17-Hydroxypregnenolone 30-Minute Timed Specimen
Also known as: OHPRGN 30
Use
The 17-Hydroxypregnenolone 30-Minute Timed Specimen test is used primarily for diagnosing disorders related to adrenal and gonadal steroid biosynthesis, including congenital adrenal hyperplasia. It measures the level of 17-Hydroxypregnenolone in the blood, which is a precursor in the synthesis of cortisol, androgens, and estrogens. This test can be crucial for evaluating patients with ambiguous genitalia or other signs of hormonal imbalance.
Special Instructions
Not provided.
Limitations
The test is not FDA-approved and is conducted in a CLIA-certified laboratory. Results may vary based on pre-test preparation, specimen handling, and timing of specimen collection. Ambient and refrigerated conditions are unacceptable, which could influence the specimen integrity and subsequently, the test results.
New York Approved
Methodology
Mass Spectrometry
Biomarkers
17-Hydroxypregnenolone
Analyte
LOINC Codes
- 56522-6 - 17OH-Preg 30M p chal SerPl-mCnc
Result Turnaround Time
1-5 days
Related Documents
For more information, please review the documents below
Specimen
Serum
Volume
0.5 mL
Minimum Volume
0.25 mL
Container
ARUP Standard Transport Tube
Collection Instructions
Separate serum or plasma from cells ASAP or within 2 hours of collection. Freeze immediately.
Causes for Rejection
Refrigerated or room temperature specimens.
Stability Requirements
| Temperature | Period |
|---|---|
| Frozen | 6 months |
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