Androstenedione
Also known as: ANDRO TMS
Use
The Androstenedione test aids in the investigation of virilizing endocrinopathies and in managing congenital adrenal hyperplasia. It is utilized in conjunction with other sex steroids to provide a comprehensive understanding of the hormonal imbalance. However, this test is not recommended for initial evaluation of polycystic ovarian syndrome.
Special Instructions
Specimen should be collected between 6-10 a.m. and transferred to an ARUP standard transport tube with a minimum of 0.3 mL.
Limitations
This test was developed by ARUP Laboratories and its performance characteristics determined, but it is not cleared or approved by the US Food and Drug Administration. The test should be used for clinical purposes and not as a standalone diagnostic tool. Interpretation should be in the context of the clinical setting and alongside other diagnostic information.
New York Approved
Methodology
Mass Spectrometry
Biomarkers
LOINC Codes
- 1854-9
Result Turnaround Time
1-5 days
Related Documents
For more information, please review the documents below
Specimen
Serum
Volume
1 mL
Minimum Volume
0.3 mL
Container
ARUP standard transport tube
Patient Preparation
Specimen should be collected between 6-10 a.m.
Storage Instructions
Refrigerated.
Stability Requirements
| Temperature | Period |
|---|---|
| Room Temperature | 24 hours |
| Refrigerated | 1 week |
| Frozen | 6 months |
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