Periodontitis
(PD)
is
a
dysbiosis-triggered
chronic
inflammation
affecting
the
tooth-supporting
tissue.
Growing
evidence
indicates
that
there
an
association
between
periodontitis
and
rheumatoid
arthritis
(RA).
RA
autoimmune
disease
characterised
by
of
synovial
membrane
joint
destruction
with
unclear
aetiology.
The
PD
can
be
explained
by,
amongst
others,
shared
risk
factors
like
genetic
predisposition
smoking,
high
local
systemic
inflammatory
burden
induction
autoimmunity
inflammation.
Anti-citrullinated
proteins
antibodies
(ACPA)
factor
(RF)
are
hallmarks
seropositive
RA.
presence
ACPA
RF
have
been
reported
to
emerge
in
serum
years
before
clinically
diagnosed
indicating
role
extra-articular
site
as
inducing
site.
aim
this
study
was
explore
presumed
links
emphasis
on
gingival
crevicular
fluid
(GCF)
microbiome.
results
showed:
(1)
patients
increased
circulating
GCF
levels
pro‐inflammatory
cytokines
proteins,
despite
anti‐rheumatic
treatment
biological
DMARDs.
accompanied
higher
cytokine
protein
levels,
(2)
IgA‐ACPA
present
healthy
associated
periodontal
could
involved
progression
RA,
(3)
no
exist
against
P
gingivalis,
A
actinomycetemcomitans
RA-specific
autoantibodies,
(4)
certain
taxa,
including
Porphyromonas,
seem
periodontium.
Gut,
Journal Year:
2023,
Volume and Issue:
72(9), P. 1664 - 1677
Published: Jan. 5, 2023
Gut
microbiota
dysbiosis
is
closely
linked
to
the
pathogenesis
of
rheumatoid
arthritis
(RA).
We
aimed
identify
potential
probiotic
gut
microbes
that
can
ameliorate
development
RA.Microbiota
profiling
in
patients
with
RA
and
healthy
individuals
was
investigated
via
16S
rDNA
bacterial
gene
sequencing
shotgun
metagenomics.
Collagen-induced
arthritic
mice
TNF-α
transgenic
were
used
evaluate
roles
commensal
Parabacteroides
distasonis
RA.
The
effects
P.
distasonis-derived
microbial
metabolites
on
differentiation
CD4+
T
cells
macrophage
polarisation
also
investigated.The
relative
abundance
new-onset
history
disease
downregulated
this
decrease
negatively
correlated
Disease
Activity
Score-28
(DAS28).
Oral
treatment
live
(LPD)
considerably
ameliorated
pathogenesis.
LPD-derived
lithocholic
acid
(LCA),
deoxycholic
(DCA),
isolithocholic
(isoLCA)
3-oxolithocholic
(3-oxoLCA)
had
similar
synergistic
In
addition
directly
inhibiting
Th17
cells,
3-oxoLCA
isoLCA
identified
as
TGR5
agonists
promoted
M2
macrophages.
A
specific
synthetic
inhibitor
bile
salt
hydrolase
attenuated
antiarthritic
LPD
by
reducing
production
these
four
acids.
natural
product
ginsenoside
Rg2
exhibited
its
anti-RA
promoting
growth
distasonis.P.
might
represent
prebiotic
agents
Biomedicines,
Journal Year:
2022,
Volume and Issue:
10(3), P. 671 - 671
Published: March 14, 2022
The
oral
microbiome,
forming
a
biofilm
that
covers
the
structures,
contains
high
number
of
microorganisms.
Biofilm
formation
starts
from
salivary
pellicle
allows
bacterial
adhesion-colonization-proliferation,
co-aggregation
and
maturation
in
complex
microbial
community.
There
is
constant
bidirectional
crosstalk
between
human
host
its
microbiome.
paper
presents
fundamentals
regarding
microbiome
relationship
to
modulator
factors,
systemic
health.
modern
studies
microorganisms
relationships
with
benefits
are
based
on
genomics,
transcriptomics,
proteomics
metabolomics.
Pharmaceuticals
such
as
antimicrobials,
prebiotics,
probiotics,
surface
active
or
abrasive
agents
plant-derived
ingredients
may
influence
Many
found
associations
dysbiosis
disorders,
including
autoimmune
diseases,
cardiovascular,
diabetes,
cancers
neurodegenerative
disorders.
We
outline
general
individual
factors
influencing
host-microbial
balance
possibility
use
analysis
prevention,
diagnosis
treatment
personalized
medicine.
Future
therapies
should
take
account
restoration
normal
symbiotic
relation
Bone Research,
Journal Year:
2023,
Volume and Issue:
11(1)
Published: May 22, 2023
Abstract
Rheumatoid
arthritis
(RA)
and
periodontitis
are
chronic
inflammatory
diseases
leading
to
increased
bone
resorption.
Preventing
this
resorption
is
a
major
health
challenge.
Both
share
immunopathogenic
similarities
common
environment.
The
autoimmune
response
or
periodontal
infection
stimulates
certain
immune
actors,
in
both
cases
inflammation
that
perpetuates
Moreover,
RA
have
strong
epidemiological
association
could
be
explained
by
microbial
dysbiosis.
This
dysbiosis
believed
involved
the
initiation
of
via
three
mechanisms.
(i)
dissemination
pathogens
triggers
systemic
inflammation.
(ii)
Periodontal
can
induce
generation
citrullinated
neoepitopes,
anti-citrullinated
peptide
autoantibodies.
(iii)
Intracellular
danger-associated
molecular
patterns
accelerate
local
Therefore,
promote
sustain
distant
inflamed
joints.
Interestingly,
conditions,
existence
osteoclasts
distinct
from
“classical
osteoclasts”
has
recently
been
reported.
They
proinflammatory
origins
functions.
Several
populations
osteoclast
precursors
described
RA,
such
as
classical
monocytes,
dendritic
cell
subtype,
arthritis-associated
osteoclastogenic
macrophages.
aim
review
synthesize
knowledge
on
their
especially
periodontitis.
Special
attention
will
given
recent
data
related
potential
value
due
between
two
diseases.
Improving
our
understanding
these
pathogenic
mechanisms
should
lead
identification
new
therapeutic
targets
pathological
associated
with
Biocell,
Journal Year:
2024,
Volume and Issue:
48(1), P. 9 - 19
Published: Jan. 1, 2024
Rheumatoid
arthritis
(RA)
is
a
prevalent
autoimmune
disease
whose
main
features
include
chronic
synovial
inflammation,
bone
destruction,
and
joint
degeneration.Neutrophils
are
often
considered
to
be
the
first
responders
inflammation
key
presence
in
inflammatory
milieu
of
RA.Neutrophil
extracellular
traps
(NETs),
meshwork
DNA-histone
complexes
proteins
released
by
activated
neutrophils,
widely
involved
pathophysiology
diseases,
especially
RA,
addition
playing
role
neutrophil
innate
immune
response.NETs
have
been
found
an
important
source
citrullinated
autoantigen
antibodies
factor
release,
which
can
activate
RA
fibroblasts
(FLS)
cause
damage.This
article
reviews
NETs
demonstrating
application
multiple
molecules
with
various
therapies,
view
informing
discovery
development
novel
biomarkers
therapeutic
targets
for
RA.
Physiological Research,
Journal Year:
2022,
Volume and Issue:
71(6), P. 719 - 738
Published: Nov. 25, 2022
Hundreds
of
studies
in
last
decades
have
aimed
to
compare
the
microbiome
patients
suffering
from
diverse
diseases
with
that
healthy
controls.
The
microbiome-related
component
was
additionally
identified
pathophysiology
many
formerly
considered
depend
only
on
host
physiology.
This,
however,
opens
important
questions
like:
“What
is
microbiome?”
or
“Is
it
possible
define
unequivocally?”.
In
this
review,
we
describe
main
hindrances
complicating
definition
“healthy
microbiome”
terms
microbiota
composition.
We
discuss
human
perspective
classical
ecology
and
advocate
for
shift
stress
composition
functions
ensures
host.
Finally,
propose
leave
concept
ideal
replace
by
focus
advantageous
host,
which
always
depends
specific
context
like
age,
genetics,
dietary
habits,
body
site
physiological
state.
Cell Biochemistry and Function,
Journal Year:
2024,
Volume and Issue:
42(2)
Published: Jan. 30, 2024
Abstract
Both
the
epigenetic
changes
and
gut
microbiota
(GM)
have
attracted
a
growing
interest
in
establishing
effective
diagnostics
potential
therapeutic
strategies
for
number
of
diseases.
These
disorders
include
metabolic,
central
nervous
system‐related
diseases,
autoimmune,
gastrointestinal
infections
(GI).
Despite
studies,
there
is
no
extensive
review
that
connects
epigenetics
modifications
GM
as
biomarkers
could
confer
treatment
options.
To
this
end,
hopes
to
give
detailed
information
on
connecting
GM.
An
updated
connection
between
factors
influence
diseases
are
given.
In
addition,
showed
some
associations
maternal
offspring
health.
Finally,
limitations
concept
prospects
into
new
emerging
discipline
were
also
looked
into.
Although
elucidated
diet
response
health
with
respect
modifications,
still
exist
various
newly
discipline.
addition
integrating
complementary
multi‐omics
data,
longitudinal
sampling
will
aid
identification
functional
mechanisms
may
serve
targets.
gave
perspective
harnessing
disease
diagnostics,
prevention
options
through
Microorganisms,
Journal Year:
2024,
Volume and Issue:
12(7), P. 1387 - 1387
Published: July 9, 2024
Rheumatoid
arthritis
(RA)
is
a
chronic,
autoimmune
rheumatic
disease
characterized
by
synovial
joint
inflammation
with
subsequent
destruction
as
well
systemic
manifestation,
leading
to
impaired
mobility
and
quality
of
life.
The
etiopathogenesis
RA
still
unknown,
genetic,
epigenetic
environmental
factors
(incl.
tobacco
smoking)
contributing
susceptibility.
link
between
genetic
like
"shared
epitope
alleles"
the
development
known.
However,
why
only
some
carriers
have
break
in
self-tolerance
develop
autoimmunity
needs
be
clarified.
presence
autoantibodies
patients'
serum
months
years
prior
onset
clinical
manifestations
has
moved
focus
possible
factors,
including
triggers
that
could
contribute
initiation
perpetuation
inflammatory
reaction
RA.
Over
past
several
years,
role
microorganisms
at
mucosal
sites
(i.e.,
microbiome)
emerged
an
essential
mediator
An
increasing
number
studies
revealed
microbial
immunopathogenesis
diseases.
Interaction
host
immune
system
microbiota
initiates
loss
immunological
tolerance
autoimmunity.
alteration
microbiome
composition,
so-called
dysbiosis,
associated
Immune
dysfunction
caused
dysbiosis
sustains
chronic
inflammation.
This
review
aims
provide
critical
summary
literature
findings
related
hypothesis
reciprocal
relation
system.
Available
data
from
reveal
pivotal
pathogenesis.