Medicina,
Год журнала:
2024,
Номер
60(12), С. 1920 - 1920
Опубликована: Ноя. 22, 2024
Background
and
Objectives:
Recurrent
pregnancy
loss
(RPL)
affects
numerous
couples
worldwide
has
traditionally
been
attributed
mainly
to
maternal
factors.
However,
recent
evidence
highlights
significant
paternal
influences
on
viability
outcomes.
This
review
aims
comprehensively
examine
male
contributions
loss,
focusing
underlying
mechanisms,
novel
biomarkers,
integrated
strategies
for
improved
reproductive
success.
Materials
Methods:
A
comprehensive
narrative
was
conducted
by
searching
databases
including
PubMed
Embase
the
literature
published
from
January
2004
October
2024.
Studies
in
RPL—encompassing
oxidative
stress,
genetic
epigenetic
health
conditions,
lifestyle
factors,
environmental
exposures,
advancements
sperm
proteomics—were
included.
Inclusion
criteria
were
peer-reviewed
articles
English
that
directly
addressed
factors
RPL;
studies
not
meeting
these
excluded.
Results:
The
identified
such
as
advanced
age,
metabolic
cardiovascular
issues,
chronic
diseases,
habits
(e.g.,
smoking,
alcohol
consumption,
poor
diet),
exposures
significantly
affect
integrity
through
mechanisms
like
DNA
fragmentation,
alterations.
Advanced
age
conditions
are
associated
with
increased
risks
of
miscarriage
adverse
Novel
proteomic
biomarkers
have
identified,
offering
potential
enhanced
diagnostics
personalized
interventions.
Integrated
approaches
involving
multidisciplinary
assessments,
preventive
strategies,
counseling
essential
effectively
addressing
RPL.
Conclusions:
Integrating
into
clinical
evaluations
is
crucial
recurrent
loss.
Recognizing
modifying
risk
changes,
medical
interventions,
management
can
improve
findings
underscore
need
incorporating
assessments
standard
care
highlight
importance
future
research
standardizing
diagnostic
protocols,
expanding
contributions,
integrating
practice
facilitate
treatment
strategies.
BMC Pregnancy and Childbirth,
Год журнала:
2024,
Номер
24(1)
Опубликована: Окт. 29, 2024
Recurrent
pregnancy
loss
(RPL),
also
known
as
recurrent
implantation
failure
(RIF),
is
a
distressing
condition
affecting
women
characterized
by
two
or
more
consecutive
miscarriages
the
inability
to
carry
beyond
20
weeks.
Immunological
factors
and
genetic
variations,
particularly
in
Vit
D
Binding
Protein
(VDBP),
have
gained
attention
potential
contributors
RPL.
This
study
aimed
provide
insight
into
immunological,
genetic,
metabolic
networks
underlying
RPL,
placing
particular
emphasis
on
interactions
between
VDBP,
HLA-G1,
CTLA-4,
ENTPD1,
adenosine-fetal-maternal
conflict
crosstalk.
A
retrospective
included
198
with
three
spontaneous
abortions.
Exclusion
criteria
comprised
uterine
abnormalities,
endocrine
disorders,
parental
chromosomal
infectious
factors,
autoimmune
diseases,
connective
tissue
diseases.
interplay
was
investigated
162
female
participants,
divided
groups
based
their
levels:
normal
D-RPL
low
D-RPL.
Various
laboratory
techniques
were
employed,
including
LC/MS/MS
for
measurement,
ELISA
protein
detection,
flow
cytometry
immune
function
analysis,
molecular
docking
protein–ligand
interaction
assessment.
General
characteristics
significant
regarding
glucose
levels.
Low
levels
associated
decreased
NK
cell
activity
downregulation
of
HLA-G1
HLA-G5
proteins,
while
CTLA-4
revealed
upregulation.
VDBP
significantly
downregulated
group.
Our
findings
highlight
intricate
relationship
status
adenosine
metabolism
SGLT1,
NT5E,
key
components
metabolism,
suggests
that
deficiency
may
disrupt
regulation
levels,
leading
an
impaired
reproductive
outcome.
HNF1β,
negative
regulator
upregulated,
HNF1α,
positive
regulator,
after
Molecular
analysis
crucial
residues
involved
HNF1β.
Collectively,
these
underscore
importance
modulating
pathways
relevant
maintenance,
highlighting
need
further
research
elucidate
mechanisms
therapeutic
interventions
improving
outcomes
individuals
International Journal of Molecular Sciences,
Год журнала:
2025,
Номер
26(3), С. 1326 - 1326
Опубликована: Фев. 4, 2025
Recurrent
pregnancy
loss
(RPL)
of
unknown
genesis
is
a
complex
condition
with
multifactorial
origins,
including
genetic,
hormonal,
and
immunological
factors.
However,
the
specific
mechanisms
underlying
endocervical
cell
proliferation
disorders
in
women
RPL
remain
inadequately
understood,
particularly
concerning
role
microbiota
viral
infections.
The
aim
this
study
was
to
investigate
by
examining
microbiota,
human
papillomavirus
(HPV)
typing,
expression
levels
key
molecular
biological
markers,
p16/Ki-67,
BCL-2,
miR-145,
miR-34a.
A
prospective
observational
comparative
executed
on
healthy
pregnant
controls
full
ethical
approval.
Samples
were
collected
for
HPV
typing
immunocytochemical
analysis
evaluate
p16,
Ki-67,
anti-oncogenic
microRNAs
(miR-145
miR-34a).
mRNA
progesterone
receptor
(PGR-A)
also
assessed,
alongside
local
immune
status
proinflammatory
T-lymphocytes
(Th17/Th1)
regulatory
CD4+
Tregs.
Overexpression
BCL-2
observed
52.5%
who
had
an
ASC-US/LSIL
cytogram,
average
double
p16/Ki-67
being
three
times
higher
than
group.
significant
decrease
PGR-A
endocervix
noted,
accompanied
dysregulated
characterized
increased
prevalence
Th17/Th1
cells
reduction
Additionally,
miR-145
miR-34a
endometrium
significantly
differed
from
physiological
group,
context
high-risk
infection.
findings
describe
that
are
associated
overexpression
impaired
regulation,
altered
microRNA
profiles.
These
alterations
may
contribute
pathophysiology
RPL,
highlighting
need
further
research
into
targeted
interventions
could
improve
reproductive
outcomes
affected
individuals.
International Journal of Medical Laboratory,
Год журнала:
2024,
Номер
unknown
Опубликована: Март 2, 2024
Recurrent
pregnancy
loss
(RPL),
which
is
also
known
as
repeated
miscarriage,
affects
around
2-3%
of
women
who
are
trying
to
conceive.
While
some
factors
contributing
RPL
have
been
identified,
the
cause
almost
half
all
cases
remains
unknown.
Immunological
proposed
one
potential
causes
such
miscarriages.
However,
it
hard
track
common
leading
since
individual
genomic
identity
aborted
fetuses
different
in
a
family
like
other
siblings.
The
immunological
involved
pathogenesis
miscarriage
generally
result
from
either
function
maternal
immune
system
attributable
her
background
or
fetal
origination
established
by
both
and
paternal
backgrounds
that
constitute
genome.
Toxicology Reports,
Год журнала:
2024,
Номер
12, С. 546 - 563
Опубликована: Май 9, 2024
Recurrent
pregnancy
Loss
(RPL)is
a
frequent
and
upsetting
condition.
Besides
the
prevalent
cause
of
RPL
including
chromosomal
defects
in
embryo,the
effect
translational
elements
like
alterations
epigenetics
are
great
importance.
The
emergence
has
offered
fresh
outlook
on
causes
treatment
by
focusing
examination
DNA
methylation.
may
arise
as
result
aberrant
methylation
imprinted
genes,
placenta-specific
immune-related
sperm
DNA,
which
have
direct
or
indirect
impact
embryo
implantation,
growth,
development.
Moreover,
distinct
immunological
tolerogenic
milieu
established
at
interface
between
mother
fetus
plays
crucial
role
sustaining
pregnancy.
Given
this,
there
been
deal
interest
regulation
cellular
components
maternal-fetal
milieu.
research
methylation's
incidence
control
mother-fetal
is
summed
up
this
review.
Heliyon,
Год журнала:
2024,
Номер
10(15), С. e35345 - e35345
Опубликована: Июль 27, 2024
Recurrent
pregnancy
loss
(RPL),
often
known
as
spontaneous
miscarriages
occurring
two
or
more
times
in
a
row,
is
reproductive
disease
that
affects
certain
couples.
The
cause
of
RPL
unknown
many
cases,
leading
to
difficulties
therapy
and
increased
psychological
suffering
Toll-like
receptors
(TLR)
have
been
identified
crucial
regulators
inflammation
various
human
tissues.
occurrence
during
parturition
indicates
receptor
activity
tissues
related
may
play
role
the
onset
continuation
normal
function,
well
complications
like
infection-related
preterm.
TLRs
their
signaling
molecules
serve
effective
therapeutic
targets
for
inhibiting
premature
activity.
At
maternal-fetal
interface,
are
found
both
immune
non-immune
cells,
such
trophoblasts
decidual
cells.
TLR
expression
patterns
influenced
by
phases
pregnancy.
In
this
way,
translational
combinations
epigenetics,
indicated
impact
on
TLRs.Importantly,
abnormal
DNA
methylation
histone
alterations
an
impressive
performance
decreasing
fertility
influencing
gene
required
molecular
cellular
activities
which
vital
embryonic
process.
TLRs,
central
duty
innate
system
can
regulate
epigenetic
elements
different
pathways.
potential
roles
epigenetics
factors
ability
identify
react
infections,
place
will
all
be
covered
narrative
review
essay.
Thrombosis Journal,
Год журнала:
2024,
Номер
22(1)
Опубликована: Фев. 13, 2024
Abstract
Background
Inherited
thrombophilia
(IT)
has
a
complex
pathophysiology
and
is
associated
with
recurrent
miscarriage
(RM)
by
causing
placental
insufficiency
inhibiting
fetal
development.
However,
screening
in
unexplained
RM
cases
still
questionable.
This
study
aimed
to
investigate
the
association
between
common
eight
IT
mutations
their
combinations
among
Palestinian
women
RM.
Methods
an
unmatched
case-control
200
(100
cases,
100
controls).
Eight
namely
Factor
V
Leiden
(FVL),
prothrombin
gene
(FII)
G202120A,
Methylenetetrahydrofolate
Reductase
(MTHFR)
(C677T
A1298C),
B-fibrinogen
−
455G
>
A,
FV
HR2
A4070G,
Plasminogen
activator
inhibitor
1
(PAI1)
5G/4G
XIIIA
(FXIIIA)
V34L;
were
analyzed.
The
first
five
analyzed
Restriction
Fragment
Length
Polymorphism
PCR
other
three
using
Amplification
Refractory
Mutation
System
PCR.
Results
prevalence
of
control
group
was
order
PAI1
(69%),
MTHFR
C677T
(53%)
A1298C
(47%),
BFG
A
(35%),
FVL
(each
18%),
FXIIIA
V34L
(16%)
FII
G20210A
(3%).
Patients
had
higher
percentage
(heterozygotes
mutant
homozygote)
compared
controls
(
p
=
0.016).
Frequencies
alleles
<
0.001)
0.009)
patients
controls.
No
significant
differences
observed
for
all
or
alleles.
Most
(75%)
have
2–4
out
8
studied,
while
1%
2%
zero
None
most
often
studied
(FVL,
G20210A,
C1677T,
A1298C)
showed
difference
Conclusions
There
V34L.
combination
both
studied.
report
that
evaluates
inherited
alleles’
cases.