Girish Mahajan (Editor)

Ursodeoxycholic acid

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AHFS/Drugs.com
  
Monograph

Routes of administration
  
oral

MedlinePlus
  
a699047

Ursodeoxycholic acid

Trade names
  
Actigall, Udcasid, others

License data
  
US DailyMed: 19396 US FDA: Ursodiol

Pregnancy category
  
AU: B3 US: B (No risk in non-human studies)

Ursodeoxycholic acid (INN, BAN and AAN), also known as ursodiol (USAN) and the abbreviation UDCA, from the root-word for bear urso, as bear bile contains the substance, is one of the secondary bile acids, which are metabolic byproducts of intestinal bacteria.

Contents

Endogenous effects

Primary bile acids are produced by the liver and stored in the gall bladder. When secreted into the intestine, primary bile acids can be metabolized into secondary bile acids by intestinal bacteria. Primary and secondary bile acids help the body digest fats. Ursodeoxycholic acid helps regulate cholesterol by reducing the rate at which the intestine absorbs cholesterol molecules while breaking up micelles containing cholesterol. Because of this property, ursodeoxycholic acid is used to treat (cholesterol) gallstones non-surgically. It is also used to relieve itching in pregnancy for some women who suffer obstetric cholestasis.

While some bile acids are known to be colon tumor promoters (e.g. deoxycholic acid), others such as ursodeoxycholic acid are thought to be chemopreventive, perhaps by inducing cellular differentiation and/or cellular senescence in colon epithelial cells.

It is believed to inhibit apoptosis.

Ursodeoxycholic acid has also been shown experimentally to suppress immune response such as immune cell phagocytosis. Prolonged exposure and/or increased quantities of systemic (throughout the body, not just in the digestive system) ursodeoxycholic acid can be toxic.

Medical uses

An incomplete list of the current uses is as follows:

  • Reduction in gallstone formation, either in patients with gallstones unfit for cholecystectomy, or obese patients undergoing rapid weight loss to prevent gallstone formation.
  • For the treatment of primary biliary cholangitis (PBC).
  • To aim to improve bile flow in patients with cystic fibrosis (controversial)
  • In newborn infants with impaired bile flow
  • Meta-analyses have borne out conflicting results on the mortality benefit of UDCA in PBC, however analyses that exclude trials of short duration (i.e. < 2 years) have demonstrated a survival benefit and are generally considered more clinically relevant. Ursodiol is the only FDA approved drug to treat primary biliary cirrhosis.

    Ursodiol may be used for biliary stasis, [also known as intrahepatic cholestasis of pregnancy, to relieve the symptoms of itching, and to decrease infant mortality rate, which is generally believed to be 10% when Urso is not administered in this fairly rare, and largely undiagnosed pregnancy related disorder. Maternal mortality from hemorrhage is another outcome of the disease, but Urso is not believed to be the preventive cure for this outcome], and to decrease bile absorption.

    In children, ursodeoxycholic acid use is not licensed, as its safety and effectiveness have not been established. Evidence is accumulating that ursodeoxycholic acid is ineffective and unsafe in neonatal hepatitis and neonatal cholestasis.

    There is insufficient evidence to justify routine use of ursodeoxycholic acid in cystic fibrosis, especially that available data for analysis of long-term outcomes such as death or need for liver transplantation is lacking.

    In double the recommended daily dose ursodeoxycholic acid reduces elevated liver enzyme levels in those with primary sclerosing cholangitis, but its use was associated with an increased risk of serious adverse events (the development of cirrhosis, varices, death or liver transplantation) in patients who received ursodeoxycholic acid compared with those who received placebo. Serious adverse events, were more common in the ursodeoxycholic acid group than the placebo group. The risk was 2.1 times greater for death, transplantation, or minimal listing criteria in patients on ursodeoxycholic acid than for those on placebo.

    It is concluded that ursodeoxycholic acid use is associated with improved serum liver tests that do not always correlate with improved liver disease status. WHO Drug Information advises against its use in primary sclerosing cholangitis in unapproved doses beyond 13–15 mg/kg/day.

    Mechanism of action

    The drug reduces cholesterol absorption and is used to dissolve (cholesterol) gallstones in patients who want an alternative to surgery. If the patient stops taking the drug the gallstones tend to recur if the condition that gave rise to their formation does not change. For these reasons, it has not supplanted surgical treatment by cholecystectomy.

    Also used to relieve itching in intrahepatic cholestasis of pregnancy (naltrexone may also be used).

    Trade names

    Ursodeoxycholic acid can be chemically synthesized and is marketed under multiple trade names, including Actigall, Biliver, Coric, Deursil, Egyurso, Udcasid, Udiliv, Udoxyl, Urso, Urso Forte, Ursocol, Ursofalk, Ursosan, Ursoserinox, Udimarin, Ursonova, and Stenerh.

    References

    Ursodeoxycholic acid Wikipedia