Journal of the Endocrine Society,
Journal Year:
2024,
Volume and Issue:
9(1)
Published: Nov. 14, 2024
Abstract
Introduction
Congenital
and
acquired
damage
to
hypothalamic
nuclei
or
neuronal
circuits
controlling
satiety
energy
expenditure
results
in
obesity
(HO).
To
date,
successful
weight
loss
has
only
been
achieved
a
limited
number
of
affected
patients
across
multiple
drug
trials.
Glucagon-like
peptide-1
(GLP-1)
acts
via
central
pathways
that
are
independent
from
the
hypothalamus
induce
satiety.
GLP-1
receptor
agonists
(GLP-1RAs)
may
provide
an
alternative
approach
treating
HO.
Methods
We
performed
comprehensive
search
Medline,
Google
Scholar,
clinical
trials
registries
(ClinicalTrials.gov;
clinicaltrialsregister.eur).
This
nonsystematic
literature
review
was
conducted
identify
scientific
papers
published
January
2005
February
2024
using
Pubmed
Embase
databases.
Key
words
used
were
GLP-1,
GLP-1RA,
obesity,
suprasellar
tumor,
craniopharyngioma.
Results
Our
identified
7
case
studies,
5
series,
2
relating
use
GLP-1RAs
All
studies
demonstrated
improved
metabolic
function.
In
contrast,
series
variable,
with
some
showing
no
others
demonstrating
moderate
significant
parameters.
ECHO
trial,
nearly
half
subjects
randomized
weekly
exenatide
showed
reduced
body
mass
index
(BMI).
Paradoxically,
BMI
reduction
greater
more
extensive
injuries.
Conclusion
potentially
offer
new
There
is
need
stratify
who
likely
respond.
Further
controlled
required
determine
their
efficacy
either
isolation
combined
other
therapies.
Nutrients,
Journal Year:
2024,
Volume and Issue:
16(22), P. 3841 - 3841
Published: Nov. 9, 2024
Sodium-glucose
cotransporter
2
inhibitors
(SGLT2is)
induce
body
weight
loss,
but
their
effect
on
skeletal
muscle
mass
(SMM)
and
strength
needs
to
be
better
elucidated.
International Journal of Molecular Sciences,
Journal Year:
2024,
Volume and Issue:
25(7), P. 3832 - 3832
Published: March 29, 2024
Glucagon-like
peptide
1
(GLP-1)
and
glucose-dependent
insulinotropic
polypeptide
(GIP)
are
incretins
that
regulate
postprandial
glucose
regulation,
stimulating
insulin
secretion
from
pancreatic
β-cells
in
response
to
food
ingestion.
Modified
GLP-1
receptor
agonists
(GLP-1RAs)
being
administered
for
the
treatment
of
obesity
type
2
diabetes
mellitus
(T2DM).
Strongly
related
those
disorders,
metabolic
dysfunction-associated
steatotic
liver
disease
(MASLD),
especially
its
aggressive
form,
defined
as
steatohepatitis
(MASH),
is
a
major
healthcare
burden
associated
with
high
morbidity
extrahepatic
complications.
GLP-1RAs
have
been
explored
MASH
patients
evident
improvement
dysfunction
enzymes,
glycemic
control,
weight
loss.
Importantly,
combination
GIP
and/or
glucagon
RAs
may
be
even
more
effective
via
synergistic
mechanisms
amelioration
metabolic,
biochemical,
histological
parameters
MASLD
but
also
has
beneficial
impact
on
MASLD-related
In
this
current
review,
we
aim
provide
an
overview
incretins’
physiology,
action,
signaling.
Furthermore,
insight
into
key
pathophysiological
through
which
they
aspects,
well
analyze
clinical
data
human
interventional
studies.
Finally,
discuss
challenges
future
perspectives
pertinent
growing
area
research
medicine.
JMIR Research Protocols,
Journal Year:
2024,
Volume and Issue:
13, P. e62667 - e62667
Published: July 11, 2024
Older
adults
with
type
2
diabetes
mellitus
(T2DM)
or
prediabetes
are
at
increased
risk
of
adverse
changes
in
body
composition,
physical
function,
and
aging-related
biomarkers
compared
to
those
normal
glucose
tolerance.
Semaglutide
is
a
glucagon-like
peptide
1
receptor
agonist
that
has
been
approved
for
T2DM
chronic
weight
management.
Although
semaglutide
effective
loss
management,
its
effects
on
lean
mass,
aging
understudied
older
adults.
Expert Opinion on Drug Safety,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Oct. 19, 2024
This
study
evaluates
the
risk
of
ocular
adverse
events
(AEs)
associated
with
glucagon-like
peptide-1
receptor
agonists
(GLP-1
RAs)
by
analyzing
data
from
FDA
Adverse
Event
Reporting
System
(FAERS)
and
employing
network
pharmacology
methods.
Journal of the Endocrine Society,
Journal Year:
2024,
Volume and Issue:
9(1)
Published: Nov. 14, 2024
Abstract
Introduction
Congenital
and
acquired
damage
to
hypothalamic
nuclei
or
neuronal
circuits
controlling
satiety
energy
expenditure
results
in
obesity
(HO).
To
date,
successful
weight
loss
has
only
been
achieved
a
limited
number
of
affected
patients
across
multiple
drug
trials.
Glucagon-like
peptide-1
(GLP-1)
acts
via
central
pathways
that
are
independent
from
the
hypothalamus
induce
satiety.
GLP-1
receptor
agonists
(GLP-1RAs)
may
provide
an
alternative
approach
treating
HO.
Methods
We
performed
comprehensive
search
Medline,
Google
Scholar,
clinical
trials
registries
(ClinicalTrials.gov;
clinicaltrialsregister.eur).
This
nonsystematic
literature
review
was
conducted
identify
scientific
papers
published
January
2005
February
2024
using
Pubmed
Embase
databases.
Key
words
used
were
GLP-1,
GLP-1RA,
obesity,
suprasellar
tumor,
craniopharyngioma.
Results
Our
identified
7
case
studies,
5
series,
2
relating
use
GLP-1RAs
All
studies
demonstrated
improved
metabolic
function.
In
contrast,
series
variable,
with
some
showing
no
others
demonstrating
moderate
significant
parameters.
ECHO
trial,
nearly
half
subjects
randomized
weekly
exenatide
showed
reduced
body
mass
index
(BMI).
Paradoxically,
BMI
reduction
greater
more
extensive
injuries.
Conclusion
potentially
offer
new
There
is
need
stratify
who
likely
respond.
Further
controlled
required
determine
their
efficacy
either
isolation
combined
other
therapies.