Editora Científica Digital eBooks,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Jan. 1, 2024
Esta
quarta
edição
foi
pensada
a
dar
continuidade
ao
trabalho
realizado
pelo
laboratório
multidisciplinar
de
estudos
e
escrita
científica
em
ciências
da
saúde
–
LaMEECCS
Universidade
Federal
do
Acre
devidamente
registrada
núcleo
CNPQ.
Nós
desenvolvemos
os
mais
variados
na
grande
área
com
nossos
colaboradores,
bem
como
especialistas
todo
o
Brasil,
incluindo
exterior.
Nosso
objetivo
nesta
versão
é
oportunidade
aos
pesquisadores
publicarem
seus
produtos
intelectuais,
dando
maior
visibilidade
conhecimento
nosso
mundo
científico.
Procuramos
avaliar
forma
criteriosa
possível,
qualidade
material
sem
fugir
das
normas
referida
editora.
Nossa
intenção
desenvolver
três
volumes
ano,
inclusive
entre
uma
edições,
serem
somente
trabalhos
conclusões
dos
cursos
graduação
saúde,
estimulando
isso,
que
eles
possam
criar
interesse
as
pesquisas
científicas.
Agradecemos
colaboradores
Brasil
submeterem
edição,
nas
próximas,
continuem
apresentando
suas
obras
futuros.
Eu,
professor
Pós
Dr.
Mauro
José
Deus
Morais,
agradeço
também
outros
revisores
desta
obra
por
contribuir
análises
parcerias,
e,
esperando
mesmos
no
apoio
nossas
futuras.
Cardiovascular Diabetology,
Journal Year:
2023,
Volume and Issue:
22(1)
Published: July 31, 2023
Abstract
Type
2
diabetes
(T2D),
cardiovascular
disease
(CVD)
and
chronic
kidney
(CKD),
are
recognized
among
the
most
disruptive
public
health
issues
of
current
century.
A
large
body
evidence
from
epidemiological
clinical
research
supports
existence
a
strong
interconnection
between
these
conditions,
such
that
unifying
term
cardio-metabolic-renal
(CMR)
has
been
defined.
This
coexistence
remarkable
epidemiological,
pathophysiologic,
prognostic
implications.
The
mechanisms
hyperglycemia-induced
damage
to
cardio-renal
system
well
validated,
as
those
tie
cardiac
renal
together.
Yet,
it
remains
controversial
how
what
extent
CVD
CKD
can
promote
metabolic
dysregulation.
aim
this
review
is
recapitulate
epidemiology
CMR
connections;
discuss
well-established,
putative
emerging
implicated
in
interplay
three
entities;
provide
pathophysiological
background
for
an
integrated
therapeutic
intervention
aiming
at
interrupting
vicious
crosstalks.
Molecular Aspects of Medicine,
Journal Year:
2023,
Volume and Issue:
93, P. 101194 - 101194
Published: June 27, 2023
Heart
failure
is
a
leading
cause
of
mortality
and
hospitalization
worldwide.
Cardiac
fibrosis,
resulting
from
the
excessive
deposition
collagen
fibers,
common
feature
across
spectrum
conditions
converging
in
heart
failure.
Eventually,
either
reparative
or
reactive
nature,
long-term
cardiac
fibrosis
contributes
to
development
progression
associated
with
poor
clinical
outcomes.
Despite
this,
specific
antifibrotic
therapies
are
lacking,
making
an
urgent
unmet
medical
need.
In
this
context,
better
patient
phenotyping
needed
characterize
heterogenous
features
advance
toward
its
personalized
management.
review,
we
will
describe
different
phenotypes
focus
on
potential
usefulness
imaging
techniques
circulating
biomarkers
for
non-invasive
characterization
condition
tracking
impact.
We
also
recapitulate
effects
existing
non-heart
drugs
discuss
strategies
under
preclinical
targeting
activation
fibroblasts
at
levels,
as
well
additional
extracardiac
processes.
Diabetes & Metabolism Journal,
Journal Year:
2024,
Volume and Issue:
48(1), P. 19 - 36
Published: Jan. 4, 2024
Insulin
resistance
has
been
regarded
as
a
hallmark
of
diabetes
heart
disease
(DHD).
Numerous
studies
have
shown
that
insulin
can
affect
blood
circulation
and
myocardium,
which
indirectly
cause
cardiac
hypertrophy
ventricular
remodeling,
participating
in
the
pathogenesis
DHD.
Meanwhile,
hyperinsulinemia,
hyperglycemia,
hyperlipidemia
associated
with
directly
impair
metabolism
function
heart.
Targeting
is
potential
therapeutic
strategy
for
prevention
Currently,
role
pathogenic
development
DHD
still
under
active
research,
pathological
roles
involved
are
complex
not
yet
fully
understood,
related
approaches
well
developed.
In
this
review,
we
describe
add
recent
advances
major
physiological
changes
underlying
mechanisms
by
leads
to
myocardial
remodeling
dysfunction
diabetic
heart,
including
exosomal
dysfunction,
ferroptosis,
epigenetic
factors.
addition,
discuss
improve
accelerate
cardiovascular
protection
drugs.
Frontiers in Pharmacology,
Journal Year:
2024,
Volume and Issue:
14
Published: Jan. 8, 2024
Rhodiola
rosea
is
a
valuable
functional
medicinal
plant
widely
utilized
in
China
and
other
Asian
countries
for
its
anti-fatigue,
anti-aging,
altitude
sickness
prevention
properties.
Salidroside,
most
active
constituent
derived
from
,
exhibits
potent
antioxidative,
hypoxia-resistant,
anti-inflammatory,
anticancer,
anti-aging
effects
that
have
garnered
significant
attention.
The
appreciation
of
the
pharmacological
role
salidroside
has
burgeoned
over
last
decade,
making
it
beneficial
option
treatment
multiple
diseases,
including
atherosclerosis,
Alzheimer’s
disease,
Parkinson’s
cardiovascular
more.
With
renoprotective
effects,
parallel
with
inhibition
oxidative
stress
inflammation,
holds
promise
as
potential
therapeutic
agent
kidney
damage.
This
article
provides
an
overview
microinflammatory
state
disease
discuss
current
strategies,
particular
focus
on
highlighting
recent
advancements
utilizing
renal
disease.
mechanisms
action
are
primarily
associated
regulation
gene
protein
expression
glomerular
endothelial
cells,
podocytes,
tubule
mesangial
cells
cell
carcinoma
cell,
TNF-α,
TGF-β,
IL-1β,
IL-17A,
IL-6,
MCP-1,
Bcl-2,
VEGF,
ECM
protein,
caspase-3,
HIF-1α,
BIM,
well
modulation
AMPK/SIRT1,
Nrf2/HO-1,
Sirt1/PGC-1α,
ROS/Src/Cav-1,
Akt/GSK-3β,
TXNIP-NLRP3,
ERK1/2,
TGF-β1/Smad2/3,
PI3K/Akt,
Wnt1/Wnt3a
β-catenin,
TLR4/NF-κB,
MAPK,
JAK2/STAT3,
SIRT1/Nrf2
pathways.
To
best
our
knowledge,
this
review
first
to
comprehensively
cover
protective
diverse
suggests
great
be
developed
drug
metabolic
syndrome,
cerebrovascular
diseases
complications.
Antioxidants,
Journal Year:
2024,
Volume and Issue:
13(6), P. 687 - 687
Published: June 3, 2024
Affecting
millions
of
people
worldwide,
chronic
kidney
disease
is
a
serious
medical
problem.
It
results
in
decrease
glomerular
filtration
rate
below
60
mL/min/1.73
m,
albuminuria,
abnormalities
urine
sediment
and
pathologies
detected
by
imaging
studies
lasting
minimum
3
months.
Patients
with
CKD
develop
uremia,
as
result
the
accumulation
uremic
toxins
body,
patients
can
be
expected
to
suffer
from
number
consequences
such
progression
renal
fibrosis,
development
atherosclerosis
or
increased
incidence
cardiovascular
events.
Another
key
element
pathogenesis
oxidative
stress,
resulting
an
imbalance
between
production
antioxidants
reactive
oxygen
species.
Oxidative
stress
contributes
damage
cellular
proteins,
lipids
DNA
increases
inflammation,
perpetuating
dysfunction.
Additionally,
fibrogenesis
involving
fibrous
tissue
kidneys
occurs.
In
our
review,
we
also
included
examples
forms
therapy
for
CKD.
To
improve
condition
patients,
pharmacotherapy
used,
described
review.
Among
drugs
that
prognosis
CKD,
include:
GLP-1
analogues,
SGLT2
inhibitors,
Finerenone
monoclonal
antibody—Canakinumab
Sacubitril/Valsartan.
Pharmaceutics,
Journal Year:
2023,
Volume and Issue:
15(5), P. 1343 - 1343
Published: April 27, 2023
The
diabetes
epidemic
and
the
increasing
number
of
patients
with
diabetic
chronic
vascular
complications
poses
a
significant
challenge
to
health
care
providers.
Diabetic
kidney
disease
is
serious
diabetes-mediated
complication
represents
burden
for
both
society
in
general.
not
only
major
cause
end
stage
renal
but
also
paralleled
by
an
increase
cardiovascular
morbidity
mortality.
Any
interventions
delay
development
progression
are
important
reduce
associated
burden.
In
this
review
we
will
discuss
five
therapeutic
tools
prevention
treatment
disease:
drugs
inhibiting
renin–angiotensin–aldosterone
system,
statins,
more
recently
recognized
sodium-glucose
co-transporter-2
inhibitors,
glucagon-like
peptide
1
agonists,
novel
non-steroidal
selective
mineralocorticoid
receptor
antagonist.
Frontiers in Endocrinology,
Journal Year:
2023,
Volume and Issue:
14
Published: June 30, 2023
Diabetic
kidney
disease
(DKD)
is
a
common
microangiopathy
in
diabetic
patients
and
the
main
cause
of
death
patients.
The
manifestations
DKD
are
proteinuria
decreased
renal
filtration
capacity.
glomerular
rate
urinary
albumin
level
two
most
important
hallmarks
progression
DKD.
classical
treatment
controlling
blood
glucose
pressure.
However,
commonly
used
clinical
therapeutic
strategies
existing
biomarkers
only
partially
slow
roughly
predict
progression.
Therefore,
novel
methods,
targets
urgently
needed
to
meet
requirements.
In
recent
years,
increasing
attention
has
been
given
role
epigenetic
modification
pathogenesis
Epigenetic
variation
mainly
includes
DNA
methylation,
histone
changes
noncoding
RNA
expression
profile,
which
deeply
involved
DKD-related
inflammation,
oxidative
stress,
hemodynamics,
activation
abnormal
signaling
pathways.
Since
reversible
at
certain
stages,
it
valuable
identify
modifications
as
early
diagnosis
prevent
end-stage
(ESRD).
Because
current
understanding
mechanism
not
comprehensive,
purpose
this
review
summarize
occurrence
development
evaluate
value
therapies
Journal of the American Heart Association,
Journal Year:
2024,
Volume and Issue:
13(12)
Published: June 6, 2024
The
mineralocorticoid
receptor
plays
a
significant
role
in
the
development
of
chronic
kidney
disease
(CKD)
and
associated
cardiovascular
complications.
Classic
steroidal
antagonists
are
therapeutic
option,
but
their
use
clinic
is
limited
due
to
risk
hyperkalemia
patients
with
CKD.
Finerenone
nonsteroidal
antagonist
that
has
been
recently
investigated
2
large
phase
III
clinical
trials
(FIDELIO-DKD
[Finerenone
Reducing
Kidney
Failure
Disease
Progression
Diabetic
Disease]
FIGARO-DKD
Cardiovascular
Mortality
Morbidity
Disease]),
showing
reductions
outcomes.
Pragmatic and Observational Research,
Journal Year:
2025,
Volume and Issue:
Volume 16, P. 27 - 37
Published: Feb. 1, 2025
This
study
aimed
to
describe
the
characteristics,
treatment
patterns,
adverse
events
(AEs),
and
clinical
outcomes
of
patients
starting
steroidal
mineralocorticoid
receptor
antagonists
(sMRAs)
in
real-world
settings.
The
RELICS
study,
complementing
survey-based
RELICS-PS
was
a
retrospective
cohort
conducted
using
Healthcare
Integrated
Research
Database
(HIRD®),
single-payer
healthcare
database
with
medical
pharmacy
claims
from
health
insurance
plans
across
United
States.
A
adults
initiating
sMRAs
January
2016
June
2021
divided
into
six
subgroups:
three
mutually
exclusive
heart
failure
(HF)
subgroups,
two
chronic
kidney
disease
(CKD)
"all
other
patients"
subgroup,
which
included
those
without
documented
HF
or
CKD.
Outcomes
assessed
first
sMRA
fill
until
death,
health-plan
disenrollment,
2022
(whichever
came
first)
analysis
AEs,
outcomes.
Factors
associated
discontinuation
were
evaluated
multivariate
logistic
regression.
Of
224,100
initiators
identified,
76.4%
did
not
have
CKD
(ie,
subgroup).
subgroup
younger
primarily
female.
Across
all
initiators,
72.3%
nonadherent,
73.0%
discontinued
within
median
90
days
initiation.
these
discontinuers,
44.2%
restarted
91
discontinuation.
decreasing
odds
most
subgroups
higher
comorbidity
burden,
use
cardiovascular
medications,
cardiologist
prescribing.
These
findings
consistent
subgroups.
AEs
varied
line
baseline
profiles.
Patients
such
as
both
T2D
rather
than
alone,
experienced
worse
High
rates
subsequent
restart
observed
implying
fluctuating
use.
However,
heightened
risk
may
decrease