Lab Guide
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Test ID: Bile Acid
Bile Acid
Useful For
  • Assessment of enterohepatic cholestasis of pregnancy.
  • Indicator of portal venous circulation and hepatic function.
Method name and description

Enzymatic colorimetric assay manufactured by Randox performed on the Roche cobas c-systems. In the presence of Thio-NAD, the enzyme 3-α hydroxysteroid dehydrogenase (3-α HSD) converts bile acids to 3-keto steroids and Thio-NADH. The reaction is reversible and 3-α HSD can convert 3-keto steroids and Thio-NADH to bile acids and Thio-NAD. In the presence of excess NADH, the enzyme cycling occurs efficiently and the rate of formation of Thio-NADH is determined by measuring specific change of absorbance at 405nm.

Reporting name

Bile Acid

Clinical information

Bile acids are formed in the liver from cholesterol, conjugated primarily to glycine and taurine, stored and concentrated in the gallbladder, and secreted into the intestine after the ingestion of a meal. Fasting serum bile acids can be used in the diagnosis and prognosis of liver disease. Levels rise in many liver diseases, for example hepatitis and liver cirrhosis. Abnormal levels in fasting patients or immediately after a meal can be used to detect liver disease and damage, impaired liver function, intestinal dysfunction and perhaps a gall bladder blockage. Their measurement may detect some forms of liver disease earlier than standard liver tests because bile acids levels correspond to liver function, rather than liver damage. Bile acids are measured in cholestasis during pregnancy. Patients always present with symptoms of itchiness. If left untreated cholestasis could lead to still birth.

Specimen type / Specimen volume / Specimen container

Specimen type: Serum, Plasma

Minimum volume of sample: 1 mL

Serum: Plain tube (red or yellow top)

Plasma: Li‑heparin tube


 

Collection instructions / Special Precautions / Timing of collection

Preferably patient on fasting.

Storage and transport instructions

Storage: 1 week at 2-8°C

               3 months at -20°C


Transport: 2-25°C  
 

Specimen Rejection Criteria
  • Grossly hemolyzed specimen.
  • Icteric specimen.
  • Lipemic specimen.
  • Wrong collection container.
  • Specimen with insufficient quanitity .
Biological reference intervals and clinical decision values
Gender Age Reference Range (umol/L)
Female/Male 0 Mintues - 150 Years 2.0 – 10.0

 

Turnaround time / Days and times test performed / Specimen retention time

Daily (24/7)

Turn-around time:

Routine: One working day

Specimen Retention: 4 days