Diabetology,
Journal Year:
2025,
Volume and Issue:
6(2), P. 12 - 12
Published: Feb. 11, 2025
Background:
The
prospective
relationship
between
coffee
and
tea
consumption
the
risk
of
developing
type
2
diabetes
mellitus
(T2DM)
is
seldom
assessed
in
older
adults.
This
study
investigated
association
10-year
incidence
T2DM
Australian
Method:
Data
were
collected
from
participants
aged
49
years
or
above
at
baseline
Blue
Mountains
Eye
Study
(n
=
1668).
Coffee
intakes
using
a
validated
food
frequency
questionnaire.
was
ascertained
by
self-reported
history,
fasting
blood
glucose
≥
7.0
mmol/L,
use
medication.
Associations
discrete-time
logistic
regression,
adjusting
for
lifestyle
demographic
factors.
Results:
Compared
to
no
consumption,
intake
1
cup/day
associated
with
lower
(multivariate-adjusted
HR:
0.46,
95%
CI:
0.23,
0.91)
follow-up
period.
However,
2–3
cups/day
(HR:
0.66,
0.37,
1.18)
≥4
1.04,
0.52,
2.08)
showed
significant
association.
Tea
any
level
not
significantly
incidence.
Results
similar
after
excluding
implausible
energy
intake.
Conclusions:
In
adults,
moderate
(1
cup/day)
incidence,
while
higher
not.
lack
dose-dependent
effect
warrants
further
investigation.
These
findings
should
be
verified
larger
studies,
considering
different
types
potential
age-related
genetic
iScience,
Journal Year:
2024,
Volume and Issue:
27(3), P. 109221 - 109221
Published: Feb. 15, 2024
Fat
infiltration
in
skeletal
muscle
(also
known
as
myosteatosis)
is
now
recognized
a
distinct
disease
from
sarcopenia
and
directly
related
to
declining
capacity.
Hence,
understanding
the
origins
regulatory
mechanisms
of
fat
vital
for
maintaining
development
improving
human
health.
In
this
article,
we
summarized
triggering
factors
such
aging,
metabolic
diseases
syndromes,
nonmetabolic
diseases,
injury
that
all
induce
muscle.
We
discussed
recent
advances
on
cellular
found
several
cell
types
including
myogenic
cells
non-myogenic
contribute
myosteatosis.
Furthermore,
reviewed
molecular
mechanism,
detection
methods,
intervention
strategies
Based
current
findings,
our
review
will
provide
new
insight
into
regulating
function
lipid
metabolism
treating
muscle-related
diseases.
Cell Reports Medicine,
Journal Year:
2024,
Volume and Issue:
5(1), P. 101372 - 101372
Published: Jan. 1, 2024
Insulin
sensitivity
and
metabolic
flexibility
decrease
in
response
to
bed
rest,
but
the
temporal
causal
adaptations
human
skeletal
muscle
metabolism
are
not
fully
defined.
Here,
we
use
an
integrative
approach
assess
during
rest
provide
a
multi-system
analysis
of
how
circulatory
system
adapt
short-
long-term
(German
Clinical
Trials:
DRKS00015677).
We
uncover
that
intracellular
glycogen
accumulation
after
short-term
accompanies
rapid
reduction
systemic
insulin
less
GLUT4
localization
at
cell
membrane,
preventing
further
deposition
rest.
evidence
link
between
triglycerides,
lipotoxic
ceramides,
sphingomyelins
altered
mitochondrial
structure
function
An
nutrient
overload
therefore
represents
crucial
determinant
for
insensitivity
alterations
prolonged
European Heart Journal,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 20, 2025
Abstract
Background
and
Aims
Skeletal
muscle
(SM)
fat
infiltration,
or
intermuscular
adipose
tissue
(IMAT),
reflects
quality
is
associated
with
inflammation,
a
key
determinant
in
cardiometabolic
disease.
Coronary
flow
reserve
(CFR),
marker
of
coronary
microvascular
dysfunction
(CMD),
independently
body
mass
index
(BMI),
inflammation
risk
heart
failure,
myocardial
infarction,
death.
The
relationship
between
SM
quality,
CMD,
cardiovascular
outcomes
not
known.
Methods
Consecutive
patients
(n
=
669)
undergoing
evaluation
for
artery
disease
cardiac
stress
positron
emission
tomography
demonstrating
normal
perfusion
preserved
left
ventricular
ejection
fraction
were
followed
over
median
6
years
major
adverse
events
(MACEs),
including
death
hospitalization
infarction
failure.
was
calculated
as
stress/rest
blood
flow.
Subcutaneous
(SAT),
SM,
IMAT
areas
(cm2)
obtained
from
simultaneous
attenuation
correction
computed
using
semi-automated
segmentation
at
the
12th
thoracic
vertebra
level.
Results
Median
age
63
years,
70%
female,
46%
nonwhite.
Nearly
half
obese
(46%,
BMI
30–61
kg/m2),
correlated
highly
SAT
(r
.84
r
.71,
respectively,
P
<
.001)
moderately
.52,
.001).
Decreased
increased
IMAT,
but
SAT,
remained
decreased
CFR
(adjusted
.03
.04,
respectively).
In
adjusted
analyses,
both
lower
higher
MACE
[hazard
ratio
1.78
(95%
confidence
interval
1.23–2.58)
per
−1
U
1.53
(1.30–1.80)
+10
cm2
.002
.0001,
respectively],
while
protective
.89
(.81–.97)
.94
(.91–.98)
.01
.003,
respectively].
Every
1%
increase
fatty
[IMAT/(SM
+
IMAT)]
conferred
an
independent
2%
odds
CMD
[CFR
<2,
1.02
(1.01–1.04),
.04]
7%
1.07
(1.04–1.09),
.001].
There
significant
interaction
BMI,
such
that
demonstrated
highest
.02).
Conclusions
Increased
conventional
factors.
presence
infiltration
identified
novel
at-risk
phenotype.
Cell Reports Medicine,
Journal Year:
2025,
Volume and Issue:
unknown, P. 101968 - 101968
Published: Feb. 1, 2025
Highlights•Physical
activity
helps
protect
against
age-related
decline
in
physical
performance•Physical
boosts
mitochondrial
energetics
while
aging
per
se
has
no
impact•Mitochondrial
ROS
production
is
unaffected
by
both
active
and
inactive
men•Mitochondrial
calcium
handling
declines
with
age
linked
to
muscle
performanceSummaryAging-related
atrophy
weakness
contribute
loss
of
mobility,
falls,
disability.
Mitochondrial
dysfunction
widely
considered
a
key
contributing
mechanism
aging.
However,
mounting
evidence
positions
as
confounding
factor,
making
unclear
whether
mitochondria
accumulate
bona
fide
defects
To
disentangle
from
activity-related
adaptations,
we
functionally
profiled
skeletal
51
88
men
aged
20–93.
Physical
status
confers
partial
protection
performance.
respiration
remains
unaltered
participants,
indicating
that
does
not
alter
respiratory
capacity.
reactive
oxygen
species
(ROS)
higher
participants.
In
contrast,
retention
capacity
decreases
regardless
correlates
mass,
performance,
the
stress-responsive
metabokine/mitokine
growth
differentiation
factor
15
(GDF15).
Targeting
may
hold
promise
for
treating
aging-related
impairments.Graphical
abstract
JHEP Reports,
Journal Year:
2023,
Volume and Issue:
6(2), P. 100963 - 100963
Published: Nov. 14, 2023
Metabolic
dysfunction-associated
steatotic
liver
disease
(MASLD)
is
associated
with
an
increased
risk
of
multisystemic
complications,
including
muscle
changes
such
as
sarcopenia
and
myosteatosis
that
can
reciprocally
affect
function.
We
conducted
a
systematic
review
to
highlight
innovative
assessment
tools,
pathophysiological
mechanisms
metabolic
consequences
related
in
MASLD,
based
on
original
articles
screened
from
PUBMED,
EMBASE
COCHRANE
databases.
Forty-six
manuscripts
(14
pre-clinical
32
clinical
studies)
were
included.
Microscopy
(8/14)
tissue
lipid
extraction
are
the
two
main
techniques
used
measure
content
studies.
In
studies,
imaging
most
tool
included
CT
(14/32),
MRI
(12/32)
ultrasound
(4/32).
Assessed
muscles
varied
across
studies
but
mainly
paravertebral
(4/14
pre-clinical;
13/32
lower
limb
(10/14
preclinical;
studies).
Myosteatosis
already
highly
prevalent
non-cirrhotic
stages
MASLD
correlates
activity
when
using
density
assessed
by
CT.
Numerous
found
included:
high-fat
high-fructose
diet,
dysregulation
fatty
acid
transport
ketogenesis,
endocrine
disorders
impaired
microRNA122
pathway
signalling.
this
we
also
uncover
several
potential
insulin
resistance,
progression
steatosis
steatohepatitis
loss
strength.
conclusion,
data
available.
Screening
for
could
be
relevant
context
considering
its
correlation
well
consequences.
Molecular Aspects of Medicine,
Journal Year:
2024,
Volume and Issue:
97, P. 101277 - 101277
Published: May 24, 2024
Excessive
accumulation
of
intermuscular
adipose
tissue
(IMAT)
is
a
common
pathological
feature
in
various
metabolic
and
health
conditions
can
cause
muscle
atrophy,
reduced
function,
inflammation,
insulin
resistance,
cardiovascular
issues,
unhealthy
aging.
Although
IMAT
results
from
fat
muscle,
the
mechanisms
underlying
its
onset,
development,
cellular
components,
functions
remain
unclear.
levels
are
influenced
by
several
factors,
such
as
changes
environment,
type
origin,
extent
duration
trauma,
persistent
activation
fibro-adipogenic
progenitors
(FAPs).
FAPs
diverse
transcriptionally
heterogeneous
population
stromal
cells
essential
for
maintenance,
neuromuscular
stability,
regeneration.
However,
cases
chronic
inflammation
conditions,
expand
differentiate
into
adipocytes,
resulting
development
abnormal
ectopic
IMAT.
This
review
discusses
role
adipogenesis
how
they
remodel
It
highlights
evidence
supporting
FAP-derived
adipocytes
constituents
IMAT,
emphasizing
their
significance
maintenance
well
involvement
disorders,
pathologies
diseases.
We
also
investigated
intricate
molecular
pathways
cell
interactions
governing
FAP
behavior,
adipogenesis,
diseases
deconditioning.
Finally,
we
hypothesize
that
impaired
flexibility
dysfunctional
muscles
impacts
FAPs,
leading
to
A
deeper
understanding
biology
regulating
behavior
fate
new
therapeutic
strategies
debilitating
conditions.