Identification of common signature genes and pathways underlying the pathogenesis association between nonalcoholic fatty liver disease and heart failure
Gerui Li,
No information about this author
Zhengjie Lu,
No information about this author
Ze Chen
No information about this author
et al.
Frontiers in Immunology,
Journal Year:
2024,
Volume and Issue:
15
Published: Sept. 16, 2024
Background
Non-alcoholic
fatty
liver
disease
(NAFLD)
and
heart
failure
(HF)
are
related
conditions
with
an
increasing
incidence.
However,
the
mechanism
underlying
their
association
remains
unclear.
This
study
aimed
to
explore
shared
pathogenic
mechanisms
common
biomarkers
of
NAFLD
HF
through
bioinformatics
analyses
experimental
validation.
Methods
HF-related
transcriptome
data
were
extracted
from
Gene
Expression
Omnibus
(GEO)
database
(GSE126848
GSE26887).
Differential
analysis
was
performed
identify
differentially
expressed
genes
(co-DEGs)
between
HF.
ontology
(GO),
Kyoto
Encyclopedia
Genes
Genomes
(KEGG),
gene
set
enrichment
(GSEA)
conducted
functions
regulatory
pathways
co-DEGs.
Protein-protein
interaction
(PPI)
network
support
vector
machine-recursive
feature
elimination
(SVM-RFE)
methods
used
screen
key
DEGs.
The
diagnostic
value
DEGs
assessed
by
receiver
operating
characteristic
(ROC)
curve
validated
external
datasets
(GSE89632
GSE57345).
Finally,
expression
in
mouse
models.
Results
A
total
161
co-DEGs
screened
out
patients.
GO,
KEGG,
GSEA
indicated
that
these
mainly
enriched
immune-related
pathways.
PPI
revealed
14
DEGs,
SVM-RFE
model
eventually
identified
two
(
CD163
CCR1
)
as
for
levels
significantly
down-regulated
ROC
showed
had
good
values
NAFLD.
Single-gene
suggested
engaged
immune
responses
inflammation.
Experimental
validation
unbalanced
macrophage
polarization
models,
down-regulated.
Conclusion
M2
impairment
characterized
decreased
a
pathway
downregulation
may
reflect
pathological
changes
development
progression
HF,
suggesting
potential
therapeutic
targets.
Language: Английский
Clinical utility of the Fibrosis-4 index for predicting mortality in patients with heart failure with or without metabolic dysfunction-associated steatotic liver disease: a prospective cohort study
The Lancet Regional Health - Europe,
Journal Year:
2024,
Volume and Issue:
48, P. 101153 - 101153
Published: Nov. 30, 2024
Language: Английский
The Cardiac-Kidney-Liver (CKL) syndrome: the “real entity” of type 2 diabetes mellitus
Archives of Medical Science,
Journal Year:
2024,
Volume and Issue:
20(1), P. 207 - 215
Published: Jan. 31, 2024
1.
Davies
MJ,
D'Alessio
DA,
Fradkin
J,
et
al.
Management
of
hyperglycemia
in
type
2
diabetes,
2018.
A
Consensus
Report
by
the
American
Diabetes
Association
(ADA)
and
European
for
Study
(EASD).
Care
2018;
41:
2669–701.
Google
Scholar
Language: Английский
Non-alcoholic fatty liver disease and risk of cardiovascular diseases: clinical association, pathophysiological mechanisms, and management
Cardiology Plus,
Journal Year:
2023,
Volume and Issue:
8(4), P. 217 - 226
Published: Oct. 1, 2023
Non-alcoholic
fatty
liver
disease
(NAFLD)
is
a
associated
with
metabolic
dysfunction
in
genetically
susceptible
individuals
due
to
over-nutrition
and
lack
of
exercise.
With
the
prevalence
obesity,
syndrome,
type
2
diabetes
mellitus,
NAFLD
has
become
most
common
cause
chronic
worldwide.
shares
many
risk
factors
cardiovascular
diseases
(CVDs).
increased
major
events
other
cardiac
complications
even
after
adjustment
for
traditional
factors.
The
primary
pathology
within
liver,
but
deaths
patients
CVDs.
This
review
summarizes
epidemiological
evidence
association
between
CVD
pathophysiological
mechanisms
underlying
this
association.
Current
treatment
strategies
their
potential
impact
on
are
also
discussed.
Language: Английский
Metabolic Dysfunction-Associated Steatotic Liver Disease and Heart Failure with Preserved Ejection Fraction: A Bidirectional Relationship with Clinical and Therapeutic Implications
Ana Rita Leite,
No information about this author
João Carlos Pinto Dias,
No information about this author
T Godinho
No information about this author
et al.
Deleted Journal,
Journal Year:
2024,
Volume and Issue:
unknown, P. 1 - 17
Published: Sept. 18, 2024
Background:
Metabolic
dysfunction-associated
steatotic
liver
disease
(MASLD)
is
increasingly
prevalent
and
the
most
common
cause
of
chronic
in
western
world.
It
considered
hepatic
manifestation
metabolic
syndrome
ultimately
leads
to
cardiovascular
diseases,
which
are
leading
death.
Heart
failure
with
preserved
ejection
fraction
(HFpEF)
appears
be
a
complication
MASLD
and,
conversely,
seems
exacerbate
its
severity.
This
review
focuses
on
pathophysiological
association
between
HFpEF,
as
well
their
clinical
therapeutic
implications.
Summary:
The
connection
HFpEF
intricate
bidirectional,
involving
several
mechanisms,
such
insulin
resistance,
overactivation
renin-angiotensin-aldosterone
sympathetic
nervous
systems,
systemic
inflammation,
gut
dysbiosis.
an
independent
risk
factor
for
diastolic
dysfunction
increasing
hospitalization
death
those
established
heart
failure.
Conversely,
exacerbates
severity
MASLD.
Screening
fibrosis
should
conducted
stable
euvolemic
patients
utilizing
ultrasonography
Fibrosis-4
index.
performed
measurement
natriuretic
peptides;
however,
these
may
have
lower
sensitivity
echocardiography
needed.
Therapeutic
strategies
both
limited,
but
certain
interventions
studied
also
benefit
system.
Lifestyle
interventions,
adherence
Mediterranean
diet
weight
loss,
proven
beneficial
diseases.
Sodium-glucose
cotransporter
2
inhibitors
(SGLT2i)
incretin
mimetics
show
promise
treating
conditions
synergistic
effects.
Key
Messages:
increases
incident
worsens
prognosis
HFpEF.
Given
high
prevalence
screening
crucial.
begin
peptides
when
there
suspicion.
SGLT2i
glucagon-like
peptide-1
receptor
agonists
offer
benefits
Language: Английский
Cardiac abnormalities pre- and post-liver transplantation for metabolic dysfunction-associated steatohepatitis – Evidence and special considerations
Journal of Liver Transplantation,
Journal Year:
2024,
Volume and Issue:
15, P. 100228 - 100228
Published: May 18, 2024
Metabolic
dysfunction-associated
steatotic
liver
disease
(MASLD)
has
an
alarmingly
high
global
prevalence.
Its
progressive
subtype,
metabolic
steatohepatitis
(MASH),
is
the
leading
indication
for
transplantation
overall.
Although
MASLD
been
associated
with
increased
risk
several
cardiac
abnormalities
including
arrhythmias,
structural
disease,
heart
failure,
valvular
and
coronary
artery
little
known
about
clinical
course
effects
of
these
in
post-liver
transplant
patients
MASH
as
etiology
their
cirrhosis.
This
narrative
review
presents
mechanistic
evidence
association
aforementioned
abnormalities,
well
characterizes
what
significance
post-operative
period
those
undergoing
MASH.
Additionally,
this
emphasizes
knowledge
gaps
highlights
areas
further
study
impact
Language: Английский