International Journal of Molecular Sciences,
Journal Year:
2024,
Volume and Issue:
26(1), P. 61 - 61
Published: Dec. 25, 2024
Severe
mental
disorders
(SMDs),
such
as
schizophrenia
(SZ),
bipolar
disorder
(BD),
and
major
depressive
(MDD),
are
heterogeneous
psychiatric
diseases
that
impose
a
significant
societal
burden
due
to
their
chronic
disabling
nature.
There
no
objective
reliable
diagnostic
tests
for
SMDs;
thus,
there
is
an
urgent
need
specific
biomarkers
improve
diagnosis,
treatment,
resource
allocation.
Neurofilaments,
found
in
cerebrospinal
fluid
blood,
offer
prognostic
potential.
This
review
discusses
the
link
between
neurofilament
light
chain
(NfL)
involvement
neurodegenerative
gives
insights
into
value
of
NfL
SMDs.
systematic
searched
PubMed,
Scopus,
Web
Science
databases
answer
research
question
“Are
levels
higher
individuals
with
SMDs
compared
healthy
controls?”
using
terms
related
neurofilament,
SMDs,
SZ,
BD,
depression.
Of
8577
initial
papers,
115
were
relevant.
After
exclusions
manual
additions,
17
articles
included.
Studies
indicate
elevated
controls,
suggesting
its
potential
biomarker
distinguishing
from
disorders.
However,
further
longitudinal
needed
confirm
reliability
differential
disease
prediction,
treatment
assessment
psychiatry.
Alzheimer s & Dementia,
Journal Year:
2024,
Volume and Issue:
20(11), P. 7989 - 8001
Published: Oct. 6, 2024
Abstract
INTRODUCTION
People
with
neurodegenerative
disorders
(ND)
frequently
face
diagnostic
delay
and
misdiagnosis.
We
investigated
blood
cerebrospinal
fluid
(CSF)
neurofilament
light
chain
(NfL)
to
distinguish
ND
from
primary
psychiatric
(PPD),
a
common
challenge
in
clinical
settings.
METHODS
Plasma
CSF
NfL
levels
were
measured
compared
between
groups,
adjusting
for
age,
sex,
weight.
RESULTS
A
total
of
337
participants
included:
136
ND,
77
PPD,
124
Controls.
was
2.5‐fold
elevated
PPD
had
strong
performance
(area
under
the
curve,
[AUC]:
0.86,
81%/85%
specificity/sensitivity)
that
comparable
(2‐fold
elevated,
AUC:
0.89,
95%/71%
specificity/sensitivity).
Diagnostic
especially
younger
people
(40–
<
60
years).
Additional
findings
cutoffs
optimized
sensitivity
specificity,
issues
important
future
translation.
CONCLUSIONS
This
study
adds
evidence
simple
blood‐based
biomarker
assist
as
screening
test
neurodegeneration
distinction
Highlights
significantly
higher
versus
PPD.
showed
performance,
NfL,
people,
where
challenges
are
greater.
Further
research
is
needed
on
analytical
reference
range
factors,
These
support
neurodegeneration.
Ecotoxicology and Environmental Safety,
Journal Year:
2025,
Volume and Issue:
289, P. 117670 - 117670
Published: Jan. 1, 2025
Population
exposure
to
plastics
is
increasing,
and
plasticizers
are
frequently
detected
in
humans
as
important
ingredients
of
plastic
products.
However,
patterns
harmful
their
effects
on
neurofilament
light
chain
(NFL),
a
marker
active
brain
pathology,
currently
inconclusive.
Herein,
we
employed
range
statistical
methods
thoroughly
investigate
the
impact
24
hazardous
varying
NFL
concentrations
blood
general
population
533
participants.
Generalized
linear
model
revealed
positive
correlation
between
Mono-isononyl
phthalate
Mono
(2-Ethyl-
5-Hydroxyhexyl)
Phthalate
(MEHHP)
with
NFL.
Furthermore,
significant
dose-response
relationship
was
observed
MEHHP
NFL,
while
Butyl
paraben
(Hydroxy-Isononyl)
Ester
exhibited
distinct
"inverted
U-shaped"
nonlinear
pattern
Additionally,
Weighted
Quantile
Sum
allowed
us
identify
mixed
all
ingredients,
Mono(2-Ethyl-5-Oxohexyl)
Phthalate,
Mono-isobutyl
phthalate,
Mon
butyl
Propyl
Triclosan
occupying
prominent
positions.
Finally,
latent
profile
analysis
categorized
exposures
into
high,
medium,
low
patterns,
confirming
that
higher
posed
risk
factor
for
elevated
levels
blood.
Exposure
significantly
increases
present
contributes
early
detection
intervention
reduce
incidence
neurodevelopmental
disorder.
Journal of Clinical Laboratory Analysis,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 15, 2025
Neurofilament
light
chain
(NfL)
is
one
of
the
most
important
biomarkers
in
field
clinical
neurochemistry.
Several
analytical
methods
have
been
developed
last
decade.
Recently,
Fujirebio
introduced
a
ready-to-use
assay
kit
for
measuring
NfL
levels
cerebrospinal
fluid
(CSF)
on
fully
automated
LUMIPULSE
G
System.
In
this
study,
we
established
decisional
cutoffs
CSF
NfL.
We
performed
retrospective
observational
study
including
patients
with
cognitive
decline.
were
measured
by
two
methods:
NF-light
ELISA
(UmanDiagnostics)
and
Lumipulse
G1200
system
(Fujirebio).
calculated
Lumipulse,
starting
from
consolidated
method
each
age
using
equation
obtained
regression
analysis.
The
population
consisted
100
median
776.5
±
772.6
pg/mL
473.5
443.5
pg/mL,
respectively,
significantly
different
(p
<
0.001).
Spearman's
rank
correlation
coefficient
was
0.962,
indicating
robust
positive
between
measurement
methods.
derived
Passing-Bablok
analysis
CLEIA
=
-61.16
+
1.83
×
ELISA.
Based
equation,
defined
cutoff
values.
Decisional
are
fundamental
tools
guiding
clinicians
to
use
biomarkers'
results
interpretation
appropriately.
This
first
establishing
value
platform
widely
used
laboratories.
Brain Sciences,
Journal Year:
2025,
Volume and Issue:
15(3), P. 241 - 241
Published: Feb. 25, 2025
Background/Objectives:
Multiple
system
atrophy
(MSA)
presents
a
challenging
diagnosis
due
to
its
clinical
overlap
with
other
neurodegenerative
disorders,
especially
α-synucleinopathies.
The
main
purpose
of
this
systematic
review
and
meta-analysis
was
assess
neurofilament
light
chain
(NfL)
differences
in
the
CSF
blood
patients
MSA
versus
healthy
control
group
(HC),
Parkinson’s
disease
(PD)
Lewy
body
dementia
(LBD).
Secondarily,
diagnostic
metrics
circulating
NfL
HC,
PD,
LBD,
progressive
supranuclear
palsy
(PSP)
corticobasal
degeneration
(CBD)
were
discussed.
Methods:
MEDLINE
EMBASE
thoroughly
searched
for
relevant
case-control
studies.
Standardized
mean
(SMDs)
calculated
separately
per
comparison.
Statistical
heterogeneity
assessed
based
on
Q
I^2
statistics.
Results:
Twenty-five
studies
retrieved.
Quantitative
syntheses
revealed
elevated
levels
individuals
HC
[SMD
=
1.80
(95%CI
1.66,
1.94)
SMD
2.00
1.36,
2.63),
respectively]
PD
1.65
1.26,
2.03)
1.63
0.84,
2.43),
as
well
LBD
1.17,
0.71,
1.63)
0.65
0.30,
1.00),
respectively].
Diagnostic
accuracy
outstanding
it
moderate
LBD.
On
hand,
suboptimal
vs.
PSP
CBD.
Conclusions:
Both
are
compared
To
achieve
optimal
properties,
further
work
is
required
standardization
processes
establishment
reference
intervals
and/or
thresholds.
International Journal of Molecular Sciences,
Journal Year:
2025,
Volume and Issue:
26(6), P. 2629 - 2629
Published: March 14, 2025
We
aimed
to
determine
whether
transient
global
amnesia
(TGA)
is
associated
with
alterations
in
central
nervous
system
(CNS)
injury
biomarkers—serum
neurofilament
light
chain
(sNfL)
and
serum
glial
fibrillary
acidic
protein
(sGFAP).
In
a
prospective
cohort
of
TGA
patients,
blood
samples
were
obtained
within
24–48
h
onset
(t0)
6
weeks
thereafter
(t1).
assessed
sNfL
sGFAP
levels
using
the
highly
sensitive
single-molecule
array
assay
calculated
Z-scores
adjusted
for
age,
gender,
body
mass
index
(BMI).
Demographics,
electroencephalography
(EEG),
cerebral
magnetic
resonance
imaging
(cMRI)
findings
also
collected.
A
total
20
patients
included
(median
age:
66
years,
70%
women).
No
significant
changes
or
at
t0
t1
observed.
Median
0.45
(interquartile
range
[IQR]
−0.09,
1.19)
0.60
(IQR
−0.61,
t1.
0.27
−0.45,
0.76)
0.44
−0.27,
0.75)
Similarly,
subgroup
diffusion-weighted
(DWI)-positive
hippocampal
lesions
(n
=
5/20[25%]),
no
elevations
biomarkers
detected.
Our
pilot
study
on
neurological
supports
benign
nature
TGA,
indicating
that
CNS
tissue
damage
occurs.
Bipolar Disorders,
Journal Year:
2025,
Volume and Issue:
unknown
Published: April 23, 2025
ABSTRACT
Background
Recent
advances
now
allow
detection
of
brain‐specific
proteins
in
blood,
including
neurofilament
light
chain
(NfL),
a
marker
axonal
pathology,
and
glial
fibrillary
acidic
protein
(GFAP),
indicative
astrocytic
activation.
Given
the
evidence
astroglial
pathology
neuronal
dysfunction
bipolar
disorder,
ongoing
debates
on
neuroprogression,
we
investigated
plasma
NfL
GFAP
levels
affected
individuals.
Methods
This
study
analysed
measured
216
individuals
using
Simoa.
We
used
bootstrapped
general
linear
models
(GLM)
to
compare
between
people
with
depression
(
n
=
120)
healthy
controls
96),
adjusting
for
age,
sex,
weight.
examined
associations
these
biomarkers
clinical
variables
while
multiple
comparisons.
For
sensitivity
analyses,
predictors
were
evaluated
Bayesian
model
averaging
(BMA).
Results
Plasma
β
0.21
[0.07,
0.35],
p
0.006)
0.06
[0.01,
0.10],
0.028)
elevated
depression.
Illness
duration
was
positively
associated
r
2.97,
0.002),
further
supported
by
BMA
analysis
(posterior
inclusion
probability,
PIP
0.85).
Age
onset
0.246
0.041),
which
also
(PIP
0.67).
Conclusions
These
findings
indicate
increased
disorder.
Our
support
neuroprogression
hypothesis,
where
prolonged
illness
contributes
neuroaxonal
damage.
Elevated
those
later
suggests
role
neuroinflammation,
potentially
linked
cardiovascular
metabolic
comorbidities.