medRxiv (Cold Spring Harbor Laboratory),
Год журнала:
2024,
Номер
unknown
Опубликована: Апрель 6, 2024
Abstract
Background
Cerebral
white
matter
lesions
(WMLs)
in
people
with
multiple
sclerosis
(pwMS)
are
associated
the
death
of
myelin-producing
oligodendrocytes.
MS
treatment
strategies
aim
to
limit
WML
accumulation
and
disability
progression.
It
is
commonly
accepted
that
nutrition
one
possible
environmental
factors
involved
pathogenesis
MS,
but
its
role
as
a
complementary
unclear
and,
large
extent,
ignored.
Objective
A
pilot
case
control
study
over
10
year
period
ascertain
whether
dietary-
lifestyle
modification
Program
pwMS
reduces
or
prevents
formation.
Methods
MRI
was
performed
at
baseline
after
an
interval
least
years
longer
22
pwMS.
volumes
were
determined
using
Sequence
Adaptive
Multimodal
SEGmentation
(SAMSEG)
software,
part
FreeSurfer
7.2.
Other
variables
include
age
MRI,
disease
duration,
status
medication.
Results
PwMS
(n=13)
who
had
followed
for
more
than
years,
significantly
smaller
lesion
(mm
3
)
compared
did
not
adhere
(n=9)
(4950
±
5303
vs
17934
11139;
p=0.002).
(p=0.02)
(EDSS)
(p=0.350),
duration
(p=0.709),
Interferon-β
(p=0.70).
Conclusion
Dietary-
changes
may
lower
risk
developing
cerebral
WMLs
potentially
slow
down
Larger
studies
required
confirm
effectiveness
such
interventions
Importance
Vitamin
D
deficiency
is
a
risk
factor
for
multiple
sclerosis
(MS)
and
associated
with
the
of
disease
activity,
but
data
on
benefits
supplementation
are
conflicting.
Objective
To
evaluate
efficacy
high-dose
cholecalciferol
as
monotherapy
in
reducing
activity
patients
clinically
isolated
syndrome
(CIS)
typical
MS.
Design,
Setting,
Participants
The
D-Lay
MS
trial
was
parallel,
double-blind,
randomized
placebo-controlled
clinical
36
centers
France.
Patients
were
enrolled
from
July
2013
to
December
2020
(final
follow-up
January
18,
2023).
Untreated
CIS
aged
18
55
years
duration
less
than
90
days,
serum
vitamin
concentration
100
nmol/L,
diagnostic
magnetic
resonance
imaging
(MRI)
meeting
2010
criteria
dissemination
space
or
2
more
lesions
presence
oligoclonal
bands
recruited.
Intervention
1:1
receive
oral
000
IU
(n
=
163)
placebo
153)
every
weeks
24
months.
Main
Outcomes
Measures
primary
outcome
measure
defined
occurrence
relapse
and/or
MRI
(new
contrast-enhancing
lesions)
over
months
follow-up,
also
analyzed
separate
secondary
outcomes.
Results
Of
316
participants
(median
[IQR]
age,
34
[28-42]
years;
70%
women),
analysis
included
303
(95.9%)
who
took
at
least
1
dose
study
drug
288
(91.1%)
ultimately
completed
24-month
trial.
Disease
observed
94
(60.3%)
group
109
(74.1%)
(hazard
ratio
[HR],
0.66
[95%
CI,
0.50-0.87];
P
.004),
median
time
longer
(432
vs
224
days;
log-rank
.003).
All
3
outcomes
reported
significant
differences
favoring
group:
(89
[57.1%]
96
[65.3%];
HR,
0.71
0.53-0.95];
.02),
new
(72
[46.2%]
87
[59.2%];
0.61
0.44-0.84];
.003),
(29
[18.6%]
50
[34.0%];
0.47
0.30-0.75];
.001).
10
showed
no
difference,
including
relapse,
which
occurred
28
(17.9%)
32
(21.8%)
(HR,
0.69
0.42-1.16];
.16).
similar
subset
247
updated
2017
relapsing-remitting
treatment
initiation.
Severe
adverse
events
17
13
group,
none
related
cholecalciferol.
Conclusions
Relevance
Oral
significantly
reduced
early
These
results
warrant
further
investigation,
potential
role
pulse
add-on
therapy.
Trial
Registration
ClinicalTrials.gov
Identifier:
NCT01817166
International Journal of Molecular Sciences,
Год журнала:
2023,
Номер
24(5), С. 4689 - 4689
Опубликована: Фев. 28, 2023
Vitamin
D
is
a
secosteroid
hormone
that
highly
involved
in
bone
health.
Mounting
evidence
revealed
that,
addition
to
the
regulation
of
mineral
metabolism,
vitamin
implicated
cell
proliferation
and
differentiation,
vascular
muscular
functions,
metabolic
Since
discovery
receptors
T
cells,
local
production
active
was
demonstrated
most
immune
addressing
interest
clinical
implications
status
surveillance
against
infections
autoimmune/inflammatory
diseases.
together
with
B
are
seen
as
main
cells
autoimmune
diseases;
however,
growing
currently
focused
on
innate
compartment,
such
monocytes,
macrophages,
dendritic
natural
killer
initiation
phases
autoimmunity.
Here
we
reviewed
recent
advances
onset
Graves’
Hashimoto’s
thyroiditis,
vitiligo,
multiple
sclerosis
relation
role
their
crosstalk
acquired
cells.
Nutrients,
Год журнала:
2023,
Номер
15(13), С. 2978 - 2978
Опубликована: Июнь 30, 2023
Multiple
sclerosis
(MS)
is
a
complex
neurological
condition
that
involves
both
inflammatory
demyelinating
and
neurodegenerative
components.
MS
research
treatments
have
traditionally
focused
on
immunomodulation,
with
less
investigation
of
neuroprotection,
this
holds
true
for
the
role
vitamin
D
in
MS.
Researchers
already
established
plays
an
anti-inflammatory
modulating
immune
system
More
recently,
researchers
begun
investigating
potential
neuroprotective
The
active
form
D,
1,25(OH)2D3,
has
range
properties,
which
may
be
important
remyelination
and/or
prevention
demyelination.
most
notable
finding
relevant
to
1,25(OH)2D3
promotes
stem
cell
proliferation
drives
differentiation
neural
cells
into
oligodendrocytes,
carry
out
remyelination.
In
addition,
counteracts
neurodegeneration
oxidative
stress
by
suppressing
activation
reactive
astrocytes
M1
microglia.
also
expression
various
factors,
including
neurotrophins
antioxidant
enzymes.
decreases
blood–brain
barrier
permeability,
reducing
leukocyte
recruitment
central
nervous
system.
These
effects,
stimulated
all
enhance
neuronal
survival.
This
review
summarizes
connects
current
evidence
supporting
D-mediated
mechanisms
action
neuroprotection
Frontiers in Immunology,
Год журнала:
2023,
Номер
14
Опубликована: Июль 24, 2023
Compelling
evidence
indicates
that
Epstein
Barr
virus
(EBV)
infection
is
a
prerequisite
for
multiple
sclerosis
(MS).
The
disease
may
arise
from
complex
interplay
between
latent
EBV
infection,
genetic
predisposition,
and
various
environmental
lifestyle
factors
negatively
affect
immune
control
of
the
infection.
Evidence
gene-environment
interactions
epigenetic
modifications
triggered
by
in
genetically
susceptible
individuals
supports
this
view.
This
review
gives
short
introduction
to
host
immunity
discusses
indicating
as
MS.
role
risk
factors,
their
interactions,
MS
pathogenesis
reviewed
put
context
Finally,
possible
preventive
measures
are
discussed
based
on
findings
presented.
Journal of Clinical Medicine,
Год журнала:
2024,
Номер
13(3), С. 835 - 835
Опубликована: Фев. 1, 2024
Vitamin
D
is
known
for
its
role
in
modulating
calcium
and
phosphate
homeostasis
implicated
both
bone
mineralization
immune
system
regulation.
The
immune-modulatory
of
vitamin
impact
on
multiple
sclerosis
(MS)
courses
are
still
debated.
aim
this
review
was
to
check
the
effect
supplementation
cytokine
profile
regulation
people
with
MS.
A
significant
increase
serum
concentrations
interleukin
(IL)-10
Transforming
growth
factor
(TGF)-β1
after
demonstrated
most
studies,
some
them
reporting
a
reduction
disability
scores
an
inverse
correlation
between
IL-10
levels
disability.
IL-17
IL-6
controversial;
different
results
across
studies
could
be
explained
by
variability
treatment
duration,
route,
frequency
administration,
as
well
dosage
supplementation,
responses
reached
including
methods
used
analysis
cell
types
investigated,
MS
phenotype,
disease
phase
(active
vs.
non-active)
concomitant
disease-modifying
therapies.
Nevertheless,
TGF-β1,
suggests
anti-inflammatory
supplementation.
Journal of Neuroinflammation,
Год журнала:
2024,
Номер
21(1)
Опубликована: Фев. 17, 2024
Abstract
Establishing
biomarkers
to
predict
multiple
sclerosis
diagnosis
and
prognosis
has
been
challenging
using
a
single
biomarker
approach.
We
hypothesised
that
combination
of
would
increase
the
accuracy
prediction
models
differentiate
from
other
neurological
disorders
enhance
prognostication
for
people
with
sclerosis.
measured
24
fluid
in
blood
cerebrospinal
77
80
disorders,
ELISA
or
Single
Molecule
Array
assays.
Primary
outcomes
were
versus
any
diagnosis,
time
first
relapse,
disability
milestone
(Expanded
Disability
Status
Scale
6),
adjusted
age
sex.
Multivariate
calculated
area
under
curve
value
diagnostic
prediction,
concordance
statistics
(the
percentage
each
pair
events
are
correctly
ordered
Cox
regression
models)
prognostic
predictions.
Predictions
combinations
considerably
better
than
The
[chitinase-3-like-1
+
TNF-receptor-1
CD27]
serum
[osteopontin
MCP-1]
had
an
0.97
sclerosis,
compared
best
discriminative
marker
(osteopontin:
0.84)
(chitinase-3-like-1
0.84).
Prediction
next
relapse
was
optimal
fluid[vitamin
D
binding
protein
Factor
I
C1inhibitor]
serum[Factor
B
Interleukin-4
(concordance
0.80),
Expanded
6
[C9
Neurofilament-light]
serum[chitinase-3-like-1
CCL27
vitamin
0.98).
A
higher
significantly
improved
development
sustained
Serum
rivalled
those
fluid,
holding
promise
non-invasive
utility
our
can
only
be
established
by
robust
validation
different
varied
cohorts.
Brain and Behavior,
Год журнала:
2024,
Номер
14(2)
Опубликована: Фев. 1, 2024
Abstract
Objective
Vitamin
D
deficiency
is
a
risk
factor
for
Parkinson's
disease
(PD)
and
vitamin
supplementation
robustly
alleviates
neurodegeneration
in
PD
models.
However,
the
mechanisms
underlying
this
effect
require
further
clarification.
Current
evidence
suggests
that
harnessing
regulatory
T
cells
(Treg)
may
mitigate
neuronal
degeneration.
In
study,
we
investigated
therapeutic
effects
of
receptor
activation
by
calcitriol
on
PD,
specifically
focusing
its
role
Treg.
Methods
Hemiparkinsonian
mice
model
was
established
through
injection
6‐OHDA
into
striatum.
Mice
were
pretreated
with
before
injection.
The
motor
performance,
dopaminergic
survival,
contents
dopamine,
dopamine
metabolites
evaluated.
pro‐inflammatory
cytokines
levels,
T‐cell
infiltration,
mRNA
expression
indicated
microglial
M1/M2
phenotypic
markers,
marker
midbrain
detected.
Populations
Treg
splenic
tissues
assessed
using
flow
cytometry
assay.
PC61
monoclonal
antibody
applied
to
deplete
vivo.
Results
We
show
notably
improved
performance
reduced
degeneration
6‐OHDA‐induced
model.
Mechanistically,
promoted
anti‐inflammatory/neuroprotective
inhibited
pro‐inflammatory/neurodestructive
effector
generation
This
process
significantly
infiltration
midbrain,
restrained
activation,
M1
polarization,
decreased
release.
more
favorable
inflammatory
microenvironment
rescued
To
verify
anti‐inflammatory
are
associated
expansion,
an
antibody‐mediated
depletion
As
predicted,
diminished
following
depletion.
Conclusion
These
findings
suggest
calcitriol's
neuroprotective
potential
boost
expansion.