Ursodeoxycholic acid therapy in cystic fibrosis liver disease - a retrospective long-term follow-up case-control study

• Published in: Alimentary pharmacology & therapeutics Vol. 36; no. 3; pp. 266 - 273
• Main Authors: Kappler, M., Espach, C., Schweiger-Kabesch, A., Lang, T., Hartl, D., Hector, A., Glasmacher, C., Griese, M.
• Format: Journal Article
• Language: English
• Published: Oxford Blackwell Publishing Ltd 01.08.2012; Blackwell
• Subjects: Adolescent; Adult; Biological and medical sciences; Case-Control Studies; Chemical and Drug Induced Liver Injury - etiology; Child; Child, Preschool; Cholagogues and Choleretics - adverse effects; Cholagogues and Choleretics - therapeutic use; Cystic Fibrosis - complications; Cystic Fibrosis - drug therapy; Digestive system; Errors of metabolism; Female; Gastroenterology. Liver. Pancreas. Abdomen; Humans; Infant; Liver Function Tests; Liver. Biliary tract. Portal circulation. Exocrine pancreas; Longitudinal Studies; Male; Medical sciences; Metabolic diseases; Miscellaneous hereditary metabolic disorders; Other diseases. Semiology; Pharmacology. Drug treatments; Retrospective Studies; Ursodeoxycholic Acid - adverse effects; Ursodeoxycholic Acid - therapeutic use; Young Adult; Hepatic fibrosis; Human; Respiratory disease; Metabolic diseases; Hepatic disease; Cystic fibrosis; Case control study; Long term; Retrospective; Genetic disease; Ursodeoxycholic acid; Treatment; Follow up study; Bile acid; Digestive diseases; Pancreatic disease
• DOI: 10.1111/j.1365-2036.2012.05177.x
• ISSN: 0269-2813; 1365-2036

Summary Background The prevention and treatment of liver disease associated with cystic fibrosis remain a significant unresolved problem. Aim To assess the long‐term effects of continuous ursodeoxycholic acid (UDCA) therapy in cystic fibrosis patients with constantly elevated serum liver enzymes. Methods The primary endpoint was the incidence of overt liver disease. Between 1989 and 2005, UDCA treatment was started in 98 subjects from a cohort of 382 cystic fibrosis patients. These subjects were compared with a historic control group of 352 subjects who attended our centre between 1975 and 1989 before UDCA became standard treatment. For the long‐term comparison of liver function and lung function tests, a group of 98 matched contemporary cystic fibrosis patients were compared with the 98 subjects treated with UDCA. Results Overt liver disease developed in only one of the 382 patients who was treated with UDCA for increased serum liver enzymes compared with nine patients in the historic control group (P < 0.05). Serum liver enzyme levels declined in most patients receiving UDCA treatment during the 17‐year follow‐up (87/98, P < 0.05). No difference was seen in lung function between subjects with cystic fibrosis‐related liver disease and the matched controls. Conclusions Regular and systematic screening for liver involvement enables early introduction of UDCA therapy in affected cystic fibrosis patients, reduces the development of severe liver disease and leads to a significant and persistent improvement in serum liver tests, without impairing long‐term pulmonary outcome.