Conclusions
These
observations
provide
support
studies
on
administration
thyroid
therapeutics
liver‐specific
receptor
agonists
across
continuum.
Liver International,
Journal Year:
2024,
Volume and Issue:
44(5), P. 1129 - 1141
Published: March 1, 2024
Abstract
Background
Metabolic
dysfunction‐associated
fatty
liver
disease
(MAFLD)
is
an
emerging
risk
factor
for
chronic
kidney
(CKD).
N‐terminal
propeptide
of
collagen
type
3
(PRO‐C3)
a
biomarker
advanced
fibrosis
in
MAFLD
and
PRO‐C3
may
be
involved
renal
fibrosis.
We
aimed
to
use
measurements
generate
new
algorithmic
score
test
the
prediction
with
(MAFLD–CKD).
Methods
A
derivation
independent
validation
cohort
750
129
Asian
patients
biopsy‐confirmed
were
included.
Serum
concentration
was
measured
regression
analyses
performed
examine
associations
MAFLD–CKD.
derivative
algorithm
MAFLD–CKD
evaluated
receiver
operator
characteristic
(ROC)
curve
analysis.
Results
The
study
included
two
cohorts
(
n
=
180
MAFLD–CKD;
mean‐eGFR:
94.93
mL/min/1.73
m
2
;
median‐urinary
albumin‐to‐creatinine
ratio:
6.58
mg/mmol).
associated
severity
MAFLD‐CKD
independently
(adjusted
odds
ratio
1.16,
95%
confidence
interval
[CI]:
1.08–1.23,
p
<
.001).
non‐invasive
(termed
PERIOD)
including
efficiently
predicted
(AUROC
.842,
CI:
.805–.875).
Accuracy,
specificity
negative
predictive
values
80.2%,
85.1%
88.4%,
respectively.
In
cohort,
PERIOD
had
good
diagnostic
performance
.807,
.691–.893)
similar
results
all
patient
subgroups.
subgroup,
accuracy
identifying
further
improved
by
combining
PRO‐C3‐based
ADAPT
Agile
3+
scores
.90,
.836–.964).
Conclusions
helpful
accurately
predicting
can
also
used
assess
people
Metabolism and Target Organ Damage,
Journal Year:
2024,
Volume and Issue:
4(3)
Published: June 26, 2024
Metabolic
dysfunction-associated
steatotic
liver
disease
(MASLD)
stands
as
an
independent
risk
factor
for
cardiovascular
(CVD),
which
is
the
leading
cause
of
mortality
among
MASLD
patients.
The
diverse
spectrum
cardio-nephro-metabolic
and
vascular
manifestations
inherent
in
highlights
complex
profile
CVD
associated
with
this
condition.
However,
current
approaches
to
assessing
lack
specificity,
predominantly
relying
on
traditional
markers.
Although
it
widely
accepted
that
patients
advanced
fibrosis
are
more
prone
risk,
recent
evidence
suggests
isolated
focus
may
overlook
remarkable
phenotypic
variability
across
entire
population.
Emerging
data
indicate
a
progressive
escalation
parallel
severity
MASLD,
highlighting
need
precise
staging
inform
accurate
assessment.
To
address
challenge,
we
propose
novel
sequential
approach
assessment
MASLD.
While
factors
remain
essential,
incorporating
liver-specific
parameters
enhances
stratification
guides
targeted
interventions
mitigate
substantial
burden
vulnerable
This
involves
initial
screening
using
FIB-4
NAFLD
score,
followed
by
imaging-based
non-invasive
techniques
individuals
at
intermediate-high
fat
quantification
low-risk
individuals.
Future
prospective
investigations
should
simultaneous
use
biomarkers
imaging
modalities
evaluate,
sex-specific
manner,
efficacy
proposed
determine
optimal
thresholds
steatosis