Implications of cytokine genes polymorphisms in Jordanian patients with obsessive compulsive disorder
Egyptian Journal of Medical Human Genetics,
Journal Year:
2025,
Volume and Issue:
26(1)
Published: Jan. 14, 2025
Abstract
Background
Obsessive–compulsive
disorder
(OCD)
is
a
common
and
often
highly
debilitating
chronic
neuropsychiatric
condition.
There
substantial
evidence
that
immune
system
genetic
changes
are
involved
in
OCD
pathogenesis.
Only
few
studies
have
been
encountered
the
literature
this
field.
We
aimed
at
providing
experimental
for
single
nucleotide
polymorphisms
(SNPs)
candidate
cytokine
genes
etiology
of
OCD.
Methods
A
total
52
patients
54
healthy
controls
were
randomly
recruited
from
Jordanian
population.
Age
ranged
between
16
55
years
(35.5
±
13.72
33.5
10.48
years)
controls,
respectively.
Five
polymorphic
positions
four
interleukin
(IL-1β;
rs16944
rs1143634,
IL-6;
rs1800795,
IL-10;
rs1800896
rs1800795)
genotyped
using
polymerase
chain
reaction–restriction
fragment
length
polymorphism
(PCR–RFLP)
method.
The
tumor
necrosis
factor-α
(TNF-α)
SNP
(rs1800629)
DNA
was
sequenced
by
Sanger
obtained
data
analyzed
GraphPad
Prism
Results
no
statistically
significant
differences
alleles
genotypes
opposite
groups.
However,
there
positive
association
incidence
studied
non-OCD
individuals.
two
SNPs
(IL-1β
+
3954
C
>
T
TNF-α-308
G
A)
more
predominant
positively
correlated
with
higher
risk
women.
In
contrast,
link
gender
occurrence
mutant
other
IL-1β
(−
511
T);
IL-6
174
C);
IL-10
1082
G);
819
robust
males
than
corresponding
females.
Conclusion
observed
different
groups
may
be
due
to
an
tested
samples
rather
true
association.
But,
possibility
critical
effect
still
exists.
One
might
want
explore
further
repeating
study
larger
sample
size.
Language: Английский
Autoimmune hepatitis under the COVID-19 veil: an analysis of the nature of potential associations
Frontiers in Immunology,
Journal Year:
2025,
Volume and Issue:
16
Published: Jan. 31, 2025
In
recent
years,
the
novel
coronavirus
infectious
disease
2019
(COVID-19),
caused
by
severe
acute
respiratory
syndrome
coronavirus-2
(SARS-CoV-2),
has
led
to
over
670
million
infections
and
nearly
7
deaths
worldwide.
The
global
pandemic
of
COVID-19
precipitated
a
significant
public
health
crisis.
prevalence
liver
function
abnormalities
associated
with
SARS-CoV-2
is
as
high
53%
among
healthy
individuals
or
patients
autoimmune
hepatitis
(AIH)
shows
positive
correlation
severity;
moreover,
specific
adaptive
immune
responses
can
influence
trajectory
outcomes
COVID-19.
For
instance,
may
impact
autoimmunity
through
mechanisms
such
excessive
stimulation
molecular
mimicry,
particularly
in
genetically
predisposed
individuals.
Currently,
overall
mutational
trend
indicates
heightened
infectivity
evasion
capabilities.
Consequently,
vaccination
remains
crucial
for
universal
protection
against
this
disease.
Nevertheless,
alongside
widespread
implementation
programs
globally,
an
increasing
number
cases
have
been
documented
where
appears
trigger
new-onset
hepatitis;
yet
definitive
evidence
still
pending
elucidation
regarding
causality.
review,
we
analyse
clinical-immunological
characteristics,
risks
progression,
prognosis
AIH
infected
SARS-CoV-2;
discuss
detrimental
effects
exerted
on
hepatic
function;
summarise
attributes
leading
AIH;
well
provide
insights
into
how
interfere
processes.
We
continue
underscore
significance
while
aiming
enhance
awareness
concerning
potential
it-this
could
facilitate
better
management
strategies
diseases
along
appropriate
adjustments
protocols.
Although
precise
triggering
mechanism
linking
COVID-19-related
events
unclear,
existing
suggests
that
relationship
far
from
coincidental.
Language: Английский
IFNL1 rs30461 polymorphism as a risk factor for COVID-19 severity: A cross-sectional study
Cytokine,
Journal Year:
2024,
Volume and Issue:
176, P. 156500 - 156500
Published: Jan. 24, 2024
Language: Английский
The role of inflammatory gene polymorphisms in severe COVID-19: a review
J Yip,
No information about this author
Adrian Oo,
No information about this author
Yan Ling Ng
No information about this author
et al.
Virology Journal,
Journal Year:
2024,
Volume and Issue:
21(1)
Published: Dec. 20, 2024
The
COVID-19
pandemic,
caused
by
the
novel
coronavirus
SARS-CoV-2,
has
profoundly
impacted
global
healthcare
systems
and
spurred
extensive
research
efforts
over
past
three
years.
One
critical
aspect
of
disease
is
intricate
interplay
between
virus
host
immune
response,
particularly
role
inflammatory
gene
expression
in
severe
COVID-19.
While
numerous
previous
studies
have
explored
genetic
polymorphisms
COVID-19,
specifically
focusing
on
genes
their
associations
with
severity
remains
limited.
This
review
explores
relationship
outcomes
within
key
genes.
By
investigating
impact
variations
responses,
which
include
cytokine
production
downstream
signalling
pathways,
we
aim
to
provide
a
comprehensive
overview
how
contribute
variability
presentation.
Through
an
in-depth
analysis
existing
literature,
shed
light
potential
therapeutic
targets
personalized
approaches
that
may
enhance
our
understanding
pathogenesis
treatment
strategies.
Language: Английский
HLA-DQ2/8 and COVID-19 in celiac disease: Boon or Bane
Published: Nov. 17, 2023
The
SARS-CoV-2
pandemic
continues
to
pose
a
global
threat.
While
its
virulence
has
subsided,
it
persisted
due
the
continual
emergence
of
new
mutations.
Although
many
high-risk
conditions
related
COVID-19
have
been
identified,
understanding
protective
factors
remains
limited.
Intriguingly,
epidemiological
evidence
suggests
low
incidence
COVID-19-infected
CD
patients.
present
study
explores
whether
their
genetic
background,
namely
associated
HLA-DQs,
offers
protection
against
severe
outcomes.
We
hypothesize
that
HLA-DQ
2/8
alleles
may
shield
patients
from
and
subsequent
effects,
possibly
memory
CD4
T
cells
primed
by
previous
exposure
human-associated
common
cold
coronaviruses
(CCC)
higher
affinity
those
allele's
groove.
In
this
context,
we
examined
potential
cross-reactivity
between
epitopes
CCC
assessed
binding
(BA)
these
2/8.
Using
computational
methods,
analyzed
sequence
similarity
four
distinct
CCC.
Of
924
unique
immunodominant
15-mer
with
at
least
67%
identity,
37
exhibited
significant
BA
2/8,
suggesting
effect.
various
mechanisms
might
explain
role
HLA-DQ2/8
in
COVID-19-afflicted
If
substantiated,
insights
could
enhance
our
gene-environment
enigma
viral-host
relationship,
guiding
therapeutic
innovations
ongoing
pandemic.
Language: Английский
HLA-DQ2/8 and COVID-19 in Celiac Disease: Boon or Bane
Microorganisms,
Journal Year:
2023,
Volume and Issue:
11(12), P. 2977 - 2977
Published: Dec. 13, 2023
The
SARS-CoV-2
pandemic
continues
to
pose
a
global
threat.
While
its
virulence
has
subsided,
it
persisted
due
the
continual
emergence
of
new
mutations.
Although
many
high-risk
conditions
related
COVID-19
have
been
identified,
understanding
protective
factors
remains
limited.
Intriguingly,
epidemiological
evidence
suggests
low
incidence
COVID-19-infected
CD
patients.
present
study
explores
whether
their
genetic
background,
namely,
associated
HLA-DQs,
offers
protection
against
severe
outcomes.
We
hypothesize
that
HLA-DQ2/8
alleles
may
shield
patients
from
and
subsequent
effects,
possibly
memory
CD4
T
cells
primed
by
previous
exposure
human-associated
common
cold
coronaviruses
(CCC)
higher
affinity
those
allele's
groove.
In
this
context,
we
examined
potential
cross-reactivity
between
epitopes
CCC
assessed
binding
(BA)
these
HLA-DQ2/8.
Using
computational
methods,
analyzed
sequence
similarity
four
distinct
CCC.
Of
924
unique
immunodominant
15-mer
with
at
least
67%
identity,
37
exhibited
significant
BA
HLA-DQ2/8,
suggesting
effect.
various
mechanisms
might
explain
role
in
COVID-19-afflicted
If
substantiated,
insights
could
enhance
our
gene-environment
enigma
viral-host
relationship,
guiding
therapeutic
innovations
ongoing
pandemic.
Language: Английский