Rare Diseases Symptoms Automatic Extraction
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Evaluation of polymorphisms in predicted target sites for micro RNAs differentially expressed in endometriosis.
[wolf-hirschhorn syndrome]
Previous
microarray
analyses
identified
22
microRNAs
(
miRNAs
)
differentially
expressed
in
paired
ectopic
and
eutopic
endometrium
of
women
with
and
without
endometriosis
.
To
investigate
further
the
role
of
these
miRNAs
in
women
with
endometriosis
,
we
conducted
an
association
study
aiming
to
explore
the
relationship
between
endometriosis
risk
and
single
-nucleotide
polymorphisms
(
SNPs
)
in
miRNA
target
sites
for
these
differentially
expressed
miRNAs
.
A
panel
of
102
SNPs
in
the
predicted
miRNA
binding
sites
were
evaluated
for
an
endometriosis
association
study
and
an
ingenuity
pathway
analysis
was
performed
.
Fourteen
rare
variants
were
identified
in
this
study
.
We
found
SNP
rs
14647
in
the
Wolf-
Hirschhorn
syndrome
candidate
gene
1
(
WHSC
1
)
3
'
UTR
(
untranslated
region
)
was
associated
with
endometriosis
-related
infertility
presenting
an
odds
ratio
of
12
.
2
(
95
%
confidence
interval
=
2
.
4
-
60
.
7
,
P
=
9
.
03
×
10
(
-
5
)
)
.
SNP
haplotype
AGG
in
the
solute
carrier
family
22
,
member
23
(
SLC
22
A
23
)
3
'
UTR
was
associated
with
endometriosis
-related
infertility
and
more
severe
disease
.
With
the
individual
genotyping
data
,
ingenuity
pathways
analysis
identified
the
tumour
necrosis
factor
and
cyclin-dependant
kinase
inhibitor
as
major
factors
in
the
molecular
pathways
.
Significant
associations
between
WHSC
1
alleles
and
endometriosis
-related
infertility
and
SLC
22
A
23
haplotypes
and
the
disease
severe
stage
were
identified
.
These
findings
may
help
focus
future
research
on
subphenotypes
of
this
disease
.
Replication
studies
in
independent
large
sample
sets
to
confirm
and
characterize
the
involvement
of
the
gene
variation
in
the
pathogenesis
of
endometriosis
are
needed
.
Diseases
Validation
Diseases presenting
"infertility"
symptom
achondroplasia
congenital adrenal hyperplasia
kallmann syndrome
krabbe disease
monosomy 21
wolf-hirschhorn syndrome
This symptom has already been validated