Kidney Medicine,
Journal Year:
2024,
Volume and Issue:
7(2), P. 100947 - 100947
Published: Dec. 15, 2024
Pure
red
cell
aplasia
(PRCA)
is
a
rare
complication
of
erythropoietin
(EPO)
therapy,
characterized
by
severe
deficiency
in
blood
production.
There
no
guideline
on
the
treatment
for
PRCA
because
there
have
been
too
few
cases
to
perform
prospective
cohort
studies.
The
main
treatments
include
immediate
cessation
EPO,
restrictive
transfusion,
and
immunosuppressive
therapies.
A
35-year-old
male
patient
with
type
1
diabetic
nephropathy
was
diagnosed
PRCA.
Enarodustat
roxadustat
were
administered
successively
after
discontinuation
but
anemia
did
not
improve,
maintained
weekly
transfusions.
Subsequently,
EPO-mimetic
peptide
pegmolesatide
administered,
patient's
hemoglobin
started
increase
week
increased
from
50
g/L
92
over
approximately
3
months.
Based
these
findings,
we
speculate
that
can
provide
safe,
effective,
convenient
therapeutic
strategy
Chinese
patients
chronic
kidney
disease.
Nephrology Dialysis Transplantation,
Journal Year:
2025,
Volume and Issue:
40(Supplement_2), P. ii54 - ii63
Published: March 1, 2025
ABSTRACT
Cancer
and
kidney
diseases
(KD)
intersect
in
many
ways
resulting
worse
outcomes.
Both
conditions
are
correlated
with
cognitive
impairment,
which
can
be
exacerbated
cancer
patients
by
known
effects
of
antineoplastic
drugs
on
cognition,
leading
to
a
phenomenon
as
chemotherapy-related
impairment
(CRCI).
This
manifests
poor
attention
span,
disturbed
short-term
memory,
general
mental
sluggishness.
literature
review
explores
CRCI
investigates
the
potential
impact
KD
this
phenomenon.
Additionally,
we
highlight
shared
pathogenetic
mechanisms
(including
neurotoxicity,
neuroinflammation,
oxidative
stress,
vascular
disease,
electrolyte,
acid-base
imbalances),
clinical
presentation
imaging
findings
between
CRCI.
The
disruption
blood–brain
barrier
might
key
mechanism
for
increased
brain
permeability
anticancer
nephropathic
cancer.
Based
existing
knowledge,
found
heightened
neurotoxicity
synergistic
potentiation
KD.
However,
further
translational
research
is
urgently
required
validate
hypothesis.
European Journal of Clinical Investigation,
Journal Year:
2025,
Volume and Issue:
unknown
Published: April 11, 2025
Cognitive
impairment
is
a
prevalent
complication
in
chronic
kidney
disease
(CKD),
ranging
from
mild
deficits
early
stages
to
more
severe
conditions,
such
as
cognitive
and
dementia
advanced
stages.
CKD
patients
exhibit
reduced
performance
memory,
attention,
language,
visuospatial
abilities
executive
functions.
Contributing
factors
include
uraemic
toxins,
structural
brain
changes,
blood-brain
barrier
dysfunction,
anaemia
comorbidities
like
diabetes
mellitus.
Malnutrition,
affecting
nearly
half
of
patients,
exacerbates
decline
through
inflammation,
oxidative
stress
protein-energy
wasting.
Nutritional
deficiencies,
particularly
protein,
vitamin
D,
B
vitamins,
omega-3
fatty
acids
antioxidants,
are
linked
impaired
cognition.
Emerging
evidence
highlights
the
role
gut-brain
axis,
with
gut-derived
toxins
microbiome
alterations
contributing
dysfunction.
Processed
foods
microplastics
further
compound
risks
by
promoting
inflammation
neurotoxicity.
Dialysis
transplantation
offer
opportunities
for
recovery,
though
challenges
remain,
haemodialysis
patients.
interventions,
including
tailored
protein
intake,
micronutrient
supplementation
dietary
counselling,
critical
mitigating
decline.
Addressing
comorbidities,
targeted
nutritional
pharmacological
strategies,
improves
outcomes.
Integrating
psychological
social
support
enhances
quality
life,
given
high
prevalence
anxiety
depression
Future
research
should
focus
on
personalized
nutrition,
gut
microbiota
modulation
routine
assessments
optimise
care.
A
holistic
approach
combining
medical,
psychosocial
strategies
essential
improving
overall
health
Clinical Kidney Journal,
Journal Year:
2024,
Volume and Issue:
18(2)
Published: Sept. 30, 2024
Cognitive
impairment
is
a
prevalent
and
debilitating
complication
in
patients
with
chronic
kidney
disease
(CKD).
This
position
paper,
developed
by
the
Decline
Nephro-Neurology:
European
Cooperative
Target
network,
provides
guidance
on
epidemiology,
risk
factors,
pathophysiology,
diagnosis
clinical
management
of
CKD-related
cognitive
impairment.
significantly
more
common
CKD
compared
general
population,
particularly
those
undergoing
haemodialysis.
The
development
influenced
complex
interplay
including
uraemic
neurotoxins,
electrolytes
acid-base
disorders,
anaemia,
vascular
damage,
metabolic
disturbances
comorbidities
like
diabetes
hypertension.
Effective
screening
diagnostic
strategies
are
essential
for
early
identification
utilizing
assessment
tools,
neuroimaging
circulating
biomarkers.
impact
various
drug
classes,
antiplatelet
therapy,
oral
anticoagulants,
lipid-lowering
treatments
antihypertensive
drugs,
function
evaluated.
Management
encompass
pharmacological
non-pharmacological
interventions,
recommendations
optimizing
while
managing
complications.
highlights
importance
addressing
through
detection,
careful
medication
tailored
therapeutic
to
improve
patient
outcomes.
Nephrology Dialysis Transplantation,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Oct. 14, 2024
ABSTRACT
Cognitive
decline
is
common
in
patients
with
acute
or
chronic
kidney
disease.
Several
areas
of
brain
function
can
be
affected,
including
short-
and
long-term
memory,
attention
inhibitory
control,
sleep,
mood,
eating
control
motor
function.
disease
shares
risk
factors
cognitive
dysfunction
people
without
disease,
such
as
diabetes,
high
blood
pressure,
sedentary
lifestyle
unhealthy
diet.
However,
additional
kidney-specific
may
contribute,
uremic
toxins,
electrolyte
imbalances,
inflammation,
acid–base
disorders
endocrine
dysregulation.
Traditional
interact
to
cause
damage
the
blood–brain
barrier,
induce
vascular
neurotoxicity
neuroinflammation.
Here,
we
discuss
recent
insights
into
pathomechanisms
from
animal
models
novel
avenues
for
prevention
therapy.
We
focus
on
a
several
that
influence
cognition:
barrier
disruption,
role
skeletal
muscle,
physical
activity
factor
irisin,
emerging
therapeutic
sodium-glucose
cotransporter
2
(SGLT2)
inhibitors
glucagon-like
peptide
1
(GLP-1)
receptor
agonists.
Taken
together,
these
studies
demonstrate
importance
providing
mechanistic
understanding
this
complex
condition
their
potential
explain
mechanisms
therapies.
Pharmaceutical Development and Technology,
Journal Year:
2024,
Volume and Issue:
unknown, P. 1 - 15
Published: Sept. 28, 2024
Erythropoietin
(EPO)
is
a
pivotal
hormone
that
regulates
red
blood
cell
production,
predominantly
synthesized
by
the
kidneys
and
also
produced
liver.
Since
introduction
of
recombinant
human
EPO
(rh-EPO)
in
1989
through
DNA
technology,
therapeutic
landscape
for
anemia
has
been
improved.
rh-EPO's
market
expansion
substantial,
with
its
application
extending
across
various
conditions
such
as
chronic
kidney
disease,
cancer-related
anemia,
other
disorders.
Despite
success,
significant
concerns
remain
regarding
stability
EPO,
which
critical
preserving
biological
activity
ensuring
efficacy
under
diverse
environmental
conditions.
Instability
issues,
including
degradation
loss
activity,
challenge
both
drug
development
treatment
outcomes.
Factors
contributing
to
instability
include
temperature
fluctuations,
light
exposure,
interactions
substances.
To
overcome
these
challenges,
pharmaceutical
research
focused
on
developing
innovative
strategies
stabilizing
agents,
advanced
formulation
techniques,
optimized
storage
This
review
article
explores
multifaceted
aspects
stability,
examining
impact
clinical
development.
It
provides
comprehensive
current
stabilization
strategies,
use
excipients,
lyophilization,
novel
delivery
systems.