Immediatley following collection, mix sample by gently inverting 5 times
Red:
Lavender:
Frozen (preferred) - 2 years
Refrigerated - 1 day
Ambient - 6 hours
High-pressure liquid chromatography (HPLC) tandem mass spectrometry.
Premature (26 - 28 weeks) day 4: 375−3559 ng/dL
Premature (31 - 35 weeks) day 4: 64−2380 ng/dL
3 days: 10−829 ng/dL
1 - 5 months: 36−763 ng/dL
6 - 11 months: 42−540 ng/dL
12 - 23 months: 14−207 ng/dL
24 months - 5 years: 10−103 ng/dL
6 - 9 years: 10−186 ng/dL
Pubertal: 44−235 ng/dL
Adults: 53−357 ng/dL
In humans, the adrenal glands and the gonads produce steroid hormones. The formation of pregnenolone from cholesterol is the first step in steroidogenesis. Steroidogenesis continues along two paths from pregnenolone. 17-Hydroxypregnenolone is produced from pregnenolone through the enzymatic action of 17 alpha-hydroxylase (17 alpha-H). 3 beta-hydroxysteroid dehydrogenase (3 beta-HSD) mediates the conversion of 17-hydroxypregnenolone to 17-hydroxyprogesterone. Alternatively, the enzyme 17,20 lyase can convert 17-hydroxypregnenolone to dehydroepiandrosterone (DHEA). 17 alpha-H and 17,20 lyase activity are both mediated by a single microsomal cytochrome P450 complex.
17-hydroxypregnenelone levels have been shown to remain in the normal range in patients with Cushing. Levels can be suppressed with dexamethasone inhibition and increased with exogenous ACTH stimulation. Levels during the follicular phase of the menstrual cycle tend to be higher than during the luteal phase. 17-hydroxypregnenelone levels have been shown to be elevated in patients with idiopathic hirsutism.