European Journal of Clinical Investigation,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Dec. 20, 2024
Both
chronic
kidney
disease
(CKD)
and
type
2
diabetes
mellitus
(T2DM)
confer
a
high
risk
of
cardiovascular
mortality.
These
entities
frequently
coincide.
The
separate
joint
impact
CKD
T2DM
on
the
major
events
(MACE)
survival
is
unclear.
Frontiers in Endocrinology,
Journal Year:
2025,
Volume and Issue:
16
Published: Feb. 21, 2025
Chronic
kidney
disease
(CKD)
is
a
serious
complication
of
diabetes,
and
the
global
burden
gradually
increasing.
This
study
systematically
analyzed
trends
future
projections
worldwide
chronic
caused
by
type
1
2
diabetes
mellitus
based
on
Global
Burden
Disease
Study
(GBD)
using
data
from
1990
to
2021.
Number
deaths,
Age-standardized
mortality
rates,
disability-adjusted
life
years
(DALYs),
age-standardized
DALYs
rate
were
used
estimate
burden.
The
Estimated
Annual
Percentage
Changes
(EAPCs)
calculate
in
each
subtype
different
regions
assessed
impact
various
age
groups
metabolic
factors
due
diabetes.
ARIMA
model
was
further
predict
Diabetic
nephropathy
2022
2050.
results
showed
that
its
EAPCs
varied
significantly
distribution
across
Sociodemographic
Index
subgroups
countries
as
well
among
204
worldwide.
In
addition,
influence
also
significant
variability.
effects
number
deaths
positively
correlated
with
age.
Different
have
CKD
predicts
will
continue
increase
absence
interventions.
To
effectively
manage
more
accurate
cost-effective
diagnostic
tools
interventions
are
needed
future,
especially
low
-
middle-income
poor
healthcare
resources.
Cardiovascular Diabetology,
Journal Year:
2025,
Volume and Issue:
24(1)
Published: March 20, 2025
Abstract
Background
Familial
hypercholesterolemia
(FH)
is
a
genetic
condition
characterized
by
elevated
LDL-C
and
increased
cardiovascular
risk.
Beyond
levels,
the
impact
of
genotype
on
glucose
homeostasis
has
not
been
well
evaluated.
We
aimed
to
evaluate
glycemic
status
atherosclerotic
injury
in
FH
subjects.
Methods
conducted
cross-sectional
study
322
subjects
lipid-lowering
therapy
without
history
disease.
Biochemical
analyses
as
vascular
profile
assessment
were
obtained
from
all
The
population
was
divided
into
two
groups
according
genotype:
LDL
receptor
(LDLR)
group
non-LDLR
(NLDLR)
group.
Results
LDLR
exhibited
higher
prevalence
low
(LGS)
than
NLDLR
(44.1%
vs.
26%,
p
<
0.01),
whereas
high
(HGS)
more
prevalent
compared
with
(74%
55.9%,
0.01).
peripheral
plaques
(93.4%
73%,
0.05),
while
coronary
artery
calcification
(CAC)
presence
(74.7%
48%,
In
secondary
analysis
stratified
three
based
NLDLR,
defective,
null
groups.
LGS
progressively
group,
HGS
showed
an
inverse
trend
(
for
0.05).
Peripheral
plaque
decreased
CAC
Logistic
regression
that
mutation
inversely
associated
both
0.01)
strongest
association.
Conclusions
mutations
worse
profile,
association
HGS.
integrations
genetic,
lipid
data
could
be
useful
better
identify
metabolic
atherosclerosis
distribution
Graphical
abstract
Research
insights
What
currently
known
about
this
topic?
levels.
protected
pancreatic
β-cells
cholesterol
accumulation.
NGS
improved
diagnosis
genes
implicated
disorder.
key
research
question?
(monogenic
or
mutation/polygenic)
status?
new?
heterogeneous
mutation.
plasma
modulate
subclinical
atherosclerosis.
How
might
studyinfluence
clinical
practice?
Genetic,
lipid,
profiles
FH.
Biomolecules,
Journal Year:
2024,
Volume and Issue:
14(6), P. 687 - 687
Published: June 13, 2024
The
increasing
utilization
of
Glucagon-like
Peptide-1
receptor
agonists
(GLP-1
RAs)
in
managing
type
2
diabetes
mellitus
has
raised
interest
regarding
their
impact
on
thyroid
function.
In
fact,
while
these
agents
are
well
known
for
efficacy
glycemic
control
and
weight
management,
association
with
disorders
requires
clarification
due
to
the
complex
interplay
between
hormones
metabolic
pathways.
Thyroid
dysfunction
commonly
co-occurs
conditions
such
as
obesity,
suggesting
a
profound
interconnection
systems.
This
review
aims
contribute
deeper
understanding
interaction
GLP-1
RAs
clarify
safety
diabetic
patients
disorders.
By
synthesizing
existing
evidence,
this
highlights
that,
despite
various
studies
exploring
topic,
current
evidence
is
inconclusive,
conflicting
results.
It
important
note
that
drugs
relatively
recent,
longer-term
larger
sample
sizes
likely
needed
draw
clearer
conclusions.
Currently,
no
guidelines
provide
definitive
directions
clinical
issue;
however,
it
advisable
include
function
tests
routine
screening
patients,
particularly
those
treated
Ras,
goal
optimizing
patient
care
management.
Cell Communication and Signaling,
Journal Year:
2024,
Volume and Issue:
22(1)
Published: July 5, 2024
Abstract
Background
Accompanied
by
activation
of
the
NOD-like
receptor
protein
3
(NLRP3)
inflammasome,
aberrant
connexin
43
(Cx43)
hemichannel-mediated
ATP
release
is
situated
upstream
inflammasome
assembly
and
inflammation
contributes
to
multiple
secondary
complications
diabetes
associated
cardiometabolic
comorbidities.
Evidence
suggests
there
may
be
a
link
between
Cx43
hemichannel
activity
in
diabetic
kidney.
The
consequences
blocking
tubular
priming/activation
NLRP3
model
kidney
disease
(DKD)
was
investigated.
We
examined
downstream
markers
proinflammatory
chemoattractant
role
secretome
on
macrophage
recruitment
activation.
Methods
Analysis
human
transcriptomic
data
from
Nephroseq
repository
correlated
gene
expression
renal
function
DKD.
Primary
proximal
tubule
epithelial
cells
(RPTECs)
monocyte-derived
macrophages
(MDMs)
were
cultured
high
glucose
inflammatory
cytokines
as
DKD
assess
activity,
epithelial-to-macrophage
paracrine-mediated
crosstalk.
Tonabersat
assessed
for
hemichannels.
Results
Transcriptomic
analysis
biopsies
patients
with
showed
that
increased
declining
glomerular
filtration
rate
(GFR)
proteinuria.
In
vitro,
blocked
glucose/cytokine-dependant
increases
reduced
RPTECs.
observed
reciprocal
relationship
which
exacerbated
release,
events
driven
nuclear
factor
kappa-B
(NFκB)-mediated
priming
opening,
changes
Tonabersat.
Conditioned
media
(CM)
RPTECs
treated
glucose/cytokines
MDMs,
an
effect
when
pre-treated
Co-culture
using
conditioned
Tonabersat-treated
dampened
marker
migration.
Conclusion
Using
DKD,
we
report
first
time
trigger
instigate
NLRP3-induced
Recapitulating
observations
previously
reported
retinopathy,
these
suggest
blockers
(i.e.,
Tonabersat)
dampen
multi-system
damage
diabetes.
Renal Failure,
Journal Year:
2025,
Volume and Issue:
47(1)
Published: Feb. 23, 2025
Objectives
Diabetic
kidney
disease
(DKD)
is
driven
by
mitochondrial
dysfunction
and
immune
dysregulation,
yet
the
mechanistic
interplay
remains
poorly
defined.
This
study
aimed
to
identify
key
molecular
networks
linking
pathways
DKD
progression,
with
a
focus
on
uncovering
biomarkers
therapeutic
targets.
Frontiers in Endocrinology,
Journal Year:
2025,
Volume and Issue:
16
Published: March 24, 2025
Background
Alpha-1-acid
glycoprotein
(AGP)
is
a
vital
acute
phase
reactant
that
increases
when
glomerular
filtration
impaired,
making
it
potential
biomarker
of
kidney
disease.
The
urine
albumin-to-creatinine
ratio
(UACR)
sensitive
indicator
proteinuria
and
frequently
used
to
screen
for
disease
in
its
early
stage.
aim
this
study
was
explore
their
correlation
order
advance
our
understanding
the
mechanisms
underlying
damage.
Methods
This
included
2579
female
participants
with
serum
AGP
UACR
from
National
Health
Nutrition
Examination
Survey
(2015-2018).
We
divided
all
equally
into
three
groups
based
on
concentration.
univariate
multivariate
regression
models
were
assessing
between
UACR.
Subgroup
analyses
then
performed
effect
each
covariate
correlation.
Smoothing
splines
utilized
nonlinear
identify
thresholds
within
it.
Results
After
adjusting
models,
significantly
positively
associated
(p<0.0001).
identified
specific
cohort
non-Hispanic
Black
individuals
under
20
years
age,
characterized
by
BMI
below
25
kg/m²
waist
circumference
80
cm
or
more.
Within
cohort,
those
hypertension
sleep
disorders
but
without
hypercholesterolemia
diabetes
exhibited
higher
(p
<
0.001).
Furthermore,
we
discovered
an
L-shaped
concentration
Specifically,
less
than
140
mg/dL,
plateaued.
Conclusions
first
address
found
threshold
mg/dl.
could
be
target
intervention
reduce
risk
Aging and Disease,
Journal Year:
2025,
Volume and Issue:
unknown, P. 0 - 0
Published: Jan. 1, 2025
Diabetic
retinopathy
(DR)
is
a
leading
cause
of
vision
impairment
and
blindness
among
individuals
with
diabetes
mellitus.
Current
clinical
diagnostic
criteria
mainly
base
on
visible
vascular
structure
changes,
which
are
insufficient
to
identify
diabetic
patients
without
DR
(NDR)
but
dysfunctional
retinopathy.
This
review
focuses
retinal
endothelial
cells
(RECs),
the
first
sense
respond
elevated
blood
glucose.
As
glucose
rises,
RECs
undergo
compensatory
transitional
phases,
correspondingly
altered
molecules
likely
become
biomarkers
targets
for
early
prediction
treatment
NDR
article
elaborated
possible
pathophysiological
processes
focusing
summarized
recently
published
reliable
screening
emerging
intervention
strategies
Additionally,
references
medication
selection
lifestyle
recommendations
this
population
provided.
aims
deepen
understanding
REC
biology
pathophysiology,
emphasizes
importance
detection
intervention,
points
out
future
directions
improve
diagnosis
reduce
occurrence
DR.