From Genomics to Metabolomics: Molecular Insights into Osteoporosis for Enhanced Diagnostic and Therapeutic Approaches
Qingmei Li,
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Jihan Wang,
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Congzhe Zhao
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et al.
Biomedicines,
Journal Year:
2024,
Volume and Issue:
12(10), P. 2389 - 2389
Published: Oct. 18, 2024
Osteoporosis
(OP)
is
a
prevalent
skeletal
disorder
characterized
by
decreased
bone
mineral
density
(BMD)
and
increased
fracture
risk.
The
advancements
in
omics
technologies—genomics,
transcriptomics,
proteomics,
metabolomics—have
provided
significant
insights
into
the
molecular
mechanisms
driving
OP.
These
technologies
offer
critical
perspectives
on
genetic
predispositions,
gene
expression
regulation,
protein
signatures,
metabolic
alterations,
enabling
identification
of
novel
biomarkers
for
diagnosis
therapeutic
targets.
This
review
underscores
potential
these
multi-omics
approaches
to
bridge
gap
between
basic
research
clinical
applications,
paving
way
precision
medicine
OP
management.
By
integrating
technologies,
researchers
can
contribute
improved
diagnostics,
preventative
strategies,
treatments
patients
suffering
from
related
conditions.
Language: Английский
The Association of Systemic and Mandibular Bone Mineral Density in Postmenopausal Females with Osteoporosis
Ioana Duncea,
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Cecilia Bacali,
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Smaranda Buduru
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et al.
Medicina,
Journal Year:
2024,
Volume and Issue:
60(8), P. 1313 - 1313
Published: Aug. 14, 2024
Background/Objectives:
Osteoporosis
is
a
common
general
disease
that
mostly
affects
the
skeletal
system,
including
jawbone.
There
link
between
systemic
and
mandibular
osteoporosis.
This
study
aimed
at
assessing
association
(lumbar
spine
L1–L4,
femoral
neck,
total
hip)
bone
mineral
density
(BMD)
mandible
BMD
sites
in
Romanian
postmenopausal
females.
Methods:
A
of
97
menopausal
patients
were
studied,
62
with
osteoporosis
35
females
no
For
each
patient,
dual-energy
X-ray
absorptiometry
(DXA)
assessments
mandible,
proximal
femur,
hip,
lumbar
(L1–L4)
performed.
Mandibular
measurements
performed
using
distal
forearm
software,
followed
by
manual
analysis
after
contour
was
defined
case.
Results:
Comparing
control
groups,
there
significant
differences
examined
location.
The
(1.125
±
0.181506
g/cm2)
group
considerably
smaller
than
(1.35497
0.244397
g/cm2).
Correlations
different
significant:
neck
(r
=
0.738,
p
<
0.0001),
hip
0.735,
0.506,
0.891,
0.482,
0.466,
0.0001).
Conclusions:
correlations
spine,
BMD,
suggesting
density.
locations
may
help
predict
probability
Language: Английский
Meta-analysis of proteomics data from osteoblasts, bone, and blood: Insights into druggable targets, active factors, and potential biomarkers for bone biomaterial design
Journal of Tissue Engineering,
Journal Year:
2024,
Volume and Issue:
15
Published: Jan. 1, 2024
Non-healing
bone
defects
are
a
pressing
public
health
concern
accounting
for
one
main
cause
decreased
life
expectancy
and
quality.
An
aging
population
accompanied
with
increasing
incidence
of
comorbidities,
foreshadows
worsening
this
socio-economic
problem.
Conventional
treatments
non-healing
prove
ineffective
5%–10%
fractures.
Those
challenges
not
only
increase
the
patient’s
burden
but
also
complicate
medical
intervention,
underscoring
need
more
effective
treatment
strategies
identification
patients
at
risk
before
selection.
To
address
this,
our
proteomic
meta-analysis
aims
to
identify
universally
affected
proteins
functions
in
context
regeneration
that
can
be
utilized
as
novel
bioactive
biomaterial
functionalizations,
drug
targets
or
therapeutics
well
analytical
endpoints,
biomarkers
implant
design
testing,
respectively.
We
compiled
29
studies
covering
cellular
models,
extracellular
vesicles,
matrix,
tissue,
liquid-biopsies
different
tissue
hierarchies
species.
innovative,
integrated
framework
consisting
data
harmonization,
candidate
protein
selection,
network
construction,
functional
enrichment
repurposing
scoring
metrics
was
developed.
make
widely
applicable
other
research
questions,
we
have
published
detailed
tutorial
process.
identified
51
potentially
important
healing.
This
includes
well-known
ECM
components
such
collagens,
fibronectin
periostin,
less
explored
biology
like
YWHAE,
HSPG2,
CCN1,
HTRA1,
IGFBP7,
LGALS1,
TGFBI,
C3,
SERPINA1,
ANXA1
might
future
development.
Furthermore,
discovered
compounds
trifluoperazine,
phenethyl
isothiocyanate,
quercetin,
artenimol,
which
target
key
S100A4,
YWHAZ,
MMP2,
TPM4
providing
option
manipulate
undesired
processes
regeneration.
may
open
new
ways
options
face
pressure
defects.
Language: Английский