Virology Journal,
Journal Year:
2024,
Volume and Issue:
21(1)
Published: March 25, 2024
Abstract
Background
Several
observational
studies
demonstrated
that
pregnant
individuals
with
COVID-19
had
a
higher
risk
of
preeclampsia
and
preterm
birth.
We
aimed
to
determine
whether
women
diagnosis
adverse
pregnancy
outcomes.
Methods
A
two-sample
Mendelian
randomization
(MR)
analysis
in
this
study
was
used
evaluate
the
casual
relationships
between
infection
obstetric-related
diseases
based
on
genome-wide
association
(GWAS)
dataset.
Inverse-variance
weighted
(IVW),
MR-Egger
MR-PRESSO
were
infer
connection
estimate
pleiotropy
respectively.
Results
The
significant
observed
placental
disorders
beta
IVW
1.57
odds
ratio
(OR)
4.81
(95%
confidence
interval
[CI]:
1.05–22.05,
p
=
0.04).
However,
there
no
associations
gestational
diabetes
mellitus
(GDM)
(OR
1.12;
95%
CI:
0.85–1.45,
0.41),
other
amniotic
fluid
membranes
0.90;
0.61–1.32,
0.59),
Intrahepatic
Cholestasis
Pregnancy
(ICP)
1.42;
0.85–2.36,
0.18),
birth
weight
1.02;
0.99–1.05,
0.19),
hypertension
1.00;
1.00–1.00,
0.85),
spontaneous
miscarriages
0.96–1.04,
0.90)
stillbirth
0.98–1.01,
0.62).
Conclusion
There
direct
causal
relationship
maternal
neonatal
poor
Our
could
alleviate
anxiety
under
pandemic
conditions
partly.
Frontiers in Immunology,
Journal Year:
2022,
Volume and Issue:
13
Published: Sept. 27, 2022
SARS-CoV-2
infected
pregnant
women
are
at
increased
risk
of
severe
COVID-19
than
non-pregnant
and
have
a
higher
adverse
pregnancy
outcomes
like
intrauterine/fetal
distress
preterm
birth.
However,
little
is
known
about
the
impact
infection
on
maternal
neonatal
immunological
profiles.
In
this
study,
we
investigated
inflammatory
humoral
responses
to
in
cord
blood
paired
samples.
Thirty-six
were
recruited
delivery
Hospital
Sant
Joan
de
Déu,
Barcelona,
Spain,
between
April-August
2020,
before
having
available
vaccines.
Maternal
variables,
as
well
perinatal
outcomes,
recorded
questionnaires.
Nasopharyngeal
swabs
samples
collected
for
detection
by
rRT-PCR
serology,
respectively.
We
measured
IgM,
IgG
IgA
levels
6
antigens
(spike
[S],
S1,
S2,
receptor-binding
domain
[RBD],
nucleocapsid
[N]
full-length
C-terminus),
N
from
4
human
coronaviruses
(OC43,
HKU1,
229E
NL63),
concentrations
30
cytokines,
chemokines
growth
factors
Luminex.
Mothers
classified
or
non-infected
based
serology
results.
Sixty-four
%
with
(positive
during
third
trimester
and/or
just
after
delivery).
None
newborns
tested
positive
rRT-PCR.
mothers
had
virus-specific
antibodies
several
cytokines.
Those
symptoms
cytokine
levels.
IFN-α
was
mothers,
symptomatic
EGF,
FGF,
IL-17
IL-15
increased,
whereas
RANTES
decreased.
showed
correlations
their
counterparts
blood.
lower
transfer
SARS-CoV-2-specific
IgGs,
stronger
effect
when
closer
delivery.
carrying
male
fetus
antibody
IL-7
concentrations.
Our
results
show
that
induces
robust
response
causes
significant
reduction
IgGs
transplacental
transfer,
negative
Cureus,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Feb. 16, 2024
In
this
systematic
review
and
meta-analysis,
we
aimed
to
the
characteristics
outcomes
of
newborns
Coronavirus
disease
2019
(COVID-19)
infected
pregnant
women.
We
conducted
an
online
bibliographic
search
using
following
electronic
databases:
MEDLINE
via
PubMed,
Scopus,
Web
Science,
Cochrane
Central.
Studies
were
deemed
eligible
if
they
recruited
from
mothers
with
confirmed
COVID-19
reported
perinatal
neonatal
cases.
A
total
20
studies
included.
Neonates
born
positive
results
have
been
shown
significantly
lower
birth
weights
(mean
difference,
MD
=
-48.54
g,
p
0.04),
increased
risks
fetal
distress
(odds
ratio,
OR
1.76,
<
0.00001),
respiratory
(OR
1.96,
0.006),
premature
2.08,
death
2.20,
0.004),
a
5-minute
Apgar
score
1.44,
0.02).
Additionally,
more
likely
be
admitted
intensive
care
unit
(NICU)
2.25,
0.007)
test
for
themselves
9.88,
0.03).
However,
other
parameters,
such
as
malformations,
mechanical
ventilation,
hypoglycemia,
sepsis,
appeared
comparable
between
two
groups.
Maternal
infection
during
pregnancy
is
associated
several
outcomes,
some
which
are
adverse
others
that
do
not
show
significant
deviation
norms.
While
our
meta-analysis
clearly
illustrates
heightened
birth,
reduced
weight,
challenges,
it
also
emphasizes
all
can
directly
attributed
maternal
SARS-CoV-2
infection.
International Journal of Environmental Research and Public Health,
Journal Year:
2020,
Volume and Issue:
17(21), P. 8277 - 8277
Published: Nov. 9, 2020
Pregnant
women
seem
to
be
at
risk
for
developing
complications
from
COVID-19.
Given
the
limited
knowledge
about
impact
of
COVID-19
on
pregnancy,
management
guidelines
are
fundamental.
Our
aim
was
examine
obstetrics
released
December
2019
April
2020
compare
their
recommendations
and
assess
how
useful
they
could
maternal
health
workers.
We
reviewed
11
management,
assessing
four
domains:
(1)
timeliness:
time
between
declaration
pandemics
by
WHO
a
guideline
release
update;
(2)
accessibility:
readiness
access
searching
it
common
browser;
(3)
completeness:
amount
foundational
topics
covered;
(4)
consistency:
agreement
among
different
guidelines.
In
terms
timeliness,
Royal
College
Obstetricians
Gynaecologists
(RCOG)
first
organization
recommendation.
Only
were
accessible
with
one
click,
while
only
6/11
covered
more
than
80%
30
we
identified.
For
consistency,
study
highlights
existence
10
points
conflict
recommendations.
The
present
research
revealed
lack
uniformity
resulting
in
potentially
challenging
decisions
healthcare
providers.
American Journal of Obstetrics and Gynecology,
Journal Year:
2021,
Volume and Issue:
225(3), P. 301.e1 - 301.e14
Published: March 30, 2021
Severe
acute
respiratory
syndrome
coronavirus
2,
the
disease-causing
pathogen
of
disease
2019
pandemic,
has
resulted
in
morbidity
and
mortality
worldwide.
Pregnant
women
are
more
susceptible
to
severe
at
higher
risk
preterm
birth
than
uninfected
pregnant
women.
Despite
this
evidence,
immunologic
effects
2
infection
during
pregnancy
remain
understudied.
medRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2020,
Volume and Issue:
unknown
Published: Nov. 16, 2020
Abstract
Importance
The
effects
of
SARS-CoV-2
infection
on
immune
responses
during
pregnancy
have
not
been
systematically
evaluated.
Objective
To
assess
the
impact
inflammatory
and
humoral
in
maternal
fetal
samples
compare
antibody
to
among
pregnant
non-pregnant
women.
Design
Immune
were
analyzed
using
from
women
who
had
either
tested
positive
or
negative
for
SARS-CoV-2.
We
measured,
proinflammatory
placental
cytokine
mRNAs,
neonatal
Fc
receptor
(FcRn)
expression,
tetanus
transfer
cord
blood
samples.
Additionally,
we
measured
anti-spike
(S)
IgG,
anti-S-receptor
binding
domain
(RBD)
neutralizing
(nAb)
serum
plasma
collected
women,
blood.
Setting
Johns
Hopkins
Hospital
(JHH)
Participants
Pregnant
recruited
through
JHH
outpatient
obstetric
clinics
Labor
&
Delivery
unit.
Non-pregnant
after
receiving
testing
within
Health
System,
USA.
Adult
with
RT-PCR
results
SARS-CoV-2,
age
range
18-48
years,
included
study.
Exposures
Main
Outcomes
Measures
Participant
demographic
characteristics,
titers,
mRNA
FcRn
expression.
Results
SARS-COV-2
expressed
more
IL1β
,
but
IL6
14
days
versus
>
a
confirmed
test,
similar
patterns
observed
side
placentas,
particularly
asymptomatic
also
reduced
anti-S-RBD
IgG
titers
less
likely
detectable
nAb
as
compared
Although
did
disrupt
expression
placenta,
was
inhibited
by
pregnancy.
Conclusions
Relevance
characterized
inflammation
antiviral
responses,
which
may
efficacy
COVID-19
therapeutics
long-term
implications
health
requires
greater
consideration.
NeuroImmunoModulation,
Journal Year:
2021,
Volume and Issue:
28(1), P. 1 - 21
Published: Jan. 1, 2021
Coronavirus
disease
2019
(COVID-19)
caused
by
severe
acute
respiratory
syndrome-related
coronavirus
2
(SARS-CoV-2)
has
devastating
effects
on
the
population
worldwide.
Given
this
scenario,
extent
of
impact
more
vulnerable
individuals,
such
as
pregnant
women,
is
great
concern.
Although
pregnancy
may
be
a
risk
factor
in
virus
infections,
there
are
no
considerable
differences
regarding
COVID-19
severity
observed
between
and
nonpregnant
women.
In
these
circumstances,
an
emergent
concern
possibility
neurodevelopmental
neuropsychiatric
harm
for
offspring
infected
mothers.
Currently,
stronger
evidence
indicating
vertical
transmission
SARS-CoV-2;
however,
exacerbated
inflammatory
response
could
lead
to
several
impairments
offspring’s
brain.
Furthermore,
face
historical
knowledge
possible
long-term
consequences
progeny’s
brain
after
infection
viruses,
we
must
consider
that
might
another
deleterious
facet
COVID-19.
light
neuroimmune
interactions
at
maternal-fetal
interface,
review
here
harmful
outcomes
brains
mothers
SARS-CoV-2.
BMC Medical Genomics,
Journal Year:
2023,
Volume and Issue:
16(1)
Published: Oct. 30, 2023
Abstract
Background
During
gestation,
stressors
to
the
fetus,
including
viral
exposure
or
maternal
psychological
distress,
can
fundamentally
alter
neonatal
epigenome,
and
may
be
associated
with
long-term
impaired
developmental
outcomes.
The
impact
of
in
utero
COVID-19
pandemic
on
newborn
epigenome
has
yet
described.
Methods
This
study
aimed
determine
whether
there
are
unique
epigenetic
signatures
newborns
who
experienced
otherwise
healthy
pregnancies
that
occurred
during
(Project
RESCUE).
pre-pandemic
control
cohorts
RESCUE)
included
this
part
a
prospective
observational
longitudinal
cohort
evaluates
elevated
prenatal
stress
early
childhood
neurodevelopment.
Using
buccal
swabs
collected
at
birth,
differential
DNA
methylation
analysis
was
performed
using
Infinium
MethylationEPIC
arrays
linear
regression
analysis.
Pathway
gene
ontology
enrichment
were
resultant
lists.
Results
Widespread
found
between
neonates
exposed
neonates.
In
contrast,
no
apparent
differences
infection
pregnancy.
Differential
observed
among
genomic
sites
underpin
important
neurological
pathways
have
been
previously
reported
literature
differentially
methylated
because
stress,
such
as
NR3C1
.
Conclusions
present
reveals
potential
associations
pregnancy
subsequent
changes
epigenome.
While
finding
warrants
further
investigation,
it
is
point
should
considered
any
assessing
studies
obtained
period,
even
pregnancies.