Journal of Medical Virology,
Journal Year:
2023,
Volume and Issue:
95(11)
Published: Nov. 1, 2023
Please
note:
The
publisher
is
not
responsible
for
the
content
or
functionality
of
any
supporting
information
supplied
by
authors.
Any
queries
(other
than
missing
content)
should
be
directed
to
corresponding
author
article.
Viruses,
Journal Year:
2024,
Volume and Issue:
16(1), P. 112 - 112
Published: Jan. 12, 2024
This
study
investigates
the
intricate
interplay
between
Metabolic-associated
Fatty
Liver
Disease
(MAFLD)
and
COVID-19,
exploring
impact
of
MAFLD
on
disease
severity,
outcomes,
efficacy
antiviral
agent
Paxlovid
(nirmatrelvir/ritonavir).
MAFLD,
affecting
a
quarter
global
population,
emerges
as
potential
risk
factor
for
severe
yet
underlying
pathophysiological
mechanisms
remain
elusive.
focuses
clinical
significance
Paxlovid,
first
orally
bioavailable
granted
Emergency
Use
Authorization
in
United
States.
Notably,
outcomes
from
phase
II/III
trials
exhibit
an
88%
relative
reduction
COVID-19-associated
hospitalization
or
mortality
among
high-risk
patients.
Despite
conflicting
data
association
COVID-19
this
research
strives
to
bridge
gap
by
evaluating
effectiveness
patients
with
addressing
scarcity
relevant
studies.
Frontiers in Genetics,
Journal Year:
2024,
Volume and Issue:
15
Published: Sept. 4, 2024
This
study
investigated
the
influence
of
single
nucleotide
polymorphisms
(SNPs)
in
genes
associated
with
interferon
pathway
(IFNAR2
rs2236757),
antiviral
response
(OAS1
rs10774671,
OAS3
rs10735079),
and
viral
entry
(ACE2
rs2074192)
on
COVID-19
severity
their
association
nonalcoholic
fatty
liver
disease
(MAFLD).
We
did
not
observe
a
significant
between
SNPs
severity.
While
IFNAR2
rs2236757
A
allele
was
correlated
higher
creatinine
levels
upon
admission
G
lower
band
neutrophils
discharge,
these
findings
require
further
investigation.
The
distribution
OAS
gene
(rs10774671
rs10735079)
differ
MAFLD
patients
non-MAFLD
patients.
Our
population's
ACE2
rs2074192
genotypes
alleles
differed
from
that
European
reference
population.
Overall,
our
suggest
specific
may
be
major
contributors
to
patient
population,
highlighting
potential
role
other
genetic
factors
environmental
influences.
Viruses,
Journal Year:
2024,
Volume and Issue:
16(6), P. 985 - 985
Published: June 19, 2024
Metabolic-associated
fatty
liver
disease
(MAFLD)
is
a
risk
factor
for
severe
COVID-19.
This
study
explores
the
potential
influence
of
gut
hormone
receptor
and
immune
response
gene
expression
on
COVID-19
outcomes
in
MAFLD
patients.
Infection,
Journal Year:
2025,
Volume and Issue:
unknown
Published: April 10, 2025
Abstract
Purpose
Steatotic
liver
diseases
(SLD)
have
become
more
prevalent
over
the
last
decade
and
are
associated
not
only
with
cardiometabolic
but
also
psychological
symptoms
(depression,
fatigue).
These
common
in
post-COVID
syndrome
(PCS).
Therefore,
aim
of
study
was
to
analyze
burden
SLD
PCS
patients.
Methods
We
systematically
screened
all
patients
from
our
outpatient
clinic
using
transient
elastography,
structured
questionnaires
for
neurocognitive
evaluation
blood
sample
analysis.
Controls
without
known
were
recruited
assessed
same
approach.
Results
560
103
healthy
controls
included.
The
overall
prevalence
high
both
cohorts
(57
vs.
53%).
frequently
male
(41
24%),
older
(52
44
years)
had
(87.0
46.4%).
Cognitive
impairment
related
than
no-SLD
group
(OR:
1.68,
CI:
1.14–2.46,
p
=
0.008).
presence
severe
COVID-19
hospitalization
2.91,
1.85–4.56,
<
0.001).
Within
1
year
follow-up,
152
289
described
a
resolution
irrespective
or
absence
(log-rank
0.96).
Conclusions
is
cognitive
dysfunction
PCS.
Longitudinal
studies
needed
assess
role
hepatic
steatosis,
development
post-acute
infection
regulation
(e.g.,
SARS-CoV-2)
differentiate
between
SLD-associated
Viruses,
Journal Year:
2023,
Volume and Issue:
15(10), P. 2093 - 2093
Published: Oct. 14, 2023
Coronavirus
disease
(COVID-19)
and
its
outcomes
remain
one
of
the
most
challenging
problems
today.
COVID-19
in
children
could
be
asymptomatic,
but
can
result
a
fatal
outcome;
therefore,
predictions
severity
are
important.
The
goal
was
to
investigate
human
genetic
factors
that
associated
with
children.
Single-nucleotide
polymorphisms
following
genes
were
studied:
ACE2
(rs2074192),
IFNAR2
(rs2236757),
TYK2
(rs2304256),
OAS1
(rs10774671),
OAS3
(rs10735079),
CD40
(rs4813003),
FCGR2A
(rs1801274)
CASP3
(rs113420705).
In
case-control
study
30
mild
or
moderate
course
disease;
severe
symptoms
multisystem
inflammatory
syndrome
(MIS-C)
15
who
healthy,
did
not
have
SARS-CoV-2
(PCR
negative,
Ig
G
negative).
revealed
rs2074192
(allele
T),
rs2236757
A),
rs10774671
rs4813003
C),
rs113420705
C)
male
sex
contribute
MIS-C
85.6%
cases.
World
Health
Organization
reported
new
variants
may
cause
previously
unseen
Although
has
limitations
due
cohort
size,
findings
help
provide
better
understanding
infection
proactive
pediatric
patient
management.
Metabolic-associated
fatty
liver
disease
(MAFLD)
is
a
risk
factor
for
severe
COVID-19.
This
study
explores
the
potential
influence
of
gut
hormone
receptor
and
immune
response
gene
expression
on
COVID-19
outcomes
in
MAFLD
patients.
Methods:
We
investigated
levels
AHR,
FFAR2,
FXR,
TGR5
patients
with
compared
to
controls.
examined
associations
between
clinical
outcomes.
Results:
displayed
altered
AHR
expression,
potentially
impacting
recovery.
Downregulated
correlated
increased
coagulation
parameters.
Elevated
FFAR2
linked
specific
cell
populations
hospital
stay
duration.
Significantly
lower
FXR
was
observed
both
Conclusion:
Our
findings
suggest
modulatory
roles
MAFLD.
Frontiers in Microbiology,
Journal Year:
2025,
Volume and Issue:
16
Published: April 25, 2025
Metabolic
dysfunction-associated
fatty
liver
disease
(MAFLD)
is
a
complex
metabolic
disorder
characterized
by
hepatic
lipid
accumulation
and
subsequent
inflammation.
This
condition
closely
linked
to
syndrome
obesity,
with
its
prevalence
rising
due
sedentary
lifestyles
high-calorie
diets.
The
pathogenesis
of
MAFLD
involves
multiple
factors,
including
insulin
resistance,
lipotoxicity,
oxidative
stress,
inflammatory
responses.
gut
microbiota
plays
crucial
role
in
development,
dysbiosis
contributing
inflammation
through
various
mechanisms,
such
as
enhanced
intestinal
permeability
the
translocation
bacterial
products
like
lipopolysaccharide
(LPS).
Microbial
metabolites,
short-chain
acids
(SCFAs)
bile
acids,
influence
function
immune
responses,
potential
implications
for
progression.
Specific
microbiome
signatures
have
been
identified
patients,
offering
diagnostic
therapeutic
targets.
Moreover,
gut-derived
toxins,
endotoxins,
lipopolysaccharides,
trimethylamine-N-oxide
significantly
damage
inflammation,
highlighting
interplay
between
health.
review
comprehensively
examines
MAFLD,
focusing
on
underlying
pathogenic
biomarkers,
emerging
microbiome-targeted
strategies
management.
Viruses,
Journal Year:
2024,
Volume and Issue:
16(12), P. 1938 - 1938
Published: Dec. 18, 2024
Metformin,
a
widely
used
antidiabetic
medication,
has
emerged
as
promising
broad-spectrum
antiviral
agent
due
to
its
ability
modulate
cellular
pathways
essential
for
viral
replication.
By
activating
AMPK,
metformin
depletes
energy
reserves
that
viruses
rely
on,
effectively
limiting
the
replication
of
pathogens
such
influenza,
HIV,
SARS-CoV-2,
HBV,
and
HCV.
Its
role
in
inhibiting
mTOR
pathway,
crucial
protein
synthesis
reactivation,
is
particularly
significant
managing
infections
caused
by
CMV,
EBV.
Furthermore,
reduces
oxidative
stress
reactive
oxygen
species
(ROS),
which
are
critical
replicating
arboviruses
Zika
dengue.
The
drug
also
regulates
immune
responses,
differentiation,
inflammation,
disrupting
life
cycle
HPV
potentially
other
viruses.
These
diverse
mechanisms
suppress
replication,
enhance
system
functionality,
contribute
better
clinical
outcomes.
This
multifaceted
approach
highlights
metformin’s
potential
an
adjunctive
therapy
treating
wide
range
infections.
This
study
investigated
the
influence
of
single
nucleotide
polymorphisms
(SNPs)
in
genes
asso-ciated
with
interferon
pathway
(IFNAR2
rs2236757),
antiviral
response
(OAS1
rs10774671,
OAS3
rs10735079),
and
viral
entry
(ACE2
rs2074192)
on
COVID-19
severity
their
association
non-alcoholic
fatty
liver
disease
(MAFLD).
We
did
not
observe
a
significant
between
SNPs
severity.
While
IFNAR2
rs2236757
A
allele
correlated
higher
creatinine
levels
upon
admission
G
lower
band
neu-trophils
discharge,
these
findings
require
further
investigation.
The
distribution
OAS
gene
(rs10774671,
rs10735079
differ
MAFLD
non-MAFLD
patients.
Our
population's
ACE2
rs2074192
genotypes
alleles
differed
from
European
reference
population.
Overall,
our
suggest
that
specific
may
be
major
contributors
to
patient
population,
highlighting
potential
role
other
genetic
factors
environmental
influences.
CHILD`S HEALTH,
Journal Year:
2024,
Volume and Issue:
19(3), P. 162 - 174
Published: May 26, 2024
The
literature
review
highlights
the
issue
of
genetic
risk
factors
associated
with
development
metabolic
dysfunction-associated
fatty
liver
disease.
Human
examinations
revealed
132
genes
among
which
32
loci
are
strongly
pathogenesis
It
has
been
found
that
developing
disease
is
carried
by
single-nucleotide
variants
various
whose
products
involved
in
lipid
and
carbohydrate
metabolism,
maintenance
redox
state,
inflammation
fibrosis
tissue,
components
reactome.
authors
presented
a
detailed
list
singling
out
those
influence
directly
steatohepatitis
fibrosis.
Also,
they
emphasized
it
protein
3
containing
patatin-like
phospholipase
domain,
transmembrane
6
superfamily
member
2,
17b-hydroxysteroid
dehydrogenase
type
13
characterized
highest
degree
association
(odds
ratio
>
1.6)
compared
to
other
identified
gene
studies.
combination
several
polymorphisms
increases
severity
additive
steatogenic
effect
domain
2
probably
due
an
increased
expression
de
novo
lipogenesis.
emphasize
need
for
assessment
disease,
should
include
molecular
testing
at
early
stage
examination.