17-Hydroxypregnenolone Quantitative by LC-MS/MS, Serum or Plasma
Ordering Recommendation
New York DOH Approval Status
Specimen Required
Serum separator tube. Also acceptable: Plain red, lavender (EDTA), pink (K2EDTA), or green (sodium or lithium heparin).
Separate serum or plasma from cells ASAP or within 2 hours of collection. Transfer two 0.5 mL serum or plasma specimens to an ARUP Standard Transport Tube and freeze immediately. (Min: 0.25 mL/container)
CRITICAL FROZEN. Separate specimens must be submitted when multiple tests are ordered.
Refrigerated or room temperature specimens.
After separation from cells: Ambient: Unacceptable; Refrigerated: Unacceptable; Frozen: 6 months
Methodology
Quantitative High Performance Liquid Chromatography-Tandem Mass Spectrometry
Performed
Mon-Fri
Reported
1-5 days
Reference Interval
Age |
Female |
Male |
---|---|---|
Premature (26-28 weeks) | 1219-9799 ng/dL | 1219-9799 ng/dL |
Premature (29-36 weeks) | 346-8911 ng/dL | 346-8911 ng/dL |
Full Term (1-5 months) | 229-3104 ng/dL | 229-3104 ng/dL |
6-12 months | less than or equal to 917ng/dL | less than or equal to 917ng/dL |
13-23 months | less than or equal to 592 ng/dL | less than or equal to 592 ng/dL |
2-4 years | less than or equal to 280 ng/dL | less than or equal to 249 ng/dL |
5-6 years | less than or equal to 350 ng/dL | less than or equal to 319 ng/dL |
7-9 years | less than or equal to 212 ng/dL | less than or equal to 187 ng/dL |
10-12 years | less than or equal to 398 ng/dL | less than or equal to 392 ng/dL |
13-15 years | less than or equal to 407 ng/dL | 35-465 ng/dL |
16-17 years | less than or equal to 423 ng/dL | 32-478 ng/dL |
18 years and older | Less than 226 ng/dL | Less than 442 ng/dL |
Tanner Stage I | less than or equal to 235 ng/dL | less than or equal to 208 ng/dL |
Tanner Stage II | less than or equal to 367 ng/dL | less than or equal to 355 ng/dL |
Tanner Stage III | less than or equal to 430 ng/dL | less than or equal to 450 ng/dL |
Tanner Stage IV-V | less than or equal to 412 ng/dL | 35-478 ng/dL |
Interpretive Data
This test was developed and its performance characteristics determined by ARUP Laboratories. It has not been cleared or approved by the US Food and Drug Administration. This test was performed in a CLIA certified laboratory and is intended for clinical purposes.
Laboratory Developed Test (LDT)
Note
Hotline History
Hotline History
CPT Codes
84143
Components
Component Test Code* | Component Chart Name | LOINC |
---|---|---|
0092333 | 17-Hydroxypregnenolone Quant, MS/MS, Ser | 6765-2 |