|Category||Biochemistry >> Endocrinology|
Androstenedione, produced in the adrenal glands and gonads, is a precursor to the androgen testosterone and the oestrogens oestrone and oestradiol. Androstenedione may accumulate in CAH due to 21-hydroxylase or 11β hydroxylase deficiency or in PCOS through increased testosterone turnover. Its secretion may also be elevated by ovarian and adrenal tumours.
Monitoring treatment of patients with CAH Diagnosis of 17-hydroxysteroid dehydrogenase deficiency. May be useful in differential diagnosis of hyperandrogenism Limited use in diagnosis of CAH, inappropriate to investigations of PCOS
0-9 nmol/L; <3 nmol/L prior to adrenarche
|Sample & container required||Serum (red top)|
|Sample volume||0.5 mL|
|Transport storage||Stable at 2-8°C for 72 hours. Please freeze pending dispatch for analysis.
Sample can be sent by first class post.
|Turnaround time||10 days|
Grossly haemolysed samples are unsuitable for this assay.