17-Hydroxypregnenolone Quantitative by LC-MS/MS, Serum or Plasma
Also known as: OHPRGNLON
Use
The 17-Hydroxypregnenolone Quantitative by LC-MS/MS test is primarily used for assessing adrenal gland function and diagnosing conditions related to abnormal steroid production such as congenital adrenal hyperplasia (CAH), adrenal tumors, or polycystic ovary syndrome (PCOS). It measures the level of 17-hydroxypregnenolone, a precursor steroid hormone, in serum or plasma, providing valuable insights into the hormonal status of the patient across different life stages and in response to ACTH stimulation.
Special Instructions
Not provided.
Limitations
This test has not been cleared or approved by the US Food and Drug Administration (FDA) but is performed in a CLIA-certified laboratory. Assay results may be affected by improper specimen handling, such as delayed separation from cells or incorrect storage conditions. The reference intervals may vary based on age, gender, and tanner stage, which should be considered when interpreting results.
New York Approved
Methodology
Mass Spectrometry
Biomarkers
17-Hydroxypregnenolone
Analyte
LOINC Codes
- 6765-2 - 17OH-Preg 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
Collect in a serum separator tube. Also acceptable: Plain red, lavender (EDTA), pink (K2EDTA), or green (sodium or lithium heparin) tubes. Separate serum or plasma from cells ASAP or within 2 hours of collection.
Storage Instructions
CRITICAL FROZEN. Separate specimens must be submitted when multiple tests are ordered.
Causes for Rejection
Refrigerated or room temperature specimens.
Stability Requirements
| Temperature | Period |
|---|---|
| Room Temperature | Unacceptable |
| Refrigerated | Unacceptable |
| Frozen | 6 months |
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