International Journal of Molecular Sciences,
Journal Year:
2023,
Volume and Issue:
24(13), P. 10615 - 10615
Published: June 25, 2023
In
the
context
of
neurodegenerative
disorders,
cognitive
decline
is
frequently
reported
in
older
population.
Recently,
numerous
metabolic
pathways
have
been
implicated
neurodegeneration,
including
signaling
disruption
insulin
and
other
glucose-regulating
hormones.
fact,
Alzheimer's
disease
has
now
considered
as
"type-3
diabetes".
this
review,
we
tried
to
clarify
role
sleep
impairment
third
major
player
complex
relationship
between
diseases.
Altered
may
trigger
or
perpetuate
these
vicious
mechanisms,
leading
development
both
dementia
type
2
diabetes
mellitus.
Finally,
analyzed
reciprocal
interactions
considering
emerging
gut
microbiota
modulating
same
processes.
Conditions
dysbiosis
linked
circadian
rhythm
disruption,
alterations,
release
neurotoxic
products,
all
contributing
neurodegeneration.
a
future
prospective,
could
provide
contribution
explaining
tangled
diabetes.
Frontiers in Neuroendocrinology,
Journal Year:
2024,
Volume and Issue:
73, P. 101131 - 101131
Published: Feb. 16, 2024
This
systematic
review
and
meta-analysis
aimed
to
determine
the
association
between
use
of
sodium-glucose
cotransporter
2
(SGLT-2)
inhibitors
dementia
onset
as
well
cognitive
function
in
patients
with
diabetes
mellitus.
We
comprehensively
searched
MEDLINE,
Embase,
CENTRAL
databases
select
relevant
studies
published
up
August
2023.
The
SGLT-2
significantly
lowers
risk
compared
SGLT-2i
non-users
(Hazard
ratio:
0.68,
95
%
CI:
0.50-0.92).
Furthermore,
our
findings
indicated
a
positive
effect
inhibitor
on
score
improvement,
demonstrated
by
standardized
mean
difference
0.88
(95
0.32-1.44),
particularly
among
populations
mild
impairment
or
dementia.
indicate
potential
role
reducing
These
underscore
need
for
well-controlled
large
clinical
trials
future
research
this
field.
Biomedicines,
Journal Year:
2024,
Volume and Issue:
12(8), P. 1750 - 1750
Published: Aug. 3, 2024
Dementia
is
an
age-related
syndrome
characterized
by
the
progressive
deterioration
of
cognition
and
capacity
for
independent
living.
Diabetes
often
associated
with
cognitive
decline
shares
similar
pathophysiological
mechanisms
dementia,
such
as
systemic
inflammation,
oxidative
stress,
insulin
resistance,
advanced
glycation
end-products
formation.
Therefore,
adequate
diabetes
management
may
reduce
risk
decline,
especially
in
patients
other
comorbidities
factors.
The
sodium
glucose
cotransporter
inhibitors
(SGLT2i)
regulate
renal
reabsorption
blocking
SGLT2
cotransporters
located
proximal
tubules,
causing
glycosuria
intraglomerular
pressure
reduction.
Their
use
helps
to
lower
blood
modifying
water
homeostasis;
these
drugs
are
also
commonly
used
treatment
heart
failure
chronic
kidney
disease,
while
recently,
a
potential
neuroprotective
role
central
nervous
system
has
been
suggested.
aim
our
scoping
review
analyze
current
evidence
about
effects
SGLT2i
adult
patients.
We
performed
literature
evaluate
effect
on
mild
impairment
(MCI)
Alzheimer's
disease
incidence
progression.
screening
process
was
through
different
searches
PubMed
EMBASE,
evaluating
original
works
published
up
January
2024.
In
conclusion,
could
be
diabetes,
reducing
or
progression
MCI
dementia.
Further
prospective
studies
needed
validate
this
hypothesis
effectiveness
class
normal
glycemic
profile
BMJ,
Journal Year:
2024,
Volume and Issue:
unknown, P. e079475 - e079475
Published: Aug. 28, 2024
To
compare
the
risk
of
dementia
associated
with
sodium-glucose
cotransporter-2
(SGLT-2)
inhibitors
versus
dipeptidyl
peptidase-4
(DPP-4)
in
adults
aged
40-69
years
type
2
diabetes.
Annals of Pharmacotherapy,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Feb. 23, 2025
Background:
Adults
with
type
2
diabetes
mellitus
(T2DM)
are
at
an
increased
risk
for
certain
brain
or
psychiatric
disorders,
as
those
without
chronic
kidney
disease
heart
failure.
Whether
sodium-glucose
cotransporter
(SGLT2)
inhibitors
associated
these
diseases
is
unclear.
Objective:
This
systematic
review
and
meta-analysis
aimed
to
investigate
the
effects
of
SGLT2
on
nervous
system
disorders.
Methods:
We
searched
PubMed,
ClinicalTrials.gov,
Web
Science
randomized,
double-blind
placebo-controlled
trials
least
≥24
weeks.
used
Mantel–Haenszel
statistical
method,
ratio
(RR),
95%
confidence
interval
(CI)
dichotomous
variables.
Results:
included
52
publications/trials
covering
111
376
participants
(SGLT2
62
192;
Placebo
49
184).
Sodium-glucose
had
no
significant
effect
ischaemic
stroke
(RR
=
0.97;
CI
0.87-1.09;
P
0.64),
cerebrovascular
accident
1.05;
0.91-1.22;
0.50),
dementia
1.29;
0.78-2.12;
0.32),
carotid
artery
occlusion/carotid
stenosis
1.18;
CI:
0.92-1.53;
0.20),
haemorrhagic
0.84;
0.62-1.12;
0.23),
transient
attack
0.82-1.15;
0.73)
compared
placebo.
No
heterogeneity
was
observed.
However,
showed
slight
reduce
Parkinson’s
(major
failure
subgroup).
Empagliflozin
dapagliflozin
significantly
syncope
1.65;
1.15-2.38;
<
0.01)
1.04-2.61;
0.03),
respectively.
Conclusion
Relevance:
disorders
There
reduced
Disease
observed
in
some
specific
populations.
In
addition,
risks
empagliflozin
concerning
worth
attention.
JAMA Neurology,
Journal Year:
2025,
Volume and Issue:
unknown
Published: April 7, 2025
Importance
The
association
between
glucagon-like
peptide-1
receptor
agonists
(GLP-1RAs)
and
sodium-glucose
cotransporter-2
inhibitors
(SGLT2is)
risk
of
Alzheimer
disease
related
dementias
(ADRD)
remains
to
be
confirmed.
Objective
To
assess
the
ADRD
associated
with
GLP-1RAs
SGLT2is
in
people
type
2
diabetes
(T2D).
Design,
Setting,
Participants
This
target
trial
emulation
study
used
electronic
health
record
data
from
OneFlorida+
Clinical
Research
Consortium
January
2014
June
2023.
Patients
were
50
years
or
older
T2D
no
prior
diagnosis
antidementia
treatment.
Among
396
963
eligible
patients
T2D,
33
858
included
GLP-1RA
vs
other
glucose-lowering
drug
(GLD)
cohort,
34
185
SGLT2i
GLD
24
117
cohort.
Exposures
Initiation
treatment
a
GLP-1RA,
SGLT2i,
second-line
GLD.
Main
Outcomes
Measures
was
identified
using
clinical
codes.
Hazard
ratios
(HRs)
95%
CIs
estimated
Cox
proportional
hazard
regression
models
inverse
probability
weighting
(IPTW)
adjust
for
potential
confounders.
Results
cohort
(mean
age,
65
years;
53.1%
female),
65.8
49.3%
63.8
51.7%
female).
In
IPTW-weighted
cohorts,
incidence
rate
lower
initiators
compared
(rate
difference
[RD],
−2.26
per
1000
person-years
[95%
CI,
−2.88
−1.64]),
yielding
an
HR
0.67
(95%
0.47-0.96).
had
than
(RD,
−3.05
−3.68
−2.42]),
0.57
0.43-0.75).
There
SGLT2is,
RD
−0.09
−0.80
0.63)
0.97
0.72-1.32).
Conclusion
Relevance
both
statistically
significantly
decreased
GLDs,
observed
drugs.
Diabetes Obesity and Metabolism,
Journal Year:
2023,
Volume and Issue:
26(2), P. 441 - 462
Published: Oct. 23, 2023
Abstract
Aims
The
objective
of
this
umbrella
review
and
meta‐analysis
was
to
evaluate
the
effect
diabetes
on
risk
dementia,
as
well
mitigating
antidiabetic
treatments.
Materials
Methods
We
conducted
a
systematic
its
treatment,
focusing
treatment.
searched
MEDLINE/PubMed,
Embase,
PsycINFO,
CINAHL
Cochrane
Library
for
reviews
meta‐analyses
assessing
cognitive
decline/dementia
in
individuals
with
until
2
July
2023.
random‐effects
obtain
ratios
95%
confidence
intervals
estimating
association
metformin,
thiazolidinediones,
pioglitazone,
dipeptidyl
peptidase‐4
inhibitors,
α‐glucosidase
meglitinides,
insulin,
sulphonylureas,
glucagon‐like
peptide‐1
receptor
agonists
(GLP1RAs)
sodium‐glucose
cotransporter‐2
inhibitors
(SGLT2is)
dementia
from
cohort/case‐control
studies.
subgroups
analysed
included
country
world
region.
Risk
bias
assessed
AMSTAR
tool
Newcastle‐Ottawa
Scale.
Results
100
27
studies
(N
=
3
046
661).
Metformin,
GLP1RAs
SGLT2is
were
associated
significant
reduction
dementia.
When
examining
metformin
divided
by
country,
only
United
States.
Moreover,
Western
but
not
Eastern
populations.
No
observed
or
while
meglitinides
sulphonylureas
increased
risk.
Conclusions
reduced
More
longitudinal
aimed
at
determining
their
relative
benefit
different
populations
should
be
conducted.
Diabetes Therapy,
Journal Year:
2024,
Volume and Issue:
15(3), P. 663 - 675
Published: Feb. 10, 2024
Dementia
is
quite
prevalent
and
among
the
leading
causes
of
death
worldwide.
According
to
earlier
research,
diabetes
may
increase
possibility
developing
dementia.
However,
association
between
antidiabetic
agents
dementia
not
yet
clear.
This
investigation
examines
use
sodium-glucose
transporter
2
inhibitors
(SGLT2i)
risk
in
patients
with
diabetes.
Up
April
18,
2023,
four
databases—Europe
PMC,
Medline,
Scopus,
Cochrane
Library—were
searched
for
relevant
literature.
We
included
all
studies
that
examine
adults
who
SGLT2i.
Random-effect
models
were
used
compute
outcomes
this
investigation,
producing
pooled
odds
ratios
(OR)
95%
confidence
intervals
(CI).
Pooled
data
from
seven
observational
revealed
SGLT2i
was
linked
a
lower
people
(OR
0.45,
CI
0.34–0.61;
p
<
0.00001,
I2
=
97%).
The
reduction
due
SGLT2i's
neuroprotective
effect
only
significantly
affected
by
dyslipidemia
(p
0.0004),
but
sample
size
0.2954),
study
duration
0.0908),
age
0.0805),
sex
0.5058),
hypertension
0.0609),
cardiovascular
disease
0.1619),
or
stroke
0.2734).
taking
reduces
incidence
having
beneficial
impact.
Randomized
controlled
trials
(RCTs)
are
still
required
order
verify
findings
our
research.
Diabetes/Metabolism Research and Reviews,
Journal Year:
2024,
Volume and Issue:
40(2)
Published: Feb. 1, 2024
Abstract
Aims
The
effectiveness
of
sodium‐glucose
co‐transporter‐2
inhibitors
(SGLT2i)
on
incident
dementia
in
patients
with
diabetes
and
atrial
fibrillation
(AF)
remains
unknown.
This
study
aimed
to
investigate
the
association
between
SGLT2i
risk
diabetic
AF,
explore
interactions
oral
anticoagulants
or
dipeptidyl
peptidase‐4
(DPP4i).
Materials
Methods
We
conducted
a
cohort
using
Taiwan's
National
Health
Insurance
Research
Database.
Patients
AFwithout
prior
history
established
cardiovascular
diseases,
were
identified.
Using
propensity
score
matching,
810
receiving
matched
1620
not
SGLT2i.
primary
outcome
was
dementia,
secondary
outcomes
included
composite
events
mortality.
Results
After
up
5
years
follow‐up,
use
associated
significantly
lower
(hazard:
0.71,
95%
confidence
interval:
0.51–0.98),
particularly
vascular
(HR:
0.44,
CI:
0.24–0.82).
related
reduced
risks
AF‐related
hospitalisation
0.72,
0.56–0.93),
stroke
0.75,
0.60–0.94),
all‐cause
death
0.33,
0.24–0.44).
protective
effects
consistent
irrespective
concurrent
non‐vitamin
K
antagonist
(NOACs)
DPP4i.
Conclusions
In
hospitalisation,
stroke,
death.
independent
either
NOACs