Genes,
Journal Year:
2023,
Volume and Issue:
14(6), P. 1167 - 1167
Published: May 27, 2023
Inflammatory
bowel
diseases
(IBDs)
are
a
group
of
chronic
characterized
by
recurring
periods
exacerbation
and
remission.
Fibrosis
the
intestine
is
one
most
common
complications
IBD.
Based
on
current
analyses,
it
evident
that
genetic
factors
mechanisms,
as
well
epigenetic
factors,
play
role
in
induction
progression
intestinal
fibrosis
Key
mechanisms
appear
to
be
significant
include
NOD2,
TGF-β,
TLRs,
Il23R,
ATG16L1.
Deoxyribonucleic
acid
(DNA)
methylation,
histone
modification,
ribonucleic
(RNA)
interference
primary
mechanisms.
Genetic
which
seem
important
pathophysiology
IBD,
may
potentially
used
targeted
therapy
future.
Therefore,
aim
this
study
was
gather
discuss
selected
factors.
Journal of Evidence-Based Medicine,
Journal Year:
2024,
Volume and Issue:
17(2), P. 409 - 433
Published: June 1, 2024
Abstract
Inflammatory
bowel
disease
(IBD)
is
a
chronic
and
relapsing
immune‐mediated
of
the
gastrointestinal
tract
with
gradually
increasing
global
incidence
prevalence.
A
prolonged
course
IBD
leads
to
decline
in
patient
quality
life
creation
substantial
economic
burden
on
society.
Owing
lack
specific
diagnostic
markers,
diagnosis
still
needs
gold
standard
based
combination
clinical
manifestations,
imaging,
laboratory,
endoscopic
results.
Accordingly,
current
goals
treatment
are
alleviate
symptoms
reduce
recurrence
rates.
Therefore,
it
imperative
develop
set
procedures
diagnose
treat
IBD.
In
this
review,
we
summarize
prominent
emerging
studies,
outline
classical
contemporary
approaches
diagnosing
managing
IBD,
integrate
multiple
guidelines.
Furthermore,
propose
possibility
establishing
an
early
comprehensive
workflow
personalized
management
strategy
future.
We
aim
enhance
standardization
for
International Journal of Molecular Sciences,
Journal Year:
2024,
Volume and Issue:
25(13), P. 7062 - 7062
Published: June 27, 2024
In
inflammatory
bowel
diseases
(IBDs),
such
as
Crohn's
disease
(CD)
and
ulcerative
colitis
(UC),
the
immune
system
relentlessly
attacks
intestinal
cells,
causing
recurrent
tissue
damage
over
lifetime
of
patients.
The
etiology
IBD
is
complex
multifactorial,
involving
environmental,
microbiota,
genetic,
immunological
factors
that
alter
molecular
basis
organism.
Among
these,
microbiota
cells
play
pivotal
roles;
generates
antigens
recognized
by
antibodies,
while
autoantibodies
target
attack
membrane,
exacerbating
inflammation
damage.
Given
altered
framework,
analysis
multiple
biomarkers
in
patients
proves
exceedingly
valuable
for
diagnosing
prognosing
IBD,
including
markers
like
C
reactive
protein
fecal
calprotectin.
Upon
detection
classification
patients,
specific
treatments
are
administered,
ranging
from
conventional
drugs
to
new
biological
therapies,
antibodies
neutralize
molecules
tumor
necrosis
factor
(TNF)
integrin.
This
review
delves
into
targets,
biomarkers,
treatment
options,
monitoring
techniques,
and,
ultimately,
current
challenges
management.
Current Issues in Molecular Biology,
Journal Year:
2024,
Volume and Issue:
46(1), P. 469 - 484
Published: Jan. 3, 2024
Inflammatory
diseases
are
a
global
health
problem
affecting
millions
of
people
with
wide
range
conditions.
These
diseases,
including
inflammatory
bowel
disease
(IBD),
rheumatoid
arthritis
(RA),
osteoarthritis
(OA),
gout,
and
diabetes,
impose
significant
burden
on
patients
healthcare
systems.
A
complicated
interaction
between
genetic
variables,
environmental
stimuli,
dysregulated
immune
responses
shows
the
complex
biological
foundation
various
diseases.
This
review
focuses
molecular
mechanisms
underlying
function
inflammasomes
inflammation.
We
investigate
impact
factors
progression
explore
connection
inflammation
inflammasome
activation,
examine
incidence
in
relation
to
inflammasomes.
Cells,
Journal Year:
2024,
Volume and Issue:
13(5), P. 381 - 381
Published: Feb. 23, 2024
At
the
intestinal
front,
several
lines
of
defense
are
in
place
to
resist
infection
and
injury,
mucus
layer,
gut
microbiome
strong
epithelial
junctions,
name
a
few.
Their
collaboration
creates
resilient
barrier.
In
disorders,
such
as
inflammatory
bowel
disease
(IBD),
barrier
function
is
compromised,
which
results
rampant
inflammation
tissue
injury.
response
destruction,
epithelium
releases
adenosine,
small
but
powerful
nucleoside
that
functions
an
alarm
signal.
Amidst
chaos
inflammation,
adenosine
aims
restore
order.
Within
scope
its
effects
ability
regulate
integrity.
This
review
define
contributions
production,
microbiome-dependent
protection,
tight
junction
dynamics,
chloride
secretion
acid–base
balance
reinforce
importance
International Journal of Molecular Sciences,
Journal Year:
2024,
Volume and Issue:
25(5), P. 2789 - 2789
Published: Feb. 28, 2024
The
advent
of
biologic
drugs
has
revolutionized
the
treatment
Inflammatory
Bowel
Disease,
increasing
rates
response
and
mucosal
healing
in
comparison
to
conventional
therapies
by
allowing
corticosteroid-refractory
cases
reducing
corticosteroid-related
side
effects.
However,
(anti-TNFα
inhibitors,
anti-α4β7
integrin
anti-IL12/23)
are
still
burdened
that
hover
around
40%
(in
biologic-naïve
patients)
or
lower
(for
biologic-experienced
patients).
Moreover,
knowledge
mechanisms
underlying
drug
resistance
loss
is
scarce.
Several
cellular
molecular
determinants
implied
therapeutic
failure;
genetic
predispositions,
form
single
nucleotide
polymorphisms
sequence
cytokines
Human
Leukocyte
Antigen,
an
altered
expression
other
molecules
involved
inflammation
cascade,
play
most
important
role.
Accessory
include
gut
microbiota
dysregulation.
In
this
narrative
review
current
recent
literature,
we
shed
light
on
mentioned
failure
order
pave
way
for
a
more
personalized
approach
could
help
avoid
unnecessary
treatments
toxicities.
International Journal of Molecular Sciences,
Journal Year:
2024,
Volume and Issue:
25(7), P. 3717 - 3717
Published: March 27, 2024
Inflammatory
bowel
disease
(IBD)
is
a
chronic
inflammatory
disorder
of
the
digestive
tract
usually
characterized
by
diarrhea,
rectal
bleeding,
and
abdominal
pain.
IBD
includes
Crohn’s
ulcerative
colitis
as
main
entities.
debilitating
condition
that
can
lead
to
life-threatening
complications,
involving
possible
malignancy
surgery.
The
available
therapies
aim
achieve
long-term
remission
prevent
progression.
Biologics
are
bioengineered
therapeutic
drugs
mainly
target
proteins.
Although
they
have
revolutionized
treatment
IBD,
their
potential
benefits
limited
due
large
interindividual
variability
in
clinical
response
terms
efficacy
toxicity,
resulting
high
rates
failure.
It
therefore
important
find
biomarkers
provide
tailor-made
strategies
allow
for
patient
stratification
maximize
minimize
adverse
events.
Pharmacogenetics
has
optimize
biologics
selection
identifying
genetic
variants,
specifically
single
nucleotide
polymorphisms
(SNPs),
which
underlying
factors
associated
with
an
individual’s
drug
response.
This
review
analyzes
current
knowledge
variants
biological
agent
(infliximab,
adalimumab,
ustekinumab,
vedolizumab)
IBD.
An
online
literature
search
various
databases
was
conducted.
After
applying
inclusion
exclusion
criteria,
28
reports
from
1685
results
were
employed
review.
most
significant
SNPs
potentially
useful
predictive
linked
immunity,
cytokine
production,
immunorecognition.
Diagnostics,
Journal Year:
2023,
Volume and Issue:
13(20), P. 3183 - 3183
Published: Oct. 12, 2023
Delayed
diagnosis
is
a
challenge
in
the
management
of
inflammatory
bowel
disease
(IBD).
Several
studies
show
significant
association
between
diagnostic
delay
and
progression
to
complications
surgery,
especially
Crohn’s
(CD).
What
risk
factors
are
associated
with
IBD
remains
unclear.
In
order
reduce
delay,
Red
Flags
Index
has
been
developed
validated.
The
combination
score
non-invasive
biomarkers
such
as
fecal
calprotectin
seems
be
highly
accurate
screening
patients
underlying
referred
for
further
workup
eventual
early
effective
treatment
strategies.
Our
literature
review
aims
obtain
comprehensive
overview
impacts
on
potential
IBD,
how
tools
may
reducing
future
perspectives
this
field.
Frontiers in Immunology,
Journal Year:
2024,
Volume and Issue:
15
Published: April 29, 2024
Background
The
inflammatory
response
plays
an
essential
role
in
the
tumor
microenvironment
(TME)
of
colorectal
cancer
(CRC)
by
modulating
growth,
progression,
and
to
therapy
through
recruitment
immune
cells,
production
cytokines,
activation
signaling
pathways.
However,
molecular
subtypes
risk
score
prognostic
model
based
on
remain
be
further
explored.
Methods
Inflammation-related
genes
were
collected
from
signature
database
identified
using
nonnegative
matrix
factorization
TCGA
cohort.
We
compared
clinicopathological
features,
infiltration,
somatic
mutation
profile,
survival
prognosis,
drug
sensitivity
between
subtypes.
was
developed
LASSO
multivariate
Cox
regression
above
results
independently
validated
GEO
Moreover,
we
explored
biological
functions
hub
gene,
receptor
interacting
protein
kinase
2
(RIPK2),
leveraging
proteomics
data,
vivo
,
vitro
experiments.
Results
two
inflammation-related
(inflammation-low
inflammation-high)
have
excellent
internal
consistency
stability.
Inflammation-high
subtype
showed
higher
cell
infiltration
increased
common
chemotherapeutic
drugs,
while
inflammation-low
may
more
suitable
for
immunotherapy.
Besides,
differ
significantly
pathway
enrichment
functions.
In
addition,
11-gene
constructed
strong
assessment
power
could
serve
as
a
novel
marker
predict
CRC
patients.
Finally,
RIPK2
crucial
promoting
malignant
proliferation
experiment.
Conclusions
This
study
provides
new
insights
into
heterogeneity
opportunities
treatment
development
clinical
decision
making.