Medicina,
Год журнала:
2024,
Номер
60(12), С. 2030 - 2030
Опубликована: Дек. 9, 2024
Chronic
respiratory
disorders
are
the
third
leading
cause
of
mortality
globally.
Consequently,
there
is
a
continuous
pursuit
effective
therapies
beyond
those
currently
available.
The
therapeutic
potential
glucagon-like
peptide-1
(GLP-1)
and
glucose-dependent
insulinotropic
polypeptide/GLP-1
(GIP/GLP-1)
receptor
agonists
extends
regulation
glycemia,
including
glucometabolic,
cardiovascular,
renal
effects,
rendering
them
viable
candidates,
due
to
their
mechanisms
action,
for
possible
treatment
disorders.
This
manuscript
aims
provide
comprehensive
evaluation
evidence
on
direct
(cellular)
indirect
(metabolic)
actions
GLP-1
GIP/GLP-1
within
pulmonary
systems.
In
addition,
it
examines
efficacy
in
addressing
prevalent
disorders,
specifically
chronic
obstructive
disease
(COPD),
asthma,
pneumonia,
sleep
apnea,
hypertension,
lung
cancer,
transplantation.
Finally,
seeks
identify
avenues
further
focused
research
this
field.
Diabetology & Metabolic Syndrome,
Год журнала:
2025,
Номер
17(1)
Опубликована: Янв. 10, 2025
Type
2
diabetes
mellitus
(T2DM)
is
usually
complicated
by
cardiovascular
diseases,
hyperglycemia,
and
obesity,
which
worsen
the
outcome
for
patient.
Since
recent
evidence
underlines
epigenetic
role
of
glucagon-like
peptide-1
receptor
agonists
(GLP-1RAs)
in
management
these
comorbidities,
this
study
compared
effects
agents,
namely
liraglutide,
semaglutide,
dulaglutide,
exenatide,
on
miRNA
regulation
T2DM.
GLP-1RAs
modify
expression
miRNAs
involved
endothelial
function,
sugar
metabolism,
adipogenesis,
including
but
not
limited
to
miR-27b,
miR-130a,
miR-210.
Baseline
miR-15a-5p
predict
weight
loss,
while
higher
miR-378-3p
miR-126-3p
levels
are
related
better
glycemic
control
lower
HbA1c
FPG
at
one
year
post-treatment.
miR-375-5p
was
also
reported
as
a
predictor
levels.
Liraglutide
has
protecting
effect
against
pancreatic
β-cell
apoptosis
downregulating
miR-139-5p.
The
highly-expressed
miR-375
islets
can
be
considered
biomarker
assessing
cytoprotective
action
β-cells.
enhance
responsiveness
promoting
GLP-1
through
suppression
miR-204.
While
dulaglutide
reduce
both
systolic
diastolic
blood
pressures,
lixisenatide
exenatide
QW
did
reveal
such
an
effect.
long-acting
exenatide-induced
miR-29b-3p
required
protection
diabetic
cardiomyopathy.
modulates
critical
regulators
cell
function
atherosclerosis,
miR-93-5p,
miR-26a-5p,
miR-181a-5p.
Eventually,
exosomal
miRNAs,
miR-192,
implicated
development
fibrosis
inflammation
T2DM
micro-cardiovascular
outcomes
like
DKD
DR.
Additional
studies
will
needed
elucidation
relations
between
GLP-1RA-induced
clinical-laboratory
findings
concerning
diverse
populations,
gender,
presence
other
comorbid
states
treated
patients
with
Biomedicines,
Год журнала:
2024,
Номер
12(9), С. 2112 - 2112
Опубликована: Сен. 16, 2024
Obesity
is
a
significant
predisposing
factor
for
heart
failure
with
preserved
ejection
fraction
(HFpEF).
Although
substantial
proportion
of
individuals
HFpEF
also
have
obesity,
those
obesity
are
under-represented
in
clinical
trials
failure.
In
turn,
current
guidelines
provided
limited
recommendations
the
medical
management
this
patient
population.
Both
and
diabetes
induce
pro-inflammatory
state
that
can
contribute
to
endothelial
dysfunction
coronary
microvascular
impairment,
finally
resulting
HFpEF.
Additionally,
leads
increased
epicardial
chest
wall
adiposity,
which
enhances
ventricular
interdependence.
This
condition
further
aggravated
by
plasma
blood
volume
expansion
excessive
vasoconstriction,
ultimately
worsening
Despite
well-documented
benefits
GLP-1
receptor
agonists
subjects
diabetes,
or
both,
their
role
obesity-related
remains
unclear.
light
recently
published
literature,
review
aims
investigate
potential
mechanisms
synthesize
available
evidence
regarding
patients
Frontiers in Clinical Diabetes and Healthcare,
Год журнала:
2025,
Номер
5
Опубликована: Янв. 9, 2025
In
recent
years,
glucagon-like
peptide-1
(GLP-1)
receptor
agonists
have
gained
widespread
popularity
not
only
as
effective
agents
in
the
management
of
type
2
diabetes
but
also
for
their
beneficial
impact
on
weight
loss.
Additionally,
this
surge
interest
has
been
underpinned
by
pleiotropic
effects
and
spurred
further
investigation
into
potential
applications
beyond
care.
However,
expanding
adoption
GLP-1
brings
with
it
a
set
challenges
complications.
With
promising
therapeutic
comes
an
increased
scrutiny
side
effects.GLP-1
mimic
action
native
peptide,
enhancing
insulin
secretion,
suppressing
glucagon
release,
slowing
gastric
emptying,
increasing
satiety.
Initially
introduced
to
treat
diabetes,
they
were
found
important
effect
loss;
paradigm
shift
medical
obesity
may
-in
fact
-be
imminent,
per
opinion
non-medical
pundits
[1][2][3].
Drugs
like
semaglutide,
liraglutide
or
tirzepatide
(a
dual
GIP
analog)
led
significant
reduction
participants
clinical
trials
real-world
settings,
making
them
popular
patients
physicians
alike.The
success
lies
multifaceted
mechanisms,
which
address
complex
physiological
pathways
hunger,
satiety,
glucose
metabolism.
These
drugs
target
pancreas
gut
brain's
hypothalamic
appetite-regulating
centers.
Some
analogs
be
attributed
actions
central
nervous
system
neurotransmitter
secretion/action;
enhance
gamma-aminobutyric
acid
(GABA)
activity,
restore
dopaminergic
activity
act
parallel
peptide
YY
(PYY)
[4][5][6].
sense,
are
redefining
approach
metabolic
disease
addressing
glycemic
control
influencing
body
cardiovascular
health.
Currently,
long-term
consequences
analog
use
over
1.5
-2
years
look
promising;
published
meta-analyses,
reduced
morbidity
mortality
noted,
whereas
no
appearance
gastrointestinal
neoplasia
observed
[7][8].The
foster
ongoing
research
new
indications.Evidence
suggests
these
benefits,
studies
indicating
risk
among
people
who
[9][10][11][12].
explored
GLP-1[3]
liver
health,
including
benefit
treatment
dysfunction
associated
fatty
(MASLD)
[13][14].
The
anti-inflammatory
neuroprotective
properties
being
investigated,
implications
neurodegenerative
conditions
Alzheimer's
[15][16][17].
Such
raises
possibility
broader
agonists,
influence
extends
traditional
management.As
exciting
advancements
are,
raise
critical
questions
about
society's
preference
pharmacological
solutions
lifestyle
interventions
diet
exercise.
mindset
many
practitioners,
allure
weight-loss
medications
indeed
outweigh
need
changes,
despite
evidence
that
physical
fundamental
components
sustainable
Surveys
internet
worldwide
indicated
frank
increase
searches
[18][19].
revealed
more
interested
pharmaceutical
loss
than
modifications.
This
trend
is
fueled
relative
ease
accessibility
medications,
coupled
perception
can
yield
rapid,
visible
results
(traditional
social
media
statements
"celebrities"
add
trend).Pharmaceutical
companies
responded
demand
pipeline
drugs,
based
mechanisms
agonists.
focus
pharmacotherapy,
however,
risks
overshadowing
essential
role
nonpharmacological
chronic
prevention
management.
It
healthcare
providers
emphasize
while
play
valuable
plans,
substitutes
balanced
diet,
regular
other
modifications.While
largely
considered
safe,
usage
drawn
attention
rare
adverse
events.
Nonarteritic
anterior
ischemic
optic
neuropathy
(NAION),
idiopathic
injury
nerve
head,
marked
sudden,
painless
vision
eye
swelling
disc,
reported
association
agonists'
use,
though
such
cases
remain
[20].
might
trigger
NAION
yet
fully
understood,
necessary
determine
whether
causal
[4]
relationship
exists.
practice,
experiencing
visual
disturbances
therapy
should
evaluated
promptly,
consideration
given
discontinuing
medication
if
link
suspected.Pancreatitis
known
Although
absolute
low,
pancreatitis
severe
even
life-threatening.
receptors
expressed
pancreas,
researchers
hypothesize
pancreatic
function
ways
could
predispose
certain
individuals
inflammation.
Studies
yielded
mixed
negative
[21-23],
there
definitive
linking
higher
incidence
pancreatitis,
remains
listed
effect.Other
events,
possibly
linked
analogs,
include
muscle
mass
loss,
dermatological/hypersensitivity
reactions,
heart
rate,
left
ventricular
ejection
fraction
depressionThe
emergence
safety
concerns
reinforces
importance
individualized
patient
assessment
before
prescribing
particularly
those
history
disorders
factors.
Healthcare
must
engage
thorough
discussions
patients,
weighing
benefits
against
ensuring
understand
signs
symptoms
events.The
advent
represents
milestone
obesity,
presents
challenge
balancing
drive
innovation
safety.
landscape,
devoid
risks,
detract
from
comprehensive,
While
offer
much
promise,
underscore
reality
pharmacotherapy
alone
cannot
root
causes
diseases.
As
we
move
forward,
will
crucial
develop
nuanced
prescription
drugs.
Educating
modification,
well
essential.
needed
clarify
underlying
events
identify
at
[27].[5]
transformed
landscape
management,
offering
extend
control.However,
reliance
reflects
societal
de-emphasizing
exercise
managing
although
rare,
serves
reminder
complexities
drug
careful
selection
monitoring.
our
pursuit
advancements,
innovative
pharmacotherapies
commitment
safe
responsible
practice.
providers,
responsibility
embrace
tools
modern
medicine
provides
vigilant
safeguarding
health
through
informed,
evidence-based
promise
undeniable,
so
caution
judicious
quest
improve
outcomes.
Biomedicines,
Год журнала:
2024,
Номер
12(11), С. 2503 - 2503
Опубликована: Ноя. 1, 2024
Obstructive
sleep
apnea
(OSA)
is
a
prevalent
condition
associated
with
increased
cardiovascular
risk,
particularly
in
individuals
comorbid
obesity
and
type
2
diabetes
(T2D).
Despite
the
widespread
use
of
continuous
positive
airway
pressure
(CPAP)
for
OSA
management,
adherence
remains
suboptimal,
CPAP
has
not
consistently
demonstrated
reductions
surrogate
events.
Recently,
attention
focused
on
glucagon-like
peptide-1
receptor
agonists
(GLP-1RAs)
sodium-glucose
cotransporter-2
(SGLT2)
inhibitors
as
potential
therapeutic
agents
mitigating
risk
patients.
These
agents,
originally
developed
T2D
have
pleiotropic
effects,
including
significant
weight
loss,
blood
reduction,
amelioration
endothelial
dysfunction
arterial
stiffness,
along
anti-inflammatory
benefits,
which
may
be
beneficial
OSA.
Emerging
clinical
evidence
suggests
that
GLP-1RAs
SGLT2
can
reduce
severity
improve
daytime
sleepiness,
potentially
reversing
adverse
effects
observed
This
review
explores
pathophysiological
mechanisms
linking
disease
evaluates
roles
addressing
Further
research,
long-term
trials,
necessary
to
establish
effectiveness
these
therapies
reducing
events
improving
patients'
reported
outcomes
this
population.
Clinical Pharmacology in Drug Development,
Год журнала:
2025,
Номер
unknown
Опубликована: Апрель 16, 2025
Abstract
This
phase
1,
randomized,
open‐label,
2
×
crossover
study
evaluated
the
bioequivalence
of
fixed‐dose
combination
(FDC)
formulations
alogliptin
(ALO)
and
metformin
extended‐release
(MET
XR)
compared
to
their
individual
assessed
effect
food
on
FDC
pharmacokinetics
in
healthy
participants.
The
comprised
high‐dose
(ALO
25
mg/MET
XR
1000
mg)
low‐dose
12.5
500
mg),
both
conducted
under
fasting
conditions,
fed
conditions.
Among
enrolled
participants,
46
50
completed
study,
45
51
22
26
study.
Plasma
concentrations
were
analyzed
using
liquid
chromatography‐tandem
mass
spectrometry.
geometric
mean
ratios
AUC
last
C
max
for
versus
within
range
(0.80‐1.25)
ALO
MET
XR.
ALO's
unaffected
by
food,
while
exhibited
a
significant
effect,
with
increasing
factor
1.63
T
delayed
hours.
Given
these
findings,
should
be
administered
consistent
monotherapy
recommendations.
Abstract
Background
Comorbid
type
2
diabetes
mellitus
(T2DM),
severe
obesity,
and
chronic
myeloid
leukemia
(CML)
present
therapeutic
challenges,
especially
given
the
limited
data
on
glucagon-like
peptide-1
(GLP-1)
receptor
agonists
in
this
setting.
Methods
We
describe
a
33-year-old
female
with
poorly
controlled
T2DM
(HbA1c
10.7%),
obesity
(BMI
47.05
kg/m
),
stable
CML
tyrosine
kinase
inhibitor
therapy.
She
received
once-weekly
semaglutide
(0.5–1.5
mg)
for
6
months,
alongside
insulin
glargine
dapagliflozin/metformin.
Clinical,
biochemical,
molecular
parameters
were
monitored.
Results
After
her
HbA1c
declined
from
10.7
to
5.5%,
fasting
plasma
glucose
16.2
5.3
mmol/L,
body
weight
decreased
by
18
kg.
Lipid
improved,
analysis
confirmed
continued
remission
(undetectable
BCR-ABL1).
The
patient
experienced
only
mild,
transient
gastrointestinal
side
effects.
Conclusion
In
complex
case,
proved
safe
effective
achieving
glycemic
control
reduction
without
compromising
stability.
These
findings
suggest
that
GLP-1
may
be
viable
option
patients
coexisting
T2DM,
CML,
warranting
further
investigation
broader
populations.