Pregnenolone, MS

Alphabetical Test listing

Pregnenolone, MS-994

  
Pregnenolone, MS
  
994
  
LAB994
  
MSO
  

Pregnenolone levels have been shown to remain in the normal range in patients with Cushing syndrome and hyperaldosteronism. Levels can be suppressed with dexamethasone inhibition and increased with exogenous ACTH stimulation. Pregnenolone levels have been shown to be elevated in patients with idiopathic hirsutism. Since the various forms of congenital adrenal hyperplasia (CAH) result from enzymatic defects in the adrenal steroidogenic pathways, measurement of pregnenolone levels can be useful in diagnosis. Pregnenolone levels tend to be elevated in several forms of CAH, particularly in 17α-H deficiency and 3β-HSD deficiency since these enzymes catalyze steps immediately after pregnenolone in the steroidogenic pathways.

  
Serum
  
  
2.5 mL
  
1.1 mL
Note: this volume does not allow for repeat testing
  
  1. Spin and transfer serum to a  Screw-cap polypropylene frozen transport vial/tube - 4mL (LabCorp) within one (1) hour of specimen collection
  2. Freeze
  
EDTA plasma
Heparin plasma
  

Red serum vial/tube - 5 mL

Lavender (EDTA), 4mL

Dk green heparin (Li or Na), no gel

 

  
  1. Spin and transfer plasma to a  Screw-cap polypropylene frozen transport vial/tube - 4mL (LabCorp) within one (1) hour of specimen collection
  2. Freeze
  

Frozen (preferred) - 2 years

Freeze/thaw cycle: Stable x 3

Refrigerated - 2 days

Ambient - 4 hours

  
Esoterix Endocrinology (500258) via LabCorp (140707): R-NX
  
Mo - Th, Sa
  
4 - 6 days
  

High-pressure liquid chromatography (HPLC) tandem mass spectrometry

  

Adults: < 151

  

In humans, steroid hormones are produced by the adrenal glands and the gonads. The formation of pregnenolone from cholesterol is the first step in steroidogenesis and is mediated by the proteolytic enzyme, single cholesterol side-chain cleavage enzyme (P450 scc). Steroidogenesis continues along two paths from pregnenolone. 17-Hydroxypregnenolone is produced from pregnenolone through the enzymatic action of 17α-hydroxylase (17α-H).


Alternatively, pregnenolone is converted to progesterone through the enzymatic action of 3β-hydroxysteroid dehydrogenase (3β-HSD).  Pregnenolone levels have been shown to remain in the normal range in patients with Cushing syndrome and hyperaldosteronism. Levels can be suppressed with dexamethasone inhibition and increased with exogenous ACTH stimulation.


Pregnenolone levels have been shown to be elevated in patients with idiopathic hirsutism.  Since the various forms of congenital adrenal hyperplasia (CAH) result from enzymatic defects in the adrenal steroidogenic pathways, measurement of pregnenolone levels can be useful in diagnosis. Pregnenolone levels tend to be elevated in several forms of CAH, particularly in 17α-H deficiency and 3β-HSD deficiency since these enzymes catalyze steps immediately after pregnenolone in the steroidogenic pathways.

  
84140
  
Result 2837-3
  
05/24/2019
  
11/11/2021
  
05/19/2020