Semaglutide
is
a
class
of
long-acting
glucagon-like
peptide-1
receptor
agonists
(GLP1-RA)
used
for
the
treatment
type
2
diabetes
mellitus
(T2DM)
and
obesity.
We
present
31-year-old
female
patient
with
past
medical
history
T2DM
without
complication
no
long-term
or
current
use
insulin,
3
obesity,
hypertension,
hyperlipidemia,
polycystic
ovary
syndrome
(PCOS),
anxiety,
who
underwent
an
esophagogastroduodenoscopy
(EGD)
in
preparation
bariatric
surgery
while
taking
semaglutide.
Despite
appropriately
following
preoperative
fasting
guidelines
American
Society
Anesthesiologists
(ASA),
endoscopy
revealed
food
residue
gastric
body,
necessitating
abortion
procedure
to
reduce
risk
intraoperative
pulmonary
aspiration.
Given
lack
patients
on
semaglutide
date,
delayed
emptying
being
known
side
effect
among
semaglutide,
anesthesiologists
should
be
aware
alternative
methods
ensure
stomach
mitigate
aspiration
during
general
anesthesia.
Diabetes Obesity and Metabolism,
Год журнала:
2022,
Номер
25(1), С. 18 - 35
Опубликована: Окт. 18, 2022
Obesity
is
a
chronic,
relapsing
disease
associated
with
multiple
complications
and
substantial
morbidity,
mortality
health
care
burden.
Pharmacological
treatments
for
obesity
provide
valuable
adjunct
to
lifestyle
intervention,
which
often
achieves
only
limited
weight
loss
that
difficult
maintain.
The
Semaglutide
Treatment
Effect
in
People
(STEP)
clinical
trial
programme
evaluating
once-weekly
subcutaneous
semaglutide
2.4
mg
(a
glucagon-like
peptide-1
analogue)
people
overweight
or
obesity.
Across
STEP
1,
3,
4
8,
was
mean
losses
of
14.9%-17.4%
individuals
without
type
2
diabetes
from
baseline
week
68;
69%-79%
participants
achieved
≥10%
(vs.
12%-27%
placebo)
51%-64%
≥15%
5%-13%
placebo).
In
5,
-15.2%
versus
-2.6%
placebo
104.
(individuals
obesity,
diabetes),
-9.6%
-3.4%
68.
Improvements
cardiometabolic
risk
factors,
including
high
blood
pressure,
atherogenic
lipids
benefits
on
physical
function
quality
life
were
seen
mg.
safety
profile
consistent
across
trials,
primarily
gastrointestinal
adverse
events.
magnitude
reported
the
trials
offers
potential
clinically
relevant
improvement
obesity-related
diseases.
The
development
of
glucagon-like
peptide
1
receptor
agonists
(GLP-1RA)
for
type
2
diabetes
and
obesity
was
followed
by
data
establishing
the
cardiorenal
benefits
GLP-1RA
in
select
patient
populations.
In
ongoing
trials
investigators
are
interrogating
efficacy
these
agents
new
indications,
including
metabolic
liver
disease,
peripheral
artery
Parkinson
Alzheimer
disease.
success
GLP-1–based
medicines
has
spurred
molecular
entities
combinations
with
unique
pharmacokinetic
pharmacodynamic
profiles,
exemplified
tirzepatide,
a
GIP-GLP-1
coagonist.
Simultaneously,
investigational
molecules
such
as
maritide
block
GIP
activate
GLP-1
receptor,
whereas
retatrutide
survodutide
enable
simultaneous
activation
glucagon
receptors.
Here
I
highlight
evidence
medicines,
while
discussing
that
inform
safety,
focusing
on
muscle
strength,
bone
density
fractures,
exercise
capacity,
gastrointestinal
motility,
retained
gastric
contents
anesthesia,
pancreatic
biliary
tract
disorders,
risk
cancer.
Rapid
progress
highly
efficacious
anticipated
differentiation
newer
subsets
will
provide
greater
opportunities
use
personalized
medicine
approaches
to
improve
health
people
living
cardiometabolic
disorders.
Annual Review of Medicine,
Год журнала:
2023,
Номер
74(1), С. 125 - 139
Опубликована: Янв. 27, 2023
Nearly
half
of
Americans
are
projected
to
have
obesity
by
2030,
underscoring
the
pressing
need
for
effective
treatments.
Glucagon-like
peptide
1
receptor
agonists
(GLP-1
RAs)
represent
first
agents
in
a
rapidly
evolving,
highly
promising
landscape
nascent
hormone-based
therapeutics.
With
understanding
neurobiology
expanding,
these
emerging
entero-endocrine
and
endo-pancreatic
combined
or
coformulated
with
GLP-1
RAs
herald
new
era
targeted,
mechanism-based
treatment
obesity.
This
article
reviews
previews
imminent
future
nutrient-stimulated
anti-obesity
Journal of Diabetes Investigation,
Год журнала:
2023,
Номер
14(6), С. 767 - 773
Опубликована: Март 15, 2023
Previous
studies
have
reported
that
the
glucagon-like
peptide-1
receptor
agonist
(GLP-1RA)
delays
gastric
emptying,
and
emptying
was
assessed
by
13
C
breath
test
or
paracetamol
absorption
technique.
However,
neither
of
them
is
clinically
familiar
in
real-world
clinical
practice.
The
purpose
present
study
to
investigate
association
between
GLP-1RA
treatment
residue
an
esophagogastroduodenoscopy.This
a
matched
pair
case-control
study.
population
consisted
1,128
individuals
with
diabetes
who
had
esophagogastroduodenoscopy
at
our
clinic
July
2020
June
2022.
To
account
for
differences
characteristics,
such
as
age,
sex,
insulin
glycated
hemoglobin,
we
carried
out
one-to-one
nearest
neighbor
propensity
score
matching
analysis
patients
without
treatment.
After
matching,
compared
presence
McNemar
treatment.After
selected
205
pairs.
In
score-matched
comparison,
proportion
statistically
significantly
higher
group
(0.49%
vs
5.4%,
P
=
0.004).
details
prescribed
11
were
liraglutide
once
daily
1.8
mg
(n
2),
dulaglutide
weekly
0.75
5),
semaglutide
0.5
2)
1.0
2).GLP-1RA
associated
diabetes.
EClinicalMedicine,
Год журнала:
2024,
Номер
69, С. 102475 - 102475
Опубликована: Фев. 19, 2024
BackgroundNew
obesity
medications
result
in
large
weight
losses.
However,
long-term
adherence
a
real-world
setting
is
challenging,
and
termination
of
medication
results
regain
towards
pre-treatment
body
weight.
Therefore,
we
investigated
whether
loss
improved
composition
are
sustained
better
at
1
year
after
active
treatment
with
glucagon-like
peptide-1
(GLP-1)
receptor
agonist,
supervised
exercise
program,
or
both
combined
for
year.MethodsWe
conducted
post-treatment
study
extension
randomised,
controlled
trial
Copenhagen.
Adults
(aged
18–65
years
initial
mass
index
32–43
kg/m2)
completed
an
eight-week
low-calorie
diet-induced
13.1
kg
(week
−8
to
0)
were
randomly
allocated
(1:1:1:1)
one-year
maintenance
0–52)
either
exercise,
the
GLP-1
agonist
once-daily
subcutaneous
liraglutide
3.0
mg,
combination
liraglutide,
placebo.
166
Participants
phase.
All
randomised
participants
invited
participate
outcome
assessments
one
termination,
week
104.
The
primary
assessment
was
change
from
(at
randomisation,
104)
intention-to-treat
population.
secondary
body-fat
percentage
0–104).
registered
EudraCT,
2015-005585-32,
ClinicalTrials.gov,
NCT04122716.FindingsBetween
Dec
17,
2018,
2020,
109
attended
study.
From
randomisation
0–104),
had
reduced
(−5.1
[95%
CI
−10.0;
−0.2];
P
=
0.040)
(−2.3%-points
[−4.3
−0.3];
0.026)
compared
alone.
More
who
previously
received
maintained
least
10%
placebo
(odds
ratio
[OR]
7.2
[2.4;
21.3])
(OR
4.2
[1.6;
10.8]).
3.7
[1.2;
11.1]).
During
52–104),
6.0
[2.1;
10.0]
larger
2.5
[−1.5
6.5]
treatment.InterpretationThe
addition
pharmacotherapy
seems
improve
healthy
Body
contrast
alone.FundingHelsefonden
Novo
Nordisk
Foundation.