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Higher thrombin activatable fibrinolysis inhibitor levels are associated with inflammation in attack-free familial Mediterranean fever patients.
[familial mediterranean fever]
Coagulation
abnormalities
have
been
reported
in
familial
Mediterranean
fever
(
FMF
)
patients
with
amyloidosis
and
nephrotic
syndrome
;
but
there
is
not
enough
data
about
the
continuity
of
the
thrombogenic
activity
in
FMF
patients
in
clinical
remission
.
The
purpose
of
this
study
was
to
assess
thrombin
activatable
fibrinolysis
inhibitor
(
TAFI
)
levels
and
its
relationship
with
fibrinolytic
activity
and
also
evaluate
relationships
between
mutations
and
clinical
signs
in
attack-free
patients
without
amyloidosis
.
Seventy
-
nine
FMF
patients
and
40
healthy
adults
were
included
.
The
study
group
was
divided
into
five
groups
as
follows
:
first
group
,
homozygote
M
694
V
;
second
group
,
homozygote
M
680
I
;
third
group
,
M
694
V
in
one
allele
,
the
other
allele
have
other
mutations
or
not
;
fourth
group
,
other
mutations
;
and
fifth
group
,
no
mutation
.
Serum
TAFI
levels
were
significantly
increased
in
patients
compared
with
healthy
individuals
(
116
.
64
 
±
 
21
.
8
vs
.
78
.
48
 
±
 
19
.
7
 
μg
/
mL
,
p
 
<
 
0
.
001
)
and
a
positive
correlation
was
detected
between
TAFI
antigen
level
and
erythrocyte
sedimentation
rate
and
C-
reactive
protein
levels
(
r
 
=
 
0
.
247
,
p
 
=
 
0
.
029
and
r
 
=
 
0
.
252
,
p
 
=
 
0
.
032
,
respectively
)
.
Mean
fibrinogen
and
TAFI
levels
were
significantly
higher
in
Group
1
than
the
other
groups
(
p
 
=
 
0
.
04
and
p
 
=
 
0
.
001
,
respectively
)
and
in
Group
3
it
was
higher
than
Groups
2
,
4
and
5
(
p
 
=
 
0
.
04
and
p
 
=
 
0
.
001
,
respectively
)
.
High
level
of
TAFI
antigen
in
attack-free
period
of
FMF
disease
shows
ongoing
subclinical
inflammation
and
hypercoagulability
.
Clinicians
should
be
careful
about
thrombosis
even
in
patients
at
clinical
remission
.
Also
,
genetic
tests
must
be
considered
to
predict
clinical
outcome
and
to
reduce
complications
of
FMF
disease
.
Diseases
Validation
Diseases presenting
"fmf disease"
symptom
familial mediterranean fever
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