Test Code 7AC4 7AC4, Bile Acid Synthesis, Serum
Reporting Name
7AC4, Bile Acid Synthesis, SPerforming Laboratory
Mayo Clinic Laboratories in RochesterUseful For
Screening for bile acid malabsorption in patients with irritable bowel syndrome with diarrhea
Method Name
Liquid Chromatography Tandem Mass Spectrometry (LC-MS/MS)
Specimen Required
Patient Preparation:
1. Patient must fast for at least 12 hours prior to collection; fasting morning specimen is preferred.
2. Patient should not be taking bile acid sequestrants for 24 hours prior to collection or statins for 5 days prior to collection.
Collection Container/Tube:
Preferred: Serum gel
Acceptable: Red top
Submission Container/Tube: Plastic vial
Specimen Volume: 1 mL
Collection Instructions:
1. Centrifuge and aliquot 1 mL of serum into plastic vial.
2. Send specimen frozen.
Specimen Type
SerumSpecimen Minimum Volume
0.5 mL
Specimen Stability Information
Specimen Type | Temperature | Time | Special Container |
---|---|---|---|
Serum | Frozen (preferred) | 90 days | |
Refrigerated | 72 hours | ||
Ambient | 24 hours |
Reject Due To
All specimens will be evaluated at Mayo Clinic Laboratories for test suitability.Reference Values
≥18 years: 2.5-63.2 ng/mL
Reference values have not been established for patients who are <18 years of age.
Interpretation
In patients with irritable bowel syndrome with diarrhea, elevated 7alpha-hydroxy-4-cholesten-3-one (7aC4) is consistent with bile acid diarrhea (BAD). A result of 17.6 ng/mL or greater is 83% sensitive and 53% specific for BAD. In these cases, a confirmatory 48-hour fecal bile acid test could be considered. A result above 52.5 ng/mL is 40% sensitive and 85% specific for BAD.
Interpretation of 7aC4 results in patients with chronic diarrhea (bile acid malabsorption: BAM):
Below 17.6 |
17.6 or above |
Above 52.5 |
BAM unlikely, consider other conditions |
BAM indeterminate, consider confirmatory fecal bile acids test or trial of bile acid sequestrant |
BAM likely, consider bile acid sequestrant therapy |
Serum 7aC4 can be used in combination with a random (single collection) stool bile acid assessment for increased sensitivity and specificity for BAM detection. See BAMRP / Bile Acids Malborption Panel, Serum and Feces.
Day(s) Performed
Monday, Thursday
Report Available
5 daysTest Classification
This test was developed and its performance characteristics determined by Mayo Clinic in a manner consistent with CLIA requirements. It has not been cleared or approved by the US Food and Drug Administration.CPT Code Information
82542
LOINC Code Information
Test ID | Test Order Name | Order LOINC Value |
---|---|---|
7AC4 | 7AC4, Bile Acid Synthesis, S | 94866-1 |
Result ID | Test Result Name | Result LOINC Value |
---|---|---|
65504 | 7AC4, Bile Acid Synthesis, S | 94866-1 |
Forms
If not ordering electronically, complete, print, and send Gastroenterology and Hepatology Test Request (T728) with the specimen
Testing Algorithm
For more information see Ordering Guide: Bile Acid-Associated Tests.