Microbiological and Metabolomic Analysis of Biomarkers for Grades A and B in Stage II Periodontitis
Inflammation,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Feb. 27, 2025
Periodontitis
is
a
chronic
inflammatory
disease
characterized
by
inflammation
of
the
periodontal
soft
tissues
and
loss
alveolar
bone.
In
oral
environment,
subgingival
microorganisms
salivary
metabolites
reflect
host's
health
status.
This
study
aimed
to
understand
periodontitis
severity
progression
rate
analyzing
microflora
identify
potential
biomarkers.
Fifty-three
volunteers
with
stage
II
were
graded
using
bone
(%)/age
index
into
two
grades:
33
in
grade
A
(<
0.25)
20
B
(0.25–1.00).
Using
case–control
study,
simultaneously
analyzed
biomarkers
associated
periodontitis.
The
red
complex,
orange
Campylobacter
spp.,
uncultured
Candidatus
Saccharibacteria
such
as
5-Aminovaleric
acid,
N1-Acetylspermine
showed
significant
positive
correlation
clinical
parameters.
Furthermore,
we
identified
four
differential
(DL-Leucineamide,
Dodecanedioic
L-Tyrosine
methyl
ester
Phenylpyruvic
acid)
that
may
serve
for
predicting
progression.
These
results
complex
significantly
correlated
influenced
changes
metabolites.
Additionally,
indicating
predominantly
amino
acid
derivatives,
confirming
interactions
between
exacerbate
development.
Language: Английский
Evaluation of annexin A1, carbonic anhydrase 1, and elongation factor 1-gamma levels in periodontal diseases
Bilge Cansu Uzun Saylan,
No information about this author
Büşra Yılmaz,
No information about this author
Veli Özgen Öztürk
No information about this author
et al.
BMC Oral Health,
Journal Year:
2025,
Volume and Issue:
25(1)
Published: May 2, 2025
Periodontitis
arises
from
dysbiotic
subgingival
microbiota
and
an
unresolved
inflammatory
response.
Annexin
A1
(ANXA1),
Carbonic
Anhydrase
I
(CA1),
Elongation
Factor
1-gamma
(EF1-Ɣ)
may
play
a
role
in
periodontal
inflammation
disease
pathogenesis.
This
study
aimed
to
investigate
the
levels
of
these
molecules
gingival
crevicular
fluid
(GCF)
individuals
with
different
conditions.
GCF
samples
were
collected
20
patients
Stage
III
Grade
B
periodontitis,
C
19
gingivitis
patients,
21
periodontally
healthy
individuals.
ANXA1,
CA1,
EF1-Ɣ
measured
using
ELISA.
Clinical
parameters
significantly
higher
periodontitis
groups
compared
(p
<
0.001).
total
amount
differed
among
groups,
control
Elevated
found
III/B
III/C
ANXA1
CA1
similar
across
>
0.05).
Within
limitations
this
study,
it
might
be
suggested
that
decreased
diseased
sites
its
elevated
are
associated
pathogenesis
disease.
Language: Английский
Characterisation of the periodontal proteome in gingival crevicular fluid and saliva using SWATH-MS
Frontiers in Cellular and Infection Microbiology,
Journal Year:
2025,
Volume and Issue:
15
Published: May 2, 2025
Introduction
Proteomic
techniques
are
useful
to
analyse
the
periodontal
proteome
in
gingival
crevicular
fluid
(GCF)
and
saliva.
However,
few
investigations
have
assessed
compared
GCF
salivary
proteomes.
Therefore,
this
research
aims
structure
compare
protein
expression
these
fluids
between
individuals
with
health
those
periodontitis.
Methods
saliva
were
collected
from
44
periodontally
healthy
subjects
41
periodontitis
(stages
III-IV).
Samples
analysed
using
sequential
window
acquisition
of
all
theoretical
mass
spectra
(SWATH-MS),
proteins
identified
employing
UniProt
database.
The
was
principal
component
analysis
(PCA).
Differential
defined
as
an
adjusted
p-value
<0.05
combined
a
fold-change
≥2
(upregulated)
or
≤0.5
(downregulated).
Results
250
abundant
quantified
377
(238
common).
different
both
oral
fluids.
In
GCF,
63
(25.2%)
differentially
expressed,
38
upregulated
25
downregulated
most
overexpressed
haemoglobin
subunits
(Hbs)
beta
(fold-change
5.06)
alpha
(4.35),
carbonic
anhydrase
1
(4.28),
S100-P
(4.27).
Among
underexpressed
proteins,
14
keratins,
type
II
cytoskeletal
6B
being
(0.10),
together
glyceraldehyde-3-phosphate
dehydrogenase
(0.12)
zymogen
granule
16
homolog
B
(0.13).
saliva,
59
(15.7%)
55
four
Twenty-nine
showed
≥4,
highlighting
beta-2-microglobulin
(44.14),
keratin,
I
13
(36.23),
neutrophil
defensin
(25.08),
S100-A9
(12.30),
A8
(10.61),
A12
(4.76),
P
(4.72),
annexin
A1
(9.34),
lysozyme
C
(4.98),
immunoglobulin
heavy
constant
(4.45),
resistin
(4.37),
Hbs
(4.20)
(4.06).
lipocalin-1
(0.35).
Fourteen
expressed
where
seven
keratins
but
Conclusion
Periodontitis
alters
numerous
vary
qualitatively
quantitatively,
indicating
patterns
Language: Английский
Diagnostic Accuracy of Novel Protein Biomarkers in Saliva to Detect Periodontitis Using Untargeted ‘SWATH’ Mass Spectrometry
Journal Of Clinical Periodontology,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Dec. 27, 2024
ABSTRACT
Aim
To
discover
new
salivary
biomarkers
to
diagnose
periodontitis
and
evaluate
the
impact
of
age
smoking
on
predictive
capacity.
Material
Methods
Saliva
samples
were
collected
from
44
healthy
periodontal
individuals
41
with
periodontitis.
Samples
analysed
by
sequential
window
acquisition
all
theoretical
mass
spectra
(SWATH‐MS),
proteins
identified
employing
UniProt
database.
The
diagnostic
capacity
molecules
was
determined
generalized
additive
models.
models
obtained
single‐protein
unadjusted
adjusted
for
status,
besides
two‐protein
combinations.
Results
Eight
single
had
a
bias‐corrected
accuracy
(bc‐ACC)
78.8%–86.8%
(bc‐sensitivity/bc‐specificity
62.5%–86.9%/60.9%–98.1%)
Predictive
increased
more
adjusting
(bc‐ACC:
94.1%–98.2%;
bc‐sensitivity/bc‐specificity:
90.2%–98.6%/93.6%–97.2%)
than
83.9%–90.4%;
73.6%–89.9%/76.2%–96.4%).
These
keratin,
type
II
cytoskeletal
1,
protein
S100‐A8,
β‐2‐microglobulin,
neutrophil
defensin
lysozyme
C,
ubiquitin‐60S
ribosomal
L40,
isoform
2
tropomyosin
α‐3
chain
resistin.
Two
dual
combinations
showed
bc‐sensitivity/bc‐specificity
>
90%:
β‐2‐microglobulin
profilin‐1,
C
zymogen
granule
16
homologue
B.
Conclusions
New
show
good
or
excellent
ability
Age
has
significant
influence
smoking,
results
comparable
Language: Английский