Gut Microbiota Serves as a Crucial Independent Biomarker in Inflammatory Bowel Disease (IBD)
Bharti Sharma,
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George Agriantonis,
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Kate Twelker
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et al.
International Journal of Molecular Sciences,
Journal Year:
2025,
Volume and Issue:
26(6), P. 2503 - 2503
Published: March 11, 2025
Inflammatory
bowel
disease
(IBD),
encompassing
Crohn’s
(CD),
ulcerative
colitis
(UC),
and
IBD
unclassified
(IBD-U),
is
a
complex
intestinal
disorder
influenced
by
genetic,
environmental,
microbial
factors.
Recent
evidence
highlights
the
gut
microbiota
as
pivotal
biomarker
modulator
in
pathogenesis.
Dysbiosis,
characterized
reduced
diversity
altered
composition,
hallmark
of
IBD.
A
consistent
decrease
anti-inflammatory
bacteria,
such
Faecalibacterium
prausnitzii,
an
increase
pro-inflammatory
species,
including
Escherichia
coli,
have
been
observed.
Metabolomic
studies
reveal
decreased
short-chain
fatty
acids
(SCFAs)
secondary
bile
acids,
critical
for
homeostasis,
alongside
elevated
metabolites.
The
interacts
with
host
immune
pathways,
influencing
morphogens,
glycosylation,
podoplanin
(PDPN)
expression.
disruption
glycosylation
impairs
mucosal
barriers,
while
aberrant
PDPN
activity
exacerbates
inflammation.
Additionally,
alterations
contribute
to
oxidative
stress,
further
destabilizing
barriers.
These
molecular
cellular
disruptions
underscore
role
microbiome
pathophysiology.
Emerging
therapeutic
strategies,
probiotics,
prebiotics,
dietary
interventions,
aim
restore
balance
mitigate
Advanced
on
microbiota-targeted
therapies
their
potential
reduce
severity
improve
patient
outcomes.
Nevertheless,
research
needed
elucidate
bidirectional
interactions
between
responses
translate
these
insights
into
clinical
applications.
This
review
consolidates
current
findings
microbiota’s
IBD,
emphasizing
its
diagnostic
implications,
advocates
continued
exploration
microbiome-based
interventions
combat
this
debilitating
disease.
Language: Английский
Salting-out assisted liquid-liquid extraction for UPLC-MS/MS determination of bile acids and kynurenine-, indole- and serotonin-pathway metabolites of tryptophan in human serum of healthy probands
Celine Oanes,
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Marina Alexeeva,
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Kjetil Søreide
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et al.
Journal of Chromatography B,
Journal Year:
2025,
Volume and Issue:
1255, P. 124519 - 124519
Published: Feb. 11, 2025
Language: Английский
Rosuvastatin inhibits carcinogenesis through Ca2+ triggered endoplasmic reticulum stress pathway in pancreatic cancer
Cellular Signalling,
Journal Year:
2025,
Volume and Issue:
unknown, P. 111753 - 111753
Published: March 1, 2025
Language: Английский
Exploring the genetic link between gastroesophageal reflux disease and pancreatic cancer: insights from Mendelian randomization
Chen Yang,
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Fan Ge,
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Mengye Peng
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et al.
BMC Cancer,
Journal Year:
2025,
Volume and Issue:
25(1)
Published: April 18, 2025
Gastroesophageal
reflux
disease
(GERD)
is
increasingly
recognized
for
its
associations
with
extragastric
diseases,
yet
potential
role
in
pancreatic
cancer
(PC)
etiology
remains
underexplored.
This
study
investigates
the
genetic
causal
relationship
between
GERD
and
PC
using
Mendelian
randomization
(MR),
a
method
designed
to
reduce
confounding
factors.
A
two-sample
MR
analysis
was
conducted
genome-wide
association
studies
(GWAS)
data.
The
inverse
variance
weighted
(IVW)
applied,
additional
sensitivity
analyses
performed
evaluate
pleiotropy
heterogeneity.
IVW
demonstrated
significant
signature
predisposing
an
increased
risk
of
(OR:
1.36,
95%
CI:
1.04-1.80,
P
=
0.03).
There
no
evidence
(P
0.71)
or
heterogeneity
0.94).
Our
provides
robust
supporting
that
predisposition
associated
PC.
These
findings
emphasize
necessity
integrating
into
assessments
encourage
further
research
elucidate
underlying
biological
mechanisms.
insight
holds
inform
strategies
early
detection,
prevention,
personalized
management
patients.
Language: Английский