Digestive Diseases and Sciences,
Год журнала:
2023,
Номер
68(11), С. 4212 - 4220
Опубликована: Сен. 8, 2023
The
rs641738
C
>
T
single-nucleotide
polymorphism
of
MBOAT7
has
been
associated
with
hepatocellular
carcinoma
(HCC)
and
nonalcoholic
fatty
liver
disease
(NAFLD).
Latin
Americans
have
high
rates
HCC
NAFLD,
but
no
assessment
between
performed
in
this
population.
We
provide
the
first
impact
on
risk
Americans.
Patients
were
prospectively
recruited
into
ESCALON
network,
designed
to
collect
samples
from
American
patients
6
South
countries
(Argentina,
Ecuador,
Brazil,
Chile,
Peru,
Colombia).
A
European
cohort
general
Hispanic
population
gnomAD
database
included
for
comparison.
Associations
evaluated
using
logistic
regression.
In
total,
310
cases
493
cirrhosis
without
assessed.
TT
genotype
was
not
predictive
(TT
vs
CC
OR
adjusted
=
1.15,
95%
CI
0.66–2.01,
p
0.610)
or
Europeans
1.20,
0.59–2.43,
0.621).
No
significant
association
noted
subgroup
analysis
viral
hepatitis,
alcohol-related
disease.
increased
NAFLD-cirrhosis
compared
a
non-cirrhotic
NAFLD
+
CT
2.75,
1.10–6.87,
0.031).
rs631738
allele
Europeans.
An
increase
NAFLD.
Annals of Hepatology,
Год журнала:
2022,
Номер
28(1), С. 100874 - 100874
Опубликована: Ноя. 10, 2022
Obesity
is
a
risk
factor
for
developing
nonalcoholic
fatty
liver
disease
(NAFLD),
and
the
associated
molecular
mechanisms
could
be
targeted
with
nutrient-based
strategies.
Therefore,
it
necessary
to
review
current
propose
further
treatments.
facilitates
onset
of
insulin
resistance,
lipidic
abnormalities,
hepatic
fat
accumulation,
lipid
peroxidation,
mitochondrial
dysfunction,
excessive
reactive
oxygen
species
(ROS)
production,
inflammation,
all
related
steatosis
progression
fibrosis.
Microbiota
alterations
can
also
influence
by
translocation
pathogenic
bacteria,
energy
extraction
from
short
chain
acids
(SCFAs),
intestinal
suppression
expression
fasting-induced
adipose
(FIAF),
reduction
bile
acids,
altered
choline
metabolism.
There
are
genetic
polymorphisms
in
metabolic
proteins
that
predispose
higher
diseases,
such
as
those
found
patatin-like
phospholipase
domain-containing
3
(PNPLA3),
transmembrane
6
superfamily
member
2
(TM6SF2),
membrane-bound
O-acyltransferase
7
(MBOAT7)
or
known
lysophosphatidylinositol
acyltransferase
1
(LPIAT1),
channel-like
4
genes
(TMC4),
mass
obesity-associated
protein
(FTO),
b
Klotho
(KLB)
carboxylesterase
(CES1).
No
clear
dietary
guidelines
target
NAFLD
development
progression.
However,
carbohydrate
intake
restriction,
regular
physical
exercise,
supplementation
antioxidants,
restoration
gut
microbiota
seem
have
beneficial
effects
on
new
proposed
features
NAFLD.
BMJ Open,
Год журнала:
2022,
Номер
12(11), С. e067203 - e067203
Опубликована: Ноя. 1, 2022
Objectives
Non-alcoholic
fatty
liver
disease
(NAFLD)
is
a
non-communicable
with
rising
prevalence
worldwide
and
large
burden
for
patients
health
systems.
To
date,
the
presence
of
unique
phenotypes
in
NAFLD
has
not
been
studied,
their
identification
could
inform
precision
medicine
public
pragmatic
implications
personalised
management
care
NAFLD.
Design
Cross-sectional
prospective
(up
to
31
December
2019)
analysis
National
Health
Nutrition
Examination
Survey
III
(1988–1994).
Primary
secondary
outcomes
measures
diagnosis
was
based
on
ultrasound.
The
following
predictors
informed
an
unsupervised
machine
learning
algorithm
(k-means):
body
mass
index,
waist
circumference,
systolic
blood
pressure
(SBP),
plasma
glucose,
total
cholesterol,
triglycerides,
enzymes
alanine
aminotransferase,
aspartate
aminotransferase
gamma
glutamyl
transferase.
We
summarised
(means)
compared
across
clusters.
used
Cox
proportional
hazard
models
quantify
all-cause
mortality
risk
associated
each
cluster.
Results
1652
(mean
age
47.2
years
51.5%
women)
were
grouped
into
3
clusters:
anthro-SBP-glucose
(6.36%;
highest
levels
anthropometrics,
SBP
glucose),
lipid-liver
(10.35%;
lipid
enzymes)
average
(83.29%;
at
levels).
Compared
phenotype,
phenotype
had
higher
(aHR=2.88;
95%
CI:
2.26
3.67);
(aHR=1.11;
0.86
1.42).
Conclusions
There
heterogeneity
NAFLD,
whom
can
be
divided
three
different
risk.
These
guide
specific
interventions
plans,
thus
advancing
Introduction
Fructose
intake
of
over
70
g/day
is
known
to
cause
dyslipidemias,
involving
multiple
metabolic
pathways
that
can
promote
an
excess
hepatic
lipid
synthesis
as
dysfunction-associated
fatty
liver
disease
(MAFLD),
formerly
non-alcoholic
disease.
Digestive Diseases and Sciences,
Год журнала:
2023,
Номер
68(11), С. 4212 - 4220
Опубликована: Сен. 8, 2023
The
rs641738
C
>
T
single-nucleotide
polymorphism
of
MBOAT7
has
been
associated
with
hepatocellular
carcinoma
(HCC)
and
nonalcoholic
fatty
liver
disease
(NAFLD).
Latin
Americans
have
high
rates
HCC
NAFLD,
but
no
assessment
between
performed
in
this
population.
We
provide
the
first
impact
on
risk
Americans.
Patients
were
prospectively
recruited
into
ESCALON
network,
designed
to
collect
samples
from
American
patients
6
South
countries
(Argentina,
Ecuador,
Brazil,
Chile,
Peru,
Colombia).
A
European
cohort
general
Hispanic
population
gnomAD
database
included
for
comparison.
Associations
evaluated
using
logistic
regression.
In
total,
310
cases
493
cirrhosis
without
assessed.
TT
genotype
was
not
predictive
(TT
vs
CC
OR
adjusted
=
1.15,
95%
CI
0.66–2.01,
p
0.610)
or
Europeans
1.20,
0.59–2.43,
0.621).
No
significant
association
noted
subgroup
analysis
viral
hepatitis,
alcohol-related
disease.
increased
NAFLD-cirrhosis
compared
a
non-cirrhotic
NAFLD
+
CT
2.75,
1.10–6.87,
0.031).
rs631738
allele
Europeans.
An
increase
NAFLD.