Cardiovascular Diabetology,
Journal Year:
2023,
Volume and Issue:
22(1)
Published: June 22, 2023
This
study
aimed
to
assess
the
long-term
effects
of
tofogliflozin,
a
sodium-glucose
cotransporter
2
(SGLT2)
inhibitor,
on
atherosclerosis
progression
and
major
clinical
parameters
in
patients
with
type
diabetes
lacking
an
apparent
history
cardiovascular
disease.This
was
prospective
observational
2-year
extension
"Using
TOfogliflozin
for
Possible
better
Intervention
against
Atherosclerosis
(UTOPIA)"
trial,
randomized
intervention
study.
The
primary
endpoints
represented
changes
carotid
intima-media
thickness
(IMT).
Secondary
included
brachial-ankle
pulse
wave
velocity
(baPWV)
biomarkers
glucose
metabolism,
lipid
renal
function,
risks.The
mean
IMT
common
artery
(IMT-CCA)
significantly
decreased
both
tofogliflozin
(-
0.067
mm,
standard
error
0.009,
p
<
0.001)
conventional
treatment
groups
0.080
SE
throughout
follow-up
period;
however,
no
significant
intergroup
differences
(0.013
95%
confidence
interval
(CI)
-
0.012
0.037,
=
0.32)
were
observed
mixed-effects
model
repeated
measures.
baPWV
increased
group
(82.7
±
210.3
cm/s,
0.008)
but
not
17.5
221.3
0.54),
resulting
difference
100.2
CI
182.8
17.5,
0.018).
Compared
group,
improved
hemoglobin
A1c
high-density
lipoprotein
cholesterol
levels,
body
mass
index,
abdominal
circumference,
systolic
blood
pressure.
frequencies
total
serious
adverse
events
did
vary
between
groups.Tofogliflozin
associated
inhibition
wall
thickening
exerted
positive
various
risk
factors
while
showing
good
safety
profile.
Equine Veterinary Education,
Journal Year:
2024,
Volume and Issue:
unknown
Published: April 8, 2024
Summary
Background
Sodium‐glucose
cotransporter
2
inhibitors
(SGLT2i)
are
being
used
increasingly
in
equine
practice.
While
there
is
emerging
clinical
evidence
of
the
safety
and
efficacy
these
drugs,
currently
no
reports
to
document
owner
experiences
with
treatment.
Objective
The
objective
study
was
report
observations
following
treatment
SGLT2i
horses.
Study
design
A
cross‐sectional
online
survey.
Methods
Horse
owners
were
recruited
via
social
media,
forums
their
veterinarians
participate
an
anonymous
survey
when
treating
horses
SGLT2i.
Results
Three
hundred
forty‐two
responses
met
inclusion
criteria.
Ertugliflozin
most
commonly
prescribed
(79.8%),
common
reasons
for
high
insulin
concentrations
(84.2%)
active
laminitis
(59.7%).
85.3%
reported
had
improved
quality
life
after
commencing
treatment,
while
9.4%
change
5.3%
a
worsening
signs.
Of
who
considered
euthanasia
prior
(
n
=
77),
80.5%
horse's
level
pain
be
either
mild
or
absent
30
days
94.8%
improved.
Most
220,
64.7%)
they
extremely
satisfied
somewhat
72,
21.2%)
Treatment
concerns
included
safety/side
effects,
medication
cost,
availability
long‐term
efficacy.
114
(33.3%)
one
more
initial
adverse
effects
upon
induction
onto
medication,
particularly
excessive
urination
70,
20.5%),
drinking
38,
11.1%),
weight
loss
34,
9.9%)
dullness
26,
7.6%).
Main
limitation
Sampling
bias
through
media
veterinary
practices
reliance
on
subjective
reports.
Conclusion
use
associated
excellent
rates
satisfaction
owner‐reported
horse;
however,
some
observed.
Hypertension Research,
Journal Year:
2024,
Volume and Issue:
47(7), P. 1789 - 1796
Published: April 10, 2024
Although
several
randomized
clinical
trials
have
reported
the
potential
benefit
of
sodium-glucose
cotransporter
2
inhibitors
(SGLT2i)
in
reducing
blood
pressure
(BP),
whether
SGLT2i
can
reduce
incident
hypertension
is
unknown.
We
analyzed
individuals
with
diabetes
who
were
newly
prescribed
or
dipeptidyl
peptidase
4
(DPP4i)
a
large-scale
epidemiological
database.
The
primary
outcome
was
incidence
hypertension.
A
propensity
score
matching
algorithm
employed
to
compare
subsequent
development
between
and
DPP4i
groups.
After
matching,
5708
well-balanced
pairs
users
identified.
administration
associated
reduced
risk
(HR
0.91,
95%
CI:
0.84-0.97).
advantage
use
over
for
generally
consistent
sensitivity
analyses,
subgroup
analyses
showed
that
significantly
lower
men,
patients
baseline
HbA1c
<7.5%,
systolic
≥127
mmHg.
Our
investigation
using
nationwide
real-world
data
demonstrated
diabetes.
Diabetes Obesity and Metabolism,
Journal Year:
2024,
Volume and Issue:
26(8), P. 3248 - 3260
Published: May 19, 2024
Abstract
Aim
To
conduct
a
post
hoc
subgroup
analysis
of
patients
with
type
2
diabetes
(T2D)
from
the
RECAP
study,
who
were
treated
sodium‐glucose
cotransporter‐2
(SGLT2)
inhibitor
and
glucagon‐like
peptide
1
receptor
agonist
(GLP‐1RA)
combination
therapy,
focusing
only
on
those
had
chronic
kidney
disease
(CKD),
to
examine
whether
composite
renal
outcome
differed
between
received
SGLT2
treatment
first
GLP‐1RA
first.
Methods
We
included
438
CKD
(GLP‐1RA‐first
group,
n
=
223;
inhibitor‐first
215)
643
T2D
in
study.
The
incidence
outcome,
defined
as
progression
macroalbuminuria
and/or
≥50%
decrease
estimated
glomerular
filtration
rate
(eGFR),
was
analysed
using
propensity
score
(PS)‐matched
model.
Furthermore,
we
calculated
win
ratio
for
these
outcomes,
which
weighted
following
order:
(1)
both
eGFR
macroalbuminuria;
(2)
only;
(3)
only.
Results
Using
PS‐matched
model,
132
each
group
paired.
outcomes
did
not
differ
two
groups
10%;
17%;
odds
1.80;
95%
confidence
interval
[CI]
0.85
4.26;
p
0.12).
GLP‐1RA‐first
versus
1.83
(95%
CI
1.71
1.95;
<
0.001).
Conclusion
Although
groups,
significant.
These
results
suggest
that,
addition
an
baseline
may
lead
more
favourable
outcomes.
Cureus,
Journal Year:
2025,
Volume and Issue:
unknown
Published: May 4, 2025
Sodium-glucose
co-transporter-2
(SGLT2)
inhibitors
have
demonstrated
significant
cardiovascular
benefits
in
patients
with
type
2
diabetes.
However,
head-to-head
comparisons
between
dapagliflozin
and
empagliflozin,
two
widely
prescribed
SGLT2
inhibitors,
remain
limited.
This
meta-analysis
aimed
to
directly
compare
the
outcomes
of
these
agents
We
conducted
a
comprehensive
literature
search
across
multiple
databases
included
eight
retrospective
studies
enrolling
280,617
(158,352
receiving
empagliflozin
122,265
dapagliflozin).
The
primary
outcome
was
major
adverse
events
(MACE),
secondary
including
all-cause
mortality,
myocardial
infarction,
stroke.
Our
pooled
analysis
revealed
no
difference
MACE
risk
(RR:
1.04;
95%
CI:
0.96
1.13).
Similarly,
differences
were
observed
for
mortality
1.05;
1.15),
infarction
0.94
1.16),
or
stroke
1.00;
0.91
1.09).
Subgroup
analyses
by
gender,
atherosclerotic
disease,
chronic
kidney
disease
status
showed
consistent
results.
heart
failure,
trend
toward
reduced
0.90;
0.82
1.00).
Despite
pharmacokinetic
agents,
our
findings
suggest
comparable
diabetes,
potentially
enhanced
those
failure.
due
lack
studies,
this
finding
should
be
interpreted
caution.
These
results
provide
valuable
insights
clinical
decision-making
when
selecting
reduction
diabetic
patients.
Further
prospective
are
warranted
confirm
explore
potential
mechanistic
agents.
Cardiovascular Diabetology,
Journal Year:
2023,
Volume and Issue:
22(1)
Published: June 22, 2023
This
study
aimed
to
assess
the
long-term
effects
of
tofogliflozin,
a
sodium-glucose
cotransporter
2
(SGLT2)
inhibitor,
on
atherosclerosis
progression
and
major
clinical
parameters
in
patients
with
type
diabetes
lacking
an
apparent
history
cardiovascular
disease.This
was
prospective
observational
2-year
extension
"Using
TOfogliflozin
for
Possible
better
Intervention
against
Atherosclerosis
(UTOPIA)"
trial,
randomized
intervention
study.
The
primary
endpoints
represented
changes
carotid
intima-media
thickness
(IMT).
Secondary
included
brachial-ankle
pulse
wave
velocity
(baPWV)
biomarkers
glucose
metabolism,
lipid
renal
function,
risks.The
mean
IMT
common
artery
(IMT-CCA)
significantly
decreased
both
tofogliflozin
(-
0.067
mm,
standard
error
0.009,
p
<
0.001)
conventional
treatment
groups
0.080
SE
throughout
follow-up
period;
however,
no
significant
intergroup
differences
(0.013
95%
confidence
interval
(CI)
-
0.012
0.037,
=
0.32)
were
observed
mixed-effects
model
repeated
measures.
baPWV
increased
group
(82.7
±
210.3
cm/s,
0.008)
but
not
17.5
221.3
0.54),
resulting
difference
100.2
CI
182.8
17.5,
0.018).
Compared
group,
improved
hemoglobin
A1c
high-density
lipoprotein
cholesterol
levels,
body
mass
index,
abdominal
circumference,
systolic
blood
pressure.
frequencies
total
serious
adverse
events
did
vary
between
groups.Tofogliflozin
associated
inhibition
wall
thickening
exerted
positive
various
risk
factors
while
showing
good
safety
profile.