Frontiers in Nutrition,
Год журнала:
2025,
Номер
12
Опубликована: Фев. 26, 2025
Body
mass
index
(BMI)
is
important
for
predicting
the
occurrence
of
metabolic
abnormality,
but
sex
differences
exist.
We
aimed
to
investigate
potential
in
predictive
value
BMI
abnormality
and
calculate
optimal
cut-offs
each
sex.
Participants
(n
=
4,623)
who
attended
a
health
check-up
centre
continuously
Eastern
China
between
January
2022
December
2023
were
evaluated
abnormalities.
calculated
proportions
different
abnormalities
sexes.
Receiver
operating
characteristic
(ROC)
curves
determine
cut-off
values
males
females.
The
recognition
rate
using
men
women
evaluated.
Among
4,623
participants
(2,234
2,389
women),
age-adjusted
prevalence
all
was
significantly
greater
among
than
females
(p
<
0.001).
23.5
kg/m2
(males)
21.8
(females).
When
≥24
used
as
rates
abnormal
factor
male
group
above
50%,
while
they
mostly
below
50%
female
group,
except
hyperglycaemia
hypertriglyceridemia.
However,
females,
when
≥22
value,
that
There
thresholds
population.
Metabolites,
Год журнала:
2025,
Номер
15(1), С. 11 - 11
Опубликована: Янв. 2, 2025
Chronic
kidney
disease
(CKD)
is
a
prevalent
global
health
concern
affecting
approximately
850
million
people
worldwide,
with
significant
and
rising
mortality
rate.
CKD
often
coexists
hyperuricemia
(HSUA),
which
also
increasingly
common
due
to
its
association
hypertension,
obesity,
diabetes.
The
interplay
between
complex;
while
in
vitro
studies
animal
models
support
role
for
uric
acid
mediating
glomerular
tubule-interstitial
damage,
HSUA
has
been
shown
predict
the
onset
progression
of
CKD,
expectations
renal
protection
by
use
urate
lowering
treatment
(ULT)
are
inconsistent.
A
challenge
managing
asymptomatic
patients
lies
determining
appropriate
SUA
threshold
values.
Recent
research,
including
URRAH
project,
sought
identify
cut-offs
predictive
cardiovascular
mortality,
but
these
thresholds
may
vary
depending
on
severity
CKD.
This
variability
complicates
establishment
universal
guidelines
treating
HSUA,
leading
lack
specific
recommendations
clinical
practice.
In
conclusion,
recognized
as
prognostic
factor
risk,
more
research
needed
refine
values
benefit
from
ULT.
Stratification
based
filtration
rate
be
necessary
tailor
treatments
improve
outcomes
this
population.
Pharmaceutics,
Год журнала:
2025,
Номер
17(1), С. 102 - 102
Опубликована: Янв. 14, 2025
The
deposition
of
monosodium
urate
(MSU)
crystals
within
joint
spaces
produces
a
painful
inflammatory
condition
known
as
gout,
specific
form
arthritis.
calls
for
combined
curative
and
preventive
management
model.
A
new
development
in
the
approach
to
gout
is
that
NLRP3-targeted
biologic
agents,
such
monoclonal
therapies,
provide
more
accurate
treatment
by
blocking
pro-inflammatory
cytokines.
Nanoparticle
drug
delivery
enhances
biological
availability
targets,
which
may
increase
therapeutic
efficacy
decrease
general
toxicity.
again
cannot
be
ignored,
mainly
keeping
up
certain
modifications
diet
weight,
along
with
pharmacological
therapies
reduce
uric
acid
(UA)
levels
frequency
acute
attacks.
advancement
genetic
profiling
patients
biomarker
discoveries
drives
trend
towards
building
individualized
medicine
care,
quickly
gaining
ground
most
effective
method
delivering
treatments
individual
patients,
moving
away
from
one-size-fits-all
treatments.
following
paper
aims
an
updated
account
focus
on
recent
developments,
order
enhance
these
approaches,
quality
life
standard
treatment.
Frontiers in Nutrition,
Год журнала:
2025,
Номер
12
Опубликована: Фев. 7, 2025
Hyperuricemia
is
associated
with
several
metabolic
and
cardiovascular
disorders,
traditional
treatments,
such
as
xanthine
oxidase
(XO)
inhibitors,
often
have
limitations,
severe
hypersensitivity
reactions
or
ineffectiveness
in
achieving
target
serum
urate
levels
some
patients.
Quercetin,
a
naturally
occurring
flavonoid,
has
shown
potential
hypouricemic
agent
through
XO
inhibition.
This
study
aims
to
evaluate
the
effect
of
Quercetin
Phytosome™
(QP)
supplementation
across
three
cohort
studies
involving
healthy
adults
various
health
profiles,
exploring
its
safe,
effective
intervention
for
hyperuricemia.
Clinical
data
collected
clinics
Italy
between
September
2021
April
2024
under
real-life
clinical
settings
from
distinct
studies,
were
analyzed.
Cohort
1
consisted
164
participants
(87
QP-treated,
77
probiotic
Streptococcus
salivarius
(S.
salivarius)
K12-treated)
who
monitored
90
days.
2
included
22
mildly
hyperuricemic
disorders
receiving
QP,
while
3
comprised
64
obese
hypercholesterolemia,
further
divided
into
moderately
QP-treated
group
(n
=
20),
Berberine
monacolins
(BM)-treated
22),
normouricemic
BM-treated
22).
QP
was
administered
at
400
mg
quercetin
daily
all
cohorts.
Primary
endpoints
reductions
uric
acid
levels,
secondary
outcomes
effects
on
lipid
profile,
glycemia,
liver
enzymes,
treatment
tolerability.
In
1,
significantly
reduced
by
15.2%
males
13.8%
females,
no
significant
changes
observed
group.
showed
13.1%
reduction
(p
<
0.01)
concurrent
10.2%
triglycerides
0.05).
3,
led
13.7%
decrease
20.8%
0.01),
well
tolerated
cohorts,
minimal,
transient
side
effects.
demonstrates
effect.
Additionally,
triglyceride-lowering
benefits
evident,
particularly
metabolically
compromised
individuals
(Cohorts
3),
where
these
statistically
significant.
With
high
tolerability,
findings
highlight
Phytosome™'s
safe
adjunctive
therapy
hyperuricemia
management,
meriting
investigation
larger,
randomized
trials
confirm
efficacy
safety.
clinicaltrials.gov,
identifier
NCT06652035.
Journal of Inflammation Research,
Год журнала:
2025,
Номер
Volume 18, С. 17 - 30
Опубликована: Янв. 1, 2025
Purpose:
Serum
uric
acid
(SUA)
is
primarily
produced
through
the
hydrolysis
of
purines
in
liver,
with
its
excretion
largely
handled
by
kidneys.
Urate
transporter
1
(URAT1)
inhibitors
are
known
to
enhance
elimination
via
kidneys,
but
they
also
increase
risk
kidney
stone
formation.
Currently,
xanthine
oxidase
(XO)
predominant
uric-lowering
medications
on
market.
Methods:
In
this
study,
we
utilized
single-cell
RNA
sequencing,
spatial
metabolomics,
plasma
flow
cytometry
explore
effects
Tigulixostat
level
and
hyperuricemic
nephropathy
(HN)
Uox-KO
mouse
model.
Results:
discovered
that
(LC350189)
more
effectively
reduced
SUA
levels
resulted
better
renal
outcomes
compared
allopurinol,
without
inducing
liver
injury
urate
knockout
(Uox-KO)
mice.
Mechanistically,
found
improved
HN
promoting
M2
macrophage
polarization.
Conclusion:
These
findings
suggest
as
a
promising
therapeutic
option
for
managing
hyperuricemia
related
conditions.
Keywords:
nephropathy,
Uox-KO,
tigulixostat,
Single-cell
Frontiers in Bioengineering and Biotechnology,
Год журнала:
2025,
Номер
12
Опубликована: Янв. 7, 2025
Uricase
replacement
therapy
is
a
promising
approach
for
managing
hyperuricemia
and
gout
but
hindered
by
challenges
such
as
short
blood
circulation
time,
reduced
catalytic
activity,
excessive
hydrogen
peroxide
(H2O2)
production.
These
limitations
necessitate
innovative
strategies
to
enhance
therapeutic
efficacy
safety.
We
designed
synthesized
RBC@SeMSN@Uri,
red
cell-coated
biomimetic
self-cascade
bioreactor,
which
encapsulates
uricase
(Uri)
selenium-based
nano-scavenger
(SeMSN)
within
RBC
membranes.
This
design
aims
reduce
immunogenicity,
extend
systemic
circulation,
maintain
enzymatic
activity.
In
vitro
assays
were
conducted
evaluate
biocompatibility,
anti-inflammatory
effects,
oxidative
stress
protection.
vivo
experiments
in
models
assessed
efficacy,
biodistribution,
biosafety.
RBC@SeMSN@Uri
effectively
degraded
uric
acid
(UA)
into
allantoin
converted
H2O2
water,
preventing
damage
inflammation.
demonstrated
excellent
biocompatibility
H2O2-induced
inflammatory
responses
compared
free
uricase.
vivo,
the
bioreactor
prolonged
significantly
levels,
alleviated
kidney
damage,
mitigated
symptoms
of
gout.
It
also
targeted
inflamed
joints,
reducing
swelling
inflammation
gouty
arthritis
models.
study
presents
novel
strategy
enzyme
By
integrating
membranes,
addresses
key
traditional
therapies,
offering
enhanced
stability,
superior
efficacy.
platform
holds
potential
broader
applications
protein
or
antibody
delivery
therapies
other
diseases.
The journal of nutrition health & aging,
Год журнала:
2025,
Номер
29(3), С. 100488 - 100488
Опубликована: Янв. 15, 2025
This
study
seeks
to
determine
the
association
between
serum
uric
acid
(SUA)
and
accelerated
aging
among
middle-aged
older
adults
in
China,
as
well
assess
relationship
SUA
trajectories
risk
of
aging.
We
utilized
data
from
China
Health
Retirement
Longitudinal
Study
(CHARLS),
selecting
participants
who
completed
follow-ups
2011
2015.
Biological
age
was
estimated
using
Klemera-Doubal
method,
determined
by
calculating
difference
an
individual's
biological
their
chronological
age.
Logistic
regression
models
were
employed
analyze
baseline
levels,
trajectories,
aging,
adjusting
for
potential
confounding
factors.
A
total
3,520
(average
59.00
years)
included.
The
results
indicated
a
significant
linear
positive
correlation
levels
Compared
group
with
lowest
those
highest
had
markedly
increased
(OR
=
1.5,
95%
CI:
1.23-1.83,
P
<
0.001).
Further
longitudinal
analysis
suggested
that
maintaining
low
level
associated
reduction
indicates
elevated
constitute
factor
adults.
Maintaining
at
low-level
help
slow
down
These
findings
highlight
importance
monitoring
this
demographic,
providing
scientific
basis
developing
interventions
delay
Abstract
Serum
uric
acid
is
an
end‐product
of
purine
metabolism.
Uric
concentrations
in
excess
the
physiological
range
may
lead
to
diseases
such
as
gout,
cardiovascular
disease,
and
kidney
injury.
The
includes
a
variety
cell
types
with
specialized
functions
fluid
electrolyte
homeostasis,
detoxification,
endocrine
functions.
Two‐thirds
excreted
through
kidney,
however,
exploration
markers
new
therapeutic
targets
renal
tissue
hyperuricemia
still
lacking.
Single‐cell
spatial
omics
techniques
represent
major
milestones
life
sciences.
combined
measurement
physical
structure
molecular
characteristics
tissues
facilitates
pathophysiological
processes
underlying
disease
development
discovery
possible
targets.
Here,
spatiotemporal
atlas
hyperuricemic
nephropathy
was
investigated
using
single‐cell
RNA
sequencing,
transcriptomics,
proteomics,
metabolomics
urate
oxidase
knockout
mouse
model.
Several
emerging
pathways
especially
ribosome
metabolism
related
excretion
were
discovered
will
be
further
studies
on
lowering
acid.