Biomedicines,
Journal Year:
2024,
Volume and Issue:
12(7), P. 1467 - 1467
Published: July 2, 2024
Cytochrome
P450
(CYP450)
is
a
group
of
enzymes
that
play
an
essential
role
in
Phase
I
metabolism,
with
57
functional
genes
classified
into
18
families
the
human
genome,
which
CYP1,
CYP2,
and
CYP3
are
prominent.
Beyond
drug
CYP
metabolize
endogenous
compounds
such
as
lipids,
proteins,
hormones
to
maintain
physiological
homeostasis.
Thus,
dysregulation
CYP450
can
lead
different
endocrine
disorders.
Moreover,
significantly
contribute
fatty
acid
cholesterol
synthesis,
bile
biosynthesis,
impacting
cellular
physiology
disease
pathogenesis.
Their
diverse
functions
emphasize
their
therapeutic
potential
managing
hypercholesterolemia
neurodegenerative
diseases.
Additionally,
implicated
onset
development
illnesses
cancer,
influencing
chemotherapy
outcomes.
Assessment
enzyme
expression
activity
aids
evaluating
liver
health
state
differentiating
between
diseases,
guiding
decisions,
optimizing
efficacy.
Understanding
roles
clinical
effect
genetic
polymorphisms
crucial
for
developing
personalized
strategies
enhancing
responses
patient
populations.
Nature Communications,
Journal Year:
2023,
Volume and Issue:
14(1)
Published: Nov. 29, 2023
Abstract
Deep
learning
transformer-based
models
using
longitudinal
electronic
health
records
(EHRs)
have
shown
a
great
success
in
prediction
of
clinical
diseases
or
outcomes.
Pretraining
on
large
dataset
can
help
such
map
the
input
space
better
and
boost
their
performance
relevant
tasks
through
finetuning
with
limited
data.
In
this
study,
we
present
TransformEHR,
generative
encoder-decoder
model
transformer
that
is
pretrained
new
pretraining
objective—predicting
all
outcomes
patient
at
future
visit
from
previous
visits.
TransformEHR’s
framework,
paired
novel
objective,
helps
it
achieve
state-of-the-art
multiple
tasks.
Comparing
model,
TransformEHR
improves
area
under
precision–recall
curve
by
2%
(
p
<
0.001)
for
pancreatic
cancer
onset
24%
=
0.007)
intentional
self-harm
patients
post-traumatic
stress
disorder.
The
high
predicting
shows
potential
building
effective
intervention
systems.
also
generalizable
be
easily
finetuned
European Journal of Gastroenterology & Hepatology,
Journal Year:
2024,
Volume and Issue:
36(4), P. 371 - 381
Published: Feb. 23, 2024
Metabolic
dysfunction-associated
steatotic
liver
disease
(MASLD)
is
a
prevalent
metabolic
disorder
characterized
by
excessive
hepatic
fat
accumulation.
Intermittent
fasting
(IF)
has
emerged
as
potential
therapeutic
strategy
with
the
ability
to
induce
weight
loss,
improve
insulin
sensitivity
and
reduce
steatosis.
We
aim
compare
efficacy
of
different
IF
regimens
for
MASLD
management.
A
systematic
review
network
meta-analysis
randomized
controlled
trials
investigating
MASLD.
PubMed
,
EMBASE
WOS
SCOPUS
Cochrane
Central
Register
Controlled
Trials
were
searched
until
10
April
2023.
Analysis
was
performed
using
R
software
meta
netmeta
packages.
Mean
difference
(MD)
used
pool
continuous
outcomes
95%
confidence
intervals
(CIs).
Our
registered
in
PROSPERO
(CRD42023418467).
included
eight
total
635
participants.
The
5
:
2
diet
significantly
improved
stiffness
(MD,
-0.32;
CI,
-0.55
-0.09;
P
<
0.01).
Time-restricted
feeding
steatosis
(controlled
attenuation
parameter
score)
-39.83;
-64.78
-14.87;
No
significant
changes
observed
asparate
aminotransferase,
gamma-glutamyl
transpeptidase,
low-density
lipoproteins
cholesterol,
triglyceride
levels,
basal
index,
blood
pressure,
Homeostatic
Model
Assessment
Insulin
Resistance,
sugar,
lean
body
mass
or
waist
circumference
across
all
regimens.
However,
alternate-day
showed
positive
results
anthropometric
measures,
including
improvements
mass,
circumference,
reduction
(
0.05).
various
effects
on
clinical
patients;
however,
these
not
consistent.
Therefore,
patient-tailored
regimen
should
be
considered.
Liver International,
Journal Year:
2025,
Volume and Issue:
45(3)
Published: Feb. 10, 2025
ABSTRACT
Objective
Drug‐induced
liver
injury
(DILI)
is
a
global
problem
and
can
develop
from
exposure
to
prescription
or
over‐the‐counter
medications
as
well
herbal
dietary
supplements.
The
diagnosis
of
DILI
clinically
challenging,
be
severe
leading
failure,
death,
transplantation.
Patients
with
underlying
chronic
diseases
(CLD)
may
at
increased
risk
for
DILI,
which
associated
factors
related
drug
disease.
Methods
This
review
summarises
current
knowledge
on
the
outcomes
in
patients
CLD.
Results
CLD
an
DILI.
Additionally
are
more
worse
after
Discussion
poor
accentuated
potentially
worst‐case
scenario
acute‐on‐chronic
failure.
We
highlight
key
observations
broad
range
high‐DILI
agents
implicated
those
populations.
Frontiers in Bioscience-Landmark,
Journal Year:
2025,
Volume and Issue:
30(3)
Published: March 17, 2025
To
date,
an
increasing
body
of
evidence
supports
the
potential
role
activated
platelets
in
pathogenesis
non-alcoholic
fatty
liver
disease
(NAFLD).
This
is
likely
due
to
their
ability
secrete
biologically
active
substances
that
regulate
regeneration
processes,
ensure
hemostasis,
and
participate
immune
response.
Additionally,
several
studies
have
demonstrated
efficacy
antiplatelet
agents
reducing
inflammation,
severity
fibrosis,
progression
fibrosis
steatohepatitis
(NASH).
Since
NAFLD
not
independent
indication
for
therapy,
primary
regarding
has
been
derived
from
using
animal
models
or
patients
with
concomitant
cardiovascular
diseases.
narrative
review
will
discuss
main
functions
platelets,
unique
interactions
cells,
outcomes
these
interactions,
as
well
results
evaluating
safety
therapy
NAFLD.
iScience,
Journal Year:
2024,
Volume and Issue:
27(3), P. 109301 - 109301
Published: Feb. 20, 2024
Persistent
liver
injury
triggers
a
fibrogenic
program
that
causes
pathologic
remodeling
of
the
hepatic
microenvironment
(i.e.,
fibrosis)
and
portal
hypertension.
The
dynamics
gene
regulation
during
disease
progression
early
regression
remain
understudied.
Here,
we
generated
transcriptome
profiles
in
two
well-established
models
at
peak
fibrosis
spontaneous
after
removal
inducing
agents.
We
linked
key
readouts,
such
as
pressure,
collagen
area,
transaminase
levels,
to
differentially
expressed
genes,
enabling
identification
transcriptomic
signatures
progressive
vs.
regressive
These
candidate
biomarkers
(e.g.,
Communications Biology,
Journal Year:
2023,
Volume and Issue:
6(1)
Published: June 24, 2023
Non-alcoholic
liver
disease
(NAFLD)
is
a
condition
caused
by
excessive
fat
accumulation
in
the
and
developed
via
multiple
pathways.
miR-27b
has
been
suggested
to
play
crucial
roles
development
of
NAFLD,
assuming
targeting
genes
involved
lipid
catabolism
anabolism.
However,
other
pathways
regulated
are
largely
unknown.
Here
we
show
that
was
induced
miR-27b-transfected
human
mouse
hepatic
cells
knockdowns
three
miR-27b-target
genes,
β-1,4-galactosyltransferase
3
(B4GALT3),
matrix
AAA
peptidase
interacting
protein
1
(MAIP1)
PH
domain
leucine
rich
repeat
phosphatase
2
(PHLPP2),
accumulation.
We
also
B4GALT3
MAIP1
were
direct
targets
overexpression
ameliorated
miR-27b-induced
In
addition,
Maip1
expression
declined
mice
fed
high-fat
diet,
suggesting
involvement
decreased
fatty
liver.
Overall,
identified
MAIP1/miR-27b
axis
as
mediator
accumulation,
potential
therapeutic
target
for
NAFLD.