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Cortical bone mineral density in patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
[congenital adrenal hyperplasia]
Prior
studies
reveal
that
bone
mineral
density
(
BMD
)
in
congenital
adrenal
hyperplasia
(
CAH
)
is
mostly
in
the
osteopaenic
range
and
is
associated
with
lifetime
glucocorticoid
dose
.
The
forearm
,
a
measure
of
cortical
bone
density
,
has
not
been
evaluated
.
We
aimed
to
evaluate
BMD
at
various
sites
,
including
the
forearm
,
and
the
factors
associated
with
low
BMD
in
CAH
patients
.
Eighty
CAH
adults
(
47
classic
,
33
nonclassic
)
underwent
dual-energy-x-
ray
absorptiometry
and
laboratory
and
clinical
evaluation
.
BMD
Z-
scores
at
the
AP
spine
,
total
hip
,
femoral
neck
,
forearm
and
whole
body
were
examined
in
relation
to
phenotype
,
body
mass
index
,
current
glucocorticoid
dose
,
average
5
-
year
glucocorticoid
dose
,
vitamin
D
,
17
-
hydroxyprogesterone
,
androstenedione
,
testosterone
,
dehydroepiandrosterone
and
dehydroepiandrosterone
sulphate
(
DHEAS
)
.
Reduced
BMD
(
T
-
score
<
-
1
at
hip
,
spine
,
or
forearm
)
was
present
in
52
%
and
was
more
common
in
classic
than
nonclassic
patients
(
P
Â
=
Â
0
·
005
)
,
with
the
greatest
difference
observed
at
the
forearm
(
P
Â
=
Â
0
·
01
)
.
Patients
with
classic
compared
to
nonclassic
CAH
,
had
higher
17
-
hydroxyprogesterone
(
P
Â
=
Â
0
·
005
)
,
lower
DHEAS
(
P
Â
=
Â
0
·
0002
)
and
higher
non-traumatic
fracture
rate
(
P
Â
=
Â
0
·
0005
)
.
In
a
multivariate
analysis
after
adjusting
for
age
,
gender
,
height
standard
deviation
,
phenotype
and
cumulative
glucocorticoid
exposure
,
higher
DHEAS
was
independently
associated
with
higher
BMD
at
the
spine
,
radius
and
whole
body
.
Classic
CAH
patients
have
lower
BMD
than
nonclassic
patients
,
with
the
most
affected
area
being
the
forearm
.
This
first
study
of
forearm
BMD
in
CAH
patients
suggests
that
low
DHEAS
may
be
associated
with
weak
cortical
bone
independent
of
glucocorticoid
exposure
.
Diseases
Validation
Diseases presenting
"femoral neck"
symptom
adrenal incidentaloma
aromatase deficiency
congenital adrenal hyperplasia
cutaneous mastocytosis
erythropoietic protoporphyria
fabry disease
familial hypocalciuric hypercalcemia
familial mediterranean fever
kallmann syndrome
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