Frontiers in Immunology,
Journal Year:
2024,
Volume and Issue:
15
Published: Oct. 18, 2024
This
study
aimed
to
investigate
the
potential
relationship
between
multiple
sclerosis
(MS)
and
coronavirus
disease
2019
(COVID-19)
outcomes
using
Mendelian
randomization
analysis.
Specifically,
it
evaluates
whether
genetic
factors,
including
single-nucleotide
polymorphism
(SNP)
rs10191329,
influence
susceptibility
of
MS
patients
three
COVID-19
[severe
acute
respiratory
syndrome
2
(SARS-CoV-2)
infection,
hospitalized
COVID-19,
severe
COVID-19].
utilized
genome-wide
association
summary
statistics
from
International
Multiple
Sclerosis
Genetics
Consortium
conduct
a
SNPs
strongly
associated
with
were
selected
examine
their
impact
on
outcomes.
The
analysis
focused
identifying
any
causal
associations
severity,
as
well
assessing
role
interferon
beta
(IFNβ)
treatment
in
modifying
these
results
suggest
an
increased
risk
but
individuals
carrying
rs10191329
SNP
appeared
less
likely
develop
COVID-19.
SNP,
located
within
DYSF-ZNF638
locus,
may
immune
responses
highlighting
its
relevance
for
personalized
strategies.
Importantly,
no
significant
was
found
IFNβ
outcomes,
indicating
that
findings
treated
differ
those
observed
untreated
patients.
suggests
offer
protective
effects
against
SARS-CoV-2
These
underscore
importance
such
shaping
clinical
context
Further
research
should
explore
targeted
therapies
approaches
managing
during
ongoing
pandemic.
Vestnik nevrologii psihiatrii i nejrohirurgii (Bulletin of Neurology Psychiatry and Neurosurgery),
Journal Year:
2025,
Volume and Issue:
1, P. 60 - 73
Published: Jan. 15, 2025
One
of
the
most
pressing
questions
regarding
COVID-19
pandemic
outbreak
is
to
determine
its
impact
on
major
neurological
diseases.
The
infection
poses
a
particular
threat
people
with
comorbidities
and
citizens
over
60
years
age.
Reports
disease
have
raised
concern
among
neurologists
treating
autoimmune
diseases,
including
multiple
sclerosis.
Previous
studies
shown
an
association
between
viral
infections,
sclerosis
relapses,
MRI
lesions.
Although
exact
mechanism
unclear,
infections
are
thought
trigger
systemic
inflammatory
response
leading
increased
expression
pro-inflammatory
cytokines
chemokines.
Changes
in
mediators
critical
pathogenesis
symptoms
may
possibly
increase
susceptibility
relapses
Given
previous
reports
as
demyelination,
it
important
investigate
whether
lead
rate
or
progression
disability.
In
this
regard,
article
reviews
current
relevant
research
observational
findings
that
relate
covid
course
Psychiatric Genetics,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Jan. 23, 2024
Background
Attention-deficit/hyperactivity
disorder
(ADHD)
and
autism
spectrum
(ASD)
are
two
neurodevelopmental
disorders
that
often
result
in
individuals
experiencing
traumatic
events.
However,
little
is
known
about
the
connection
between
ADHD/ASD
post-traumatic
stress
(PTSD).
This
study
aimed
to
investigate
genetic
associations
these
disorders.
Methods
Genetic
correlation
analysis
was
used
examine
components
shared
ADHD
(38
691
cases
275
986
controls),
ASD
(18
381
27
969
controls)
PTSD
(23
212
151
447
controls).
Two-sample
Mendelian
randomization
analyses
were
employed
explore
bidirectional
causal
relationships
PTSD.
Results
The
results
of
revealed
significant
positive
correlations
with
ADHD(r
g
=
0.70)
(r
0.34).
Furthermore,
liabilities
[odds
ratio
(OR)
1.14;
95%
confidence
interval
(CI),
1.06–1.24;
P
7.88
×
10
−4
]
(OR
1.04;
CI,
1.01–1.08;
0.014)
associated
an
increased
risk
developing
later
life.
no
evidence
supported
liability
could
elevate
or
ASD.
Conclusion
findings
this
may
increase
PTSD,
but
not
vice
versa.
BMC Psychiatry,
Journal Year:
2023,
Volume and Issue:
23(1)
Published: Dec. 8, 2023
Abstract
Background
The
severe
acute
respiratory
syndrome
coronavirus
2
(SARS-CoV-2)
can
invade
both
the
peripheral
and
central
nervous
systems
impact
function
of
brain.
Therefore,
it
is
necessary
to
evaluate
mutual
influences
between
COVID-19
outcomes
childhood
mental
disorders.
Methods
We
examined
genetic
correlations
potential
causalities
three
disorders
phenotypes
by
genetically
proxied
analyses.
included
attention-deficit/hyperactivity
disorder
(ADHD,
N
=
292,548),
Tourette’s
(TS,
14,307),
autism
spectrum
(ASD,
46,350).
traits
SARS-CoV-2
infection
(N
2,597,856),
hospitalized
2,095,324),
critical
1,086,211).
Literature-based
analysis
was
used
build
gene-based
pathways
connecting
ADHD
COVID-19.
Results
positively
correlated
with
(R
g
:
0.22
~
0.30).
Our
Mendelian
randomization
(MR)
analyses
found
that
confers
a
causal
effect
on
(odds
ratio
(OR):
1.36,
95%
confidence
interval
(CI):
1.10–1.69).
TS
(OR:
1.14,
CI:
1.04–1.25).
Genetic
liability
may
not
increase
risk
for
Pathway
identified
several
immunity-related
genes
link
COVID-19,
including
CRP
,
OXT
IL6
PON1
AR
TNFSF12
IL10
.
Conclusions
study
suggests
augment
severity
through
pathways.
However,
our
results
did
support
role
in
Clinical and Experimental Medicine,
Journal Year:
2023,
Volume and Issue:
23(7), P. 3549 - 3564
Published: July 3, 2023
Abstract
Background
Many
studies
have
shown
an
association
between
COVID-19
and
autoimmune
diseases
(ADs).
Studies
on
ADs
also
increased
significantly,
but
there
is
no
bibliometric
analysis
to
summarize
the
ADs.
The
purpose
of
this
study
was
perform
a
visual
published
related
Methods
Based
Web
Science
Core
Collection
SCI-Expanded
database,
we
utilize
Excel
2019
visualization
tools
Co-Occurrence13.2
(COOC13.2),
VOSviewer,
CiteSpace,
HistCite
for
analysis.
Results
A
total
1736
kinds
papers
were
included,
number
presented
overall
increasing
trend.
country/region
with
most
publications
USA,
institution
Harvard
Medical
School,
author
Yehuda
Shoenfeld
from
Israel,
journal
Frontiers
in
Immunology
.
Research
hotspots
include
immune
responses
(such
as
cytokines
storm),
multisystem
systemic
lupus
erythematosus,
rheumatoid
arthritis,
multiple
sclerosis),
treatment
modalities
hydroxychloroquine,
rituximab),
vaccination
mechanisms
autoantibodies,
molecular
mimicry).
future
research
direction
may
be
ideas
NF-κB,
hyperinflammation,
antiphospholipid
antibodies,
neutrophil
extracellular
traps,
granulocyte-macrophage
colony-stimulating
factor),
other
cross-diseases
inflammatory
bowel
disease,
chronic
mucocutaneous
candidiasis,
acute
respiratory
distress
syndrome).
Conclusion
growth
rate
regarding
has
risen
sharply.
Our
results
can
help
researchers
grasp
current
status
find
new
directions
future.
Frontiers in Immunology,
Journal Year:
2023,
Volume and Issue:
14
Published: July 27, 2023
Background
An
increasing
number
of
studies
have
elucidated
a
close
nexus
between
COVID-19
phenotypes
and
neuromyelitis
optica
spectrum
disorder
(NMOSD),
yet
the
causality
them
remains
enigmatic.
Methods
In
this
study,
we
conducted
Mendelian
randomization
(MR)
analysis
employing
summary
data
sourced
from
genome-wide
association
(GWAS)
pertaining
to
susceptibility,
hospitalization,
severity,
NMOSD.
The
primary
MR
employed
Inverse
variance
weighted
(IVW)
approach,
which
was
supplemented
by
MR-Egger,
median,
simple
mode,
mode
methods.
We
implemented
various
sensitivity
analyses
including
Cochran’s
Q
test,
MR-PRESSO
method,
MR-Egger
intercept,
leave-one-out
analysis,
funnel
plot.
Results
results
demonstrated
nominal
susceptibility
risk
AQP4+
NMOSD,
as
evidenced
IVW
method
(OR
=
4.958;
95%
CI:
1.322-18.585;
P
0.018).
Conversely,
no
causal
observed
or
severity
increased
AQP4-NMOSD,
comprehensive
further
bolstered
robustness
consistency
estimates.
Conclusion
Our
findings
provide
compelling
evidence
for
effect
phenotype
on
shedding
new
light
understanding
comorbidity
Brain and Behavior,
Journal Year:
2023,
Volume and Issue:
13(11)
Published: Aug. 28, 2023
Abstract
Background:
Observational
studies
have
suggested
an
association
between
coronavirus
disease
2019
(COVID‐19)
and
myasthenia
gravis
(MG).
Here,
we
aimed
to
estimate
the
genetic
correlation
causal
relationship
COVID‐19
susceptibility,
hospitalization,
severity,
MG
phenotypes
using
linkage
disequilibrium
score
regression
(LDSC)
Mendelian
randomization
(MR)
approach.
Methods
Summary
statistics
of
severity
were
used
as
instrumental
variables
for
exposure
traits.
Large‐scale
genome‐wide
study
(GWAS)
data
outcome
The
inverse
variance
weighted
approach
was
main
MR
analysis,
complemented
by
MR‐Egger,
median,
simple
mode,
mode
methods.
Sensitivity
analysis
implemented
Cochran's
Q
test,
MR‐PRESSO
method,
MR‐Egger
intercept
test.
Results
LDSC
did
not
reveal
any
among
phenotypes,
including
MG,
early‐onset
late‐onset
(
p
>
.05).
Our
provide
evidence
supporting
a
effect
or
on
Extensive
sensitivity
strengthened
robustness
consistency
estimates.
Conclusion
find
MG.
Future
with
more
GWAS
are
needed
evaluate
its
subgroups.
Medical Journal of the Islamic Republic of Iran,
Journal Year:
2024,
Volume and Issue:
unknown
Published: April 20, 2024
Background:
Case-control
studies
are
efficient
designs
for
investigating
gene-disease
associations.A
discovery
of
genome-wide
association
(GWAS)
is
that
many
genetic
variants
associated
with
multiple
health
outcomes
and
diseases,
a
phenomenon
known
as
pleiotropy.We
aimed
to
discuss
about
pleiotropic
bias
in
studies.Methods:
The
opinions
the
researchers
on
basis
literature
were
presented
critical
review.Results:
Pleiotropic
effect
can
results
if
they
use
individuals
pre-existing
diseases
control
group,
while
disease
cases
controls
have
shared
markers.The
idea
supports
conclusion
when
exposure
interest
case-control
study
marker,
from
diseased
share
similar
markers
may
increase
risk
effect.However,
not
manifesting
symptoms
among
at
time
recruitment
does
guarantee
individual
will
develop
future.Age-matched
disease-free
be
better
solution
situations.Different
analytical
techniques
also
available
used
identify
effects.Known
effects
searched
various
online
databases.Conclusion:
result
studies.Suggestions
consist
selecting
healthy
yet
agematched
considering
independent
architecture.Checking
related
databases
recommended
before
designing
study.