Extrahepatic manifestations of cholestasis
Open Access
- 7 August 2002
- journal article
- review article
- Published by Wiley in Journal of Gastroenterology and Hepatology
- Vol. 17 (9) , 938-948
- https://doi.org/10.1046/j.1440-1746.2002.02717.x
Abstract
Abstract Pruritus, fatigue and metabolic bone disease represent three major extrahepatic manifestations of chronic cholestatic liver disease that considerably affect the patient"s quality of life. The present article reviews pathogenetic aspects of and current therapeutic approaches to extrahepatic manifestations of cholestatic liver disease. Pathogenesis of pruritus of cholestasis remains poorly understood. The involvement of putative peripherally acting pruritogens, such as bile acids or endogenous opioids, is being discussed. More recently, central mechanisms, including an increased central opioidergic tone and pertubations in the serotonergic system have been proposed. Treatment of the underlying disease is beneficial also for the control of cholestasis‐associated pruritus. Current therapeutic recommendations include ursodeoxycholic acid, cholestyramine, rifampicin and opioid antagonists. Liver transplantation may be indicated when severe pruritus is refractory to medical treatment. Fatigue is being recognized as the most frequent and one of the most disabling complaints in chronic cholestasis. Fatigue is presumably of central origin and its association with other neuropsychiatric disorders (e.g. depression, obsessive –compulsive disorders) is consistent with defective central neurotransmission. No specific therapies are currently available and a healthy lifestyle, regular sleep and avoidance of unnecessary stress and other precipiting factors are recommended. Antidepressant therapy may be warranted in selected patients. Osteopenia and osteoporosis are common in chronic cholestatic liver disease, whereas osteomalacia is rare. The pathophysiology of cholestasis‐associated metabolic bone disease is regarded as multifactorial. Therapeutic recommendations include regular exercise, calcium and vitamin D supplementation in late stage disease, hormone replacement therapy in postmenopausal women and bisphosphonates.© 2002 Blackwell Publishing Asia Pty LtdKeywords
This publication has 107 references indexed in Scilit:
- Plasma from patients with the pruritus of cholestasis induces opioid receptor-mediated scratching in monkeysPublished by Elsevier ,2002
- Randomized pilot trial of vitamin K2 for bone loss in patients with primary biliary cirrhosisJournal of Hepatology, 2001
- Compactin and Simvastatin, but Not Pravastatin, Induce Bone Morphogenetic Protein-2 in Human Osteosarcoma CellsBiochemical and Biophysical Research Communications, 2000
- Long-term effects of ursodeoxycholic acid in primary biliary cirrhosis: results of a double-blind controlled multicentric trialJournal of Hepatology, 2000
- Osteoporosis is not a specific complication of primary biliary cirrhosis (PBC)Journal of Hepatology, 2000
- Hepatobiliary transportJournal of Hepatology, 2000
- Short communicationJournal of Pain and Symptom Management, 1998
- Cyclical etidronate in the prevention of bone loss in corticosteroid-treated primary biliary cirrhosis: A prospective, controlled pilot studyJournal of Hepatology, 1997
- The role of mast cell activation in cholestatic pruritusInflammation Research, 1994
- Longitudinal study on osteodystrophy in primary biliary cirrhosis (PBC) and a pilot study on calcitonin treatmentJournal of Hepatology, 1991