The Indissociable Triad: Vascular Impairment, Muscle Atrophy, and Cognitive Decline
Enzo Pereira de Lima,
No information about this author
Masaru Tanaka,
No information about this author
Caroline Barbalho Lamas
No information about this author
et al.
Published: Aug. 12, 2024
The
triad
of
vascular
impairment,
muscle
atrophy,
and
cognitive
decline
represents
critical
age-related
conditions
that
significantly
impact
health.
Vascular
impairment
disrupts
blood
flow,
precipitating
mass
reduction
seen
in
sarcopenia
the
neuronal
functions
characteristic
neurodegeneration.
Our
limited
understanding
intricate
relationships
within
this
hinders
accurate
diagnosis
effective
treatment
strategies.
This
review
ana-lyzes
interrelated
mechanisms
contribute
to
these
conditions,
with
a
specific
focus
on
ox-idative
stress,
chronic
inflammation,
impaired
nutrient
delivery.
aim
is
understand
common
pathways
involved
suggest
comprehensive
therapeutic
approaches.
dysfunctions
hinder
circulation
transportation
nutrients,
resulting
sar-copenia
characterized
by
atrophy
weakness.
dysfunction
have
negative
physical
function
quality
life.
Neurodegenerative
diseases
exhibit
comparable
pathophysiological
affect
motor
functions.
Preventive
approaches
encompass
lifestyle
adjustments,
addressing
oxidative
in-flammation,
integrated
therapies
improving
muscular
well-being.
Better
links
can
refine
strategies
yield
better
patient
out-comes.
study
emphasizes
complex
interplay
between
dysfunction,
de-generation,
decline,
highlighting
necessity
for
multidisciplinary
ap-proaches.
Advances
domain
promise
improved
diagnostic
accuracy,
more
thera-peutic
options,
enhanced
preventive
measures,
all
contributing
higher
life
elderly
population.
Language: Английский
Plasma GFAP, NfL and pTau 181 detect preclinical stages of dementia
Frontiers in Endocrinology,
Journal Year:
2024,
Volume and Issue:
15
Published: April 9, 2024
Background
Plasma
biomarkers
are
preferable
to
invasive
and
expensive
diagnostic
tools,
such
as
neuroimaging
lumbar
puncture
that
gold
standard
in
the
clinical
management
of
Alzheimer’s
Disease
(AD).
Here,
we
investigated
plasma
Glial
Fibrillary
Acidic
Protein
(GFAP),
Neurofilament
Light
Chain
(NfL)
Phosphorylated-tau-181
(pTau
181)
AD
its
early
stages:
Subjective
cognitive
decline
(SCD)
Mild
impairment
(MCI).
Material
methods
This
study
included
152
patients
(42
SCD,
74
MCI
36
AD).
All
underwent
comprehensive
neurological
assessment.
Blood
samples
were
collected
for
Apolipoprotein
E
(APOE)
genotyping
biomarker
(GFAP,
NfL,
pTau
measurements.
Forty-three
(7
27
MCI,
9
AD)
a
follow-up
(FU)
visit
after
2
years,
second
sample
was
collected.
levels
detected
using
Simoa
SR-X
technology
(Quanterix
Corp.).
Statistical
analysis
performed
SPSS
software
version
28
(IBM
Statistics).
significance
set
at
p
<
0.05.
Results
GFAP,
NfL
181
lower
SCD
than
patients.
In
particular,
GFAP
statistically
significant
different
between
(
=0.003),
=0.032).
vs
=0.026),
<0.001),
FU
p=0.033
),
p=0.011
=0.002),
=0.003)
=0.003).
concentration
significantly
=0.001),
=0.020).
APOE
ϵ4
carriers,
increase
p<0.001
)
found
p=0.014).
Moreover,
an
association
emerged
age
disease
onset
(p
=
0.021)
pTau181
0.001)
levels.
Discussion
conclusions
promising
diagnosis
prodromic
stages
prognosis
dementia.
Language: Английский
Vascular Impairment, Muscle Atrophy, and Cognitive Decline: Critical Age-Related Conditions
Enzo Pereira de Lima,
No information about this author
Masaru Tanaka,
No information about this author
Caroline Barbalho Lamas
No information about this author
et al.
Biomedicines,
Journal Year:
2024,
Volume and Issue:
12(9), P. 2096 - 2096
Published: Sept. 13, 2024
The
triad
of
vascular
impairment,
muscle
atrophy,
and
cognitive
decline
represents
critical
age-related
conditions
that
significantly
impact
health.
Vascular
impairment
disrupts
blood
flow,
precipitating
the
mass
reduction
seen
in
sarcopenia
neuronal
function
characteristic
neurodegeneration.
Our
limited
understanding
intricate
relationships
within
this
hinders
accurate
diagnosis
effective
treatment
strategies.
This
review
analyzes
interrelated
mechanisms
contribute
to
these
conditions,
with
a
specific
focus
on
oxidative
stress,
chronic
inflammation,
impaired
nutrient
delivery.
aim
is
understand
common
pathways
involved
suggest
comprehensive
therapeutic
approaches.
dysfunctions
hinder
circulation
transportation
nutrients,
resulting
characterized
by
atrophy
weakness.
dysfunction
have
negative
physical
quality
life.
Neurodegenerative
diseases
exhibit
comparable
pathophysiological
affect
motor
functions.
Preventive
approaches
encompass
lifestyle
adjustments,
addressing
integrated
therapies
improving
muscular
well-being.
Better
links
can
refine
strategies
yield
better
patient
outcomes.
study
emphasizes
complex
interplay
between
dysfunction,
degeneration,
decline,
highlighting
necessity
for
multidisciplinary
Advances
domain
promise
improved
diagnostic
accuracy,
more
options,
enhanced
preventive
measures,
all
contributing
higher
life
elderly
population.
Language: Английский
White matter injury, plasma Alzheimer's disease, and neurodegenerative biomarkers on cognitive decline in community‐dwelling older adults: A 10‐year longitudinal study
Qili Hu,
No information about this author
Xiaowen Zhou,
No information about this author
Zhenxu Xiao
No information about this author
et al.
Alzheimer s & Dementia,
Journal Year:
2025,
Volume and Issue:
21(2)
Published: Feb. 1, 2025
Abstract
INTRODUCTION
This
study
aimed
to
investigate
the
synergistic
impact
of
white
matter
injury,
Alzheimer's
disease,
and
neurodegenerative
pathology
on
long‐term
cognitive
decline
dementia
risk
in
older
adults.
METHODS
We
included
262
dementia‐free
participants
with
baseline
follow‐up
interviews
(2010–2021).
At
baseline,
peak
width
skeletonized
mean
diffusivity
(PSMD)
was
assessed
from
diffusion
tensor
imaging.
Plasma
phosphorylated
tau
217
(p‐tau217)
neurofilament
light
chain
(NfL)
were
measured
using
a
single‐molecule
immune‐array
assay.
Cognitive
function
evaluated
Mini‐Mental
State
Examination
(MMSE)
domain‐specific
tests.
RESULTS
Participants
high‐level
PSMD,
p‐tau217,
NfL
showed
fastest
MMSE
(β
=
−0.30)
highest
incidence
3.54/100
person‐years.
A
combination
model
three
markers
demonstrated
good
predictive
value
for
dementia,
incorporating
age,
sex,
education,
apolipoprotein
E
(area
under
curve
0.93,
95%
confidence
interval
0.86,
0.99).
DISCUSSION
Combining
co‐pathology
may
identify
individuals
high
decline.
Highlights
Peak
correlated
decline,
this
correlation
modified
by
plasma
(p‐tau)217
(NfL).
levels
dementia.
exhibited
incident
over
10‐year
period.
Language: Английский
Elevated plasma neurofilament light was associated with multi-modal neuroimaging features in Alzheimer’s disease signature regions and predicted future tau deposition
Qili Hu,
No information about this author
Mengqiu Shi,
No information about this author
Yunfei Li
No information about this author
et al.
BMC Neurology,
Journal Year:
2024,
Volume and Issue:
24(1)
Published: July 6, 2024
Abstract
Background
Neurofilament
Light
(NfL)
is
a
biomarker
for
early
neurodegeneration
in
Alzheimer’s
disease
(AD).
This
study
aims
to
examine
the
association
between
plasma
NfL
and
multi-modal
neuroimaging
features
across
AD
spectrum
whether
predicts
future
tau
deposition.
Methods
The
present
recruited
517
participants
comprising
Aβ
negative
cognitively
normal
(CN-)
(n
=
135),
positive
(CN
+)
(
n
64),
individuals
with
amnestic
mild
cognitive
impairment
(aMCI)
212),
those
diagnosed
dementia
106).
All
underwent
examinations.
Cross-sectional
longitudinal
associations
neuro-imaging
were
evaluated
using
partial
correlation
analysis
linear
mixed
effects
models.
We
also
used
regression
investigate
of
baseline
PET
load.
Mediation
was
explore
effect
on
cognition
mediated
by
these
imaging
biomarkers.
Results
results
showed
that
levels
rate
change
associated
deposition,
brain
atrophy,
connectome,
glucose
metabolism,
perfusion
signature
regions
P
<0.05).
In
both
CN
MCI
participants,
significant
predictive
value
elevating
burden
left
medial
orbitofrontal
cortex
para-hippocampus
(β
0.336,
0.032;
β
0.313,
0.047).
Lastly,
performance.
Conclusions
supports
AD-vulnerable
its
Language: Английский