Pharmacoepidemiology,
Journal Year:
2024,
Volume and Issue:
3(4), P. 365 - 372
Published: Nov. 20, 2024
Glucagon-like
peptide-1
receptor
agonists
(GLP-1
RAs)
have
emerged
as
a
potent
therapeutic
option
for
the
management
of
obesity,
demonstrating
exceptional
efficacy
in
several
large-scale
clinical
trials.
Despite
their
promising
outcomes,
rising
popularity
these
agents
raises
significant
concerns,
particularly
regarding
off-label
use
by
individuals
seeking
weight
loss
aesthetic
reasons
rather
than
addressing
underlying
metabolic
health
conditions.
This
article
critically
evaluates
and
safety
GLP-1
RAs
obesity
management.
Additionally,
it
explores
economic
implications
ethical
challenges
associated
with
increasing
demand
RAs.
By
dimensions,
this
aims
to
facilitate
informed
responsible
decision-making
practice,
highlighting
need
individualized
patient
assessments
careful
consideration
both
short-
long-term
risks.
British Journal of Pharmacology,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Feb. 13, 2025
Obesity
is
a
complex
and
growing
global
concern,
affecting
one
in
eight
individuals
compromising
health,
quality
of
life
expectancy.
It
carries
significant
metabolic,
cardiovascular,
oncological,
hepatorenal,
skeletal
psychiatric
risks,
imposing
substantial
costs
on
health‐care
systems.
Traditional
treatments
have
often
been
ineffective
or
led
to
relapse
after
lifestyle
changes.
Whereas
bariatric
surgery
effective,
it
also
involves
risks
such
as
mortality
hospitalisation.
Semaglutide,
licensed
2018,
synthetic
analogue
glucagon‐like
peptide
1
which
regulates
glucose
metabolism
gastrointestinal
(GI)
motility.
Studies
show
that
semaglutide,
administered
either
weekly
subcutaneously,
daily
orally,
induces
an
average
weight
loss
−11.62
kg
compared
placebo
reduces
waist
circumference
by
up
−9.4
cm.
improves
blood
pressure,
fasting
levels,
C‐reactive
protein
levels
lipid
profiles.
The
most
common
adverse
events
are
mild‐to‐moderate
GI
complaints
occurring
more
frequently
with
administration
than
doses;
hypoglycaemia
without
intervention.
Weight
regain
follows
semaglutide
withdrawal.
Furthermore,
offers
cardiovascular
benefits
for
patients
established
atherosclerotic
disease
(CVD),
lowers
the
risk
kidney
outcomes
cardiovascular‐related
death,
resolves
nonalcoholic
steatohepatitis
many
cases,
positively
impacts
mental
health
life.
In
conclusion,
therapy
could
significantly
benefit
adults
regarding
CVD
if
made
widely
accessible.
Ethical
financial
considerations
must
be
addressed
personalised
obesity
treatment
approaches.
Frontiers in Pharmacology,
Journal Year:
2025,
Volume and Issue:
15
Published: Jan. 20, 2025
Glucagon-like
peptide-1
(GLP-1)
is
a
30-amino
acid
intestinal
insulin-stimulating
factor,
which
mainly
secreted
by
L
cells
in
the
distal
ileum
and
colon.
It
has
various
physiological
functions,
such
as
promoting
insulin
secretion
synthesis,
stimulating
β-cell
proliferation,
inducing
islet
regeneration,
inhibiting
apoptosis
glucagon
release,
delaying
gastric
emptying
controlling
appetite,
etc.
plays
role
through
specific
GLP-1
receptor
(GLP-1R)
distributed
many
organs
or
tissues
participates
regulation
of
glucose
homeostasis
body.
agonists
(GLP-1RAs)
similar
function
GLP-1.
Because
its
structural
difference
from
natural
GLP-1,
it
not
easy
to
be
degraded
dipeptidyl
peptidase-4
(DPP-4),
thus
prolonging
action
time.
GLP-1RAs
have
been
recognized
new
type
hypoglycemic
drugs
widely
used
treatment
2
diabetes
mellitus
(T2DM).
Compared
with
other
non-insulin
drugs,
can
only
effectively
reduce
blood
glycosylated
hemoglobin
(HbA1c),
but
also
protect
cardiovascular
system,
nervous
system
kidney
without
causing
hypoglycemia
weight
gain.
Therefore,
good
application
prospects
potential
for
further
development.
Anesthesiology,
Journal Year:
2024,
Volume and Issue:
141(6), P. 1141 - 1161
Published: Oct. 29, 2024
This
review
discusses
recent
evidence
addressing
risks
in
patients
taking
glucagon-like
peptide-1
receptor
agonist
medications
and
proposes
a
framework
for
perioperative
management.
Biomedicines,
Journal Year:
2024,
Volume and Issue:
12(7), P. 1386 - 1386
Published: June 21, 2024
Cardiovascular
disease
(CVD)
and
kidney
are
the
main
causes
of
morbidity
mortality
in
type
2
diabetes
mellitus
(T2DM).
Globally,
incidence
T2DM
continues
to
rise.
A
substantial
increase
burden
CVD
renal
disease,
alongside
socioeconomic
implications,
would
be
anticipated.
Adopting
a
purely
glucose-centric
approach
focusing
only
on
glycemic
targets
is
no
longer
adequate
mitigate
cardiovascular
risks
T2DM.
In
past
decade,
significant
advancement
has
been
achieved
expanding
pharmaceutical
options
for
T2DM,
with
novel
agents
such
as
sodium-glucose
cotransporter
(SGLT2)
inhibitors
glucagon-like
peptide
receptor
agonists
(GLP-1
RAs)
demonstrating
robust
evidence
cardiorenal
protection.
Combinatorial
approaches
comprising
multiple
pharmacotherapies
combined
single
agent
an
emerging
promising
way
not
enhance
patient
adherence
improve
control
but
also
achieve
potential
synergistic
effects
greater
this
review,
we
provide
update
antidiabetic
appraisal
mechanisms
contributing
Additionally,
offer
glimpse
into
landscape
management
near
future
by
providing
comprehensive
summary
upcoming
early-phase
trials.
Diabetes Obesity and Metabolism,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Feb. 3, 2025
Abstract
Aims
Glucagon‐like
peptide
1
receptor
agonists
and
dual
have
changed
the
treatment
landscape
of
obesity
type
2
diabetes
(T2D),
but
significant
limitations
emerged
due
to
their
gastrointestinal
side
effects,
loss
lean
mass,
necessity
for
ongoing
subcutaneous
injections.
Our
objective
was,
therefore,
test
a
novel
small
molecule
as
different
potentially
better
tolerated
oral
medications
improve
obesity‐associated
impairment
in
glucose
homeostasis.
Materials
Methods
High‐fat
diet
(HFD)‐fed
mice
or
severely
obese,
leptin‐deficient
ob/ob
were
randomly
assigned
serve
controls
receive
TIX100,
thioredoxin‐interacting
protein
(TXNIP)
inhibitor
just
approved
by
FDA
an
investigational
new
drug
(T1D).
The
TIX100
effects
on
intolerance
weight
control
then
assessed.
Results
protected
against
HFD‐induced
intolerance,
hyperinsulinemia,
hyperglucagonemia.
also
reduced
diet‐induced
adiposity
resulting
15%
lower
treated
compared
with
HFD
(
p
<0.05),
while
preserving
mass.
Even
though
lost
mice,
improved
leading
dramatic
2.3%
reduction
HbA1C
independent
any
loss.
This
is
consistent
beneficial
non‐obese
models
its
protection
elevated
TXNIP
islet
cell
stress
common
all
types.
Conclusions
Thus,
may
provide
novel,
therapy
T2D
that
targets
underlying
disease
pathology
including
dysfunction
hyperglucagonemia
promotes
metabolic
health
without
aggressive
Nutrients,
Journal Year:
2025,
Volume and Issue:
17(6), P. 1047 - 1047
Published: March 17, 2025
As
the
prevalence
of
chronic
diseases
persists
at
epidemic
proportions,
health
practitioners
face
ongoing
challenges
in
providing
effective
lifestyle
treatments
for
their
patients.
Even
those
patients
on
GLP-1
agonists,
nutrition
counseling
remains
a
crucial
strategy
managing
these
conditions
over
long
term.
This
paper
aims
to
address
concerns
and
who
are
interested
low-carbohydrate
or
ketogenic
diet,
but
have
about
its
efficacy,
safety,
long-term
viability.
The
authors
this
used
approach
researchers
engaged
study.
reflects
our
opinion
is
not
meant
review
diets
systematically.
In
addressing
common
concerns,
we
hope
show
that
has
been
well
researched
can
no
longer
be
seen
as
“fad
diet”
with
adverse
effects
such
impaired
renal
function
increased
risk
heart
disease.
We
also
persistent
questions
patient
adherence,
affordability,
environmental
sustainability.
perspective
clinicians
study
application
dietary
interventions.
While
systematic
review,
all
factual
claims
substantiated
citations
from
peer-reviewed
literature
most
rigorous
recent
science.
To
knowledge,
first
potential
misconceptions
comprehensively.
BMJ Open Gastroenterology,
Journal Year:
2025,
Volume and Issue:
12(1), P. e001704 - e001704
Published: April 1, 2025
Objective
The
use
of
glucagon-like
peptide
1
receptor
agonists
has
been
associated
with
gastroparesis,
but
little
is
known
about
the
risk
gastroparesis
in
those
obesity
without
type
2
diabetes
(T2D),
and
how
that
compares
other
treatment
modalities
for
obesity.
This
study
aims
to
characterise
relationship
between
different
a
population
pre-existing
T2D.
Methods
A
retrospective
cohort
using
Merative
MarketScan
Research
Databases
individuals
who
underwent
semaglutide,
bupropion-naltrexone
or
sleeve
gastrectomy
from
January
2018
31
December
2022.
incidence
diagnosis
was
evaluated
International
Classification
Diseases,
Version
10
codes.
compared
three
intervention
groups
Cox
proportional
hazards
regression
models.
Results
Of
55
460
included,
36
990
(66.7%)
were
treated
7369
(13.3%)
11
101
(13.7%)
gastrectomy.
Gastroparesis
rates
among
semaglutide
versus
6.5
per
1000
person-years
(PY)
vs
2.1
PY
1.1
PY,
respectively.
After
adjusting
baseline
characteristics,
had
higher
than
(adjusted
HR
3.33,
95%
CI
2.27,
4.98)
6.14,
3.94,
9.57).
Conclusions
There
an
increased
T2D
are
as
Understanding
these
potential
side
effects,
though
rare,
may
help
guide
personalised
regimens.