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Assays / Hormones / 11-Deoxycortisol
(serum)
Clinical Use
1 Diagnosis of, and monitoring
therapeutic response in, congenital adrenal hyperplasia due to 11b-hydroxylase
deficiency.
2 Assessment of adrenal response in the
metyrapone test.
Applications
1 Congenital adrenal hyperplasia.
11-Deoxycortisol, the immediate precursor of
cortisol, accumulates in the peripheral circulation when there is
a deficiency of adrenal 11b-hydroxylase
activity. The assay should be requested when congenital adrenal
hyperplasia is suspected on clinical grounds, but serum 17a-hydroxyprogesterone
values are equivocal (14 - 100 nmol/L).
2 Long metyrapone test.
In the differential diagnosis of Cushing's syndrome,
metyrapone is given to inhibit 11b-hydroxylation.
Subsequent changes in serum concentrations of 11-deoxycortisol and
cortisol provide strong (but not absolute) indicators of the site
of the primary lesion.
3 Overnight metyrapone test.
This, by assessing the 11-deoxycortisol response
to the metyrapone-induced decrease in cortisol, provides an assessment
of pituitary response.
Patient Preparation
1 Diagnosis of congenital adrenal hyperplasia.
Take blood (5 mL) at 09.00h.
2 Long metyrapone test
The drug (750 mg orally 6-hourly for 2 days)
is usually given combined with a snack to minimise epigastric discomfort.
Glucocorticoid insufficiency may be precipitated, especially in
patients with adrenal tumours. Take blood (5 mL) before administration
of the first metyrapone dose (baseline sample) and 48h later.
3 Overnight metapyrone test
Metyrapone (30 mg/kg) is given orally with a
snack at midnight. At 09.00h the next morning take 5 mL blood for
the measurement of 11-deoxycortisol and cortisol.
Sample Preparation
1 Diagnosis of congenital adrenal
hyperplasia.
Send serum (2 mL) to the SAS laboratory.
2 Long metyrapone test.
Send a portion (0.5 mL) of each serum sample
to the local laboratory for measurement of cortisol. Send the remaining
sample to the SAS laboratory. Record on the SAS request form the
time of sampling and the serum cortisol concentration.
3 Overnight metyrapone test.
Send a portion (0.5 mL) of the serum sample
to the local laboratory for the measurement of cortisol. Send the
remaining sample to the SAS laboratory. Record on the SAS request
form the time of sampling and the serum cortisol concentration.
Reference Ranges
1 Diagnosis of 11b-hydroxylase
deficiency.
Unaffected adults (09.00h): 7-18 nmol/L;
Unaffected neonates (>48h after birth): <20
nmol/L;
Patients with untreated 11b-hydroxylase
deficiency: >100 nmol/L.
2 Long metyrapone test.
(a) Serum 11-deoxycortisol concentration >300
nmol/L at 48h, associated with a normal serum cortisol concentration,
is strongly suggestive of Cushing's disease (pituitary lesion).
(b) Serum 11-deoxycortisol concentration <150
nmol/L at 48h, associated with a subnormal cortisol value, suggests
an adrenal adenoma.
(c) Serum 11-deoxycortisol concentration >300
nmol/L at 48h, associated with subnormal or normal serum cortisol
concentration, suggests that an ectopic source of ACTH exists. There
is an overlap in the results of this test with those from patients
with Cushing's disease.
3 Overnight metyrapone test.
A normal response of 11-deoxycortisol is regarded
as >200 nmol/L. For the test to be valid the corresponding cortisol
concentration should be <200 nmol/L. A subnormal response is
suggestive of inadequate pituitary/ adrenal function.
Centre offering this assay
London
(St. Thomas').
Reference
Fiad TM, Kirby JM, Cunningham SK,
McKenna TJ. The overnight single-dose metyrapone test is a simple
and reliable index of the hypothalamic-pituitary-adrenal axis. Clin
Endocrinol 1994; 40: 603-609.
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