JBMR Plus,
Journal Year:
2024,
Volume and Issue:
9(2)
Published: Dec. 10, 2024
Lipocalin-2
(LCN2),
a
hormone
produced
by
adipocytes,
osteoblasts,
and
renal
tubular
cells,
is
implicated
in
age-related
diseases,
including
cardio-metabolic
disease.
To
understand
the
role
LCN2
may
play
pathological
states,
we
first
need
to
elucidate
relationship
between
circulating
with
indices
of
health
during
"normal"
aging.
This
study
examined
serum
levels
LCN2,
age,
measures
across
adult
lifespan
males
females.
We
conducted
pooled
cohort
analysis
124
community-dwelling
(n
=
52)
females
72)
(age
20-87
yr,
median
BMI
25.92
[23.04,
29.81]
kg/m2).
Serum
was
analyzed
using
two-step
chemiluminescent
microparticle
monoclonal
immunoassay.
The
age
evaluated
linear
regression
cubic
spline.
Simple
regressions
were
performed
investigate
following
variables:
BMI,
VO2peak,
glucose,
body
composition
(DXA).
For
every
1
yr
increase
0.26
mg/L
higher
(P
.007,
95%
CI
[0.07,
0.45]).
Each
unit
(kg/m2)
associated
0.88
.027,
[0.10,
1.66])
each
VO2peak
(mL/kg/min)
0.38
lower
(p
.003,
[-0.63,
-0.13]).There
no
significant
sex,
glucose
or
(all
p
>
.05).
increased
linearly
while
it
decreased
as
fitness
level
increased.
Future
research
should
build
on
these
findings
determine
whether
can
be
used
biomarker
for
chronic
disease
if
exercise
mitigate
changes.
The Journal of Physiology,
Journal Year:
2024,
Volume and Issue:
603(1), P. 211 - 237
Published: July 26, 2024
Exercise
is
a
potent
stimulus
for
combatting
skeletal
muscle
ageing.
To
study
the
effects
of
exercise
on
in
preclinical
setting,
we
developed
combined
endurance-resistance
training
mice
called
progressive
weighted
wheel
running
(PoWeR).
PoWeR
improves
molecular,
biochemical,
cellular
and
functional
characteristics
promotes
aspects
partial
epigenetic
reprogramming
when
performed
late
life
(22-24
months
age).
In
this
investigation,
leveraged
pan-mammalian
DNA
methylome
arrays
tandem
mass-spectrometry
proteomics
to
provide
detailed
information
late-life
adaptations
female
relative
age-matched
sedentary
controls
(n
=
7-10
per
group).
Differential
CpG
methylation
at
conserved
promoter
sites
was
related
transcriptional
regulation
genes
as
well
Nr4a3,
Hes1
Hox
after
PoWeR.
Using
holistic
method
-omics
integration
binding
expression
target
analysis
(BETA),
changes
were
associated
with
upregulated
proteins
global
mitochondrial
translation
(P
0.03).
Specifically,
BETA
implicated
control
ribosomal,
mitoribosomal,
complex
I
protein
abundance
training.
may
also
influence
LACTB,
MIB1
UBR4
induction
-
all
are
mechanistically
linked
health.
Computational
cistrome
predicted
several
transcription
factors
including
MYC
regulators
trained
methylome-proteome
landscape,
corroborating
prior
transcriptome
data.
Correlating
proteome
mass
fatigue
resistance
revealed
positive
relationships
VPS13A
NPL
levels,
respectively.
Our
findings
expose
differential
proteomic
translational
that
could
function
aged
mice.
KEY
POINTS:
Late-life
from
22-24
age
shown
improve
vivo
promote
mitigation.
Integration
36k
using
(which
contain
ageing
clock
sites)
exploratory
extends
our
work
reveals
coordinated
widespread
initiation,
ribosomal
(mitoribosomal)
voluntary
sizeable
cohort
group
analysis).
Multi-omics
serine
β-lactamase-like
(LACTB
tumour
muscle),
mind
bomb
1
(MIB1
satellite
cell
type
2
fibre
maintenance)
ubiquitin
ligase
E3
component
N-recognin
4
(UBR4
quality
control)
identified
regulator
proteome,
agreement
analyses.
Vacuolar
sorting
13
homolog
A
(VPS13A)
positively
correlated
mass,
glycoprotein/glycolipid
sialylation
enzyme
N-acetylneuraminate
pyruvate
lyase
(NPL)
resistance.
International Journal of Environmental Research and Public Health,
Journal Year:
2025,
Volume and Issue:
22(4), P. 637 - 637
Published: April 18, 2025
Physical
activity
(PA)
and
body
composition
are
important
lifestyle
factors
that
influence
public
health.
Research
suggests
DNA
regions
(CpG
site
locations)
differentially
methylated
in
a
physically
active
population.
This
meta-analysis
aimed
to
identify
CpG
sites
associated
with
various
levels
of
PA
metabolic
pathways.
The
followed
PRISMA
guidelines
using
PubMed,
SportDISCUS,
Embase,
Scopus,
Cochrane
Web
Science.
Epigenomic
analyses
performed
on
participants
no
underlying
health
conditions
were
included.
Articles
screened
Rayyan
AI
extracted
sites,
their
location
confirmed
the
EWAS
catalogue.
Six
studies
comprising
770
subjects
included
this
meta-analysis.
was
clinical
metrics
from
six
showed
BMI,
blood
pressure,
insulin
glucose
testing
significantly
improved
upon
intervention.
Amongst
studies,
total
257
participants,
134
CpGs
located
92
genes
obesity-related
identified
either
belonged
lipid
metabolism
or
signalling
pathway.
which
regulated
multiple
tissue
types
JAZF1
(insulin
signalling,
carbohydrate
pathways)
NAV1
(mTOR
pathway).
In
conclusion,
current
epigenomic
induce
differential
methylation
signatures
affect
metabolism.
To
understand
positive
molecular
effects
PA,
further
research
above
candidate
needs
be
conducted
amongst
bioRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2024,
Volume and Issue:
unknown
Published: March 17, 2024
Abstract
This
study
is
the
first
systematic
meta-analysis
of
epigenetic
age
acceleration
largest
publicly
available
DNA
methylation
data
for
healthy
samples
(93
datasets,
23K
samples),
focusing
on
geographic
and
ethnic
aspects
different
countries
(25
countries)
populations
(31
ethnicities)
around
world.
The
most
popular
tools
assessing
were
examined
in
detail,
their
quality
metrics
analyzed,
ability
to
extrapolate
from
tissue
types
ranges
training
these
models
was
explored.
In
cases,
are
not
consistent
with
each
other
show
signs
acceleration,
PhenoAge
model
tending
systematically
underestimate
versions
GrimAge
overestimate
prediction
subjects.
Although
GEO
open-access
database,
represented,
datasets
use
criteria
determining
controls.
Because
this,
it
difficult
fully
isolate
contribution
“geography/environment”,
“ethnicity”
“healthiness”
acceleration.
However,
DunedinPACE
metric,
which
measures
aging
rate,
adequately
reflects
standard
living
socioeconomic
indicators
countries,
although
can
be
applied
only
blood
data.
When
comparing
males
faster
than
females
considered.
iScience,
Journal Year:
2023,
Volume and Issue:
27(1), P. 108638 - 108638
Published: Dec. 5, 2023
Exercise
training
has
tremendous
systemic
tissue-specific
health
benefits,
but
the
molecular
adaptations
to
long-term
exercise
are
not
completely
understood.
We
investigated
skeletal
muscle
proteome
of
highly
endurance-trained,
strength-trained,
and
untrained
individuals
performed
exercise-
sex-specific
analyses.
Of
6,000+
proteins
identified,
>650
were
differentially
expressed
in
endurance-trained
compared
with
controls.
Strikingly,
92%
shared
higher
expression
both
male
female
endurance
groups
known
mitochondrial.
In
contrast
findings
individuals,
minimal
differences
found
strength-trained
between
females
males.
Lastly,
a
co-expression
network
comparative
literature
analysis
revealed
key
pathways
related
benefits
exercise,
which
primarily
mitochondrial
proteins.
This
is
available
as
an
interactive
database
resource
where
investigators
can
correlate
clinical
data
global
gene
protein
for
hypothesis
generation.
Journal of Applied Physiology,
Journal Year:
2024,
Volume and Issue:
136(4), P. 721 - 738
Published: Feb. 15, 2024
Chronic
alcohol
intoxication
decreases
muscle
strength/function
and
causes
mitochondrial
dysfunction.
Aerobic
exercise
training
improves
oxidative
capacity
increases
mass
strength.
Presently,
the
impact
of
chronic
on
aerobic
exercise-induced
adaptations
was
investigated.
Female
C57BL/6Hsd
mice
were
randomly
assigned
to
one
four
groups:
control
sedentary
(CON
SED;