Perioperative Biomarkers: Updates, Utility, and Future Directions
International Anesthesiology Clinics,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Feb. 4, 2025
Language: Английский
Exploring the interplay of glucose metabolism, insulin resistance, and neurodegenerative pathologies: insights from streptozotocin and hypoglycaemic in vitro models
Journal of Neural Transmission,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Feb. 11, 2025
Language: Английский
Diagnostic performance of S100B assay for intracranial hemorrhage detection in patients with mild traumatic brain injury under antiplatelet or anticoagulant therapy
Paul-André Poislane,
No information about this author
Mathilde Papin,
No information about this author
Damien Masson
No information about this author
et al.
Scientific Reports,
Journal Year:
2025,
Volume and Issue:
15(1)
Published: Feb. 17, 2025
The
sampling
of
S100B
protein
has
been
proposed
as
a
screening
tool
to
identify
patients
with
low
risk
post-traumatic
intracranial
hemorrhage.
Its
performance
for
on
antiplatelet
agents
or
anticoagulants
is
still
debatable.
This
exploratory
study
evaluates
the
diagnostic
accuracy
concentrations,
measured
within
3
h
head
trauma,
rule
out
hemorrhage
in
adults
anticoagulant
therapy.
prospective
enrolled
adult
presenting
trauma
last
and
under
antiplatelets
anticoagulants.
We
hypothesized
that
concentration
0,100
µg.L-1
negative
predictive
value
over
0,99.
Sensitivity,
specificity,
positive
were
analyzed.
From
June
2020
January
2023,
155
included.
119
had
level
at
over.
8
an
sensitivity
was
1
(95%CI
0,68-1),
specificity
0,25
0,18
-
0,32),
0,07
0.03-0.13),
0,90
1).
suggests
when
performed
3-hour
period
after
mild
measurement
accurate
treated
Language: Английский
Author Response: Blood Astrocyte Biomarkers in Alzheimer Disease: A Systematic Review and Meta-Analysis
Neurology,
Journal Year:
2025,
Volume and Issue:
104(6)
Published: Feb. 21, 2025
Language: Английский
Editors' Note: Blood Astrocyte Biomarkers in Alzheimer Disease: A Systematic Review and Meta-Analysis
Neurology,
Journal Year:
2025,
Volume and Issue:
104(6)
Published: Feb. 21, 2025
Language: Английский
Reader Response: Blood Astrocyte Biomarkers in Alzheimer Disease: A Systematic Review and Meta-Analysis
Neurology,
Journal Year:
2025,
Volume and Issue:
104(6)
Published: Feb. 21, 2025
Language: Английский
Short sleep and obesity in midlife and the risk of cognitive decline and incident dementia in later life: the Whitehall II cohort study
Wellcome Open Research,
Journal Year:
2025,
Volume and Issue:
10, P. 91 - 91
Published: Feb. 21, 2025
Obesity
and
short
sleep
duration
have
both
been
associated
with
an
increased
risk
of
dementia,
but
their
combined
impact
the
underlying
mechanisms
are
not
yet
fully
understood.
Our
aim
is
to
investigate
separate
associations
obesity
cognitive
decline
dementia
risk,
whether
these
mediated
by
neuroinflammatory
responses
metabolic
disturbances,
as
indicated
blood-based
biomarkers.
This
a
prospective
cohort
study
adults
who
were
free
had
data
on
BMI
at
baseline
in
1997-1999,
tracked
for
diagnoses
until
2023
via
linkage
electronic
health
records.
Participants
will
be
divided
into
four
groups:
(1)
reference
group
(2)
(≤6
hours)
non-obese
weight;
(3)
normal
(≥30kg/m2);
(4)
obesity,
main
exposure
group.
Baseline
biomarkers
include
glial
fibrillary
acidic
protein
(GFAP),
chitinase-3-like
(YKL-40),
triggering
receptor
expressed
myeloid
cells
2
(TREM2),
neurofilament-light
chain
(NfL),
brain-derived
neurotrophic
factor
(BDNF),
measured
from
EDTA
plasma,
well
insulin
resistance
fasting
serum
samples.
Cognitive
status,
using
tests
executive
function,
memory,
phonemic
fluency
semantic
fluency,
was
assessed
2002-2004,
2007-2009,
2012-2013,
2015-2016.
We
use
linear
mixed-effects
models
Cox
proportional
hazard
examine
change
functioning
respectively.
To
partially
mediate
associations,
formal
mediation
analyses
performed,
estimating
proportion
excess
individually
combination.
The
results
this
may
shed
light
pathomechanisms
terms
neuroinflammation.
Language: Английский
Systematic review and meta‐analysis of bulk RNAseq studies in human Alzheimer's disease brain tissue
Alzheimer s & Dementia,
Journal Year:
2025,
Volume and Issue:
21(3)
Published: March 1, 2025
We
systematically
reviewed
and
meta-analyzed
bulk
RNA
sequencing
(RNAseq)
studies
comparing
Alzheimer's
disease
(AD)
patients
to
controls
in
human
brain
tissue.
searched
PubMed,
Web
of
Science,
Scopus
for
RNAseq
studies,
excluding
re-analyses
limited
small
RNAs
or
gene
panels.
developed
10
criteria
quality
assessment
performed
a
meta-analysis
on
three
high-quality
datasets.
Of
3266
records,
24
qualified
the
systematic
review,
one
study
with
datasets
meta-analysis.
The
identified
571
differentially
expressed
genes
(DEGs)
temporal
lobe
189
frontal
lobe,
including
CLU
GFAP.
Pathway
analysis
suggested
reactivation
developmental
processes
adult
AD
brain.
Limited
data
availability
constrained
These
findings
underscore
need
rigorous
methods
transcriptomic
research
better
identify
changes
advance
biomarker
therapeutic
development.
This
review
is
registered
PROSPERO
(CRD42023466522).
Comprehensive
review:
Conducted
first
non-demented
using
primary
Identified
AD,
revealing
potential
targets.
discovery:
Highlighted
key
overlapping
pathways
such
as
"tube
morphogenesis"
"neuroactive
ligand-receptor
interaction"
that
may
play
critical
roles
AD.
Emphasized
importance
methodological
rigor
tools
guide
future
Acknowledged
access
complete
tables
lack
diversity
existing
datasets,
which
some
analysis.
Language: Английский
Systematic review and meta-analysis of bulk RNAseq studies in human Alzheimer's disease brain tissue
bioRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2024,
Volume and Issue:
unknown
Published: Nov. 8, 2024
Abstract
Objective
To
systematically
review
and
meta-analyze
bulk
RNA
sequencing
studies
comparing
Alzheimer’s
disease
(AD)
patients
with
controls
in
human
brain
tissue,
assessing
study
quality
identifying
key
genes
pathways.
Methods
We
searched
PubMed,
Web
of
Science,
Scopus
on
September
23,
2023,
for
using
RNAseq
primary
tissue
from
AD
controls.
Excluded
were
non-primary
re-analyses
without
new
data,
limited
types
gene
panels.
Quality
was
assessed
a
10-category
tool.
Meta-analysis
used
high-quality
datasets.
Results
From
3,266
records,
24
met
criteria.
found
571
differentially
expressed
(DEGs)
temporal
lobe
189
frontal
lobe;
overlapping
pathways
included
"Tube
morphogenesis"
"Neuroactive
ligand-receptor
interaction."
Limitations
Study
heterogeneity
data
tables
constrained
the
review.
Conclusions
Rigorous
methods
are
vital
transcriptomic
studies.
Findings
enhance
understanding
changes,
aiding
biomarker
therapeutic
development.
Registration
PROSPERO
(CRD42023466522).
Language: Английский