Alzheimer s & Dementia,
Journal Year:
2024,
Volume and Issue:
20(9), P. 6008 - 6031
Published: July 28, 2024
Abstract
INTRODUCTION
We
investigate
the
role
of
osteopontin
(OPN)
in
participants
with
Pre‐symptomatic
Alzheimer's
disease
(AD),
mild
cognitive
impairment
(MCI),
and
AD
brains.
METHODS
Cerebrospinal
fluid
(CSF)
OPN,
AD,
synaptic
biomarker
levels
were
measured
109
cognitively
unimpaired
(CU),
parental‐history
positive
Evaluation
Experimental
or
Novel
Treatments
for
Disease
(PREVENT‐AD)
participants,
167
CU
399
MCI
from
Neuroimaging
Initiative
(ADNI)
cohort.
OPN
examined
as
a
function
amyloid
beta
(Aβ)
tau
positivity.
Survival
analyses
investigated
link
between
rate
conversion
to
AD.
RESULTS
In
PREVENT‐AD,
CSF
was
positively
correlated
biomarkers.
PREVENT‐AD
ADNI,
elevated
Aβ
42/40
(+)/total
tau(+)
(+)/phosphorylated
tau181(+)
individuals.
increased
Aβ(+)
positron
emission
tomography
(PET)
PET
individuals,
associated
an
accelerated
autopsy‐confirmed
DISCUSSION
Strong
associations
key
markers
pathophysiology
suggest
significant
neurobiology,
particularly
early
stages
disease.
Highlights
cohort,
we
discovered
that
cerebrospinal
can
indicate
dysfunction,
deposition,
neuronal
loss
elderly
parental
history.
is
beta(+)
Elevated
(AD).
decline
on
Assessment
Scale‐Cognitive
subscale
13,
Montreal
Cognitive
Assessment,
Mini‐Mental
State
Examination,
Clinical
Dementia
Rating
Scale
Sum
Boxes.
mRNA
protein
are
significantly
upregulated
frontal
cortex
Alzheimer s & Dementia,
Journal Year:
2022,
Volume and Issue:
19(1), P. 307 - 317
Published: Oct. 9, 2022
Abstract
Introduction
The
Alzheimer's
Disease
Neuroimaging
Initiative
(ADNI)
aims
to
validate
biomarkers
for
disease
(AD)
clinical
trials.
To
improve
generalizability,
ADNI4
enroll
50‐60%
of
its
new
participants
from
underrepresented
populations
(URPs)
using
biofluid
and
digital
technologies.
has
received
funding
the
National
Institute
on
Aging
beginning
September
2022.
Methods
will
recruit
URPs
community‐engaged
approaches.
An
online
portal
screen
20,000
participants,
4000
whom
(50‐60%
URPs)
be
tested
plasma
APOE
.
From
this,
500
undergo
in‐clinic
assessment
joining
ADNI3
rollover
participants.
Remaining
(∼3500)
longitudinal
cognitive
testing.
add
MRI
sequences
PET
tracers.
Project
1
optimize
in
AD
Results
Discussion
generalizability
results,
use
remote
blood
screening,
continue
providing
clinical,
biomarker,
autopsy
data
investigators.
Alzheimer s & Dementia,
Journal Year:
2023,
Volume and Issue:
19(12), P. 5860 - 5871
Published: Aug. 31, 2023
Abstract
With
the
increase
in
large
multimodal
cohorts
and
high‐throughput
technologies,
potential
for
discovering
novel
biomarkers
is
no
longer
limited
by
data
set
size.
Artificial
intelligence
(AI)
machine
learning
approaches
have
been
developed
to
detect
interactions
complex
sets.
We
discuss
exemplar
uses
evaluate
current
applications
limitations
of
AI
discover
biomarkers.
Remaining
challenges
include
a
lack
diversity
sets
available,
sheer
complexity
investigating
interactions,
invasiveness
cost
some
biomarkers,
poor
reporting
studies.
Overcoming
these
will
involve
collecting
from
underrepresented
populations,
developing
more
powerful
approaches,
validating
use
noninvasive
adhering
guidelines.
By
harnessing
rich
through
international
collaborative
innovation,
we
are
well
positioned
identify
clinically
useful
that
accurate,
generalizable,
unbiased,
acceptable
clinical
practice.
Highlights
may
accelerate
dementia
biomarker
discovery.
suitability
due
size
bias
cohort
selection.
Multimodal
data,
diverse
sets,
improved
real‐world
validation,
interdisciplinary
collaboration
required.
Alzheimer s & Dementia,
Journal Year:
2024,
Volume and Issue:
20(11), P. 8074 - 8096
Published: Oct. 12, 2024
Abstract
INTRODUCTION
Blood
tests
have
the
potential
to
improve
accuracy
of
Alzheimer's
disease
(AD)
clinical
diagnosis,
which
will
enable
greater
access
AD‐specific
treatments.
This
study
compared
leading
commercial
blood
for
amyloid
pathology
and
other
AD‐related
outcomes.
METHODS
Plasma
samples
from
Disease
Neuroimaging
Initiative
were
assayed
with
AD
C2N
Diagnostics,
Fujirebio
ALZPath,
Janssen,
Roche
Quanterix.
Outcomes
measures
positron
emission
tomography
(PET),
tau
PET,
cortical
thickness,
dementia
severity.
Logistic
regression
models
assessed
classification
accuracies
individual
or
combined
plasma
biomarkers
binarized
outcomes,
Spearman
correlations
evaluated
continuous
relationships
between
RESULTS
Measures
p‐tau217,
either
individually
in
combination
biomarkers,
had
strongest
all
DISCUSSION
identified
biomarker
analytes
assays
that
most
accurately
classified
Highlights
p‐tau217
status.
Aβ42/Aβ40
relatively
low
higher
thickness
than
NfL.
Correlations
symptoms
low.
Alzheimer s & Dementia,
Journal Year:
2024,
Volume and Issue:
20(8), P. 5262 - 5270
Published: June 25, 2024
Abstract
INTRODUCTION
Identification
of
individuals
with
mild
cognitive
impairment
(MCI)
who
are
at
risk
developing
Alzheimer's
disease
(AD)
is
crucial
for
early
intervention
and
selection
clinical
trials.
METHODS
We
applied
natural
language
processing
techniques
along
machine
learning
methods
to
develop
a
method
automated
prediction
progression
AD
within
6
years
using
speech.
The
study
design
was
evaluated
on
the
neuropsychological
test
interviews
n
=
166
participants
from
Framingham
Heart
Study,
comprising
90
progressive
MCI
76
stable
cases.
RESULTS
Our
best
models,
which
used
features
generated
speech
data,
as
well
age,
sex,
education
level,
achieved
an
accuracy
78.5%
sensitivity
81.1%
predict
MCI‐to‐AD
years.
DISCUSSION
proposed
offers
fully
procedure,
providing
opportunity
inexpensive,
broadly
accessible,
easy‐to‐administer
screening
tool
prediction,
facilitating
development
remote
assessment.
Highlights
Voice
recordings
exams
coupled
basic
demographics
can
lead
strong
predictive
models
dementia
impairment.
leveraged
AI
recognition
processed
resulting
text
models.
developed
AI‐powered
pipeline
assessment
that
could
enable
cost‐effective
prognosis
Alzehimer's
disease.
Alzheimer s & Dementia,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 8, 2025
Abstract
INTRODUCTION
The
Alzheimer's
Association
and
the
Society
of
Nuclear
Medicine
Molecular
Imaging
convened
a
multidisciplinary
workgroup
to
update
appropriate
use
criteria
(AUC)
for
amyloid
positron
emission
tomography
(PET)
develop
AUC
tau
PET.
METHODS
identified
key
research
questions
that
guided
systematic
literature
review
on
clinical
amyloid/tau
Building
this
review,
developed
17
scenarios
in
which
or
PET
may
be
considered.
A
modified
Delphi
approach
was
used
rate
each
scenario
by
consensus
as
“rarely
appropriate,”
“uncertain,”
“appropriate.”
Ratings
were
performed
separately
stand‐alone
modalities.
RESULTS
For
PET,
seven
rated
appropriate,
two
uncertain,
eight
rarely
appropriate.
five
six
DISCUSSION
provide
expert
recommendations
these
technologies
evolving
landscape
diagnostics
therapeutics
disease.
Highlights
updated
goal
is
assist
clinicians
identifying
useful
guiding
diagnosis
management
patients
who
have,
are
at
risk
for,
cognitive
decline
These
intended
dementia
specialists
spend
significant
proportion
their
effort
caring
with
complaints,
well
serve
general
reference
broader
audience
interested
implementation
practice.
Journal of Nuclear Medicine,
Journal Year:
2025,
Volume and Issue:
unknown, P. jnumed.124.268756 - jnumed.124.268756
Published: Jan. 8, 2025
The
Alzheimer's
Association
and
the
Society
of
Nuclear
Medicine
Molecular
Imaging
convened
a
multidisciplinary
workgroup
to
update
appropriate
use
criteria
(AUC)
for
amyloid
positron
emission
tomography
(PET)
develop
AUC
tau
PET.
Methods:
identified
key
research
questions
that
guided
systematic
literature
review
on
clinical
amyloid/tau
Building
this
review,
developed
17
scenarios
in
which
or
PET
may
be
considered.
A
modified
Delphi
approach
was
used
rate
each
scenario
by
consensus
as
"rarely
appropriate,"
"uncertain,"
"appropriate."
Ratings
were
performed
separately
stand-alone
modalities.
Results:
For
PET,
7
rated
appropriate,
2
uncertain,
8
rarely
appropriate.
5
6
Conclusion:
provide
expert
recommendations
these
technologies
evolving
landscape
diagnostics
therapeutics
disease.
Alzheimer s & Dementia,
Journal Year:
2023,
Volume and Issue:
20(1), P. 652 - 694
Published: Sept. 12, 2023
The
Alzheimer's
Disease
Neuroimaging
Initiative
(ADNI)
aims
to
improve
disease
(AD)
clinical
trials.
Since
2006,
ADNI
has
shared
clinical,
neuroimaging,
and
cognitive
data,
biofluid
samples.
We
used
conventional
search
methods
identify
1459
publications
from
2021
2022
using
data/samples
reviewed
291
impactful
studies.
This
review
details
how
studies
improved
progression
understanding
trial
efficiency.
Advances
in
subject
selection,
detection
of
treatment
effects,
harmonization,
modeling
trials
plasma
biomarkers
like
phosphorylated
tau
showed
promise
for
use.
Biomarkers
amyloid
beta,
tau,
neurodegeneration,
inflammation,
others
were
prognostic
with
individualized
prediction
algorithms
available
online.
Studies
supported
the
cascade,
emphasized
importance
neuroinflammation,
detailed
widespread
heterogeneity
disease,
linked
genetic
vascular
risk,
co-pathologies,
sex,
resilience.
Biological
subtypes
consistently
observed.
Generalizability
results
is
limited
by
lack
cohort
diversity,
an
issue
ADNI-4
address
enrolling
a
diverse
cohort.
Communications Medicine,
Journal Year:
2023,
Volume and Issue:
3(1)
Published: July 25, 2023
Abstract
Background
Racial
and
ethnic
minoritized
groups
are
disproportionately
at
risk
for
Alzheimer’s
Disease
(AD),
but
not
sufficiently
recruited
in
AD
neuroimaging
research
the
United
States.
This
is
important
as
sample
composition
impacts
generalizability
of
findings,
biomarker
cutoffs,
treatment
effects.
No
studies
have
quantified
breadth
race/ethnicity
representation
literature.
Methods
review
identified
median
US-based
samples
available
free
full-text
articles
on
PubMed.
Two
types
published
were
analyzed:
that
directly
report
data
(i.e.,
direct
studies),
do
used
from
a
cohort
study/database
does
this
information
indirect
studies).
Results
Direct
(
n
=
719)
88.9%
white
or
87.4%
Non-Hispanic
white,
7.3%
Black/African
American,
3.4%
Hispanic/Latino
ethnicity,
with
0%
Asian
Native
Hawaiian/Pacific
Islander,
American
Indian/Alaska
Native,
Multiracial,
Other
Race
participants.
Cohort
studies/databases
44)
which
1745)
derived
more
diverse,
84.2%
83.7%
11.6%
4.7%
Hispanic/Latino,
1.75%
Notably,
94%
derive
just
10
studies/databases.
Comparisons
two
time
periods
using
split
publication
year,
1994–2017
2018–2022,
indicate
diversity
has
improved
recently,
particularly
participants
(3.39%
8.29%
2018-2022).
Conclusions
There
still
underrepresentation
all
relative
to
Census
data,
especially
individuals.
The
literature
will
benefit
increased
representative
recruitment
ethnic/racial
minorities.
More
transparent
reporting
needed.